As promised, here is the video I made on my Hyperthyroidism/Graves Disease and all the symptoms I had: th-cam.com/video/i6M3pH6nA08/w-d-xo.html Please use the comments section to share your own personal stories 💕 And please be kind to each other. It is my hope for this video that it will bring people together, where we can feel supported, and just SHARE, because for a lot of us, sharing is healing. And I'd like this page to be a place where people can come to get ideas and feel inspired! My love to you all, XO ⭐ I am wearing the wig called Mesmerized. Watch my review/try-on here: th-cam.com/video/ARYCmQJHPd0/w-d-xo.html&feature=sharea ✨ I purchased the Mesmerized wig here 👉 wigs.pxf.io/Mesmerized_ ⬆ When you use this link above, you will receive an automatic 30% off at purchase! 💗
I have hyperthyroidism too. 18 months taking carbimazole and stopped the meds for 1 year I thought I'm also on remission but after 1 year of not taking meds it came back so I'm now on meds again. 😢 Everyday I'm wishing and praying to get my life back, the best version of myself, the better me version. That's the only thing that I wanted now, nothing else in this world.
Am going through the same thing. I have taking carbimazole for a year, I stopped the medicine and my heart beat is something else and are bulging, I just can't take it, am tired of hiding my face. I really want to be oke
I also was diagnosed with Graves' disease and hyperthyroidism and was given methimazole that I rejected...told my doctor to give me time to do it my way and if that doesn't work I'll take her meds. I started with exercise at the gym and walking minimum of 2miles a day , 5-6x per week changed my diet to Whole Foods only also eliminating anything white like bread , pasta etc. but most importantly I did intermitent fasting 5x per week and did a 36hour fast every other week. I did IF slowly in the beginning like 12 hours first and kept adding more hours each time and not forcing my body to do too much at once. 4 months later I saw my doctor again and my Graves was in remission and I didn't need medication at all. Discipline and sacrifice helped so much. Hope this helps you but please talk to your docotr first because only the two of you really know what's going on with your health. God bless. Oh btw I eat a lot of meat, meat products and fish too. Only grass fed and finished also wild caught fish only , I never liked the flavor of farmed fish. But overall I eat everything that comes from the ground and seas and cook it myself. No factory processed foods and no seed oils.
I was really sick as well. I had done research and knew it was my thyroid. I kept going in, they did just the TSH test. Kept telling me I was fine because I was in the “normal” range. I was done. I was too tired to keep fighting. My son was with me and he blurted out, do an ultrasound. They did. 26 nodules. The next day I found out I had thyroid cancer. You have to be your own champion in getting better. So you work with the doctor and not just follow the doctor.
oh wow! Thank you for sharing your story. This is what I've found as well! You HAVE to be your own advocate, because only you know you the best.... I'm so glad you caught the thyroid cancer. How are you doing now? Has it been many years?
I am sooooo proud of you. For you to recognize that food is such an important key in being heathy. I am 63 had RA for decades and healed by changing my diet. I eat a whole food plant based diet , no sugar no oils, and I feel great no meds. You can now pass what you have learned onto your children so they can grow up healthy.
Thank you so much for your kind words! It’s truly inspiring to hear about your journey with RA and how changing your diet has made such a positive impact. I completely agree that food plays a crucial role in our health. I’m excited to pass on these healthy habits to the next generation. Thank you for sharing your story and for your encouragement! 🌟❤
@@cynthiajohnson798 Its. been 7 years and feel better than ever. I have learned we are what we eat and. I eat a low inflammatory diet. It's working for me. Good luck with your journey.
*Diet and lifestyle can do so much good!* My aunt struggled with hyperthyroidism and the hair loss that came with it. They put her on a synthetic hormone which helped but she wasn’t interested in being on any pill for the _rest of her life._ So she ditched it, did a lot of research and opted to start with an elimination diet: no gluten, dairy, processed sugar, caffeine/coffee and alcohol. She focused on cleaning up the gut and gentle movement of the body (walking, swimming,etc nothing HIIT related as it raises stress hormones/cortisol) and advocates getting bare feet in contact with the ground (a practice called “grounding”) and it’s made a night and day difference for her.
Thank you so much for sharing your aunt's story! It's incredible how much diet and lifestyle can impact our health. The steps she took to clean up her gut and incorporate gentle movement and grounding are truly inspiring. It's amazing to hear that she experienced such a positive transformation without relying on medication. Her journey is a powerful reminder of the potential benefits of holistic approaches. Thank you for sharing these insights! ❤
We basically have an internal alarm telling us when our lives are out of balance. This disease obligates us to live balanced lives. I see that as a positive thing now, and strive for that balance every day. It’s so rewarding when you get it right! Best wishes to you and everyone else on this journey.
Hey I was diagnosed with graves/hyperthyroidism four years ago but methimazole made me so nauseous. Instead, I went gluten free,dairy free, and caffeine free along with KETO to treat my disease. I went into remission within three months and have stayed in remission for four years. For the hair loss I started taking Hair La Vie. It has made my hair really thick again like when I was young and my natural curl is back more than ever. I just thought I would share that with everyone. Plus, I was diagnosed with osteoporosis because of the graves. I have been taking AlgaeCal bone building package and have gone from osteoporosis to mixed osteoporosis and osteopenia, to just osteopenia. I am building my bone density without one of those “bone building medications” that do NOT actually build bones and cause horrific side effects. It can be done naturally. By the way, I asked my doctor to test me for thyroid issues for nine years before she finally agreed to test me. And I was in the Air Force for 22 years and those doctors never even suspected that the racing heart, the palpitations, the tremors, and the crazy high anxiety level were indicative of a problem.
Hi there. I have been recently diagnosed and am not taking the prescribed medication because im pregnant and there are a lot of side effects. Would you mind telling me more about your diet changes and if you kept it the same after going into remission? Thank you!!
My mom has hyperthyroidism and I have the same request if you could tell us more about your diet. When you say dairy-free does that mean completely stopping all dairy products butter, milk yogurt cheese everything?
So absolutely NO dairy…no yogurt, no ice cream, no cheese, no butter, no milk, no dairy period. AND NO GLUTEN!!! You’ve got to read labels. Nothing with any wheat/flour. Plus no caffeine because it causes heart palpitations and increased anxiety. Oh and just in case you don’t know, soy is super bad if you have HYPERTHYROIDISM.
There's also eggs that make hyperthyroidism worse...I hate it..I NEED those nutrients. Idk what else I'm gonna swap it with...besides eating more cabbage from kimchi to prevent hyperthyroidism from getting worse. Cuz excess idodine from dairy and eggs
This was very interesting to me. I was diagnosed with Graves’ disease 6 years ago when I turned 40. I finally went to the dr because I had uncontrollable itching!! It felt internal and I felt like I was going crazy!! Luckily my dr knew immediately what was likely going on. My thyroid was swollen. I had rapid heartbeat and tremors. And I had lost 40 pounds in 3 months. I was on medication for about a year. They wanted me to have radiation or surgery and I just couldn’t do it. Weaned myself off the medication because I could tell I was getting better. Fast forward to yesterday. Had my levels checked for the first time in 4 years. Totally normal. Go figure!!!
I start methimazole today! I want to get better. I have a visible goiter! My biopsy came back benign but I will have my first scan in 4 month, cause dr wants to see what will happen when medication is taken. You give me hope!
I have been battling hyperthyroidism since 3-2018.. I'm doing carnivor diet. No coffee and adult beverages. And I'm on 18/6 intermittent fasting!! And to make my life like hell, I also have vertigo issues. That's ok, I love a challenge!!!! I will get over this hurdle!!!!!!
Hello from Toronto,I was diagnosed with graves disease just over 3 years ago when I suffered from a thyroid storm. I was told pretty much the same thing after I year of taking methimazole, but I did my own research and looked at treatment back decades and found out that methimazole could be taken for many years to the rest of your life if necessary. So I told the specialist that I would refuse to take the other options. I started working out and liked the fact that I couldn't grow body fat, and I developed ripped muscles because of the graves disease. I don't like the idea of operating on synthetic hormones and would rather operate on my own hormones. Besides, I see no reason to destroy the thyroid because I don't believe that it is the problem. The immune system attacks the thyroid, so why not figure out what is causing the immune system to attack the thyroid? I don't get modern medicine at all.
I was diagnosed with Graves/hyperthyroidism too. Was told I could take the iodine pill and be done. I refused, was on methimazole for a year, and metoprolol for several months...felt like a slug and gained 30 POUNDS. I went off for 6 months and back to Graves again. Took gluten out off my diet and 3 months later labs were back to normal. Take out the gluten people. My joints stopped aching, my hair improved oh and women take prenatal vitamins no matter your age, and I just felt better. Thank God, Do you homeopathic research.
@@Just.FactssI was told by my Endo that diet has nothing to do with Graves 🙄. They don’t want to find a solution, they want to get you in and out their doors and be done with you.
I was diagnosed in 2006, I had the racing heart, bulging eyes, etc. I went on meds and I was one of the few who was allergic to the meds and broke out head to toe with hives and heat rash. I ended up having the radio active iodine and it took 6 years to get my thyroid meds right. I was so depressed with hair loss and bulging eyes. Now I’m buying wigs, and still getting used to it You’re amazing and so beautiful.
Hello Steph! First of all, congratulations for being in remission, and also for having a baby. I am also suffering from hyperthyroidism since last year, I lose a lot of weight, had hair loss, my anxiety and depression was severe, same goes with fatigue. I had a surgery last year but only half was removed because my surgeon thought it was “toxic adenoma” since I had nodules as well on the left side. I also aim to be in remission, hope 2024 will be a good year for me. Thanks for sharing your story.
I was diagnosed with Graves 6 years ago, and given the same options, and not having enough information to know otherwise, i chose the radioactive iodine treatment that failed and left me with thyroid eye disease. I wish I had the information I have now, I would have made a different choice, but all I can do is try to heal it naturally without having to do the RAI again or surgery, which all the doctors have said are my only options now. I just don't believe that to be true. It is a struggle and my heart goes out to everyone here and out there in the world who are dealing with this and TED. It really affects your whole life, and so many people don't even realize it. Thank you for sharing your story and helping our community find hope.
@@2Cixth Yes I was first on methimazole and the beta blocker Propranolol. I had a severe allergic reaction to the methimazole so they put me on propylthiouracil which Im still on to this day, plus a beta blocker.
And somehow at work I'm supposed to function like everyone else and not miss work. I miss work because I'm struggling emotionally mentally physically. Not cuz I'm lazy or don't want to work ..it makes me feel normal of course I like to work..being able to do it without feeling like panicking is a different story.
You are so right… first, we have to be our own health advocates, because nobody knows our bodies better than we do ourselves, not even the doctors. Not that they don’t academically know more than we do, but finding a doctor who truly listens is literally vitally significant. And I completely agree that THE number one factor to any “dis-ease” in our bodies is due to stress. Of course what we eat and our physical activity are also important elements as is spiritual and emotional well being. I’m a senior woman now and still learning and evolving. I could be my own medical journal of things that have gone wrong with my body and mind due to my own neglect, BUT I refuse to give up, and am in a place of harmony now as I shed excess weight (75 pounds so far!) and find new ways to keep moving. That you are so young and at this level of understanding is so commendable. I’m so looking forward to watching you and learning from you as your life moves forward into new adventures, especially with you and Dan soon to welcome the little one. ❤️💕
Congratulations!!! That is great to hear! I have Graves Disease as well and I was in remission for 6 months and now I’m back to taking my meds. Took me a couple of years to be diagnosed as well. I knew something was wrong….we know our bodies!
whats remission? and also did ur heart have palpitations and did it feel heavy? I stopped taking methmizale because they think its a side effect im having from it. im having joint pains
Hello Steph. Thank you for sharing your story. I also have Graves Disease and taking Methimazole for it. It’s been exactly a year since I was diagnosed. I should have gone to see the Dr sooner. I too thought I was going crazy, I felt at times that I was possessed because I didn’t have control of my myself: mind and body. I had the shakes…like really bad to where I was embarrassed to be around others. I had to be constantly moving so that no one would see how my body trembled. I had severe heart palpitations where it was visible on my shirt. I couldn’t take it anymore. Luckily my PCP tested me for hyperthyroidism as soon as I described my symptoms. I now have the bulging eyes and I’ve lost a lot of hair, but my thyroid is making great progress and my symptoms have ceased. I hope that in the next few months I can be off the medication and go on remission. Thank you and everyone on this channel for helping me feel better about my situation. I will take the advice of ditching stress and getting on a healthy diet. I began exercising to lose weight and to get into the habit of staying active for my well being. Best of luck to everyone and God bless you ❤
I was diagnosed with Graves disease two years ago. I lost my medical and have not taken any medication for the past year. I am currently living off grid next to a national forest. I have been doing my best to stay stress free but yes, its so hard we've been waiting 15 months for electricity but it seems to be out of reach financially. The hardest part for me is trying to stay cool while living in Texas with no electricity.
I was diagnosed with graves 1,5 years ago. I was really bad and lost bone density, got heart problems etc. The first docor i met took the thyroid tests right away and sent me to an endocrinologist. I started medication right after diagnosis, and already within a week i felt my body was slowing down. Im still taking it and get tested every 6 weeks. I feel great and safe and so thankful for free healthcare, medical professionals, research and LIFE ❤.
Absolutely! That is phenomenal a doctor listened to you and had enough practice to understand what to send you out to be tested for. I'm so very glad to hear you are doing much better ❤ God bless
Thank you for this video. I'm glad to know your move has been good & that you are feeling healthy and well! You have helped me SO MUCH with the content you place on this channel, & I am sincerely grateful. After years of buying into detrimental ways to achieve "socially acceptable" hair- it became clear I would have to find alternative ways to care for my own. As it turns out, my husband was not keen on less frequent washing & no heat treatments. SO- about 8 months ago I began to try wearing wigs. Your channel is my favorite. You are very inspiring! I now see wigs as a way to protect our own hair & to step into public places with the kind of cinematically perfect hair that people enjoy seeing. Your journey proves that the human body can regain health naturally, something I have always believed. I no longer accept allopathic ideas & only work with a naturopath. Thank you so much for creating this space and for helping so many!
Hi Steph! This video came up as suggested because I had been looking for information on hyperthyroidism, as my daughter has recently been diagnosed with hyperthyroidism. You confirmed several things that I had suspected. Thank you!
Same here I was diagnosed with hyperthyroidism and hashimoto immune disease at the AGE 19, and was told I have to take insulin med FOR THE REST OF MY LIFE. Did that for a few months and decided to explore the whole ordeal in my own hands. I changed my diet, changed my living habit, lost 50 pounds, and never looked back. All the symptoms are gone once I lost the weight. I am 38 now and never had any problem with thyroid and blood work check is always normal since age 20. I maintained my habits and weight for more than 10 years too.
I believe eatin a healthy cut out sugar high salts and processed foods and eat complex carbs turkey or chicken and vegetables water, I was readin Milk has high iodine which is not good but I don’t know??
I have Graves's disease from 2007, Since I was in Grade 7. The doctors always said you will have to take medicines for your entire life. I am continuously on medicines. It became normal a few years back, but as soon as I stoppped the medication for 1 month I would get it again. It is in control by medicines but every now and then it keeps going up and down. Then I got married in 2021, and since then its never remaining constant or normal. We had a miscarriage too last year, and now the doctor have said that we should wait to concieve until the thyroid levels are normal. I had a lot of stress due to my work, so I left it in March. Taking Methimez now and trying to maintain a healthy routine with yoga, diet, sleep schedule. It has improved a little. But the doctor is unable to adjust the dose of Methimez and the thyroid levels just keep fluctuating. Its been 6 months we are waiting to concieve as I will be 31 this year and waiting for things to be normal. But I don't no what to do. Starting to get anxiety again because of all this. Please suggest.
So proud of you Steph! I don’t want to cut out my thyroid out and I don’t think I will. Thank you for this video ❤ wow that’s so wild, the adrenaline point, I have felt that perhaps my adhd, hyperactivity, dancing, running, working out, whatever would perhaps push me to the graves again 🫣😳🤯 How mental, how strange this is. I appreciate you thank you ❤🤗
I wish i never removed my gallbladder. I was healing it but docters kept telling me i was this big cancer risk so i pulled it out and guess what , I was right just like you! Deffinately mind, body, soul is connected we CAN heal our own bodies. Great job on healing yours! ❤
16:21 You are definitely reaching people. I feel grateful to people like you, who share their experience especially around not being listened to by doctors. In the interest of limiting stress, I won’t go into my journey with that because it’s not over BUT I feel strength to go on by knowing I’m not alone even if I have no idea what I have or if I’ll ever be properly diagnosed. What you said about stress and that it’s not realistic (paraphrasing) to cut it out but we can maybe absorb it differently? That’s something I’ve GOT to try to do . After over a year of feeling like I’m the only person who knows something’s wrong and the only person with no say in actions taken or not taken, I’ve reacted with so much anger inside and plenty that i’ve let out too so I’ve really isolated myself. Finally it’s gotten so bad dermatologically that they can’t say it’s “fine” anymore that people are just starting to listen to me and forced to take action but it’s after so long of being alone with it. It’s so hard for me to be okay with anyone in my orbit suggesting things with no information or assuming that the person dealing with the symptoms would have probably considered and tried ____(fill in the blank). I can’t imagine being so secure with my suggestion after hearing some symptoms and pondering it for 5 minutes as to tell someone decisively ANYTHING. So I have cut a lot of people out of my life who i guess never took me seriously to begin with. Whelp. See how angry I get? Annnnyway, LOL. So yeah I’m a real fun person to be around as you might see, I’m basically feral at this point and that’s why I appreciate your honesty about your journey and your emotions etc. This is a long and hopefully not too depressing thank you 😅
HI!!! I Love the realness of your message. I felt it deeply!!! I feel the same, and it definitely destroyed me, especially at the beginning, when people would see my thinning hair and tell me that I should take this or that vitamin, or try a hair re-growth serum…. It frustrated me SO much. Because it’s really not that simple. I honestly get exactly what you’re saying, thank you for sharing 🙏 I appreciate you!!
Just came across your channel. Thank you for your testimony. I have very similar story, like most of us with Grave’s. I totally changed my life style and fell in love with health content along the way. I’m in second year and still working on get on remission.
Thank you for sharing this. There have been many times doctors recommended things to me- surgery, medications that I refused. I’m ok and I didn’t need it. People forget they are a bu$ine$$. …. And one that has a high cost in running, so they don’t really care to help you save your health. This isn’t a personal diss to practitioners but more of a modern business model of our current healthcare system. Diet is a HUGE factor in health. Exercise is necessary for one’s body to work correctly since so much of bodily functions are greatly affected by lack of movement, primarily digestive, lymphatic and cardiovascular. And I should clear up that when I say ‘exercise’ I don’t mean CrossFit or some gym rat type life- I mean just getting active. Stress minimization is absolutely key too. These 3 things don’t always clear up a medical issue, but if you can do better in these 3 things, it will certainly help. I’m happy to hear you are doing well.
Thanks for sharing. So glad you're grave's disease has gotten better and that you're hair has grown in more. I have scarring alopecia, but even my dermatologist has admitted that sometimes treatments can help hair grow back. My hair hasn't grown back but it no longer falling out. I started wearing wigs to take the pressure off which I think will help my hair grow more and even if it doesn't I certainly feel better. I think that you are so right trying to improve things naturally instead of just going for cutting out your thyroid. You are so young and look if. You tried everything to no avail then at least you know you have done everything you could do
Hi Steph, I live in Calgary also. I am 71 years old. I started having symptoms at age 49 or even before I think but did not know it. I have graves disease and I was on medication 3 times in last 20 some years and each time went into remission. My Endo told me to get rid of it but I did not and he got very upset at me telling me, I will never feel normal again. I did not believe him at that time but I wish I did. I always felt very tired but now at my age my fatigue is worse and anxiety is very bad. I have also developed osteoporosis, high blood pressure and high cholesterol. I have decided to get surgery now because i feel i wasted a lot of my life not getting rid of the thyroid. Everyone is different and hope that your condition stays in remission. Stress can absolutely make symptoms worse so please take care of stress. My life has been very stressful. Thanks for telling us your story. Do you know of the best thyroid surgeon in calgary or a really good endocrinologist. Thank you!
Hi there! Thank you so much for sharing your story. I'm sorry to hear about the challenges you've faced with Graves' disease and the additional health issues. It’s never easy to make these decisions, but it sounds like you're taking a positive step towards better health now. I recently moved to Calgary myself and have only been here for about a year, so I don’t have personal recommendations for an endocrinologist or surgeon yet. However, I’m sure there are some excellent specialists in the area. I truly appreciate your advice about managing stress, and I will definitely keep it in mind. Thank you for reaching out and for being a part of this community. Wishing you all the best with your surgery and your journey to better health. ❤
She is 100% correct! I do not have Graves' disease, nor have they confirmed that I have it, but I do have hyperthyroidism. I was diagnosed in 2014 and had every symptom associated with it. One doctor dismissed my concerns, so I switched to another one. She immediately said that I had hyperthyroidism and had me tested to be sure. I don't remember the medication she prescribed, but it worked really well for the year or so I took it. I eventually had issues with my insurance and had to stop taking it for a few months. During that time, I went completely vegan (clean vegan). I no longer had any symptoms of hyperthyroidism until recently, which is a combination of stress and unhealthy eating. I highly recommend giving yourself a few years to change your diet. Do not let them kill or remove your thyroid until you try this. If you think that you have hyperthyroidism, please go see a doctor and see a new one if the first one is not helpful. You can 100% tell when you have it. I can't explain it, but your body just feels different, even if you are not having any of the major symptoms. I knew mine was flaring up a month before my major symptoms started. Please advocate for yourself and do not take no for an answer.
Yes, I believe if you change your life style that diet can work for some people. It depends on how severe your hyperthyroidism is. I had hyperthyroidism from 2010 but every time my doctors tried to ween me off of carbimazole my symptoms would come back right away. So earlier this year I had the radioactive iodine and I'm now hypo. I believe that more research needs to be done on graves disease to find the root cause of hyperthyroidism. Relaxing/meditation, reducing stress and diet just don't work for everyone. The sad thing about having this disease is that some people can't work because they are in a constant state of tiredness.
@@MiiFlawlassSuccess yes, right now my doctor is weening off of carbimazole and will change to my new medication next month. I am feeling so much better so far. No rapid heart beat, palpitations, my anxiety is nothing like before and I can keep down my stress level much easier. I can also do low impact exercises.
I have Hyperthyroidism, but initially my doctors ignored my abnormal lab result (TSH was .02). They basically told me I should be glad to have a disease where you lose weight since that’s what most people want (I was already underweight and had heart issues, which is why I asked for blood work in the first place). After demanding more tests, I received a T3 result (also abnormal), so they put me on methimazole. They never called me at all, I just got an alert from the pharmacy and I also received an auto message that I had an ultrasound scheduled. Then when my ultrasound came back with nodules they ignored that too, and when I reported to them that the methimazole made me extremely ill (I couldn’t talk or walk) they never responded to me. I saw 3 separate doctors at this clinic, because my PCP is always booked, so it's not just one doctor that’s a complete idiot and/or unprofessional. I'm currently waiting to see an endocrinologist, but you have to wonder how so many doctors are worthless.
Thanks for sharing your story. I have T1 diabetes, PCOS and hypothyroidism, so a real endocrine trifecta. My hair hasn’t been thick since I was a teenager probably, and trying to work with it is beyond frustrating. I also have Trichotillomania (hair pulling) that comes on in times of anxiety, and having short hair keeps that at bay. Wigs have been a godsend for so many reasons!
Thank you so much for sharing your story. I had some nervous/anxiety habits as well.... mine was biting the skin around my nails.... it's why I wear fake nails sometimes to get me to stop if I have had a stressful couple of weeks and notice me doing that bad habit again LOL....
I was diagnosed with Hyperthyroidism 2 years ago and was on Carbimazole, My dosage changes on and off for a few months after each blood test (lost weight in the beginning but have been gaining the weight back x2). I was referred by the doctor to the Endocrinology Clinic and was diagnosed with Grave Disease with Hyperthyroidism in March this year. I was given an option by the doctor to either continue with the medication that may take years to be 'normal' or go for the operation (Radioactive Iodine Treatment) that removes the thyroid gland permanently but will/might have to rely on medication for the rest of my life. Chose not to take the operation and decided to continue with being on Carbimazole. Still struggling with it due to constant weight gain and hair loss but is Staying Positive! 😁
Thank you, Steph. You are amazing. I was diagnosed with Graves a year ago and I know I had symptoms several years ago. They want me to cut out my thyroid but I have heard that there can be dramatic changes to the voice if you have the surgery. I don't want that. I love my voice.
@@timothyroman3476 I totally understand 🥹 I heard the same thing too. I also heard that taking synthetic hormone (after killing the thyroid or cutting it out) makes you feel… not great. My dad has to take synthetic hormone and he says he doesn’t feel like himself. Feels synthetic, he says. Although, maybe it’s a personal thing? Not sure. But that among other reasons is why I really just wanted to get better
That is why you can't trust most of these doctors, because it's always about medication, medication, I have learned that most disease required lifestyle change, mental, physical, spiritual . I have type 2 diabetes, my doc trying to force me to go on medication. I started researching things for myself and decided to lifestyle change ,I also found this cardiologist on TH-cam that I listened to, love this man because he is so knowledgeable and have a love for people, which is hard to find, this man has taught me how to intermittent fasting, food Choices and whole lifetime of knowledge more precious than gold, my A1C was 300, 3 months ago it's now down 105 , I also lost 15 pounds thanks to Dr Pradip Jamnadas , this man teaching is out of this world and he is also very funny.
Hi! For type 2 diabetes I would highly recommend u to try Black seed oil. It’s a wonderful natural remedy for it and for a whole list of diseases. Look it up!☺️
both my mom and grandma have graves disease and where I've never been diagnosed (because I haven't been able to afford to see a doctor in a really long time) I have all of the same symptoms they do. I've been able to manage on a high fat carnivore diet, i do find a I need a small amount of carbs though just can't do more than that. I don't think I've ever been normal :( I've never been able to gain weight, I've never weighed over 100 pounds and I'm 29. my family always tried telling me I was fine and totally normal but I've always known I wasn't. just been praying for a miracle to be able to afford to see a doctor that can help me. I feel like my life was robbed from me and I've had to try harder than most people just to be a normal functioning person. Thanks for giving me a sliver of hope that even if I spend the next several years trying it will be worth it
I'm saddened to hear your story too. I wish you the best..I too feel as you do constantly betrayed by my own body...and others. At least people (most) we can cut them out without further consequences...but our bodies our organs are there for reasons...hopefully we can heal and recover. 😢❤
Thyroid issues definitely run in the family (my mom and grandmother have it). However, once I started talking to a lot of women I know (most not related to me), I found out nearly all of them have thyroid issues. I even talked to a stranger and was told she didn't have an issue with her thyroid, but all 3 of her daughter's have it! I'm starting to think it is also environmental, like something in our food and water is causing it.
Hi... I feel really gratefull found your videos and see you in pregnant period, really boost my hope again. I thought I cann't even be pregnant. Thank you so much for make this video, some people who lived in the country that still have less literate about autoimun and thyroid problems will found this video really helpfull and inspire. I am just 2 years being diagnose hyperthyroid grave disease in still in hopeless mode before I found this video.😊
I agree with u 💯 this is what I just told my son that STRESS was the biggest factor on hyperthyroidism....and I'm like u I don't want to do the iodine radiation or surgery...I'll take the methamazol and do as u reduce /control stress(which is my husband) I was so good without him I was so healthy and no stress when I left him...I knew that the minute that I moved back in with him I started to get sick with everything!!! I keep telling everyone that he is the sole problem to my health declining...u just confirmed it...cause if ur body/mind doesn't stress then ur hormones, and all body organs work together as they should...amen🙏🏻
Yes!!! That was the same with me and my ex. I swear he made me sick…. When I left, I felt better. Whenever we came back together, I got sick again. This is 100% it. I’m so happy you’ve come to that realization for yourself too.
Freezing bread and then toasting it before you eat it gets rid of much of the starch and sugars in it. I hope this is helpful. Thank you for sharing what you have been going through. Congratulations on the baby. ♥ You have a beautiful spirit. I wish you and your family the best.
@@SparkyOne549Did you know that there are various other kinds of gluten apart from the most commonly found in wheat.,barley and rye? If you really want to be totally gluten free, you should avoid all grain. More information on dr Peter Osborne's videos.
This resonated with me so much and our story is extremely similar. I think I am just a few years behind you 😊 I am in my second time of my Graves’ disease and hyperthyroidism flaring up after just over a year of remission and I would put all of the money I have in the reason of stress and anxiety. Just like you I am a TH-camr but I also have another full time business and I have two little ones. They want to cut my thyroid out and I am refusing. I want to stay on medication again for a bit and see if I can do it again. I have never experienced losing my hair though. Everything else you explained I have at the moment. The shakes being the worst as I am an esthetician and it’s embarrassing. I am going to go and watch a few more of your videos on this subject as I get a really lovely energy from you. I hope you are well 😊
Thank you so much for making this video, would love to have another in depth food choices you had to made during and after remission, also please make a video how you reversed your eye condition and when you started noticing the change ?
Hi Steph, I am so glad that I stumbled upon all of your videos. I have been losing my hair for a few years due to alopecia. It has been very frustrating, heart wrenching, emotional, and hard. I used to have very thick, beautiful, curly hair, and now I am, almost bald and I didn’t know where to start with wigs, but I stumbled upon your videos and it has helped me so very much. I’m excited to actually learn more about wigs and to start getting some wigs so that I can feel confident again. Thank you so much for your channel. Thank you so much for your videos. I enjoy every single one of them.
Hi Valerie! Welcome to my little wig family ❤ I'm so happy to have you here. I feel everything you've just spoken to me.... oh my goodness, hair loss can be so challenging. It can be difficult to see past it sometimes. Wigs have honestly changed my life FOR THE BETTER, in SO many ways. Like, to the point where the average person doesn't know hair loss is something I struggle with, because wigs look SO real these days that nobody gives it a second thought, and it truly has given me my confidence back. I wish this exact feeling for you!!!! I can't wait to hear more from you =) XO
Seven doctors until one listened. We badly need a system rating doctors so if they're not good they get fired. They have no consequences for being terrible at their job.
Thank you so much for posting your experience. I am going through Hyperthyroidism and Graves Disease. I hear the same things from my Drs. It has been the most frustrating experience for me . I am currently trying to do exactly what you are talking about. I'm getting my diet under control, next is a exercise program. Your story is very encouraging, so I thank you ! Congratulations on your new baby ,I wish you the very best !
Breath or fresh air ❤ I was almost forced into getting mine removed or RAI , I also refused. I am on a low dose of methinazole and will be fine with it until I can also find ways to go into remission. Thank you so much !
Wow thanks for this video, I was thinking I have to live with this for life... I'm 29 male and my heart beats like crazy if I don't use my pills... Having difficult for finding clothes for my size (skinny...) I'll try your tips.
I regret taking hypothyroid medication when I was first diagnosed 7 years ago. I always wonder if I would have gotten into remission had I taken a more aggressive, holistic approach. Why? Because I saw a difference in my labs within two weeks of natural supplements, but I was still symptomatic. Unfortunately, I didn't have the guidance or support from medical providers then, despite seeing a Naturopath, which I later fired. I remember doctors telling me this is a common disease; you just need to take Levo, and you'll be fine. Essentially, dismissing the disease. Flash forward, I achieved remission once; my antibodies were under 30, which doctors consider remission. However, I was still symptomatic. Now, since seven months ago, I have lost over 70 percent of my hair. It's devasting, to say the least, especially having been dealing with it all these years. I now own two wigs.
So sorry you had so many bad doctors. It took two visits for my one doctor to diagnose me. Kick anyone who doesn't listen to the curb! I'm glad you're doing so much better!
Thank you so much for your story. I just god diagnosed less than a month ago and it’s hard and scary. I was doing fine when they gave me the medication. Its when i found out I couldn’t stop having headaches so we went to the doctors and got me to see an endocrinologist. Now I’m having joint pains that they don’t know about like when i move my arm or legs it would hurt badly but if i was still id be ok. And right now in the bed in the hospital i feel like my heart is weak and weird and heavy feels like it’s going to do something lol. Im just scared right now.. I hope people see this and understand please!
I have hyperthyroidism since 2011 (the first I was diagnosed). But I’ve had all the symptoms years before that & I’m just dealing with it as anxiety, social awkwardness etc… I’ve changed doctors 3x because with the last 2, I just got worst. I’m still on the same medication and see my doctor quarterly and she adjust my meds depending on the lab test results. She did suggest RAI therapy 2x which I refused. It’s really managing the stress and diet and exercise that makes you better. I’ve never been on remission because I still eat the food I’m not suppose to and not getting enough exercise
I was diagnosed with Graves disease Hyperthyroidism about 5 years ago. The HUGE stresser was the death of my youngest Son Austin. Depression and anxiety meds really screwed up my stomach, and now I'm taking Methimazole for my hyperthyroidism. My Endocrinologist keeps wanting to either remove or do radioactive iodine to kill my thyroid. I won't do it. He also doesn't believe that diet plays a part in healing the thyroid. I found a holistic, alternative Doctor. I wanted to get off of the meds for depression and anxiety, which I weaned off of. The holistic doctor has me taking herbs and other natural things to heal my stomach and my thyroid numbers are getting better since my stomach is healing and my diet is better. The Endo doc has slightly decreased my Methimazole. I go every 6 weeks for blood work, so we'll see what my numbers are after the next blood tests. When I saw my Endo doc a few weeks ago, I mentioned that I was seeing the holistic doctor, and wrote down what he has me taking, and my Endo doc wouldn't even acknowledge that since I started healing my stomach, AND better diet, my thyroid numbers are getting better.
I am so very sorry to hear about your son. My Endo was the same where she wouldn’t acknowledge diet, and made me feel so silly for thinking that would help me. My dad is also a doctor, although retired now, and he was really the only one in my corner that supported me and kept telling me my whole body was connected. If one thing was off, it can throw the rest off. It was that idea that kept me looking after my body, mind, stomach, and once I reached a place where I was mentally strong again, physically, and healthy with what I ate, everything changed. It took my body a long time to go into remission… but it still happened. And my Endo doc was so wrong. I saw many Endo docs (not sure if I said that in this video- but because I moved about three times, I had about three doctors who all said the same thing and wouldn’t acknowledge diet or any opinion I had on my own health.) You’re definitely doing the right thing. Especially if you’re taking all the necessary steps to feel good again; nobody knows you better than you. Thank you so much for sharing your own story with us.
I was just diagnosed with Graves & Hyperthyroidism. I'm hesitant to take the medication. I'm still learning about my diagnosis & I'm interested in how I can change my health on my own. Thank you for sharing, I definitely needed to hear what you had to say!
I have psoriasis and probably other autoimmune things going on, but the psoriasis is causing my hair to fall out. So, I am exploring the idea of wigs and am happy to find your channel. Thank you for making it!
Hello i have hyperthyrodism and i took medecin for a year,was on a remission for a year,now i am out of remission iwent under stress and depression that flared up my hyperthirodism im on medication now a week ago im considering gluten free and dairy free diet to heal my immunity i have graves basdow desease your video just put some hope inside my heart ❤
Thank you so much for your story. I just god diagnosed less than a month ago and it’s hard and scary. I was doing fine when they gave me the medication. Its when i found out I couldn’t stop having headaches so we went to the doctors and got me to see an endocrinologist. Now I’m having joint pains that they don’t know about like when i move my arm or legs it would hurt badly but if i was still id be ok. And right now in the bed in the hospital i feel like my heart is weak and weird and heavy feels like it’s going to do something lol. Im just scared right now.. I hope people see this and understand please! Oh Im also going to do radio active iodine this week so thats good I guess.
It’s so wild that they didn’t want to test your thyroid levels, when that’s part of a normal routine blood test (I have hypothyroidism and didn’t have to specifically ask for them to test for it initially; it was just part of a yearly physical exam).
My misdiagnosed Graves Disease was, in fact aspartame poisoning. It was as simple as removing aspartame from my diet and my thyroid function is normal. Aspartame is in almost EVRERYTHING labeled "sugar free" or "diet."
This is my first time watching your video I just barely found it on TH-cam I'm glad to be here I will find out and get back to you and leave a comment of how my friend got all her hair back and stuff and thank you for your videos
LOVE your video congratulations on great health and your baby. One tip Ive learned while studying GD is you need electrolytes to help the receptors on your cells during the T3 and T4 conversion. Trace minerals in drinking water is the best way to get these.
I read something about that thanks tons. I couldn't find the info to quote the guy...and also..man it doesn't make sense to cut out the thyroid just to function properly ..in extreme cases maybe..but still..and also cutting out necessary food like eggs..and meat and liver sounds bizarre to me too if our bodies need those nutrients. Same with fish...like I hear cruciferous veggies help block excess absorption of idodine from those sources.
I really am not sure why my hair has fallen. I do enjoy wigs for me it is more work but I do it because I look so much better with it. Also wear wig grip like you I feel like people can see the wig grip but it is what it is. I am thankful that I have the wigs available to me.
I love your videos Steph. You helped me so much when I first found out I had breast cancer and I’m still watching you today. It’s been several weeks since I had chemo and I still don’t have any hair. I’ve bought about 5 wigs although when I’m at home I don’t wear them either and since I’m retired I very seldom have any place to wear them but I do love them. All because I saw how real they looked on you.
I was diagnosed in December last year meds weren’t working at all making me extremely sick I have 2 kids so my only option is rai and surgery so I am scheduled for surgery Oct 1 really hoping I can go back to living normal after surgery
OMG Steph, I think that's what my Dr wants to do... cut my thyroid out and I'm not sure about the iodine.. they want to do a REE on me next week!! I feel kindred spirits with you 💕 and and the information you give is so valuable!!! I will do it your way , it's safer for my body... I don't eat much sweets but crave cinnamon graham crackers!!!🤔😳go figure 😅 congratulations on your marriage, the move to Calgary and of course your pregnancy...Step, I love your honesty, your truth and your stunning beauty.
I never heard Graves disease and hyperthyroid as two separate things, or that you can have Graves disease without hyperthyroid. I've only heard them used synonymously.
This is so helpful I was diagnosed 5 months ago after experiencing many of the symptoms you spoke of.. I’ve been given option of thyroid removal or rai as haven’t had any remission -would prefer to heal myself thanks for this - it’s encouraging to hear! Any recommendations re- diet / lifestyle appreciated ❤
Thanks for this chat Steph it's very helpful. I should like you do a chat about handling stress and anxiety please. By the way your baby bump is soo cute 💝 sounds really lovely where you live x
I have graves, dx 2 years ago. All was okay until recently and now I have TED and thinning hair, no energy. Never considered removing my thyroid until recent symptoms with my eye. I’m torn.
Wow your story sounds just like mine, I also flare up with stress, and when I get that under control I go into remission gluten free food is also key!!
I got surpriced after 12 months of keto and massive health provements and still had mild heart attack. The main cause for that was my hypothyrodism that i was diagnosed when i was in hospital few days. I had to start taking thyroxin and all the health issues that hadn´t improved doing keto disapeard. I had symptoms for that at least five years but i tought most of those were part of getting older. But i am 43 now, so i´m not that old yet that those health issues should appear. Well now it´s been over three months and i still do keto and i have recovered from that heart attack quite well. Also my thyroid hormons are great. I think that if i continue keto long enough it can fix my thyroid completly.
I’ve been diagnosed almost two months now. I’m on amlodipine, atenolol and methimazole. For side effects I am taking water pill and potassium chloride. Most days I feel completely fine. I’m actually gaining back the strength I lost in my arms and legs. I’m feeling a lot more energy overall. My biggest complaint at the moment is never feeling full and always feeling hungry after eating full meals. It’s frustrating that with Graves or a mixture of the medication has affected my gut of feeling hungry.I’ve gained weight, lost some, dealt with swelling and treated it. I guess I’ll have to figure out ways to combat my hunger.
Ketogenic diet done properly will help you to lose a lot of the hunger pains and weight, too. I used Dr. Boz's, (Annette Bosworth, M.D.), program called "Keto Continuum". Dropped 22 pounds in 3 months with 12 more to go. The Graves is what makes us so hungry.
@@lj5027thank you, I’ll look into it. Updates: All of my levels are in range now. Wow what a rollercoaster! I went from Graves to Hashis and in between. Now with meds adjusted I am in range now, thankfully 👏🙏🏽💛
Thank you for your information I too have graves hyperthyroid totally not my self you gave me such a i spratation to know things can change I have totslly giving up on my doctors ever finding answers to a problem
Hi I just want to say about the hair growing back part don't think like that if you stay positive and keep taking care of yourself living life aiming for the goal you want and are trying to achieve before you know it you will get it I have a friend of mine she lost all her hair but I'm talking about completely bald to where she couldn't even leave the house and it took a while it took years but she got all her hair back and even more thicker than she had it before and she was born with curly curly thick hair from completely losing at all she got all over the back and like I said even more all her curls and everything so forget whatever they tried to tell you that your body will never be the same yeah it won't because it will be even better
I have adult type 1 diabetes so my thyroid was well monitored. Tested in April and all was normal. In October I noticed my resting heart rate was high. Went to a cardiologist and after lots of testing could not find anything wrong. Also ended up in ER with speech difficulties that went away. Decided to test my thyroid labs. I am a nurse so was next logical step. My Endo was so shocked when it came back hyperthyroid. Wanted to do radioactive iodine but I also had thyroid eye disease. So was ruled out. Had great results with methimazole. Endo still has me on 2.5 mg a week. So that’s doable. Did have Tepezza infusions for TED and that was successful. That was not fun. Endo still asks if I want to ablate my thyroid at every visit. I’m like duh why.
I should get my larger panel back in 2 days but my current thyroid panel shows hyperthyroid. Dr said i had anxiety but i feel it is something else. I guess we will see
My eyes popped out too... In my other video I talk about all my symptoms. My eyes really bothered me... especially because one popped out more than the other. I thought it was very obvious, and unfortunately I had that symptom for a LONG time. Years. That symptom and my hair loss annoyed me the most
And just to introduce myself real quick I am 39 years old female I live here in Las Vegas but I am originally from Yugoslavia but have been in the United States for over 20 years used to live in Los Angeles but we're in Vegas now and I like it here but I do love to travel too
At the local lab -- the phleb told me they removed her thyroid due to hyperthyroidism and she gained 100# and NEVER to thst day got her thyroid balanced even when on the repacements. What a warning ⚠️
As promised, here is the video I made on my Hyperthyroidism/Graves Disease and all the symptoms I had: th-cam.com/video/i6M3pH6nA08/w-d-xo.html
Please use the comments section to share your own personal stories 💕 And please be kind to each other. It is my hope for this video that it will bring people together, where we can feel supported, and just SHARE, because for a lot of us, sharing is healing. And I'd like this page to be a place where people can come to get ideas and feel inspired! My love to you all, XO
⭐ I am wearing the wig called Mesmerized. Watch my review/try-on here: th-cam.com/video/ARYCmQJHPd0/w-d-xo.html&feature=sharea
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I have hyperthyroidism too. 18 months taking carbimazole and stopped the meds for 1 year I thought I'm also on remission but after 1 year of not taking meds it came back so I'm now on meds again. 😢 Everyday I'm wishing and praying to get my life back, the best version of myself, the better me version. That's the only thing that I wanted now, nothing else in this world.
How do you feel now?
That med nearly killed me...couldnt breath properly or walk
Take it after food it helps
Me too back with carbimazole my graves is not heal yet from 5 years ago feel hopeless and my neck is bothering me it feel uncomfortable
Am going through the same thing. I have taking carbimazole for a year, I stopped the medicine and my heart beat is something else and are bulging, I just can't take it, am tired of hiding my face. I really want to be oke
I was diagnosed 11 years ago . Still have my thyroid gland and i dont take any medications. Stay positive
How'd you do it?
I also was diagnosed with Graves' disease and hyperthyroidism and was given methimazole that I rejected...told my doctor to give me time to do it my way and if that doesn't work I'll take her meds. I started with exercise at the gym and walking minimum of 2miles a day , 5-6x per week changed my diet to Whole Foods only also eliminating anything white like bread , pasta etc. but most importantly I did intermitent fasting 5x per week and did a 36hour fast every other week. I did IF slowly in the beginning like 12 hours first and kept adding more hours each time and not forcing my body to do too much at once. 4 months later I saw my doctor again and my Graves was in remission and I didn't need medication at all. Discipline and sacrifice helped so much. Hope this helps you but please talk to your docotr first because only the two of you really know what's going on with your health. God bless. Oh btw I eat a lot of meat, meat products and fish too. Only grass fed and finished also wild caught fish only , I never liked the flavor of farmed fish. But overall I eat everything that comes from the ground and seas and cook it myself. No factory processed foods and no seed oils.
I was really sick as well. I had done research and knew it was my thyroid. I kept going in, they did just the TSH test. Kept telling me I was fine because I was in the “normal” range. I was done. I was too tired to keep fighting. My son was with me and he blurted out, do an ultrasound. They did. 26 nodules. The next day I found out I had thyroid cancer. You have to be your own champion in getting better. So you work with the doctor and not just follow the doctor.
oh wow! Thank you for sharing your story. This is what I've found as well! You HAVE to be your own advocate, because only you know you the best.... I'm so glad you caught the thyroid cancer. How are you doing now? Has it been many years?
Same, awaiting my results 😢
Ihave hprothyroidism it let me feelngnot eating gizzing and black outfeeling sickand i am medication the name of medication is carbimzole
I think it helps to have someone speak up for you.
I am sooooo proud of you. For you to recognize that food is such an important key in being heathy. I am 63 had RA for decades and healed by changing my diet. I eat a whole food plant based diet , no sugar no oils, and I feel great no meds. You can now pass what you have learned onto your children so they can grow up healthy.
Thank you so much for your kind words! It’s truly inspiring to hear about your journey with RA and how changing your diet has made such a positive impact. I completely agree that food plays a crucial role in our health. I’m excited to pass on these healthy habits to the next generation. Thank you for sharing your story and for your encouragement! 🌟❤
It will come b a ck.
@@cynthiajohnson798 Its. been 7 years and feel better than ever. I have learned we are what we eat and. I eat a low inflammatory diet. It's working for me. Good luck with your journey.
*Diet and lifestyle can do so much good!* My aunt struggled with hyperthyroidism and the hair loss that came with it. They put her on a synthetic hormone which helped but she wasn’t interested in being on any pill for the _rest of her life._ So she ditched it, did a lot of research and opted to start with an elimination diet: no gluten, dairy, processed sugar, caffeine/coffee and alcohol.
She focused on cleaning up the gut and gentle movement of the body (walking, swimming,etc nothing HIIT related as it raises stress hormones/cortisol) and advocates getting bare feet in contact with the ground (a practice called “grounding”) and it’s made a night and day difference for her.
Thank you so much for sharing your aunt's story! It's incredible how much diet and lifestyle can impact our health. The steps she took to clean up her gut and incorporate gentle movement and grounding are truly inspiring. It's amazing to hear that she experienced such a positive transformation without relying on medication. Her journey is a powerful reminder of the potential benefits of holistic approaches. Thank you for sharing these insights! ❤
Your aunt had HYPERthyroid or HYPOthyroid? They usually only give the synthetic hormone if you don't have enough, not if you have too much.
We basically have an internal alarm telling us when our lives are out of balance. This disease obligates us to live balanced lives. I see that as a positive thing now, and strive for that balance every day. It’s so rewarding when you get it right! Best wishes to you and everyone else on this journey.
Hey I was diagnosed with graves/hyperthyroidism four years ago but methimazole made me so nauseous. Instead, I went gluten free,dairy free, and caffeine free along with KETO to treat my disease. I went into remission within three months and have stayed in remission for four years. For the hair loss I started taking Hair La Vie. It has made my hair really thick again like when I was young and my natural curl is back more than ever. I just thought I would share that with everyone. Plus, I was diagnosed with osteoporosis because of the graves. I have been taking AlgaeCal bone building package and have gone from osteoporosis to mixed osteoporosis and osteopenia, to just osteopenia. I am building my bone density without one of those “bone building medications” that do NOT actually build bones and cause horrific side effects. It can be done naturally. By the way, I asked my doctor to test me for thyroid issues for nine years before she finally agreed to test me. And I was in the Air Force for 22 years and those doctors never even suspected that the racing heart, the palpitations, the tremors, and the crazy high anxiety level were indicative of a problem.
Hi there. I have been recently diagnosed and am not taking the prescribed medication because im pregnant and there are a lot of side effects. Would you mind telling me more about your diet changes and if you kept it the same after going into remission? Thank you!!
My mom has hyperthyroidism and I have the same request if you could tell us more about your diet. When you say dairy-free does that mean completely stopping all dairy products butter, milk yogurt cheese everything?
So absolutely NO dairy…no yogurt, no ice cream, no cheese, no butter, no milk, no dairy period. AND NO GLUTEN!!! You’ve got to read labels. Nothing with any wheat/flour. Plus no caffeine because it causes heart palpitations and increased anxiety. Oh and just in case you don’t know, soy is super bad if you have HYPERTHYROIDISM.
There's also eggs that make hyperthyroidism worse...I hate it..I NEED those nutrients. Idk what else I'm gonna swap it with...besides eating more cabbage from kimchi to prevent hyperthyroidism from getting worse. Cuz excess idodine from dairy and eggs
@@lesliesantos8595You can eat the egg white. The yolk has the iodine.
This was very interesting to me. I was diagnosed with Graves’ disease 6 years ago when I turned 40. I finally went to the dr because I had uncontrollable itching!! It felt internal and I felt like I was going crazy!! Luckily my dr knew immediately what was likely going on. My thyroid was swollen. I had rapid heartbeat and tremors. And I had lost 40 pounds in 3 months. I was on medication for about a year. They wanted me to have radiation or surgery and I just couldn’t do it. Weaned myself off the medication because I could tell I was getting better. Fast forward to yesterday. Had my levels checked for the first time in 4 years. Totally normal. Go figure!!!
How
Totally normal miracle cure how ?. Thanks ❤
I start methimazole today! I want to get better. I have a visible goiter! My biopsy came back benign but I will have my first scan in 4 month, cause dr wants to see what will happen when medication is taken. You give me hope!
Bless you.
I think I had the same internal itching in my chest/heart area and arm. Like I couldn’t stratch it. Hitting the muscles seemed to help a little
I have been battling hyperthyroidism since 3-2018.. I'm doing carnivor diet. No coffee and adult beverages. And I'm on 18/6 intermittent fasting!! And to make my life like hell, I also have vertigo issues. That's ok, I love a challenge!!!!
I will get over this hurdle!!!!!!
I have Graves and vertigo too. So it makes two of us :) at least . God bless you !
What helps with weightloss?
My mom also has hyperthyroidism and i have put her on a carnivore diet today. Did it work for you?
Hello from Toronto,I was diagnosed with graves disease just over 3 years ago when I suffered from a thyroid storm. I was told pretty much the same thing after I year of taking methimazole, but I did my own research and looked at treatment back decades and found out that methimazole could be taken for many years to the rest of your life if necessary. So I told the specialist that I would refuse to take the other options. I started working out and liked the fact that I couldn't grow body fat, and I developed ripped muscles because of the graves disease. I don't like the idea of operating on synthetic hormones and would rather operate on my own hormones. Besides, I see no reason to destroy the thyroid because I don't believe that it is the problem. The immune system attacks the thyroid, so why not figure out what is causing the immune system to attack the thyroid? I don't get modern medicine at all.
Did you not suffer from rapid heartbeat or weakness in the body? But awesome for the gains though! 👍
@zucifer8309 Yes, my heart rate was 186 bpm, and I had tremors and body weakness.
I was diagnosed with Graves/hyperthyroidism too. Was told I could take the iodine pill and be done. I refused, was on methimazole for a year, and metoprolol for several months...felt like a slug and gained 30 POUNDS. I went off for 6 months and back to Graves again. Took gluten out off my diet and 3 months later labs were back to normal. Take out the gluten people. My joints stopped aching, my hair improved oh and women take prenatal vitamins no matter your age, and I just felt better. Thank God, Do you homeopathic research.
I have a gluten sensitivity! I asked my doctor if that had anything to do with it and he said no. Thank you 🙏🏽
Thank you! I was diagnosed with Graves disease this morning & will make sure I don’t have gluten.
Can I ask what are some of your favorite meals to eat for breakfast lunch or dinner since you cut out gluten I guess I have to start doing this
@@Just.FactssI was told by my Endo that diet has nothing to do with Graves 🙄. They don’t want to find a solution, they want to get you in and out their doors and be done with you.
I am sensitive to gluten, casein (dairy) and eggs. I am eating a lot of burger patties (even for breakfast), and bacon@@SparkingLife111
I was diagnosed in 2006, I had the racing heart, bulging eyes, etc. I went on meds and I was one of the few who was allergic to the meds and broke out head to toe with hives and heat rash. I ended up having the radio active iodine and it took 6 years to get my thyroid meds right. I was so depressed with hair loss and bulging eyes. Now I’m buying wigs, and still getting used to it
You’re amazing and so beautiful.
For bulging eyes, Tepezza Infusion works
@@vickeeschanelthanks
@@vickeeschanel❤ thanks for information
Hello Steph! First of all, congratulations for being in remission, and also for having a baby. I am also suffering from hyperthyroidism since last year, I lose a lot of weight, had hair loss, my anxiety and depression was severe, same goes with fatigue.
I had a surgery last year but only half was removed because my surgeon thought it was “toxic adenoma” since I had nodules as well on the left side.
I also aim to be in remission, hope 2024 will be a good year for me. Thanks for sharing your story.
I was diagnosed with Graves 6 years ago, and given the same options, and not having enough information to know otherwise, i chose the radioactive iodine treatment that failed and left me with thyroid eye disease. I wish I had the information I have now, I would have made a different choice, but all I can do is try to heal it naturally without having to do the RAI again or surgery, which all the doctors have said are my only options now. I just don't believe that to be true. It is a struggle and my heart goes out to everyone here and out there in the world who are dealing with this and TED. It really affects your whole life, and so many people don't even realize it. Thank you for sharing your story and helping our community find hope.
yes that's one thing they know now, is that it exacerbates eye disease. when carbimazole would have done -
Were you on any medication at all?
@@2Cixth Yes I was first on methimazole and the beta blocker Propranolol. I had a severe allergic reaction to the methimazole so they put me on propylthiouracil which Im still on to this day, plus a beta blocker.
Check selenium and lemon balm for your eyes
And somehow at work I'm supposed to function like everyone else and not miss work. I miss work because I'm struggling emotionally mentally physically. Not cuz I'm lazy or don't want to work
..it makes me feel normal of course I like to work..being able to do it without feeling like panicking is a different story.
You are so right… first, we have to be our own health advocates, because nobody knows our bodies better than we do ourselves, not even the doctors. Not that they don’t academically know more than we do, but finding a doctor who truly listens is literally vitally significant. And I completely agree that THE number one factor to any “dis-ease” in our bodies is due to stress. Of course what we eat and our physical activity are also important elements as is spiritual and emotional well being. I’m a senior woman now and still learning and evolving. I could be my own medical journal of things that have gone wrong with my body and mind due to my own neglect, BUT I refuse to give up, and am in a place of harmony now as I shed excess weight (75 pounds so far!) and find new ways to keep moving. That you are so young and at this level of understanding is so commendable. I’m so looking forward to watching you and learning from you as your life moves forward into new adventures, especially with you and Dan soon to welcome the little one. ❤️💕
Congratulations!!! That is great to hear! I have Graves Disease as well and I was in remission for 6 months and now I’m back to taking my meds. Took me a couple of years to be diagnosed as well. I knew something was wrong….we know our bodies!
whats remission? and also did ur heart have palpitations and did it feel heavy? I stopped taking methmizale because they think its a side effect im having from it. im having joint pains
Hello Steph. Thank you for sharing your story. I also have Graves Disease and taking Methimazole for it. It’s been exactly a year since I was diagnosed. I should have gone to see the Dr sooner. I too thought I was going crazy, I felt at times that I was possessed because I didn’t have control of my myself: mind and body. I had the shakes…like really bad to where I was embarrassed to be around others. I had to be constantly moving so that no one would see how my body trembled. I had severe heart palpitations where it was visible on my shirt. I couldn’t take it anymore. Luckily my PCP tested me for hyperthyroidism as soon as I described my symptoms. I now have the bulging eyes and I’ve lost a lot of hair, but my thyroid is making great progress and my symptoms have ceased. I hope that in the next few months I can be off the medication and go on remission. Thank you and everyone on this channel for helping me feel better about my situation. I will take the advice of ditching stress and getting on a healthy diet. I began exercising to lose weight and to get into the habit of staying active for my well being. Best of luck to everyone and God bless you ❤
I was diagnosed with Graves disease two years ago. I lost my medical and have not taken any medication for the past year. I am currently living off grid next to a national forest. I have been doing my best to stay stress free but yes, its so hard we've been waiting 15 months for electricity but it seems to be out of reach financially. The hardest part for me is trying to stay cool while living in Texas with no electricity.
I was diagnosed with graves 1,5 years ago. I was really bad and lost bone density, got heart problems etc. The first docor i met took the thyroid tests right away and sent me to an endocrinologist. I started medication right after diagnosis, and already within a week i felt my body was slowing down. Im still taking it and get tested every 6 weeks. I feel great and safe and so thankful for free healthcare, medical professionals, research and LIFE ❤.
Absolutely! That is phenomenal a doctor listened to you and had enough practice to understand what to send you out to be tested for. I'm so very glad to hear you are doing much better ❤ God bless
Thank you for this video. I'm glad to know your move has been good & that you are feeling healthy and well! You have helped me SO MUCH with the content you place on this channel, & I am sincerely grateful. After years of buying into detrimental ways to achieve "socially acceptable" hair- it became clear I would have to find alternative ways to care for my own. As it turns out, my husband was not keen on less frequent washing & no heat treatments. SO- about 8 months ago I began to try wearing wigs. Your channel is my favorite. You are very inspiring! I now see wigs as a way to protect our own hair & to step into public places with the kind of cinematically perfect hair that people enjoy seeing. Your journey proves that the human body can regain health naturally, something I have always believed. I no longer accept allopathic ideas & only work with a naturopath. Thank you so much for creating this space and for helping so many!
I'm in Calgary and controlling hyperthyroid naturally. Thank you. Welcome to Calgary!!!
How?
Please how ? I don't want to undergo surgery or live on synthetic hormones 😢
Hi Steph! This video came up as suggested because I had been looking for information on hyperthyroidism, as my daughter has recently been diagnosed with hyperthyroidism. You confirmed several things that I had suspected. Thank you!
Same here I was diagnosed with hyperthyroidism and hashimoto immune disease at the AGE 19, and was told I have to take insulin med FOR THE REST OF MY LIFE. Did that for a few months and decided to explore the whole ordeal in my own hands. I changed my diet, changed my living habit, lost 50 pounds, and never looked back. All the symptoms are gone once I lost the weight. I am 38 now and never had any problem with thyroid and blood work check is always normal since age 20. I maintained my habits and weight for more than 10 years too.
What did you change your diet to?
Please explain more about the diet
Hi, thanks for sharing your health story. Why insulin? Are you type1diabetic?
I believe eatin a healthy cut out sugar high salts and processed foods and eat complex carbs turkey or chicken and vegetables water, I was readin Milk has high iodine which is not good but I don’t know??
I'm not a Doctor , I don't know everything.. What ? Believe me. Doctors don't know your body as well as you do. Get some Jesus On ! The Healer of All.
🙌🏽🙌🏽🙌🏽👏🏽👏🏽👏🏽
Absolutely. Prayer to the Most High 🙏 ❤
Amen!
I have Graves's disease from 2007, Since I was in Grade 7. The doctors always said you will have to take medicines for your entire life. I am continuously on medicines. It became normal a few years back, but as soon as I stoppped the medication for 1 month I would get it again. It is in control by medicines but every now and then it keeps going up and down. Then I got married in 2021, and since then its never remaining constant or normal. We had a miscarriage too last year, and now the doctor have said that we should wait to concieve until the thyroid levels are normal. I had a lot of stress due to my work, so I left it in March. Taking Methimez now and trying to maintain a healthy routine with yoga, diet, sleep schedule. It has improved a little. But the doctor is unable to adjust the dose of Methimez and the thyroid levels just keep fluctuating. Its been 6 months we are waiting to concieve as I will be 31 this year and waiting for things to be normal. But I don't no what to do. Starting to get anxiety again because of all this.
Please suggest.
I take 600 - 800 mg of Ashwagandha supplement 1 hour before bed 🛌 with warm organic almond milk 🥛 it seem to help with thyroid 😊😊😊😊
You can do some research on Ashwagandha supplement 😊
So proud of you Steph! I don’t want to cut out my thyroid out and I don’t think I will. Thank you for this video ❤ wow that’s so wild, the adrenaline point, I have felt that perhaps my adhd, hyperactivity, dancing, running, working out, whatever would perhaps push me to the graves again 🫣😳🤯 How mental, how strange this is. I appreciate you thank you ❤🤗
I wish i never removed my gallbladder. I was healing it but docters kept telling me i was this big cancer risk so i pulled it out and guess what , I was right just like you! Deffinately mind, body, soul is connected we CAN heal our own bodies.
Great job on healing yours! ❤
16:21 You are definitely reaching people. I feel grateful to people like you, who share their experience especially around not being listened to by doctors. In the interest of limiting stress, I won’t go into my journey with that because it’s not over BUT I feel strength to go on by knowing I’m not alone even if I have no idea what I have or if I’ll ever be properly diagnosed. What you said about stress and that it’s not realistic (paraphrasing) to cut it out but we can maybe absorb it differently? That’s something I’ve GOT to try to do . After over a year of feeling like I’m the only person who knows something’s wrong and the only person with no say in actions taken or not taken, I’ve reacted with so much anger inside and plenty that i’ve let out too so I’ve really isolated myself. Finally it’s gotten so bad dermatologically that they can’t say it’s “fine” anymore that people are just starting to listen to me and forced to take action but it’s after so long of being alone with it. It’s so hard for me to be okay with anyone in my orbit suggesting things with no information or assuming that the person dealing with the symptoms would have probably considered and tried ____(fill in the blank). I can’t imagine being so secure with my suggestion after hearing some symptoms and pondering it for 5 minutes as to tell someone decisively ANYTHING. So I have cut a lot of people out of my life who i guess never took me seriously to begin with. Whelp. See how angry I get? Annnnyway, LOL. So yeah I’m a real fun person to be around as you might see, I’m basically feral at this point and that’s why I appreciate your honesty about your journey and your emotions etc. This is a long and hopefully not too depressing thank you 😅
HI!!! I Love the realness of your message. I felt it deeply!!! I feel the same, and it definitely destroyed me, especially at the beginning, when people would see my thinning hair and tell me that I should take this or that vitamin, or try a hair re-growth serum…. It frustrated me SO much. Because it’s really not that simple.
I honestly get exactly what you’re saying, thank you for sharing 🙏 I appreciate you!!
Just came across your channel. Thank you for your testimony. I have very similar story, like most of us with Grave’s.
I totally changed my life style and fell in love with health content along the way. I’m in second year and still working on get on remission.
Thank you for sharing this. There have been many times doctors recommended things to me- surgery, medications that I refused. I’m ok and I didn’t need it. People forget they are a bu$ine$$. …. And one that has a high cost in running, so they don’t really care to help you save your health. This isn’t a personal diss to practitioners but more of a modern business model of our current healthcare system.
Diet is a HUGE factor in health. Exercise is necessary for one’s body to work correctly since so much of bodily functions are greatly affected by lack of movement, primarily digestive, lymphatic and cardiovascular. And I should clear up that when I say ‘exercise’ I don’t mean CrossFit or some gym rat type life- I mean just getting active. Stress minimization is absolutely key too. These 3 things don’t always clear up a medical issue, but if you can do better in these 3 things, it will certainly help.
I’m happy to hear you are doing well.
Thanks for sharing. So glad you're grave's disease has gotten better and that you're hair has grown in more. I have scarring alopecia, but even my dermatologist has admitted that sometimes treatments can help hair grow back. My hair hasn't grown back but it no longer falling out. I started wearing wigs to take the pressure off which I think will help my hair grow more and even if it doesn't I certainly feel better. I think that you are so right trying to improve things naturally instead of just going for cutting out your thyroid. You are so young and look if. You tried everything to no avail then at least you know you have done everything you could do
You might be interested in dr Peter Osborne's videos on alopecia and causes of hairloss in general ❤️
Hi Steph,
I live in Calgary also. I am 71 years old. I started having symptoms at age 49 or even before I think but did not know it. I have graves disease and I was on medication 3 times in last 20 some years and each time went into remission. My Endo told me to get rid of it but I did not and he got very upset at me telling me, I will never feel normal again. I did not believe him at that time but I wish I did. I always felt very tired but now at my age my fatigue is worse and anxiety is very bad. I have also developed osteoporosis, high blood pressure and high cholesterol. I have decided to get surgery now because i feel i wasted a lot of my life not getting rid of the thyroid. Everyone is different and hope that your condition stays in remission. Stress can absolutely make symptoms worse so please take care of stress. My life has been very stressful. Thanks for telling us your story. Do you know of the best thyroid surgeon in calgary or a really good endocrinologist. Thank you!
Hi there!
Thank you so much for sharing your story. I'm sorry to hear about the challenges you've faced with Graves' disease and the additional health issues. It’s never easy to make these decisions, but it sounds like you're taking a positive step towards better health now.
I recently moved to Calgary myself and have only been here for about a year, so I don’t have personal recommendations for an endocrinologist or surgeon yet. However, I’m sure there are some excellent specialists in the area.
I truly appreciate your advice about managing stress, and I will definitely keep it in mind. Thank you for reaching out and for being a part of this community. Wishing you all the best with your surgery and your journey to better health. ❤
She is 100% correct! I do not have Graves' disease, nor have they confirmed that I have it, but I do have hyperthyroidism. I was diagnosed in 2014 and had every symptom associated with it. One doctor dismissed my concerns, so I switched to another one. She immediately said that I had hyperthyroidism and had me tested to be sure. I don't remember the medication she prescribed, but it worked really well for the year or so I took it. I eventually had issues with my insurance and had to stop taking it for a few months. During that time, I went completely vegan (clean vegan). I no longer had any symptoms of hyperthyroidism until recently, which is a combination of stress and unhealthy eating. I highly recommend giving yourself a few years to change your diet. Do not let them kill or remove your thyroid until you try this.
If you think that you have hyperthyroidism, please go see a doctor and see a new one if the first one is not helpful. You can 100% tell when you have it. I can't explain it, but your body just feels different, even if you are not having any of the major symptoms. I knew mine was flaring up a month before my major symptoms started. Please advocate for yourself and do not take no for an answer.
Yes, I believe if you change your life style that diet can work for some people. It depends on how severe your hyperthyroidism is. I had hyperthyroidism from 2010 but every time my doctors tried to ween me off of carbimazole my symptoms would come back right away. So earlier this year I had the radioactive iodine and I'm now hypo. I believe that more research needs to be done on graves disease to find the root cause of hyperthyroidism. Relaxing/meditation, reducing stress and diet just don't work for everyone. The sad thing about having this disease is that some people can't work because they are in a constant state of tiredness.
@@peitrab4121 since you opted for iodine will you be on medication from here on out?
@@MiiFlawlassSuccess yes, right now my doctor is weening off of carbimazole and will change to my new medication next month. I am feeling so much better so far. No rapid heart beat, palpitations, my anxiety is nothing like before and I can keep down my stress level much easier. I can also do low impact exercises.
I have Hyperthyroidism, but initially my doctors ignored my abnormal lab result (TSH was .02). They basically told me I should be glad to have a disease where you lose weight since that’s what most people want (I was already underweight and had heart issues, which is why I asked for blood work in the first place). After demanding more tests, I received a T3 result (also abnormal), so they put me on methimazole. They never called me at all, I just got an alert from the pharmacy and I also received an auto message that I had an ultrasound scheduled. Then when my ultrasound came back with nodules they ignored that too, and when I reported to them that the methimazole made me extremely ill (I couldn’t talk or walk) they never responded to me. I saw 3 separate doctors at this clinic, because my PCP is always booked, so it's not just one doctor that’s a complete idiot and/or unprofessional. I'm currently waiting to see an endocrinologist, but you have to wonder how so many doctors are worthless.
Thanks for sharing your story. I have T1 diabetes, PCOS and hypothyroidism, so a real endocrine trifecta. My hair hasn’t been thick since I was a teenager probably, and trying to work with it is beyond frustrating. I also have Trichotillomania (hair pulling) that comes on in times of anxiety, and having short hair keeps that at bay. Wigs have been a godsend for so many reasons!
Thank you so much for sharing your story. I had some nervous/anxiety habits as well.... mine was biting the skin around my nails.... it's why I wear fake nails sometimes to get me to stop if I have had a stressful couple of weeks and notice me doing that bad habit again LOL....
I was diagnosed with Hyperthyroidism 2 years ago and was on Carbimazole, My dosage changes on and off for a few months after each blood test (lost weight in the beginning but have been gaining the weight back x2). I was referred by the doctor to the Endocrinology Clinic and was diagnosed with Grave Disease with Hyperthyroidism in March this year.
I was given an option by the doctor to either continue with the medication that may take years to be 'normal' or go for the operation (Radioactive Iodine Treatment) that removes the thyroid gland permanently but will/might have to rely on medication for the rest of my life.
Chose not to take the operation and decided to continue with being on Carbimazole. Still struggling with it due to constant weight gain and hair loss but is Staying Positive! 😁
Thank you, Steph. You are amazing. I was diagnosed with Graves a year ago and I know I had symptoms several years ago. They want me to cut out my thyroid but I have heard that there can be dramatic changes to the voice if you have the surgery. I don't want that. I love my voice.
@@timothyroman3476 I totally understand 🥹 I heard the same thing too. I also heard that taking synthetic hormone (after killing the thyroid or cutting it out) makes you feel… not great.
My dad has to take synthetic hormone and he says he doesn’t feel like himself. Feels synthetic, he says.
Although, maybe it’s a personal thing? Not sure. But that among other reasons is why I really just wanted to get better
That is why you can't trust most of these doctors, because it's always about medication, medication, I have learned that most disease required lifestyle change, mental, physical, spiritual . I have type 2 diabetes, my doc trying to force me to go on medication. I started researching things for myself and decided to lifestyle change ,I also found this cardiologist on TH-cam that I listened to, love this man because he is so knowledgeable and have a love for people, which is hard to find, this man has taught me how to intermittent fasting, food Choices and whole lifetime of knowledge more precious than gold, my A1C was 300, 3 months ago it's now down 105 , I also lost 15 pounds thanks to Dr Pradip Jamnadas , this man teaching is out of this world and he is also very funny.
Hi! For type 2 diabetes I would highly recommend u to try Black seed oil. It’s a wonderful natural remedy for it and for a whole list of diseases. Look it up!☺️
both my mom and grandma have graves disease and where I've never been diagnosed (because I haven't been able to afford to see a doctor in a really long time) I have all of the same symptoms they do. I've been able to manage on a high fat carnivore diet, i do find a I need a small amount of carbs though just can't do more than that. I don't think I've ever been normal :( I've never been able to gain weight, I've never weighed over 100 pounds and I'm 29. my family always tried telling me I was fine and totally normal but I've always known I wasn't. just been praying for a miracle to be able to afford to see a doctor that can help me. I feel like my life was robbed from me and I've had to try harder than most people just to be a normal functioning person. Thanks for giving me a sliver of hope that even if I spend the next several years trying it will be worth it
I'm saddened to hear your story too. I wish you the best..I too feel as you do constantly betrayed by my own body...and others. At least people (most) we can cut them out without further consequences...but our bodies our organs are there for reasons...hopefully we can heal and recover. 😢❤
Thyroid issues definitely run in the family (my mom and grandmother have it). However, once I started talking to a lot of women I know (most not related to me), I found out nearly all of them have thyroid issues. I even talked to a stranger and was told she didn't have an issue with her thyroid, but all 3 of her daughter's have it! I'm starting to think it is also environmental, like something in our food and water is causing it.
You have no idea the difference you have made in my life with this video. Thank you!
I’m so glad I could be of some help xoxo ❤️
I got diagnosed recently. Thanks for this video and speaking about mind body connection and adrenaline. It has really clarified a lot for me. Thanks.
I am so glad!! Wishing you health and recovery ❤️
Ditto.
Hi... I feel really gratefull found your videos and see you in pregnant period, really boost my hope again. I thought I cann't even be pregnant. Thank you so much for make this video, some people who lived in the country that still have less literate about autoimun and thyroid problems will found this video really helpfull and inspire. I am just 2 years being diagnose hyperthyroid grave disease in still in hopeless mode before I found this video.😊
I agree with u 💯 this is what I just told my son that STRESS was the biggest factor on hyperthyroidism....and I'm like u I don't want to do the iodine radiation or surgery...I'll take the methamazol and do as u reduce /control stress(which is my husband) I was so good without him I was so healthy and no stress when I left him...I knew that the minute that I moved back in with him I started to get sick with everything!!! I keep telling everyone that he is the sole problem to my health declining...u just confirmed it...cause if ur body/mind doesn't stress then ur hormones, and all body organs work together as they should...amen🙏🏻
Yes!!! That was the same with me and my ex. I swear he made me sick…. When I left, I felt better. Whenever we came back together, I got sick again. This is 100% it. I’m so happy you’ve come to that realization for yourself too.
Freezing bread and then toasting it before you eat it gets rid of much of the starch and sugars in it. I hope this is helpful. Thank you for sharing what you have been going through. Congratulations on the baby. ♥ You have a beautiful spirit. I wish you and your family the best.
It’s the gluten that does thyroid suffers in..
@@In_timeNot true for me, I am gluten free and was diagnosed with graves.
@@SparkyOne549 _“does thyroid sufferers in”_ as in _doesn’t help us._
@@SparkyOne549Did you know that there are various other kinds of gluten apart from the most commonly found in wheat.,barley and rye? If you really want to be totally gluten free, you should avoid all grain. More information on dr Peter Osborne's videos.
@@grace-dt7tu I’ve been gluten free for decades, I know what not to eat.
This resonated with me so much and our story is extremely similar. I think I am just a few years behind you 😊 I am in my second time of my Graves’ disease and hyperthyroidism flaring up after just over a year of remission and I would put all of the money I have in the reason of stress and anxiety. Just like you I am a TH-camr but I also have another full time business and I have two little ones. They want to cut my thyroid out and I am refusing. I want to stay on medication again for a bit and see if I can do it again. I have never experienced losing my hair though. Everything else you explained I have at the moment. The shakes being the worst as I am an esthetician and it’s embarrassing. I am going to go and watch a few more of your videos on this subject as I get a really lovely energy from you. I hope you are well 😊
Thank you so much for making this video, would love to have another in depth food choices you had to made during and after remission, also please make a video how you reversed your eye condition and when you started noticing the change ?
New diagnosis in Feb I went thru the storm and I'm alive but I need y'all
Same
This is a superb video!👏🏾
Thank you for sharing your testimony.
Wishing you a safe delivery and a healthy baby .
May God bless you and the baby🙏🏾
🙏AMEN🙏
Hi Steph, I am so glad that I stumbled upon all of your videos. I have been losing my hair for a few years due to alopecia. It has been very frustrating, heart wrenching, emotional, and hard. I used to have very thick, beautiful, curly hair, and now I am, almost bald and I didn’t know where to start with wigs, but I stumbled upon your videos and it has helped me so very much. I’m excited to actually learn more about wigs and to start getting some wigs so that I can feel confident again. Thank you so much for your channel. Thank you so much for your videos. I enjoy every single one of them.
Hi Valerie! Welcome to my little wig family ❤ I'm so happy to have you here. I feel everything you've just spoken to me.... oh my goodness, hair loss can be so challenging. It can be difficult to see past it sometimes. Wigs have honestly changed my life FOR THE BETTER, in SO many ways. Like, to the point where the average person doesn't know hair loss is something I struggle with, because wigs look SO real these days that nobody gives it a second thought, and it truly has given me my confidence back. I wish this exact feeling for you!!!! I can't wait to hear more from you =) XO
Seven doctors until one listened. We badly need a system rating doctors so if they're not good they get fired. They have no consequences for being terrible at their job.
Thank you so much for posting your experience. I am going through Hyperthyroidism and Graves Disease. I hear the same things from my Drs. It has been the most frustrating experience for me . I am currently trying to do exactly what you are talking about. I'm getting my diet under control, next is a exercise program. Your story is very encouraging, so I thank you ! Congratulations on your new baby ,I wish you the very best !
Breath or fresh air ❤ I was almost forced into getting mine removed or RAI , I also refused. I am on a low dose of methinazole and will be fine with it until I can also find ways to go into remission. Thank you so much !
Wow thanks for this video, I was thinking I have to live with this for life... I'm 29 male and my heart beats like crazy if I don't use my pills... Having difficult for finding clothes for my size (skinny...) I'll try your tips.
I regret taking hypothyroid medication when I was first diagnosed 7 years ago. I always wonder if I would have gotten into remission had I taken a more aggressive, holistic approach. Why? Because I saw a difference in my labs within two weeks of natural supplements, but I was still symptomatic. Unfortunately, I didn't have the guidance or support from medical providers then, despite seeing a Naturopath, which I later fired. I remember doctors telling me this is a common disease; you just need to take Levo, and you'll be fine. Essentially, dismissing the disease.
Flash forward, I achieved remission once; my antibodies were under 30, which doctors consider remission. However, I was still symptomatic. Now, since seven months ago, I have lost over 70 percent of my hair. It's devasting, to say the least, especially having been dealing with it all these years. I now own two wigs.
So sorry you had so many bad doctors. It took two visits for my one doctor to diagnose me. Kick anyone who doesn't listen to the curb! I'm glad you're doing so much better!
I hope and I pray to God that I can be healed just as you.. More power to your channel and Godbless! ❤
Taking biotin 1000 mg a day has h lord my hair grow again. My hairdresser shared this and I am so thankful!
FYI biotin interferes with thyroid tests
Thank you so much for your story. I just god diagnosed less than a month ago and it’s hard and scary. I was doing fine when they gave me the medication. Its when i found out I couldn’t stop having headaches so we went to the doctors and got me to see an endocrinologist. Now I’m having joint pains that they don’t know about like when i move my arm or legs it would hurt badly but if i was still id be ok. And right now in the bed in the hospital i feel like my heart is weak and weird and heavy feels like it’s going to do something lol. Im just scared right now.. I hope people see this and understand please!
I have hyperthyroidism since 2011 (the first I was diagnosed). But I’ve had all the symptoms years before that & I’m just dealing with it as anxiety, social awkwardness etc…
I’ve changed doctors 3x because with the last 2, I just got worst. I’m still on the same medication and see my doctor quarterly and she adjust my meds depending on the lab test results. She did suggest RAI therapy 2x which I refused. It’s really managing the stress and diet and exercise that makes you better. I’ve never been on remission because I still eat the food I’m not suppose to and not getting enough exercise
I was diagnosed with Graves disease Hyperthyroidism about 5 years ago. The HUGE stresser was the death of my youngest Son Austin. Depression and anxiety meds really screwed up my stomach, and now I'm taking Methimazole for my hyperthyroidism. My Endocrinologist keeps wanting to either remove or do radioactive iodine to kill my thyroid. I won't do it. He also doesn't believe that diet plays a part in healing the thyroid. I found a holistic, alternative Doctor. I wanted to get off of the meds for depression and anxiety, which I weaned off of. The holistic doctor has me taking herbs and other natural things to heal my stomach and my thyroid numbers are getting better since my stomach is healing and my diet is better. The Endo doc has slightly decreased my Methimazole. I go every 6 weeks for blood work, so we'll see what my numbers are after the next blood tests. When I saw my Endo doc a few weeks ago, I mentioned that I was seeing the holistic doctor, and wrote down what he has me taking, and my Endo doc wouldn't even acknowledge that since I started healing my stomach, AND better diet, my thyroid numbers are getting better.
I am so very sorry to hear about your son. My Endo was the same where she wouldn’t acknowledge diet, and made me feel so silly for thinking that would help me. My dad is also a doctor, although retired now, and he was really the only one in my corner that supported me and kept telling me my whole body was connected. If one thing was off, it can throw the rest off. It was that idea that kept me looking after my body, mind, stomach, and once I reached a place where I was mentally strong again, physically, and healthy with what I ate, everything changed. It took my body a long time to go into remission… but it still happened. And my Endo doc was so wrong. I saw many Endo docs (not sure if I said that in this video- but because I moved about three times, I had about three doctors who all said the same thing and wouldn’t acknowledge diet or any opinion I had on my own health.) You’re definitely doing the right thing. Especially if you’re taking all the necessary steps to feel good again; nobody knows you better than you. Thank you so much for sharing your own story with us.
What herbs are you using and kindly share with us what changes you have made in your diet/ lifestyle
I was just diagnosed with Graves & Hyperthyroidism. I'm hesitant to take the medication. I'm still learning about my diagnosis & I'm interested in how I can change my health on my own. Thank you for sharing, I definitely needed to hear what you had to say!
You need to start something soon. If you don’t get treatment you could get worse from the hyperthyroidism symptoms.
@blancagutierrez Thank you, I actually started taking the medication this week. Looking forward to feeling better.
@@riv30333how are you feeling now?
I started taking my medicine Bec this illness is so crazy.
@zenytamboongstark4485 it's been less than a month since I started the medication, and I already feel a lot better, and my blood work has improved!
I have psoriasis and probably other autoimmune things going on, but the psoriasis is causing my hair to fall out. So, I am exploring the idea of wigs and am happy to find your channel. Thank you for making it!
Am so glad i found your video! Everything you say and did is exactly my journey!
Hello i have hyperthyrodism and i took medecin for a year,was on a remission for a year,now i am out of remission iwent under stress and depression that flared up my hyperthirodism im on medication now a week ago im considering gluten free and dairy free diet to heal my immunity i have graves basdow desease your video just put some hope inside my heart ❤
How are you doing now
My hyperthyroidism trigger from stress!
I was in remission and had an AFIB episode please keep that in mind this condition can affect the heart
Thank you so much for your story. I just god diagnosed less than a month ago and it’s hard and scary. I was doing fine when they gave me the medication. Its when i found out I couldn’t stop having headaches so we went to the doctors and got me to see an endocrinologist. Now I’m having joint pains that they don’t know about like when i move my arm or legs it would hurt badly but if i was still id be ok. And right now in the bed in the hospital i feel like my heart is weak and weird and heavy feels like it’s going to do something lol. Im just scared right now.. I hope people see this and understand please!
Oh Im also going to do radio active iodine this week so thats good I guess.
This is so helpful! 10 years of declining health and I think I finally know what my deal is
It’s so wild that they didn’t want to test your thyroid levels, when that’s part of a normal routine blood test (I have hypothyroidism and didn’t have to specifically ask for them to test for it initially; it was just part of a yearly physical exam).
My misdiagnosed Graves Disease was, in fact aspartame poisoning. It was as simple as removing aspartame from my diet and my thyroid function is normal. Aspartame is in almost EVRERYTHING labeled "sugar free" or "diet."
This is my first time watching your video I just barely found it on TH-cam I'm glad to be here I will find out and get back to you and leave a comment of how my friend got all her hair back and stuff and thank you for your videos
LOVE your video congratulations on great health and your baby. One tip Ive learned while studying GD is you need electrolytes to help the receptors on your cells during the T3 and T4 conversion.
Trace minerals in drinking water is the best way to get these.
I read something about that thanks tons. I couldn't find the info to quote the guy...and also..man it doesn't make sense to cut out the thyroid just to function properly
..in extreme cases maybe..but still..and also cutting out necessary food like eggs..and meat and liver sounds bizarre to me too if our bodies need those nutrients. Same with fish...like I hear cruciferous veggies help block excess absorption of idodine from those sources.
I really am not sure why my hair has fallen. I do enjoy wigs for me it is more work but I do it because I look so much better with it. Also wear wig grip like you I feel like people can see the wig grip but it is what it is. I am thankful that I have the wigs available to me.
Iam also Diagoised with hyperthyroidism and recently noticed Hairfull like never before and it breaks my heart😢😢
I love your videos Steph. You helped me so much when I first found out I had breast cancer and I’m still watching you today. It’s been several weeks since I had chemo and I still don’t have any hair. I’ve bought about 5 wigs although when I’m at home I don’t wear them either and since I’m retired I very seldom have any place to wear them but I do love them. All because I saw how real they looked on you.
I was diagnosed in December last year meds weren’t working at all making me extremely sick I have 2 kids so my only option is rai and surgery so I am scheduled for surgery Oct 1 really hoping I can go back to living normal after surgery
Same for me. It's devastating for me
OMG Steph, I think that's what my Dr wants to do... cut my thyroid out and I'm not sure about the iodine.. they want to do a REE on me next week!! I feel kindred spirits with you 💕 and and the information you give is so valuable!!!
I will do it your way , it's safer for my body... I don't eat much sweets but crave cinnamon graham crackers!!!🤔😳go figure 😅 congratulations on your marriage, the move to Calgary and of course your pregnancy...Step, I love your honesty, your truth and your stunning beauty.
Double Congratulations 🎉🎉🎉
I never heard Graves disease and hyperthyroid as two separate things, or that you can have Graves disease without hyperthyroid. I've only heard them used synonymously.
This was so helpful thank you . I have the same as you . First time to hear this properly with what I am going through, stress flairs it up
I just diagnosed with a greave disease. Thank you for sharing your story
This is so helpful I was diagnosed 5 months ago after experiencing many of the symptoms you spoke of.. I’ve been given option of thyroid removal or rai as haven’t had any remission -would prefer to heal myself thanks for this - it’s encouraging to hear! Any recommendations re- diet / lifestyle appreciated ❤
Thanks for this chat Steph it's very helpful. I should like you do a chat about handling stress and anxiety please. By the way your baby bump is soo cute 💝 sounds really lovely where you live x
I have graves, dx 2 years ago. All was okay until recently and now I have TED and thinning hair, no energy. Never considered removing my thyroid until recent symptoms with my eye. I’m torn.
Thank you for your inspiring story.
When you felt that you were out of remission, how did you fix that?
Wow your story sounds just like mine, I also flare up with stress, and when I get that under control I go into remission gluten free food is also key!!
I got surpriced after 12 months of keto and massive health provements and still had mild heart attack. The main cause for that was my hypothyrodism that i was diagnosed when i was in hospital few days. I had to start taking thyroxin and all the health issues that hadn´t improved doing keto disapeard. I had symptoms for that at least five years but i tought most of those were part of getting older. But i am 43 now, so i´m not that old yet that those health issues should appear. Well now it´s been over three months and i still do keto and i have recovered from that heart attack quite well. Also my thyroid hormons are great. I think that if i continue keto long enough it can fix my thyroid completly.
I’ve been diagnosed almost two months now. I’m on amlodipine, atenolol and methimazole. For side effects I am taking water pill and potassium chloride. Most days I feel completely fine. I’m actually gaining back the strength I lost in my arms and legs. I’m feeling a lot more energy overall. My biggest complaint at the moment is never feeling full and always feeling hungry after eating full meals. It’s frustrating that with Graves or a mixture of the medication has affected my gut of feeling hungry.I’ve gained weight, lost some, dealt with swelling and treated it. I guess I’ll have to figure out ways to combat my hunger.
Ketogenic diet done properly will help you to lose a lot of the hunger pains and weight, too. I used Dr. Boz's, (Annette Bosworth, M.D.), program called "Keto Continuum". Dropped 22 pounds in 3 months with 12 more to go. The Graves is what makes us so hungry.
@@lj5027thank you, I’ll look into it.
Updates: All of my levels are in range now. Wow what a rollercoaster! I went from Graves to Hashis and in between. Now with meds adjusted I am in range now, thankfully 👏🙏🏽💛
Could you share more about what you did with your diet beyond low sugar / whole foods? Did you eliminate anything?
I've benefited a lot from dr Peter Osborne's videos on curing autoimmune diseases with a proper diet 💚
Please continue to share personal information on this and other concerns.
Thank you for your information I too have graves hyperthyroid totally not my self you gave me such a i spratation to know things can change I have totslly giving up on my doctors ever finding answers to a problem
Hi I just want to say about the hair growing back part don't think like that if you stay positive and keep taking care of yourself living life aiming for the goal you want and are trying to achieve before you know it you will get it I have a friend of mine she lost all her hair but I'm talking about completely bald to where she couldn't even leave the house and it took a while it took years but she got all her hair back and even more thicker than she had it before and she was born with curly curly thick hair from completely losing at all she got all over the back and like I said even more all her curls and everything so forget whatever they tried to tell you that your body will never be the same yeah it won't because it will be even better
I have adult type 1 diabetes so my thyroid was well monitored. Tested in April and all was normal. In October I noticed my resting heart rate was high. Went to a cardiologist and after lots of testing could not find anything wrong. Also ended up in ER with speech difficulties that went away. Decided to test my thyroid labs. I am a nurse so was next logical step. My Endo was so shocked when it came back hyperthyroid. Wanted to do radioactive iodine but I also had thyroid eye disease. So was ruled out. Had great results with methimazole. Endo still has me on 2.5 mg a week. So that’s doable. Did have Tepezza infusions for TED and that was successful. That was not fun. Endo still asks if I want to ablate my thyroid at every visit. I’m like duh why.
I should get my larger panel back in 2 days but my current thyroid panel shows hyperthyroid. Dr said i had anxiety but i feel it is something else. I guess we will see
My friend has graves disease, no hairloss but his eyes pop out
My eyes popped out too... In my other video I talk about all my symptoms. My eyes really bothered me... especially because one popped out more than the other. I thought it was very obvious, and unfortunately I had that symptom for a LONG time. Years. That symptom and my hair loss annoyed me the most
For hyperthyroid you can take shatavari capsules along with weight gain formula.
Plzz tell about weight gain formula...
@@NnaNanakak It is an herbal ayurvedic medicine prepared by planet ayurveda. You can search it and order online.
@@NnaNanakak It is a natural remedy formulated by 'planet ayurveda'. You can visit their website and order online.
And just to introduce myself real quick I am 39 years old female I live here in Las Vegas but I am originally from Yugoslavia but have been in the United States for over 20 years used to live in Los Angeles but we're in Vegas now and I like it here but I do love to travel too
At the local lab -- the phleb told me they removed her thyroid due to hyperthyroidism and she gained 100# and NEVER to thst day got her thyroid balanced even when on the repacements. What a warning ⚠️
Omg that wig suits you. You would not think its a wig. My god its liks your own hair ❤