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Dr Child's My mom who had been on Levorthtyroxine 60 mcg for the last 40 yrs . Now she switched Armour 60 mg is that the right conversion. Bcuz she for this last 3 months feels tired,Weak . she has always been active til all this. Please help. At least if at 60 mcg lev.to Armour 60
How can we get off Levrotyroxine? I've gained @ 50lbs since starting it with and I'm very active. Gym, daily walks, garden, run a house alone yet I can't l I se a pound.
I've been taking levothyroxine 25mcg for many years. I'm a Type 1 Severe Brittle Diabetes for 41 years. I've put on so much weight. I have fatigue all the time, nails issues, hair loss itchy all the time. Even scratch myself while sleeping when I sleep. Being overweight is extremely depressing don't feel good often daily. Use Iron vitamin as also Anemic among other vitamins along with prescription medication. I had taken Synthroid in beginning when started having Thyroid issues have had an overactive n underactive thyroid through the years. Was taken off Synthroid due to health insurance. Wondering if should ask my Endocrinologist to take me off levothyroxine 🤷🤷🤷🤷. I'm tired of sleeping all the time n feeling like CRAP 🥶😞
After seeing you talking with Dr. Jeffrey Welchel, I made an appointment with him. I had a near total thyroidectomy fourteen years ago, and I am having a lot of breathing and talking difficulty. I am really hoping he can help me get rid of my nodules in my neck. My ENT recommended I remove the remaining part of my thyroid.
I have been on Levothyroxine for 20 years now. I live in the UK. Since I have started I have gained weight and find it near impossible to lose. I was a healthy weight when I was diagnosed. I always feel tired and or low mood. I have my blood tested every year. I don't know why I bother. I just get given the same 100mg and 'healthcare' just keep pushing Statins (I refuse). My thyroid is NEVER discussed. I have decided to take my health into my own hands. I find channels like this and the discussions most helpful.
Me to. Been on levo 15 years and tested 1x a year. I went to the doc since I had big fatigue. He wanted a sleep study that I refused. 6 Mos later the fatigue got worse to the point I was mentally drained and it was a huge effort to get ready to go to the store and I only left home when I had no choice. I couldn't sleep no matter how often I tried but if I did sleep I'm awake 4 hours later feeling exhausted. I literally would drink a pot of tea and still not have an energy burst like when I was younger. My dog got into my pills and I can't find the bottle if levo. The dog didn't eat them or I would have found a chewed bottle. That was a good day! Been a few months since I took the pill and I'm so much better. I sleep, feel rested, don't lose as much hair, swelling in my feet/ legs have gone down. The weird shooting sensations I was having in my body quit. My thinking is more clear, I'm like a new person. When I go to the doc, I'm not telling him since I want to hear what he's says about my labs. They don't understand thyroid, think it's an easy fix and don't want to problem solve. Years back I told a nurse I was to tired, sleeping alot, she snickered and wanted to know what's wrong with it. They are A-holes and are a waste of time and money
I asked my doctor to switch me to levothyroxine plus liothyronine when my NDT was recalled. I lost weight and felt good. She freaked out when my TSH dropped too low! She sent me to an endocrinologist when she couldn’t fix my TSH and after fiddling with my dosages, which messed me up. The endocrinologist refused to do a reverse T3 when I asked her to and left me on 88 mcg levothyroxine and 5 mcg liothyronine. I gained 10 pounds almost overnight! I’ve had Hashimoto’s for years and had convinced my doctor years ago to put me on Armour thyroid, until it became difficult to get and more expensive. I thought the combo would be easier to manage, but sadly, it hasn’t been. It’s tough finding anyone who is actually knowledgeable about Hashimoto’s where I live because I follow you and other more forward-thinking doctors. Patients now know more than the stuck-in-the-past endocrinologists. I appreciate you sharing your knowledge; I’ve learned a lot. Im searching for a new doctor.
I’ve been taking this medication now for over 8 years having had a Thyroidectomy in 2009 when I lived in Canada. I went from 170 to 260lb’s I think finally watching your videos you have educated me so much. I’ve started to add extra vitamins into my body. And I’ve just gone really big on putting smoothies into my body made of fresh fruit and veggies... I pray this will help. I’m 57 and my hair is fine now but my nails are brittle. I live in the U.K. and once this lockdown is over I’m definitely going to have another chat with my Dr. My dosage is 125 a day. Thank you so much. You really really have helped me.
FYI: I started taking Collagen 3 mons ago and for the first time in my life I had long nails and they were very pretty polished. Unfortunately they were also very annoying. Anyway they r very strong now but I keep them short. Hope this helps.
Levothyroxine is working because my test show good results, but the medicine make me highly irritated and very emotional 😭 and that’s me taking .25. I’d rather try natural remedies. Good video 🤙🏼
Me too. I’m so tired of all of this. Now I can’t sit in the sun, because I break out in hives on my legs. My hair is ok for a minute then it starts to fall out. My weight is out of control too. I’m scheduled to see a endocrinologist, hopefully they can help me.
Thank you for this! I have had hashimotos for 20 plus years. I am 5’9 and went from 127 to 175 in literally 2 years. Recently had cytomel added 2x a day.. still can’t lose weight and still sluggish but running 5 miles a day
@@pamc3338 I gained over 100 pounds.. I began having fruit smoothies in morning.. Baked pond fish and salad at end of day.. I lost 30 pounds in 2-1/2 months.. I tried other diets but this is only one worked fr me.. I eat only natural foods.. No boxed or additives.. al fresh.. if you can try it.. Good luck..
I ahe hosimoto .I was in bad shape atc2l presently taking 235 mcg I weig 109 to107 Stain to not loose any more.iam 175 .feel bad have naropathy hands and legs.and feet have one hip. Replacement early dementia.
I have been diagnosed as having hypothyroidism and I started Levo this summer. But I've had problems with worsening fatigue. I felt like I was MORE tired now that I'm treating the hypothyroidism than I was before I even tried treating it. Because of that, I stopped taking them. Then I tried half a pill at nighttime (so I could sleep off some tiredness). But I started to get more tired again. It's frustrating wanting to treat it but feeling worse when getting treatment.
I am experiencing the same thing, needing to treat it but feeling worse. My doc got so frustrated with me that he accused me of making things up...so I no longer talk about it to him.
Total thyroidectomy here... My Endocrinologist was not helpful. I was prescribed many different Levo pill dosages (all colors) I stopped taking the levo because I was miserable (dangerous, not advised) My PCP took me off Levo and put me on the brand name med, Synthroid. I also take 5-10mg of cytomel . I am no longer in pain everyday! I seem to be losing weight in my abdominal area. It's only been 1 month but I am much happier. I am learning from youtube to help my doctors help me!
I got worsening of fatigue, but also sensitivity to cold air. So idk what’s wrong. I felt great the first day I took it though. Calm, clear headed, but then I didn’t so I quit
Thankful I found your videos. Left sub-total thyroidectomy 20+ years ago. Began losing hair about 2 years ago, dry and brittle. Levothyroxine @ .112mcg. I generally have to ask the doctor to check my TSH, and that's about once a year. Male pattern baldness, and serious thinning, ready to shave my head. I will look at all your videos on the thyroid to see what I can do to help myself. I was having serious fatigue and began taking Iron tabs a couple of weeks ago. I am feeling better. Will check that ferritin level. Thank you, again.
I stopped taking it for around nine weeks and my TSH levels were scary, to my doctor. I started taking it again. I don’t notice any benefits or negatives either way. However- I feel crappy all the time, every day. 🤷♀️
@@mrsmacca126I feel the same way & wonder if an additional T-3 medication might help now since my T-3 levels have gone down also. Or keep consistent w/ natural supplements first (Ashwaghanda, selenium , etc.). Don't give up & keep the faith!🙏
Thank you so much for the information you provided. You taught me everything I needed to know about hypothyroidism. I experienced side effects of this med. I have already changed my diet. The only thing that would be hard to quit is coffee, but no one ever gave me accurate information. Again, thank you so, so much.
This was so helpful. Thank you so much for doing these videos for us. It's so hard to get any answers of doctors they are not very informative. Also it's hard to find such detailed information. This is very valuable and helpful. Paula England
I had a concierge doctor tell me I had Hashimoto’s about two years ago. Come to find out, im at-risk for it but don’t have it yet. She put me on compounded T3, T4, supposedly to correct my need. In the meanwhile, I’ve progressively felt worse and worse. Now I’m trying to make sense of what the hell has happened. 17:21 yes, all of these symptoms and plus convulsive vasovagal syncope episodes, one of which resulted in a pretty serious head injury. During these epidsodes I was somewhat alert but had full on ataxia, loss of language, temperature dysregulation, vommitting, and unable to work many days. I just lay here and think about what I need to do. I didn’t even mention that I also started having tachycardia and had to have an ablation and a septoplasty, turbinate reduction surgery due to not being able to breathe. Do you think I should do something about it or just chalk it up to experience? How to I recover my body and health from being improperly medicated for this long?
i am on 175 mcg and now take 3x50 - these dyes/fillers were killing me! its hard to find someone in Calgary, Alberta that understands.... i'm very grateful for your knowledge Dr. Childs as i'm looking to a community for support. its been 27 years of struggle (started at 20years old) and i'm determined to change this. Working thur all your video and changing up my lifestyle, eating habits, diet, supplements, daily work outs and so on. Down 26lbs and feel 80% better. its been so hard - but nice to hear your thoughts & support! thank you!! i am definitely going to get all the tests redone as per your suggests as my TSH was about 310mIU/l in January prior to me taking charge on my own.
This is an older video, but exactly what I needed!!!! My Endocrinologist won’t add T3 for me and I feel awful most of the time!!! Trying to run around finding a new one in our area is nearly impossible! When in Georgia my Endo had me on a very small dose of Cytomel and I felt so much better!
For what it's worth, my pcp suggested T3, and while it did give me more energy during the day, it horribly disrupted my sleep. Then, the next day after I didn't sleep, I'd feel actively sick, irritable instead of mellow/tired (that's the one upside of being hypothyroid, for me--I'm so tired I don't have the energy to be irritable,) and after a few episodes of this, I decided it had to be the T3. It resolved when I quit taking it. I'm probably an anomaly though
A lot of people who are on levo don’t need to be on it at all. I was put on it 10 years ago when it was “drug-of-the-year.” I have slowly weaned myself from 88mcg down to 22mcg. Doing fine and looking forward to being completely off in another month or two. No, I didn’t see my doctor- who is not my body’s God.
I thought and did the same thing. I moved and didn’t have a doctor so I was off Levo for two years. I did good up until a few months ago my symptoms came back ., anxiety got really bad again also heartburn. Weight gain . I’m 5.9 207 pounds now. I was 160 lbs up until a few months ago. So be very careful coming off Levo thyroid meds . You may feel good for a year or less but then it hits again sorry too say .
I have been on this drug for 6 yrs now , and I've had no problems at all , my blood is tested every few months , I'm glad to be on it because I was ill at the time and the weight loss was bad , I have an over active thyroid and was told by my consultant I had graves decease .
Ive been on levothyroxine for about 7 years. In the beginning it made me feel better, but for last 5 years i feel bad all time with body pain allover. I exercise all time and eat small amounts and very healthy food, but cannot lose weight. I believe its the levothyroxine so i know doctor says you have to take for life, but im gonna stop taking it and see what happens.
I also am having the same symptoms as you have, Dr. said my thyroid test said my dose was to high, but I was gaining weight, with no appetite at all.., listen to this Dr. and he said instead of T4, start taking T3, so I have just started and am starting to eat a bit more and am losing weight, I went from 163 down to 148 in a few months while eating more...my weight use to be 115 to 120 lbs., 5' 7", so this extra weight was really pulling me down, it was so hard to be carring all this extra weight, and I eat like a little bird, really I never feel hungry, I have to be told to eat as I never think of eating.
I used it for 3 years. So much side effects like gaining weight, rash, breathing problems, burbing when i get outoff bed for long time...i took 75 mcg. Was so fad up of it, stopped radical to see what will happen. Within 2 weeks all side effect were gone !!! For 3 months, then my hormons started to drop....then i had to take something like tirosint. 2 y on 25 mcg. I got hartpalpitations... now i took 13 mcg more for half year but with bloodtest it had no effect totally!! If 13 mcg doesnt work what does the other 25 then??? Now i took again 13 Total 51mcg. My weight started to go up again.... i think for sure under my skin i see fat and water building up. Around my stomach is the worst. After 7 years still didnt work proper. If raising up meds doesnt do....then i try to stop with it or take less as possible like 25
I had been on levothyroxine for 30 yrs. My new gp took me off it because she said that older folks (I am 82)don't need it. In the meantime I have been dx with st. 3c endometrial cancer, had a hysterectomy and am now on chemo. My onc. put me back on levo. because my tsh went up to 9.5. I am now realizing that the symptoms I have been having may be because of levo. Onc said chemo can cause the tsh to go up. My symptoms are burning across my shoulders, bp up, anxiety.
Have you suffered some kind of side effects at that dosage? I am 25 mcg I feel stable but I sleep all day long, then I got over 50 mcg and I get energy but a little warm and sometimes it is hard to sleep. I am confused. Both doses doesn't work at their best. 😑
I'm on 75mg, 50mg, alternative, I am having progressive trimmer to shaking only on my left side, also started feeling heavy some times in my heart, other time right across my chest, other time in the lower part of my body. I'm not on any other mediation. Trimmer only affect my left side only
I've been taking synthroid for years and I have never felt any better. My hair loss didn't change and got worse. I am gradually losing more and more of my eyebrows and other body hair. I'm always exhausted, I've gained weight despite the fact that I actually don't eat a lot. I have T1 diabetes which I've had for 54 yrs. I started taking thyroid medication when I was in my 30s which was 30 yrs ago. I have never felt this was the right medication for me, but I cannot get my doctor to listen to me about it. I have a lot of other health issues and he will just put some of my symptoms down to those. I have a connective tissue disorder which causes arthritis etc and I have fibromyalgia which seems to come along with the connective tissue disorder. I have memory loss as well. I don't know how to get my doctor to consider something different.
I totally sympathise. I have been taking Levo for over 20 years. I have a blood test every year and they just give me the same dosage (100mg) and can't be bothered to discuss further. I have decided to take my health into my own hands. Forums like these help.
Frankly, I don't care if the reaction I had was due to a filler. Levothyroxin landed me in the hospital with severe heart attack symptoms. My heart was tested in every way, to the tune of many thousands of dollars out of pocket. The good news was, my heart was fine.
Interesting presentation. I am on 125 MCG, levothyroxine after being diagnosed with Grave’s Disease and having a total thyroidectomy three weeks ago for papillary thyroid cancer.. I take my medicine as prescribed but still have all of the symptoms related to Grave’s Disease and hyperthyroidism. It is very annoying because I assumed that things would instantly change once my thyroid was removed. I had my follow-up with my surgeon and we discussed the pathology report which was a confirmation of the initial diagnosis and metastasis into a few lymph nodes. I see my endocrinologist next Tuesday and will discuss this issue with her. I know I will be having radioactive iodine treatment. I just want these awful symptoms to go away.
@@meggiedemy6459 I take the medication because I have no thyroid after surgery for metastatic papillary thyroid cancer. I have to take the medication for my metabolism. The dosage has been lowered. My medication is correct.
@@tonis19891023 Before surgery, I was very hungry eating everything but losing weight. I had insomnia and horrible night sweats. There was no pain at all. When I mentioned this to my primary physician, he asked if I had any family members with thyroid problems. My mother and sister both had under active thyroids and had partial removals. He ordered blood tests that indicated an over active thyroid and I was diagnosed with Grave's Disease. I was referred to a surgeon who felt nodules on my thyroid. I had a biopsy which came back as papillary thyroid cancer with some metastasis.
Have been taking Blackstrap Molasses (2 teaspoons mixed in milk) daily. Has iron, magnesium, manganese, calcium, B6 and have always had glossy full head of hair. However since starting Levothyrixine, hair is dry, dull, and thinning....scary!!
I went through a rare they say very rare thyradic storm which almost killed me by preventing them to perform surgery on my lower intestine which split open why in the er exam room also finding out i had a hole in my intestine fo awhile and was told due to my thyroid I wouldn't survive the surgery well here I am and thank you to all the docs and nurses involved at Ben Taub Houston
Hi been diagnosed with the Hash.sevral years ago. Of course, first medication he rx-d me was the levo..I hated it I gain weight and felt tired,but my numbers were "normal"🙄 I was upset because I kept gaining weight. Currently I take a pork gland and it seems to work better for my body. My insurance stinks so it wont cover the the good stuff. Nature Thyroid isn't manufactured anymore, that was the best for me. Armour thyroid is great too! Then my new insurance kicked in and kicked that out. Lol! So now I am on NP Thyroid meh its ok, I am going to check your videos on thyroid supplements and take them in conjunction with my NP Thyroid. 😊 Thank you so much for your work. You have helped an insane amount of people. ❤
I know this is an old video, but thanks for making it. I have a history of side effects from medications. I’ve been on levothyroxine for about ten years. I have lost about 90% of the hair on my head, and have NO hair on my arms or legs. I’ve mentioned it to the doctor, and it has never really been addressed. My old provider retired, and the new guy seems to see me as an old lady waiting to die (I’m in my 60s), and isn’t much help. He just likes to write prescriptions.
I understand. I’m just getting into the thyroid hell. Tomorrow I’m having all my hormones tested, another metabolic panel, as the thyroid test is still high/ hypothyroidism, yet my symptoms are the opposite. I have enough med conditions, and this adds to it. FEDUP
Ive landed in the ER twice with this medication and had to take time off work due to the side affects, i can fuction in normal daily life eg causes my one side of my body to go numb, unbelievable nausea, head pressure, face and head numbness, feeling so so unwell but my doctor wont change it to something else, even after being in the surgery waiting room nearly passing out and crying for help on visits. What the hell can i do, i need to go back to work.
I have hypothyroid issue and take 75mcg levothyroxine.My weight was 48 kg. My problem is that after continuing my medication i starts losing my weight so fast and feel tired and irritated.i lose almost 3 to 4kg.I never gain weight even before or after medicine.Any suggestions..? I more have symptoms of hyperthyroidism like bloating,weight loss, palpitations,hair loss but my tsh is 21.
worsening fatigue is listed in both less common and more common sections :) I'm taking 50mcg of levothyroxine at the moment , i was on 25mcg a few months ago which had no impact but now on 50mcg i have some of the symptoms mentioned including feeling warm in the face area like hot flashes, i also seemed to have developed some reaction to a moisturiser i have that i never had before but using another one now ( i do have sensitive skin) skin is sometimes itchy as well around face and scalp and i still get tired too often as well . i am due another blood test next week as been on these ones for nearly 3 months so i will see if anything has changed but will mention these side effects as well. very informative video :)
@@shearosamamacita The medicine industry is a BUSINESS.. FIRST AND FOREMOST. A very lucrative one. It's a one-size fits all system. If your TSH testing is off... Levothyroxine is prescribed...it's the drug big pharma peddled to EVERYONE w thyroid symptoms. I haven't known one person taking it whose thyroid symptoms improved on that pharmaceutical. NOT ONE.
I also do the hot flashes, I’m 72, itchy skin, especially at night. I use Neutrogena Hydroboost. Then my dermatologist recommended it to me but was already using
❤❤Doctor knew I had thyroid problems for 10 years before it showed up. Had test 3 days before I had diabetes and it showed up then. I've been on lev. for 30 years. I have always taken .025 mcg. It does show up any time they check it. So what to do? I've had hair loss and cold all the time. I take it alone an hour before breakfast and some time I don't eat fir 5 or 6 hours after taking it.
Ive learned so much thru this video! Thank you! Im on Levothyroxine and struggling in almost every way mentioned here. Im gonna get another doctor and see what I can do. Ive lost so much hair. Looking forward to feeling better and getting some hair back.....
I had my whole thyroid removed 9 years ago and have never left good since. I still have traces of cancer left in my body so my doctor says that’s why my Levotgyroxine has to be so high. Do you think you could help with my situation and are you still conducting the 45 minute phone calls. PLEASE let me know thank you
Dr Childs, I'm on Levothyroxine for a few years now. Put on weight and worse all my hair thinning so much and handfuls of hair falling off in shower every day. I always had Insomnia though. Don't know what to do. I walk much every day and eat salads and chicken, fish, fruits, veggies and occasional pizza slice. I am still putting on weight especially mid section. I am Diabetic as well. 😔
My son started taking Levothyroxine at 14 he has Hashimoto’s. His hair has been falling out by the handfuls since, now leaving him almost bald at 20years old. This breaks my heart!!! His self esteem has been effected terribly as far as ever meeting someone. He says what girl wants a bald guy at 20. I’ve never heard hair loss could be caused by meds, I thought it was from having Hashimoto’s.
Awww…..this just breaks my heart! I wish you could find a Dr for your son that would help him! How unfair for him! 😢❤My son has high functioning autism and that breaks my heart too. Praying for your son and for you Stephanie! 🙏🙏🙏💕💕💕
I'm 72...been on Levo since age 30. Have felt like shit my whole life...sad. Find a sr. med student at Universiyy teaching they study and they really care.
I started taking Levothyroxine 25 MCG a year ago and feel terrible.......stiffness, soreness and pain in my whole body. I felt better when I was not taking it. Talking to my doctor to stop it.
I was diagnosed in 2009 with Hypothyroidism. Put on Levo, dose has remained at .112 mcg except for a short time that an endo had me at .125 mcg. I suffer with Chronic Fatigue Syndrome. I wake up only to take a long nap . . . . Losing weight is very hard. The CFS interferes with any exercise because I want to fall asleep! Yes, I take a multivitamin, E for hair where it has thinned up front. So what’s a woman to do?
I’m not sure what to do Levo now 150 Growing bigger and eating less Tired and I can’t walk much as I’m exhausted and itching don’t start me on that My skin is ok and hair but skin o legs flaking and I’m trembling internally all the time. Sleep well that is not great as I can feel my heart bumping sometimes. My question is if the go will not listen what the heck are we supposed to do?
This is interesting... AS I GET older, I was told my Thyroid was off kilter. Which related to the weight gain I was experiencing. Actually I always had a weight issue since I was 15. Looking back, I attributed that to the American diet. My earlier years, I never saw any photos as a kid...with me looking overweight. Actually, I was quite slender for my age. BUT when we moved back to this country (military brat) - my weight started going up. My family told me I was overeating ... but what IT was was a diet of Pastas, and more carbs. Hell...I wasn't a cook, and I relied on my family to feed me. I never once saw a salad at our dinner table. And short of eating too little - I was stuck in Teenage Hell. When I was 50, I experience 50 lb weight gain, stress from a cross country move, my Ex's car accident, and stress out of the Box... I was told, my thyroid was not working. I refused to go on drugs. I tried changing eating habits. Which was difficult, considering my ex was skinny, and wanted to NOT eat healthy. Over the past ten years - I changed my diet. More vegetables, less red meat, and overcame a sugar addiction. I dropped weight like Crazy! The only reason I gained any Weight was due to Sugar. I also suffer from some arthritis - so I gave up ALL DAIRY. Which proved to be a good thing, considering how MILK & Dairy is processed and the high rate of Estrogen in dairy products. My aches and pains are almost non existent...unless I work out to much... like mowing the yard for an hour or two. But I LOVE working like that! I do take Magnesium - and it helps me sleep. But a year ago, a doctor said he felt Nodules on my thyroid... and seem to be more tired than usual. Some of that I attributed to working too much. hahaha But I miss my Surges of Energy. Damn getting older really stinks. Man... did I mention I really hate doctors who don't consider NATURAL cures?? My poor mother was given drugs that NEVER helped her dementia...so WHO do you Trust?????
I also hate doctors that won't consider natural alternatives. They keep prescribing the same pharma profit making garbage. I've read so many comments from people who've felt terrible for years and they don't listen or take the time to try something else. I use Standard Process. Vitalogic was awesome but the company went out of business.
thank you so much!!! Had a thyroid panel drawn today, to see where I stand. Taking 88mcg levothyroxine daily now for a year, but feel very edgy and not myself. Not sleeping well and gained 10 pounds since my dose was increased from 75mcg to the 88mcg about a year ago. TSH last year was 3.51, so she increased my dose. I feel best with a TSH of 2. When all this started 7 years ago my TSH was 8, at that time I was placed on 50mcg that left me feeling like a million bucks along with a 10 pound weight loss. Over the years it has slowly crept from a happy, feel good 2, to the level of 3.51.
I am a coeliac. Have just f I understand out that the manufacturer say Levi is gluten free as there could be cross contamination . I have been ill since the pharmacist said my previous meds were going to be discontinued. No warning was issued when they gave me Levo. Not impressed.tgat I had to do research because I felt ill all the time.
Had a thyroidectomy 35 years ago. Been on Levo since. Gained 80 pounds and never lost it til I went through menopause in my 50's. It was like a switch was turned in in my body.
I switched from levothyroxine to NP thyroid ( generic armor thyroid) and cytomal and feeling good..been on dedicated pig thyroid for 8 years now since hypothyroid. My Mom was also hypothyroid. I don't have hoshimoto either
Hi Dr Childs it’s funny I should come across this today. I had been On levothyroxine 75 for about 6 months, 💎thrumy insurance from my HMO, which is another issue. Since it’s free Hmo pharmacies buy from different place. When this happened Levo tasted like cardboard since I always chewmy meds TSH was .54 on my low range is 0.40 next visit in January was 0.24 which meant I was now hyperthyroid, the hair on the top/sides of my head. The hair on my head is dry and brittle. It literally started to brake off. One side worse than the other. This was enough to make me very depressed. my Hashimotos flared up and my body started craving sugar like a crazy woman. My A1C is at 5.4 and only taking one metformin 500 a day if I really needed it a day because I was way below range and some times took nothing but the sugar cravings were not me at all. so I knew something was Sometimes none at all as I was so hyper. prior I was feeling well, I had energy and no constipation.I think my issue might be conversion, all my test had been really good, so my dr stopped the RT3 test. Anyway I text the office and explained to my Dr office what happened, so she lower my dose to 50, but by the time I saw her the damage had been done to my hair. The Dr then lowered my levo to 50 mg, but when I went back to see in her my TSH went up dramatically from 0.24 below range to 2.9. All the numbers changed for the worse which activated my Hashimoto I felt. I am on LDN 4 mg and that has been a blessing thank you for sharing the information with use. LDN took all the fibromyalgia, and back pain away. We do know 2.9 is not my spot because the I was still symptomatic, so again she added 5 more mcgs of T3 along with the levo 50 mg. I am feeling a lil better, but my hair still not growing, nails are finally growing but still brittle. We decided testing my blood every two weeks. Then I text her after I saw the new bloodwork now. TSH was 2.08 better but again, my hair is not growing and nails growing but dry and brittle. She then increased Dr. Increased her T3 to 10 mcg, and levo was left at 50 mg. I still feel hypo again not as bad. When I saw her last week I asked her if taking the generic make a difference as interactions were different. I believe because HMOs pick the cheapest cost to them because it no cost out of pocket for me. She suggested doing synthroid to give it a try. I also asked the pharmacist about the difference he explained synthroid might be better as it’s made of the same ingredients all the time. I Started today synthroid 50 mg with 10 mcg of T3 after I did my blood work today 4/24/23. We will see my bloodwork in this week. Hopefully my TSH has gone down . I still feel hypo so I feel I have not found my right spot yet. Maybe my hot spot is somewhere between 0.50- 1.50. Losing your hair is the most devastating thing for a woman our self esteem goes down the drain. Wigs here in Florida is a no with all this heat.Sorry for the long story readers should know it can take years to find your ideal spot. The only thing I haven’t tried is tiroset or T3 on its own. People if you read this pay attention to what’s going on, and to what Dr child’s is saying , don’t wait until your next drs visit! Journal your symptoms, your good days and bad says. Always have your labs done and all the tests you n Dr Child’s site! Thank you Dr Childs for all your insights. You are appreciated I hope people take what your saying seriously, as it effects the quality of your life! Thank you! 🙏
So I tried Tirosint 60mcg for 1 month. Upped to 60mcg plus doubled on weekends to 120mcg due to high TSH. THEN 2 weeks at 62.50mcg. At 62.5mcg I started to have issues. At the end of 2 weeks my face swelled up along with hands and left leg and hives. Breast pain also happened. At ER due to breast pain had complete heart exam. Heart in good condition. Drs. Advised to no longer take the Tirosint. Am back on 60mcg of Armour. It what’s sad for me as I really wanted it to work. T
Armor thyroid is much better than levothyroxine. it contains T4 and T3. Pharmaceutical companies try to claim thyroid patients have no trouble turning t4 into T3 but that is not so. Especially if the patients adrenal glands are weak. To find out if a doctor is willing to prescribe Armor Thyroid ask pharmacies which doctors they know prescribe it.
after being on 88mcg for 12 yrs it suddenly started to make me sick, my Dr lowered it to 75mcg, that didn't work so it got lowered to 50 and that didn't work.So now I'm on 50mcg of tirosint and I'm still sick I have inner trembling, anxiety, extreme, fatigue, unstable blood pressure, shortness of breath and headaches my Endo says my T4 and TSH level is normal and to keep taking it but I feel better without it. Please help😥
I am going through Menopause as well as Hypothyroid. I have felt for some time that my Levothyroxine (112mg) is too much for my system. I have hot flashes all day long, trouble sleeping, symptoms of ADD and super low energy. How do I identify the cause?
I have been taking Synthroid ( the brand) for 53 years for hypothyroidism/hashimotas disease because I can’t tolerate levothyroxine. I have not had any issues with gaining weight:
Ive been on synthroid then levothyroxine for the past 32 years so i couldn't get pregnant at 27 then started synthroid meds after being thoroughly tested. I got pregnant within 3 months of taking it. Felt great. I wasn't able unfortunately to have anymore children. Im now 61 and my levels go back and forth. Im tired, dont sleep well and have no energy. Gained an additional 11 ish pounds the last few years. Dr thinks all is good. Shes an internal medicine dr. I take mine in the morning then ready for a nap a half or so after if im not up. Im moody and unhappy.
I was on dessicated and started doing much better. I got a specialist who put me on synthroid. She made me switch tellling me “my bones wouldn’t turn over on dessicated “ and I’d end up with osteoporosis. I feel like absolute shit. Hair falling out. Severe muscle fatigue and pain and my feet are numb. I gained more weight and I’m miserable. I hate myself and I hate my life. No care health care.
I was on one thing 19 years ago after having a complete thyroidectomy, then changed to Synthroid. I started feeling all the side effects bothering me and went to a naturopathic doctor who put me on desiccated hormone. I was feeling better but, on my visits to the endocrinologist, she wasn’t happy with my decision and after some time of listening to her displeasure with my choice for treatment, I switched to another endocrinologist who over time won in my changing back to Synthroid. My dosage was messed up for more than 15 yrs. Changed doctor again and she levelled my t3&4, but because the side effects are getting worse, days ago I asked to be put on Tirosint having less fillers etc. She said she couldn’t prescribe it because it isn’t available in Canada. Given a prescription for Levo. I told her I would even cross the border to get it and was told she would have to be licensed in the USA for it to be valid, contradicting a pharmacist across the border who told me I just needed a prescription. The Levo I started today list more side effects than Synthroid….lord help us…
i have hashimoto disease and I have been on levothyroxine for about 2 months I've gain weight, i feel really bad, extremely fatigue and even my eye sight has gotten worst but lately I've been having my legs/ feet get swollen. I don't know if this is normal. have a dr appointment next month but should i make it sooner?
My sister has asked to be put on a different med because Levo is inadequate. Her doctors are firm that it is the ONLY option. I fired my doc and got one that put me on Armour, which I do pretty well on. The resistance of the so-called medical community to alternative creates an impossible situation for the patient
What's interesting is that these are not alternatives, they are prescription medications intended to treat hypothyroidism. It would be one thing if they weren't medications, but they are.
It's the drug big pharma has been peddling FOR ENDLESS DECADES...they intend for you to be on it for the rest of your life. PROFITS are their main objective.
I often wonder what the priority of Doctors actually is. The general health and well-being of the patient, or the financial incentive from the drugs manufacturer?
i just found your videos. I have been on 125 mcg of levothyroxine for over 20 years, never felt any better. I tried mentioning it to my doctor once, and since my TSH was fine according to her, she shut me down. I live in a small town, and am not able to find someone who wants to prescribe anything but levothyroxine.
Sodium Lauryl Sulphate has to be why I cannot take Levothyroxine as have had to throw out every thing with it in. I take NP THYROID now, but in UK you have to buy it yourself.
I am a T1 Diabetic with Hashimoto's and starting menopause - so wondering if my tiredness everyday could be related to these as well. My endocrinologist just keeps giving me levothyroxine. Of course it goes back to my labs saying everything is fine. But I am always fighting that extra 20 lbs, impossible to lose (I exercise, eat fairly clean) and always exhausted plus hair loss and now a puffy face especially my eyes. Considering asking for T3 change, and seeing what my doctor states. Anyway, not really sure. But I've been thinking a lot of times my doctor's just don't know.
I truly thought it was just me feeling depressed, having awful body aches, and not losing the weight I've gained with Hashimoto's! I'm on Tirosint (gluten free gel pill) 112mcg five days a week, 224 mcgs for the other two days. It helps a bit, but I'm nowhere near the activity level, mental or emotional level I was. It's a terrible disease that pecks you to death. You struggle everyday to just barely reach the minimum of your personal standards.
Excellent comments, Germaine. I have been on thyroid meds for 22 years after half of the thyroid was removed. I was so ill I was sure I was going to die, seriously. Desperate, I began titrating my dose by using parts of the various doses I had until I found a dose that made me feel human again. Finally, I thought I just might live. The doctor, at the time, lowered my dose to where I felt better. I now take .112mcg and wonder if it shouldn't be lowered as I am losing hair, along with other issues. We will see.
Subclincal hypothyroid put on 25 mcg of levo. Felt great and finally normal first day, but then started getting sensitive to the ac and worse fatigue 🤷
Dr Childs, what does it mean if levo makes somebody not able to move their body? It’s like; they take it and boom there’s like a blast and sudden energy loss, that can’t walk, can’t move.
I live in the UK and I'm entitled to free NHS healthcare. I can't afford private healthcare. The problem is, the NHS have stopped prescribing NDT and other T3 thyroid hormone drugs. Apparently now, all they offer to treat hypothyroidism is levothyroxine. And I can't get a RT3 blood test either on the NHS - my Dr says this isn't available in the UK. I think NDT is still out there but only if you go private (in the UK). So I really don't know what to do. I'm a 31 year old woman and I was diagnosed with an underactive thyroid in 2018 (when I was 28), based on 1 set of blood test results which included high TSH. But I don't know how high. I was also diagnosed with low vit D and low B12. Apparently the vit D and B12 were extremely low. I was placed on supplements for the deficiencies and test results for them have since come back normal. But since being on levothyroxine, I've felt increasingly unwell. Not once have I felt better since being on this medication. My starting dose was 50mcg. I started to have hot sweats, head aches, dizziness and feeling sick that seemed to come on all of a sudden if I'd been out just walking or gone to the shop. I thought the dose was too high so i had more bloods done. My TSH came back normal. I'm aware that can be irrelevant. But my Dr basically insisted it was all in my head and I should be feeling better. I did research and found that the fillers in levothyroxine can cause side effects. One source basically said the higher the dose the less fillers. So in the hope of feeling better I asked my Dr to increase my dose if there is room to as I still felt unwell. My dose was increased to 75mcg in November 2020. Since then I have still felt no better and I have gained more weight. And I am always hungry. I hate myself for eating, but it's as if I feel sick and dizzy when I go too long without food (which is never long at all). I have been tested several times in the last few years for diabetes too, because I seem to be urinating more at night since being on levothyroxine. I have requested that my Dr refer me to an endocrinologist. She has saud she will write to them. But I don't have high hopes as the NHS simply don't provide other options for treatment of an underactive thyroid. My hope is that I may have been subclinical hypothyroid and I don't need levothyroxine. Although my Dr did say it was my immune system attacking my thyroid. I had to do my own research to find out it's called Hashimotos thyroiditis. The Dr who originally diagnosed me told me not that much at all - apart from it's incurable and I'll have to take levothyroxine for the rest of my life. All this based on 1 set of TSH level test results. Tests since have been normal and while I've been on levothyroxine. But like I say - I feel dreadful. I also suffer EXTREME fatigue, aches and pains (which I am seeing a rheumatologist for in November as arthritis and degenerative disc disease run in my family). But I've thought, could the weight gain have caused the back and leg pain I'm suffering from. And could the weight gain be from levothyroxine. I really feel like this is the case. And if I'm genetically predisposed to back problems - it's foreseeable that getting fatter might cause it to happen sooner? I really am at the end of my tether. I have no life. I don't go out. I'm too fatigued and in pain to go at it with exercise to lose weight and feel better. I feel trapped. Drs won't listen. I stay in because going out just to the shop leaves me so exhausted and in pain. And staying in has made me even more inactive. It's a vicious circle and my weight is ballooning. I'm 5'8" and I last felt healthy when I was 13 stone. Although I know that isn't slim, I felt ok and looked good. I'm curvy and had a slim waist, skinny ankles and wrists, collarbone definition. According to BMI that's overweight, but like I say I didn't feel like I do now. I'm now 2 stone heavier, at 15 stone and I feel dreadful. Again I'm aware that's not morbidly obese for my height. But I'm sure the extra weight is putting pressure on my back and my knees - as I say, those problems run in my family. I still have slim wrists and ankles and a lot of people have said I don't look particularly dreadful. But I feel like death most days. It's rare I feel well at all. All since being on levothyroxine. I felt unwell of course, before being diagnosed with an underactive thyroid - but never as bad as I do now!!! Could that just have been the other deficiencies? Things like diet change being the cure scare me, because what are my options when I'm poor and there's very little I enjoy besides food. Meat and dairy are part of my balanced diet. I do eat enough vegetables too. But I would really struggle to cut out meat and dairy altogether. Alternative foods can be expensive and I'm already living well below the poverty line on benefits as I'm not well enough to work. I seem to often be low in vitamin b12 so surely it would be a bad idea cutting out animal products? Are there other supplements I can take, that can be bought at a reasonable price over the counter in the UK? I haven't seen iodine supplements anywhere for example. But if someone could tell me where? I want to stop taking levothyroxine completely! I feel like I'm being poisoned. I'm going to give it a try to see if I feel better. I have nothing to lose it this point. I have no faith in seeing an endocrinologist here in the UK. I feel like they will fob me off with the same bullshit. As they won't or can't even give me a RT3 test. Any help or advice from anyone would be greatly appreciated as I'm struggling to find reasons not to kill myself tbh.
I can't provide medical advice on youtube but I would strongly suggest seeking out some mental help if you are feeling suicidal. There is always hope even if it doesn't feel like you can see it right now!
If the pharmacy changed me to this medication from a different thyroid medication for finances and I've gained 40 lbs what can I do? I'm in a nursing home used to weigh 336 lbs now back up to 195 from 156 in 8 months with dieting! Have Horizon medical insurance but pharmacy switches things constantly! 😢
I was on Lovo. For a few years and came off for two years because we relocated too another city. I started getting anxiety really bad . I am 207 pounds which I’m usually 160 pounds 5.9 tall. Started losing hair and no sex drive what so ever which makes it hard in my marriage. I started taking my Levo again because I found another doctor. We did bloodwork and yes I’m low on thyroid. I feel better no anxiety but still not losing weight and NO sex drive.. I’m looking at taking the Bronephrin for weight if that’s how you spell that. Can you even take it being on thyroid meds ??
I am hashimatos with high TSH but normal T3 & T4 what ll be the best medicine... My hair falls a lot and one nails is very ugly.. Used to take Thyroxine but not regularly skipped it very often...
I got fed up with hair loss and went bald on the top of my head. It was so bad I stopped taking it. I have now changed my medication. it's improved completely. I've now got hair. Levoxine.
On my Rx bottle it says to take on empty stomach first thing in the morning 30 minutes prior to eating or drink anything. But, recently I was impatient at a hospital & my RN's gave my Levothyroxine Rx mid day. When I asked them about it, they told me it didn't make a difference. Was that a pathetic excuse, or does it really matter?
Yes. Ive been on it for 25 years and NOT ONCE did my pharmacy tell me to take it an hour before food with a glass of water. When the new formula came out i looked at the insert plus the various drs on you tube and researched it on google and since taking the thyroxine on an empty stomach.... my blood results indicate that im being over medicated. So much for pharmacists
I've had a thyroidectomy in 2016 and my doctor keeps reducing my meds to 112 mcg and I now feel miserable and put on weight. What to do. I have terrible hair loss, brittle nails, dry skin, etc. Please help me.
Hi I have been diagnosed with Graves disease 8 years ago I have been put on anti thyroid medication and within a month I went underactive and I started taking levothyroxine for over 6 years my doze was between 100 to 150 micrograms and then I relapsed and I needed to go on anti thyroid medication again and after a year of this medication I had radio iodine after the radio iodine my thyroid hormone level stayed normal for only 6 weeks after the 6 weeks I have started levothyroxine 25 micrograms and my T4 and T3 are at the normal levels but I still have fatigue, muscle aches, hair loss and I can't lose weight although I exercise and made changes in my diet choose healthy choices and eat normal portions. Do you have an idea what I can do to improve these things. I also want to say that in the 6 years period I never had these problems when my thyroid hormone levels were normal.
Can you please speak to how asthma meds like Advair and other inhaler effect thyroid meds, function, and tests? If you've already addressed this, can you point me to the video? Thanks
I am not sure how long I have been on Levothyroxine for quite a while maybe 20 years . I gain weight easily. I don't sleep well and my hair is all over the house. I get constipated more often than I ever used to. I think I take 75mg. I have asked the dr. about it but she says my numbers are good. I should do cardio and eat less. I am eating 1 meal a day. My nails are brittle and have vertical ridges my skin is dry, I have to load up on lotions. I have achy joints and developed arthritis to me there is something not right but she seems uninterested sugessted I am just getting older because my numbers are good. I asked if I should see an endocrinologist but she said I don't need one.
I guess different person,different side effect,im drinking levothyroxine by sandoz and im okay but when the pharmacy switch me to levothyroxine by Lennet this gives me a lot of problem,I feel like im running out of breath and its like i forget everything!I got brain fog and I dont have energy at all,I'm so down and I feel so depressed!.....but when I swicth back with sandoz , everything is normal again!
I'm up to 250 mcg if levo. I've gained over 60 lbs since 2007 after thyroidectomy diagnosed Hadshimoto, ice read T4 dies not always convert to enough to T3 , I bright this to my doctor, she ignored me n raised the T4 ...depression weight gain, pains , bring unstable I want real help
I am tt patient. I was on 150 t4 and 25 t3 and my tsh was 0.01 ,but my doc reduced it to 125 t4 and t3 as same as before.Now I am experiencing super brain fog and tiredness
What about people with congenial hypothyroidism without the gland? I’m eating super healthy no sugar no gluten vegetables and drink a lot of water and I’m gaining weight.
I am getting a headache and my face looks swollen. I did not change my diet so I guess I don't expect to lose weight. MY thyroid is sluggish and slow but not hoshimotos like my mom. I have been on Lev for 4 days .75 mg..I was prescribed .05 2 years ago and it did not work, so my doc prescribed this mg. I also don't eat or want any dairy in my body and I head this has lactos. Ugh, I am so sick about this. I am the heaviest weight ever and I can't seem to lose weight and not sure what diet to be on. I am plant based, but that is not enough naturally. I am so so confused. Should I just go to a natural doc instead? I need to shed this major weight gain and get rid of these headaches that I never had before. It feels like brain fog on my right side of my skull and above my right eye. maybe from the lactos? Oh no!
YEs my endochrinologist is gradually,inceasing myndosage with ONLY the 50mcg tablets I AM SURE this is why fillers and dyes.I do get scalp itching anyway and dry facial skin.
Well, trying to find a doctor who really understands thyroid in your area. Most doctor just go by the basics standard thyroid test. I keep telling my doctor my medication is not the right dose. But she won't listen and won't look up any Medical information I have suggested. All she says is the test came back find. So any suggestions for me.
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Dr Child's My mom who had been on Levorthtyroxine 60 mcg for the last 40 yrs . Now she switched Armour 60 mg is that the right conversion. Bcuz she for this last 3 months feels tired,Weak . she has always been active til all this. Please help. At least if at 60 mcg lev.to Armour 60
How can we get off Levrotyroxine? I've gained @ 50lbs since starting it with and I'm very active. Gym, daily walks, garden, run a house alone yet I can't l I se a pound.
I've been taking levothyroxine 25mcg for many years. I'm a Type 1 Severe Brittle Diabetes for 41 years. I've put on so much weight. I have fatigue all the time, nails issues, hair loss itchy all the time. Even scratch myself while sleeping when I sleep. Being overweight is extremely depressing don't feel good often daily. Use Iron vitamin as also Anemic among other vitamins along with prescription medication.
I had taken Synthroid in beginning when started having Thyroid issues have had an overactive n underactive thyroid through the years. Was taken off Synthroid due to health insurance. Wondering if should ask my Endocrinologist to take me off levothyroxine 🤷🤷🤷🤷. I'm tired of sleeping all the time n feeling like CRAP 🥶😞
@@leonardcarrico584 😹🥶IM ONLY 108 LBS. WAS , 159 LBS 😹
After seeing you talking with Dr. Jeffrey Welchel, I made an appointment with him. I had a near total thyroidectomy fourteen years ago, and I am having a lot of breathing and talking difficulty. I am really hoping he can help me get rid of my nodules in my neck. My ENT recommended I remove the remaining part of my thyroid.
I have been on Levothyroxine for 20 years now. I live in the UK. Since I have started I have gained weight and find it near impossible to lose. I was a healthy weight when I was diagnosed. I always feel tired and or low mood. I have my blood tested every year. I don't know why I bother. I just get given the same 100mg and 'healthcare' just keep pushing Statins (I refuse). My thyroid is NEVER discussed. I have decided to take my health into my own hands. I find channels like this and the discussions most helpful.
Ditto the docs here don’t care
Me too 20 years
Me to. Been on levo 15 years and tested 1x a year. I went to the doc since I had big fatigue. He wanted a sleep study that I refused. 6 Mos later the fatigue got worse to the point I was mentally drained and it was a huge effort to get ready to go to the store and I only left home when I had no choice. I couldn't sleep no matter how often I tried but if I did sleep I'm awake 4 hours later feeling exhausted. I literally would drink a pot of tea and still not have an energy burst like when I was younger. My dog got into my pills and I can't find the bottle if levo. The dog didn't eat them or I would have found a chewed bottle. That was a good day! Been a few months since I took the pill and I'm so much better. I sleep, feel rested, don't lose as much hair, swelling in my feet/ legs have gone down. The weird shooting sensations I was having in my body quit. My thinking is more clear, I'm like a new person. When I go to the doc, I'm not telling him since I want to hear what he's says about my labs. They don't understand thyroid, think it's an easy fix and don't want to problem solve. Years back I told a nurse I was to tired, sleeping alot, she snickered and wanted to know what's wrong with it. They are A-holes and are a waste of time and money
@@karenv5103Did Levo do any good for you?
God bless you for helping us
I want to cry to why most Doctor don’t elaborate those things with their patients
God bless you millions times
Bless you too, friend ☮️💐
Time and money
I asked my doctor to switch me to levothyroxine plus liothyronine when my NDT was recalled. I lost weight and felt good. She freaked out when my TSH dropped too low! She sent me to an endocrinologist when she couldn’t fix my TSH and after fiddling with my dosages, which messed me up. The endocrinologist refused to do a reverse T3 when I asked her to and left me on 88 mcg levothyroxine and 5 mcg liothyronine. I gained 10 pounds almost overnight! I’ve had Hashimoto’s for years and had convinced my doctor years ago to put me on Armour thyroid, until it became difficult to get and more expensive. I thought the combo would be easier to manage, but sadly, it hasn’t been. It’s tough finding anyone who is actually knowledgeable about Hashimoto’s where I live because I follow you and other more forward-thinking doctors. Patients now know more than the stuck-in-the-past endocrinologists. I appreciate you sharing your knowledge; I’ve learned a lot. Im searching for a new doctor.
I’ve been taking this medication now for over 8 years having had a Thyroidectomy in 2009 when I lived in Canada. I went from 170 to 260lb’s I think finally watching your videos you have educated me so much. I’ve started to add extra vitamins into my body. And I’ve just gone really big on putting smoothies into my body made of fresh fruit and veggies... I pray this will help. I’m 57 and my hair is fine now but my nails are brittle. I live in the U.K. and once this lockdown is over I’m definitely going to have another chat with my Dr.
My dosage is 125 a day. Thank you so much. You really really have helped me.
that is what I begun doing--lost 30 pounds.. changed my food..
FYI: I started taking Collagen 3 mons ago and for the first time in my life I had long nails and they were very pretty polished. Unfortunately they were also very annoying. Anyway they r very strong now but I keep them short. Hope this helps.
How are you doing now? I'm just about to start taking 125 in a few days... my level was above 150 for my test.
Levothyroxine is working because my test show good results, but the medicine make me highly irritated and very emotional 😭 and that’s me taking .25. I’d rather try natural remedies. Good video 🤙🏼
Thank you Dr. Childs for sharing this information. I had a total thyroidectomy in the late 90,s and have been going on a Rollercoaster ride since.
Me too. I’m so tired of all of this. Now I can’t sit in the sun, because I break out in hives on my legs. My hair is ok for a minute then it starts to fall out. My weight is out of control too. I’m scheduled to see a endocrinologist, hopefully they can help me.
Thank you for this! I have had hashimotos for 20 plus years. I am 5’9 and went from 127 to 175 in literally 2 years. Recently had cytomel added 2x a day.. still can’t lose weight and still sluggish but running 5 miles a day
Me too! I g ained and unable to lose a pnd
@@pamc3338 I gained over 100 pounds.. I began having fruit smoothies in morning.. Baked pond fish and salad at end of day.. I lost 30 pounds in 2-1/2 months.. I tried other diets but this is only one worked fr me.. I eat only natural foods.. No boxed or additives.. al fresh.. if you can try it.. Good luck..
@@brendamyers6320 good for you! Keep it up!
I ahe hosimoto .I was in bad shape atc2l presently taking 235 mcg I weig 109 to107
Stain to not loose any more.iam 175 .feel bad have naropathy hands and legs.and feet have one hip. Replacement early dementia.
I am hashimatos too but can’t gain ... I am 5’5 , weight 55 kgs... i want to gain little but can never gain ...falling hair is my probs😢
Wow he must speed his more recent vids up… this is so refreshing to listen to him at normal speed.
I have been diagnosed as having hypothyroidism and I started Levo this summer. But I've had problems with worsening fatigue. I felt like I was MORE tired now that I'm treating the hypothyroidism than I was before I even tried treating it. Because of that, I stopped taking them. Then I tried half a pill at nighttime (so I could sleep off some tiredness). But I started to get more tired again. It's frustrating wanting to treat it but feeling worse when getting treatment.
I am experiencing the same thing, needing to treat it but feeling worse. My doc got so frustrated with me that he accused me of making things up...so I no longer talk about it to him.
Total thyroidectomy here... My Endocrinologist was not helpful. I was prescribed many different Levo pill dosages (all colors) I stopped taking the levo because I was miserable (dangerous, not advised) My PCP took me off Levo and put me on the brand name med, Synthroid. I also take 5-10mg of cytomel . I am no longer in pain everyday! I seem to be losing weight in my abdominal area. It's only been 1 month but I am much happier. I am learning from youtube to help my doctors help me!
@@kelter1027you need a new dr
@@gencoop1000what is cytomel
I got worsening of fatigue, but also sensitivity to cold air. So idk what’s wrong. I felt great the first day I took it though. Calm, clear headed, but then I didn’t so I quit
I have been on the Levthyroxinefor about 3 weeks!No problems at all!
Thankful I found your videos. Left sub-total thyroidectomy 20+ years ago. Began losing hair about 2 years ago, dry and brittle. Levothyroxine @ .112mcg. I generally have to ask the doctor to check my TSH, and that's about once a year. Male pattern baldness, and serious thinning, ready to shave my head.
I will look at all your videos on the thyroid to see what I can do to help myself. I was having serious fatigue and began taking Iron tabs a couple of weeks ago. I am feeling better. Will check that ferritin level. Thank you, again.
when i was born,i had no thyroid,and given levothyroxine,and its kept me alive!
I'm glad you've had a good experience with it!
But how would you know since you've never been off it.
my Endo took me off for a month that's how I know I feel better without it, then he put me back on and I feel horrible😖
I stopped taking it for around nine weeks and my TSH levels were scary, to my doctor. I started taking it again. I don’t notice any benefits or negatives either way. However- I feel crappy all the time, every day. 🤷♀️
@@mrsmacca126I feel the same way & wonder if an additional T-3 medication might help now since my T-3 levels have gone down also. Or keep consistent w/ natural supplements first (Ashwaghanda, selenium , etc.). Don't give up & keep the faith!🙏
Thank you so much for the information you provided. You taught me everything I needed to know about hypothyroidism. I experienced side effects of this med. I have already changed my diet. The only thing that would be hard to quit is coffee, but no one ever gave me accurate information. Again, thank you so, so much.
This was so helpful. Thank you so much for doing these videos for us. It's so hard to get any answers of doctors they are not very informative. Also it's hard to find such detailed information. This is very valuable and helpful. Paula England
I had a concierge doctor tell me I had Hashimoto’s about two years ago. Come to find out, im at-risk for it but don’t have it yet. She put me on compounded T3, T4, supposedly to correct my need. In the meanwhile, I’ve progressively felt worse and worse. Now I’m trying to make sense of what the hell has happened.
17:21 yes, all of these symptoms and plus convulsive vasovagal syncope episodes, one of which resulted in a pretty serious head injury. During these epidsodes I was somewhat alert but had full on ataxia, loss of language, temperature dysregulation, vommitting, and unable to work many days. I just lay here and think about what I need to do. I didn’t even mention that I also started having tachycardia and had to have an ablation and a septoplasty, turbinate reduction surgery due to not being able to breathe.
Do you think I should do something about it or just chalk it up to experience? How to I recover my body and health from being improperly medicated for this long?
i am on 175 mcg and now take 3x50 - these dyes/fillers were killing me! its hard to find someone in Calgary, Alberta that understands.... i'm very grateful for your knowledge Dr. Childs as i'm looking to a community for support. its been 27 years of struggle (started at 20years old) and i'm determined to change this. Working thur all your video and changing up my lifestyle, eating habits, diet, supplements, daily work outs and so on. Down 26lbs and feel 80% better. its been so hard - but nice to hear your thoughts & support! thank you!! i am definitely going to get all the tests redone as per your suggests as my TSH was about 310mIU/l in January prior to me taking charge on my own.
This is an older video, but exactly what I needed!!!! My Endocrinologist won’t add T3 for me and I feel awful most of the time!!! Trying to run around finding a new one in our area is nearly impossible! When in Georgia my Endo had me on a very small dose of Cytomel and I felt so much better!
Try a naturopathic doctor who can prescribe it.
Find a functional medicine physician
For what it's worth, my pcp suggested T3, and while it did give me more energy during the day, it horribly disrupted my sleep. Then, the next day after I didn't sleep, I'd feel actively sick, irritable instead of mellow/tired (that's the one upside of being hypothyroid, for me--I'm so tired I don't have the energy to be irritable,) and after a few episodes of this, I decided it had to be the T3. It resolved when I quit taking it. I'm probably an anomaly though
A lot of people who are on levo don’t need to be on it at all. I was put on it 10 years ago when it was “drug-of-the-year.” I have slowly weaned myself from 88mcg down to 22mcg. Doing fine and looking forward to being completely off in another month or two. No, I didn’t see my doctor- who is not my body’s God.
I don't know if I would say a lot, but there are certainly people who fit into that category: www.restartmed.com/stop-taking-thyroid-medication/
I thought and did the same thing. I moved and didn’t have a doctor so I was off Levo for two years. I did good up until a few months ago my symptoms came back ., anxiety got really bad again also heartburn. Weight gain . I’m 5.9 207 pounds now. I was 160 lbs up until a few months ago. So be very careful coming off Levo thyroid meds . You may feel good for a year or less but then it hits again sorry too say .
If your thyroid os totally removed how would you not used it?
I have been on this drug for 6 yrs now , and I've had no problems at all , my blood is tested every few months , I'm glad to be on it because I was ill at the time and the weight loss was bad , I have an over active thyroid and was told by my consultant I had graves decease .
You have perfectly described my symptoms ‼️
Ive been on levothyroxine for about 7 years. In the beginning it made me feel better, but for last 5 years i feel bad all time with body pain allover. I exercise all time and eat small amounts and very healthy food, but cannot lose weight. I believe its the levothyroxine so i know doctor says you have to take for life, but im gonna stop taking it and see what happens.
How did you get on when you stopped taking the medication.
I am planning to do the same. Please let us know how you got on 👍
I also am having the same symptoms as you have, Dr. said my thyroid test said my dose was to high, but I was gaining weight, with no appetite at all.., listen to this Dr. and he said instead of T4, start taking T3, so I have just started and am starting to eat a bit more and am losing weight, I went from 163 down to 148 in a few months while eating more...my weight use to be 115 to 120 lbs., 5' 7", so this extra weight was really pulling me down, it was so hard to be carring all this extra weight, and I eat like a little bird, really I never feel hungry, I have to be told to eat as I never think of eating.
I used it for 3 years. So much side effects like gaining weight, rash, breathing problems, burbing when i get outoff bed for long time...i took 75 mcg. Was so fad up of it, stopped radical to see what will happen. Within 2 weeks all side effect were gone !!! For 3 months, then my hormons started to drop....then i had to take something like tirosint. 2 y on 25 mcg. I got hartpalpitations... now i took 13 mcg more for half year but with bloodtest it had no effect totally!! If 13 mcg doesnt work what does the other 25 then??? Now i took again 13 Total 51mcg. My weight started to go up again.... i think for sure under my skin i see fat and water building up. Around my stomach is the worst. After 7 years still didnt work proper. If raising up meds doesnt do....then i try to stop with it or take less as possible like 25
@@annekedam6846how’s it going?
I had been on levothyroxine for 30 yrs. My new gp took me off it because she said that older folks (I am 82)don't need it.
In the meantime I have been dx with st. 3c endometrial cancer, had a hysterectomy and am now on chemo.
My onc. put me back on levo. because my tsh went up to 9.5.
I am now realizing that the symptoms I have been having may be because of levo. Onc said chemo can cause the tsh to go up.
My symptoms are burning across my shoulders, bp up, anxiety.
I'm on 50 mg and I feel great, I've got more energy I'm losing weight and I just feel so much better and healthier.
Have you suffered some kind of side effects at that dosage? I am 25 mcg I feel stable but I sleep all day long, then I got over 50 mcg and I get energy but a little warm and sometimes it is hard to sleep. I am confused. Both doses doesn't work at their best. 😑
I'm on 75mg, 50mg, alternative, I am having progressive trimmer to shaking only on my left side, also started feeling heavy some times in my heart, other time right across my chest, other time in the lower part of my body. I'm not on any other mediation. Trimmer only affect my left side only
@@elvishart9389 that doesnt sound normal. See your dr or get 2nd opinion
Thyroid med only comes in mcg
I've been taking synthroid for years and I have never felt any better. My hair loss didn't change and got worse. I am gradually losing more and more of my eyebrows and other body hair. I'm always exhausted, I've gained weight despite the fact that I actually don't eat a lot. I have T1 diabetes which I've had for 54 yrs. I started taking thyroid medication when I was in my 30s which was 30 yrs ago. I have never felt this was the right medication for me, but I cannot get my doctor to listen to me about it. I have a lot of other health issues and he will just put some of my symptoms down to those. I have a connective tissue disorder which causes arthritis etc and I have fibromyalgia which seems to come along with the connective tissue disorder. I have memory loss as well. I don't know how to get my doctor to consider something different.
I totally sympathise. I have been taking Levo for over 20 years. I have a blood test every year and they just give me the same dosage (100mg) and can't be bothered to discuss further. I have decided to take my health into my own hands. Forums like these help.
Man I hope you’re doing better
Frankly, I don't care if the reaction I had was due to a filler. Levothyroxin landed me in the hospital with severe heart attack symptoms. My heart was tested in every way, to the tune of many thousands of dollars out of pocket. The good news was, my heart was fine.
Wow. I’m having issues right now as well
Oh, Lord! I just started today for the first time😮😮😮😢😢😢😢😬
Did you have chest pains? I had that issue. My calcium score and heart were fine however.
I’m having issues too . I hate it!! Makes me want to quit this crap of a drug
@ciaramcclellan9584 I don't recall any discomfort until I got up to walk into the kitchen & was seized with severe, stop you in your tracks pain.
"Never felt better" can be taken 2 different ways. It's a good thing you clarified that later.
Interesting presentation. I am on 125 MCG, levothyroxine after being diagnosed with Grave’s Disease and having a total thyroidectomy three weeks ago for papillary thyroid cancer.. I take my medicine as prescribed but still have all of the symptoms related to Grave’s Disease and hyperthyroidism. It is very annoying because I assumed that things would instantly change once my thyroid was removed. I had my follow-up with my surgeon and we discussed the pathology report which was a confirmation of the initial diagnosis and metastasis into a few lymph nodes. I see my endocrinologist next Tuesday and will discuss this issue with her. I know I will be having radioactive iodine treatment. I just want these awful symptoms to go away.
You have wrong medication of levothyroxine for hyoerthyrodism. Levothyroxine is a synthetic for of T4 which the not active form of thyroid hormone.
@@meggiedemy6459 I take the medication because I have no thyroid after surgery for metastatic papillary thyroid cancer. I have to take the medication for my metabolism. The dosage has been lowered. My medication is correct.
Can I ask you what type of symptoms you had before surgery ? Would appreciate any info thanks
@@tonis19891023 Before surgery, I was very hungry eating everything but losing weight. I had insomnia and horrible night sweats. There was no pain at all. When I mentioned this to my primary physician, he asked if I had any family members with thyroid problems. My mother and sister both had under active thyroids and had partial removals. He ordered blood tests that indicated an over active thyroid and I was diagnosed with Grave's Disease. I was referred to a surgeon who felt nodules on my thyroid. I had a biopsy which came back as papillary thyroid cancer with some metastasis.
@@slipdisco thanks a lot take care
Have been taking Blackstrap Molasses (2 teaspoons mixed in milk) daily. Has iron, magnesium, manganese, calcium, B6 and have always had glossy full head of hair. However since starting Levothyrixine, hair is dry, dull, and thinning....scary!!
Thank you..I have had the same side affects 25years, I'm 60 yrs old. including epilepsy since I was 8yrs old.
I went through a rare they say very rare thyradic storm which almost killed me by preventing them to perform surgery on my lower intestine which split open why in the er exam room also finding out i had a hole in my intestine fo awhile and was told due to my thyroid I wouldn't survive the surgery well here I am and thank you to all the docs and nurses involved at Ben Taub Houston
Hi been diagnosed with the Hash.sevral years ago. Of course, first medication he rx-d me was the levo..I hated it I gain weight and felt tired,but my numbers were "normal"🙄 I was upset because I kept gaining weight. Currently I take a pork gland and it seems to work better for my body. My insurance stinks so it wont cover the the good stuff. Nature Thyroid isn't manufactured anymore, that was the best for me. Armour thyroid is great too! Then my new insurance kicked in and kicked that out. Lol! So now I am on NP Thyroid meh its ok, I am going to check your videos on thyroid supplements and take them in conjunction with my NP Thyroid. 😊 Thank you so much for your work. You have helped an insane amount of people. ❤
I know this is an old video, but thanks for making it. I have a history of side effects from medications. I’ve been on levothyroxine for about ten years. I have lost about 90% of the hair on my head, and have NO hair on my arms or legs. I’ve mentioned it to the doctor, and it has never really been addressed. My old provider retired, and the new guy seems to see me as an old lady waiting to die (I’m in my 60s), and isn’t much help. He just likes to write prescriptions.
I understand. I’m just getting into the thyroid hell. Tomorrow I’m having all my hormones tested, another metabolic panel, as the thyroid test is still high/ hypothyroidism, yet my symptoms are the opposite. I have enough med conditions, and this adds to it. FEDUP
Change doctors
Ive landed in the ER twice with this medication and had to take time off work due to the side affects, i can fuction in normal daily life eg causes my one side of my body to go numb, unbelievable nausea, head pressure, face and head numbness, feeling so so unwell but my doctor wont change it to something else, even after being in the surgery waiting room nearly passing out and crying for help on visits. What the hell can i do, i need to go back to work.
I have hypothyroid issue and take 75mcg levothyroxine.My weight was 48 kg. My problem is that after continuing my medication i starts losing my weight so fast and feel tired and irritated.i lose almost 3 to 4kg.I never gain weight even before or after medicine.Any suggestions..? I more have symptoms of hyperthyroidism like bloating,weight loss, palpitations,hair loss but my tsh is 21.
worsening fatigue is listed in both less common and more common sections :) I'm taking 50mcg of levothyroxine at the moment , i was on 25mcg a few months ago which had no impact but now on 50mcg i have some of the symptoms mentioned including feeling warm in the face area like hot flashes, i also seemed to have developed some reaction to a moisturiser i have that i never had before but using another one now ( i do have sensitive skin) skin is sometimes itchy as well around face and scalp and i still get tired too often as well . i am due another blood test next week as been on these ones for nearly 3 months so i will see if anything has changed but will mention these side effects as well. very informative video :)
me to I've been on 50 sence 2010, I'm looking into alternative, I'm only 107 pounds and can't gain weight
@@shearosamamacita The medicine industry is a BUSINESS.. FIRST AND FOREMOST. A very lucrative one. It's a one-size fits all system. If your TSH testing is off... Levothyroxine is prescribed...it's the drug big pharma peddled to EVERYONE w thyroid symptoms. I haven't known one person taking it whose thyroid symptoms improved on that pharmaceutical. NOT ONE.
I also do the hot flashes, I’m 72, itchy skin, especially at night. I use Neutrogena Hydroboost. Then my dermatologist recommended it to me but was already using
❤❤Doctor knew I had thyroid problems for 10 years before it showed up. Had test 3 days before I had diabetes and it showed up then. I've been on lev. for 30 years. I have always taken .025 mcg. It does show up any time they check it. So what to do? I've had hair loss and cold all the time. I take it alone an hour before breakfast and some time I don't eat fir 5 or 6 hours after taking it.
Meant to say doesn't show up on test now either
Amazing explanation thank you dr I’m losing hair like crazy
Ive learned so much thru this video! Thank you! Im on Levothyroxine and struggling in almost every way mentioned here. Im gonna get another doctor and see what I can do. Ive lost so much hair. Looking forward to feeling better and getting some hair back.....
Multi collagen protein will grow your hair back I SWEAR. I take Levo.
I had my whole thyroid removed 9 years ago and have never left good since. I still have traces of cancer left in my body so my doctor says that’s why my Levotgyroxine has to be so high. Do you think you could help with my situation and are you still conducting the 45 minute phone calls. PLEASE let me know thank you
Dr Childs, I'm on Levothyroxine for a few years now. Put on weight and worse all my hair thinning so much and handfuls of hair falling off in shower every day. I always had Insomnia though. Don't know what to do. I walk much every day and eat salads and chicken, fish, fruits, veggies and occasional pizza slice. I am still putting on weight especially mid section. I am Diabetic as well. 😔
My son started taking Levothyroxine at 14 he has Hashimoto’s. His hair has been falling out by the handfuls since, now leaving him almost bald at 20years old. This breaks my heart!!!
His self esteem has been effected terribly as far as ever meeting someone. He says what girl wants a bald guy at 20. I’ve never heard hair loss could be caused by meds, I thought it was from having Hashimoto’s.
Awww…..this just breaks my heart! I wish you could find a Dr for your son that would help him! How unfair for him! 😢❤My son has high functioning autism and that breaks my heart too. Praying for your son and for you Stephanie! 🙏🙏🙏💕💕💕
I'm 72...been on Levo since age 30. Have felt like shit my whole life...sad. Find a sr. med student at Universiyy teaching they study and they really care.
I started taking Levothyroxine 25 MCG a year ago and feel terrible.......stiffness, soreness and pain in my whole body. I felt better when I was not taking it. Talking to my doctor to stop it.
Some people can definitely stop taking it. You can learn more here: www.restartmed.com/stop-taking-thyroid-medication/
Same.it caised me the worst pain all over my body! Like someone took a bat to the back of my neck and skull
Thank you for this excellent presentation.
It seems crazy to me that Depression and Infertility are "less serious" side effects.
I suppose it's all relative!
@@drwestinchilds According to whom?
Love that you explained all the details on levothyroxine .
Thank you
I was diagnosed in 2009 with Hypothyroidism. Put on Levo, dose has remained at .112 mcg except for a short time that an endo had me at .125 mcg. I suffer with Chronic Fatigue Syndrome. I wake up only to take a long nap . . . . Losing weight is very hard. The CFS interferes with any exercise because I want to fall asleep! Yes, I take a multivitamin, E for hair where it has thinned up front. So what’s a woman to do?
Can you take iodine ,1 to 2 drops a day with levnothyeroxine?
I wish this question can be answered
I’m not sure what to do
Levo now 150
Growing bigger and eating less
Tired and I can’t walk much as I’m exhausted and itching don’t start me on that
My skin is ok and hair but skin o legs flaking and I’m trembling internally all the time.
Sleep well that is not great as I can feel my heart bumping sometimes.
My question is if the go will not listen what the heck are we supposed to do?
Switch to NP thyroid. Natural, I had the same issues.
@@johndoes461 could you tell me more? I’m in UK
This is interesting... AS I GET older, I was told my Thyroid was off kilter. Which related to the weight gain I was experiencing. Actually I always had a weight issue since I was 15. Looking back, I attributed that to the American diet.
My earlier years, I never saw any photos as a kid...with me looking overweight. Actually, I was quite slender for my age. BUT when we moved back to this country (military brat) - my weight started going up. My family told me I was overeating ... but what IT was was a diet of Pastas, and more carbs. Hell...I wasn't a cook, and I relied on my family to feed me. I never once saw a salad at our dinner table. And short of eating too little - I was stuck in Teenage Hell.
When I was 50, I experience 50 lb weight gain, stress from a cross country move, my Ex's car accident, and stress out of the Box... I was told, my thyroid was not working. I refused to go on drugs. I tried changing eating habits. Which was difficult, considering my ex was skinny, and wanted to NOT eat healthy.
Over the past ten years - I changed my diet. More vegetables, less red meat, and overcame a sugar addiction. I dropped weight like Crazy! The only reason I gained any Weight was due to Sugar. I also suffer from some arthritis - so I gave up ALL DAIRY. Which proved to be a good thing, considering how MILK & Dairy is processed and the high rate of Estrogen in dairy products. My aches and pains are almost non existent...unless I work out to much... like mowing the yard for an hour or two. But I LOVE working like that!
I do take Magnesium - and it helps me sleep. But a year ago, a doctor said he felt Nodules on my thyroid... and seem to be more tired than usual. Some of that I attributed to working too much. hahaha But I miss my Surges of Energy. Damn getting older really stinks.
Man... did I mention I really hate doctors who don't consider NATURAL cures?? My poor mother was given drugs that NEVER helped her dementia...so WHO do you Trust?????
I also hate doctors that won't consider natural alternatives. They keep prescribing the same pharma profit making garbage. I've read so many comments from people who've felt terrible for years and they don't listen or take the time to try something else. I use Standard Process. Vitalogic was awesome but the company went out of business.
Can you address people who take these meds who have no thyroid
thank you so much!!! Had a thyroid panel drawn today, to see where I stand. Taking 88mcg levothyroxine daily now for a year, but feel very edgy and not myself. Not sleeping well and gained 10 pounds since my dose was increased from 75mcg to the 88mcg about a year ago. TSH last year was 3.51, so she increased my dose. I feel best with a TSH of 2. When all this started 7 years ago my TSH was 8, at that time I was placed on 50mcg that left me feeling like a million bucks along with a 10 pound weight loss. Over the years it has slowly crept from a happy, feel good 2, to the level of 3.51.
I feel much better Donald Trump is going to jail.
@@missadventuresmotorcycledi2773 get lost troll
@@jenniferbecca3050 Your lost not me.
@@missadventuresmotorcycledi2773 Haha. You post is unwarranted on this page. Trump and Dr. Westin have nothing in common. So bye.
I am a coeliac. Have just f I understand out that the manufacturer say Levi is gluten free as there could be cross contamination . I have been ill since the pharmacist said my previous meds were going to be discontinued. No warning was issued when they gave me Levo. Not impressed.tgat I had to do research because I felt ill all the time.
I'm in the same situation. Unwell all the time and always sleepy
Had a thyroidectomy 35 years ago. Been on Levo since. Gained 80 pounds and never lost it til I went through menopause in my 50's. It was like a switch was turned in in my body.
I switched from levothyroxine to NP thyroid ( generic armor thyroid) and cytomal and feeling good..been on dedicated pig thyroid for 8 years now since hypothyroid. My Mom was also hypothyroid. I don't have hoshimoto either
Hi Dr Childs it’s funny I should come across this today. I had been On levothyroxine 75 for about 6 months, 💎thrumy insurance from my HMO, which is another issue. Since it’s free Hmo pharmacies buy from different place. When this happened Levo tasted like cardboard since I always chewmy meds TSH was .54 on my low range is 0.40 next visit in January was 0.24 which meant I was now hyperthyroid, the hair on the top/sides of my head. The hair on my head is dry and brittle. It literally started to brake off. One side worse than the other. This was enough to make me very depressed. my Hashimotos flared up and my body started craving sugar like a crazy woman. My A1C is at 5.4 and only taking one metformin 500 a day if I really needed it a day because I was way below range and some times took nothing but the sugar cravings were not me at all. so I knew something was Sometimes none at all as I was so hyper. prior I was feeling well, I had energy and no constipation.I think my issue might be conversion, all my test had been really good, so my dr stopped the RT3 test. Anyway I text the office and explained to my Dr office what happened, so she lower my dose to 50, but by the time I saw her the damage had been done to my hair. The Dr then lowered my levo to 50 mg, but when I went back to see in her my TSH went up dramatically from 0.24 below range to 2.9. All the numbers changed for the worse which activated my Hashimoto I felt. I am on LDN 4 mg and that has been a blessing thank you for sharing the information with use. LDN took all the fibromyalgia, and back pain away. We do know 2.9 is not my spot because the I was still symptomatic, so again she added 5 more mcgs of T3 along with the levo 50 mg. I am feeling a lil better, but my hair still not growing, nails are finally growing but still brittle. We decided testing my blood every two weeks. Then I text her after I saw the new bloodwork now. TSH was 2.08 better but again, my hair is not growing and nails growing but dry and brittle. She then increased Dr. Increased her T3 to 10 mcg, and levo was left at 50 mg. I still feel hypo again not as bad. When I saw her last week I asked her if taking the generic make a difference as interactions were different. I believe because HMOs pick the cheapest cost to them because it no cost out of pocket for me. She suggested doing synthroid to give it a try. I also asked the pharmacist about the difference he explained synthroid might be better as it’s made of the same ingredients all the time. I Started today synthroid 50 mg with 10 mcg of T3 after I did my blood work today 4/24/23. We will see my bloodwork in this week. Hopefully my TSH has gone down . I still feel hypo so I feel I have not found my right spot yet. Maybe my hot spot is somewhere between 0.50- 1.50. Losing your hair is the most devastating thing for a woman our self esteem goes down the drain. Wigs here in Florida is a no with all this heat.Sorry for the long story readers should know it can take years to find your ideal spot. The only thing I haven’t tried is tiroset or T3 on its own. People if you read this pay attention to what’s going on, and to what Dr child’s is saying , don’t wait until your next drs visit! Journal your symptoms, your good days and bad says. Always have your labs done and all the tests you n Dr Child’s site! Thank you Dr Childs for all your insights. You are appreciated I hope people take what your saying seriously, as it effects the quality of your life! Thank you! 🙏
So I tried Tirosint 60mcg for 1 month. Upped to 60mcg plus doubled on weekends to 120mcg due to high TSH. THEN 2 weeks at 62.50mcg. At 62.5mcg I started to have issues. At the end of 2 weeks my face swelled up along with hands and left leg and hives. Breast pain also happened. At ER due to breast pain had complete heart exam. Heart in good condition. Drs. Advised to no longer take the Tirosint. Am back on 60mcg of Armour. It what’s sad for me as I really wanted it to work.
T
Armor thyroid is much better than levothyroxine. it contains T4 and T3. Pharmaceutical companies try to claim thyroid patients have no trouble turning t4 into T3 but that is not so. Especially if the patients adrenal glands are weak. To find out if a doctor is willing to prescribe Armor Thyroid ask pharmacies which doctors they know prescribe it.
after being on 88mcg for 12 yrs it suddenly started to make me sick, my Dr lowered it to 75mcg, that didn't work so it got lowered to 50 and that didn't work.So now I'm on 50mcg of tirosint and I'm still sick I have inner trembling, anxiety, extreme, fatigue, unstable blood pressure, shortness of breath and headaches my Endo says my T4 and TSH level is normal and to keep taking it but I feel better without it. Please help😥
I am going through Menopause as well as Hypothyroid. I have felt for some time that my Levothyroxine (112mg) is too much for my system. I have hot flashes all day long, trouble sleeping, symptoms of ADD and super low energy. How do I identify the cause?
Hot flashes could be due to estrogen withdrawal, not necessarily excess thyroid dose - though both could potentially cause hot flashes
I have been taking Synthroid ( the brand) for 53 years for hypothyroidism/hashimotas disease because I can’t tolerate levothyroxine. I have not had any issues with gaining weight:
Ive been on synthroid then levothyroxine for the past 32 years so i couldn't get pregnant at 27 then started synthroid meds after being thoroughly tested. I got pregnant within 3 months of taking it. Felt great. I wasn't able unfortunately to have anymore children. Im now 61 and my levels go back and forth. Im tired, dont sleep well and have no energy. Gained an additional 11 ish pounds the last few years. Dr thinks all is good. Shes an internal medicine dr. I take mine in the morning then ready for a nap a half or so after if im not up. Im moody and unhappy.
I was on dessicated and started doing much better. I got a specialist who put me on synthroid. She made me switch tellling me “my bones wouldn’t turn over on dessicated “ and I’d end up with osteoporosis.
I feel like absolute shit. Hair falling out. Severe muscle fatigue and pain and my feet are numb. I gained more weight and I’m miserable. I hate myself and I hate my life. No care health care.
Get tested for drug induced lupus
I was on one thing 19 years ago after having a complete thyroidectomy, then changed to Synthroid. I started feeling all the side effects bothering me and went to a naturopathic doctor who put me on desiccated hormone. I was feeling better but, on my visits to the endocrinologist, she wasn’t happy with my decision and after some time of listening to her displeasure with my choice for treatment, I switched to another endocrinologist who over time won in my changing back to Synthroid. My dosage was messed up for more than 15 yrs. Changed doctor again and she levelled my t3&4, but because the side effects are getting worse, days ago I asked to be put on Tirosint having less fillers etc. She said she couldn’t prescribe it because it isn’t available in Canada. Given a prescription for Levo. I told her I would even cross the border to get it and was told she would have to be licensed in the USA for it to be valid, contradicting a pharmacist across the border who told me I just needed a prescription. The Levo I started today list more side effects than Synthroid….lord help us…
i have hashimoto disease and I have been on levothyroxine for about 2 months I've gain weight, i feel really bad, extremely fatigue and even my eye sight has gotten worst but lately I've been having my legs/ feet get swollen. I don't know if this is normal. have a dr appointment next month but should i make it sooner?
You can reverse hashimoto with diet, check online!
And I have had type two diabetes for 17years I started taking insulin in 2011 I have no diabetes complications and my a1c is 6.
I hav been taking levothyroxin since last month.only one tab 50mcg but im feeling an increased acidity. What should i do to overcome acidoty
My sister has asked to be put on a different med because Levo is inadequate. Her doctors are firm that it is the ONLY option. I fired my doc and got one that put me on Armour, which I do pretty well on. The resistance of the so-called medical community to alternative creates an impossible situation for the patient
What's interesting is that these are not alternatives, they are prescription medications intended to treat hypothyroidism. It would be one thing if they weren't medications, but they are.
It's the drug big pharma has been peddling FOR ENDLESS DECADES...they intend for you to be on it for the rest of your life. PROFITS are their main objective.
My endocrinologist put me on armour and I love it
I often wonder what the priority of Doctors actually is. The general health and well-being of the patient, or the financial incentive from the drugs manufacturer?
@@drwestinchildsSo why are the doctors so... resistance
I am an elderly man without any thyroid problem but the provider insists that I take Levo to give me energy. Is that the right approach?
i just found your videos. I have been on 125 mcg of levothyroxine for over 20 years, never felt any better. I tried mentioning it to my doctor once, and since my TSH was fine according to her, she shut me down. I live in a small town, and am not able to find someone who wants to prescribe anything but levothyroxine.
I also had complained to doctor about fatigue and thinning hair, she didn’t even acknowledge my concerns.
Sodium Lauryl Sulphate has to be why I cannot take Levothyroxine as have had to throw out every thing with it in. I take NP THYROID now, but in UK you have to buy it yourself.
I am a T1 Diabetic with Hashimoto's and starting menopause - so wondering if my tiredness everyday could be related to these as well. My endocrinologist just keeps giving me levothyroxine. Of course it goes back to my labs saying everything is fine. But I am always fighting that extra 20 lbs, impossible to lose (I exercise, eat fairly clean) and always exhausted plus hair loss and now a puffy face especially my eyes. Considering asking for T3 change, and seeing what my doctor states. Anyway, not really sure. But I've been thinking a lot of times my doctor's just don't know.
I truly thought it was just me feeling depressed, having awful body aches, and not losing the weight I've gained with Hashimoto's! I'm on Tirosint (gluten free gel pill) 112mcg five days a week, 224 mcgs for the other two days. It helps a bit, but I'm nowhere near the activity level, mental or emotional level I was. It's a terrible disease that pecks you to death. You struggle everyday to just barely reach the minimum of your personal standards.
Excellent comments, Germaine. I have been on thyroid meds for 22 years after half of the thyroid was removed. I was so ill I was sure I was going to die, seriously. Desperate, I began titrating my dose by using parts of the various doses I had until I found a dose that made me feel human again. Finally, I thought I just might live. The doctor, at the time, lowered my dose to where I felt better. I now take .112mcg and wonder if it shouldn't be lowered as I am losing hair, along with other issues. We will see.
Very
Have you tried switching to Carnivore diet
I’m so sorry and I hope you’re doing better. God bless you.
Subclincal hypothyroid put on 25 mcg of levo. Felt great and finally normal first day, but then started getting sensitive to the ac and worse fatigue 🤷
Dr Childs, what does it mean if levo makes somebody not able to move their body? It’s like; they take it and boom there’s like a blast and sudden energy loss, that can’t walk, can’t move.
I live in the UK and I'm entitled to free NHS healthcare. I can't afford private healthcare. The problem is, the NHS have stopped prescribing NDT and other T3 thyroid hormone drugs. Apparently now, all they offer to treat hypothyroidism is levothyroxine. And I can't get a RT3 blood test either on the NHS - my Dr says this isn't available in the UK. I think NDT is still out there but only if you go private (in the UK). So I really don't know what to do.
I'm a 31 year old woman and I was diagnosed with an underactive thyroid in 2018 (when I was 28), based on 1 set of blood test results which included high TSH. But I don't know how high. I was also diagnosed with low vit D and low B12. Apparently the vit D and B12 were extremely low. I was placed on supplements for the deficiencies and test results for them have since come back normal. But since being on levothyroxine, I've felt increasingly unwell. Not once have I felt better since being on this medication. My starting dose was 50mcg. I started to have hot sweats, head aches, dizziness and feeling sick that seemed to come on all of a sudden if I'd been out just walking or gone to the shop. I thought the dose was too high so i had more bloods done. My TSH came back normal. I'm aware that can be irrelevant. But my Dr basically insisted it was all in my head and I should be feeling better. I did research and found that the fillers in levothyroxine can cause side effects. One source basically said the higher the dose the less fillers. So in the hope of feeling better I asked my Dr to increase my dose if there is room to as I still felt unwell. My dose was increased to 75mcg in November 2020. Since then I have still felt no better and I have gained more weight. And I am always hungry. I hate myself for eating, but it's as if I feel sick and dizzy when I go too long without food (which is never long at all). I have been tested several times in the last few years for diabetes too, because I seem to be urinating more at night since being on levothyroxine.
I have requested that my Dr refer me to an endocrinologist. She has saud she will write to them. But I don't have high hopes as the NHS simply don't provide other options for treatment of an underactive thyroid. My hope is that I may have been subclinical hypothyroid and I don't need levothyroxine. Although my Dr did say it was my immune system attacking my thyroid. I had to do my own research to find out it's called Hashimotos thyroiditis. The Dr who originally diagnosed me told me not that much at all - apart from it's incurable and I'll have to take levothyroxine for the rest of my life. All this based on 1 set of TSH level test results. Tests since have been normal and while I've been on levothyroxine. But like I say - I feel dreadful. I also suffer EXTREME fatigue, aches and pains (which I am seeing a rheumatologist for in November as arthritis and degenerative disc disease run in my family). But I've thought, could the weight gain have caused the back and leg pain I'm suffering from. And could the weight gain be from levothyroxine. I really feel like this is the case. And if I'm genetically predisposed to back problems - it's foreseeable that getting fatter might cause it to happen sooner?
I really am at the end of my tether. I have no life. I don't go out. I'm too fatigued and in pain to go at it with exercise to lose weight and feel better. I feel trapped. Drs won't listen. I stay in because going out just to the shop leaves me so exhausted and in pain. And staying in has made me even more inactive. It's a vicious circle and my weight is ballooning.
I'm 5'8" and I last felt healthy when I was 13 stone. Although I know that isn't slim, I felt ok and looked good. I'm curvy and had a slim waist, skinny ankles and wrists, collarbone definition. According to BMI that's overweight, but like I say I didn't feel like I do now. I'm now 2 stone heavier, at 15 stone and I feel dreadful. Again I'm aware that's not morbidly obese for my height. But I'm sure the extra weight is putting pressure on my back and my knees - as I say, those problems run in my family. I still have slim wrists and ankles and a lot of people have said I don't look particularly dreadful. But I feel like death most days. It's rare I feel well at all. All since being on levothyroxine.
I felt unwell of course, before being diagnosed with an underactive thyroid - but never as bad as I do now!!! Could that just have been the other deficiencies?
Things like diet change being the cure scare me, because what are my options when I'm poor and there's very little I enjoy besides food. Meat and dairy are part of my balanced diet. I do eat enough vegetables too. But I would really struggle to cut out meat and dairy altogether. Alternative foods can be expensive and I'm already living well below the poverty line on benefits as I'm not well enough to work. I seem to often be low in vitamin b12 so surely it would be a bad idea cutting out animal products? Are there other supplements I can take, that can be bought at a reasonable price over the counter in the UK? I haven't seen iodine supplements anywhere for example. But if someone could tell me where?
I want to stop taking levothyroxine completely! I feel like I'm being poisoned. I'm going to give it a try to see if I feel better. I have nothing to lose it this point.
I have no faith in seeing an endocrinologist here in the UK. I feel like they will fob me off with the same bullshit. As they won't or can't even give me a RT3 test.
Any help or advice from anyone would be greatly appreciated as I'm struggling to find reasons not to kill myself tbh.
I can't provide medical advice on youtube but I would strongly suggest seeking out some mental help if you are feeling suicidal. There is always hope even if it doesn't feel like you can see it right now!
If the pharmacy changed me to this medication from a different thyroid medication for finances and I've gained 40 lbs what can I do? I'm in a nursing home used to weigh 336 lbs now back up to 195 from 156 in 8 months with dieting! Have Horizon medical insurance but pharmacy switches things constantly! 😢
When can I take thyroid ? I need my morning coffee can I take it before I go to bed?
I was on Lovo. For a few years and came off for two years because we relocated too another city. I started getting anxiety really bad . I am 207 pounds which I’m usually 160 pounds 5.9 tall. Started losing hair and no sex drive what so ever which makes it hard in my marriage. I started taking my Levo again because I found another doctor. We did bloodwork and yes I’m low on thyroid. I feel better no anxiety but still not losing weight and NO sex drive.. I’m looking at taking the Bronephrin for weight if that’s how you spell that. Can you even take it being on thyroid meds ??
I am hashimatos with high TSH but normal T3 & T4 what ll be the best medicine... My hair falls a lot and one nails is very ugly.. Used to take Thyroxine but not regularly skipped it very often...
I got fed up with hair loss and went bald on the top of my head. It was so bad I stopped taking it. I have now changed my medication. it's improved completely. I've now got hair. Levoxine.
Changed to what ?
Synthroid has Acacia tree as a filler. This can cause allergic reactions as well.
I've been on Levothyroxine for 2 years. When I smoke cigarettes for a while, all symptoms come back especially, body aches and fatigue.
On my Rx bottle it says to take on empty stomach first thing in the morning 30 minutes prior to eating or drink anything. But, recently I was impatient at a hospital & my RN's gave my Levothyroxine Rx mid day. When I asked them about it, they told me it didn't make a difference. Was that a pathetic excuse, or does it really matter?
Timing is everything!
Yes. Ive been on it for 25 years and NOT ONCE did my pharmacy tell me to take it an hour before food with a glass of water. When the new formula came out i looked at the insert plus the various drs on you tube and researched it on google and since taking the thyroxine on an empty stomach.... my blood results indicate that im being over medicated. So much for pharmacists
Do you recommend to take Iodine as well
I've had a thyroidectomy in 2016 and my doctor keeps reducing my meds to 112 mcg and I now feel miserable and put on weight. What to do. I have terrible hair loss, brittle nails, dry skin, etc. Please help me.
I have iron overload where do I fall? What thyroid medication is more beneficial for patients like me?
I take synthroid levothyroxine is that the same as levothyroxine?
Hi I have been diagnosed with Graves disease 8 years ago I have been put on anti thyroid medication and within a month I went underactive and I started taking levothyroxine for over 6 years my doze was between 100 to 150 micrograms and then I relapsed and I needed to go on anti thyroid medication again and after a year of this medication I had radio iodine after the radio iodine my thyroid hormone level stayed normal for only 6 weeks after the 6 weeks I have started levothyroxine 25 micrograms and my T4 and T3 are at the normal levels but I still have fatigue, muscle aches, hair loss and I can't lose weight although I exercise and made changes in my diet choose healthy choices and eat normal portions.
Do you have an idea what I can do to improve these things. I also want to say that in the 6 years period I never had these problems when my thyroid hormone levels were normal.
Can you please speak to how asthma meds like Advair and other inhaler effect thyroid meds, function, and tests? If you've already addressed this, can you point me to the video? Thanks
I am not sure how long I have been on Levothyroxine for quite a while maybe 20 years . I gain weight easily. I don't sleep well and my hair is all over the house. I get constipated more often than I ever used to. I think I take 75mg. I have asked the dr. about it but she says my numbers are good. I should do cardio and eat less. I am eating 1 meal a day. My nails are brittle and have vertical ridges my skin is dry, I have to load up on lotions. I have achy joints and developed arthritis to me there is something not right but she seems uninterested sugessted I am just getting older because my numbers are good. I asked if I should see an endocrinologist but she said I don't need one.
In your chart it says the 25 mcg tablets have yellow dye in it but my pills are not yellow they are pink so I don't think that is correct.
I guess different person,different side effect,im drinking levothyroxine by sandoz and im okay but when the pharmacy switch me to levothyroxine by Lennet this gives me a lot of problem,I feel like im running out of breath and its like i forget everything!I got brain fog and I dont have energy at all,I'm so down and I feel so depressed!.....but when I swicth back with sandoz , everything is normal again!
I'm up to 250 mcg if levo. I've gained over 60 lbs since 2007 after thyroidectomy diagnosed Hadshimoto, ice read T4 dies not always convert to enough to T3 , I bright this to my doctor, she ignored me n raised the T4 ...depression weight gain, pains , bring unstable I want real help
I am tt patient. I was on 150 t4 and 25 t3 and my tsh was 0.01 ,but my doc reduced it to 125 t4 and t3 as same as before.Now I am experiencing super brain fog and tiredness
Make sure to check your free T3/reverse T3 ratio and sex hormone binding globulin.
What about people with congenial hypothyroidism without the gland? I’m eating super healthy no sugar no gluten vegetables and drink a lot of water and I’m gaining weight.
I am getting a headache and my face looks swollen. I did not change my diet so I guess I don't expect to lose weight. MY thyroid is sluggish and slow but not hoshimotos like my mom. I have been on Lev for 4 days .75 mg..I was prescribed .05 2 years ago and it did not work, so my doc prescribed this mg. I also don't eat or want any dairy in my body and I head this has lactos. Ugh, I am so sick about this. I am the heaviest weight ever and I can't seem to lose weight and not sure what diet to be on. I am plant based, but that is not enough naturally. I am so so confused. Should I just go to a natural doc instead? I need to shed this major weight gain and get rid of these headaches that I never had before. It feels like brain fog on my right side of my skull and above my right eye. maybe from the lactos? Oh no!
YEs my endochrinologist is gradually,inceasing myndosage with ONLY the 50mcg tablets I AM SURE this is why fillers and dyes.I do get scalp itching anyway and dry facial skin.
I was on that for one week. And my atrial fib got worse so I was changed to a different one.
Me too!
Well, trying to find a doctor who really understands thyroid in your area. Most doctor just go by the basics standard thyroid test. I keep telling my doctor my medication is not the right dose. But she won't listen and won't look up any Medical information I have suggested. All she says is the test came back find. So any suggestions for me.
I googled, it says levothyroxine is not advisable to cut into half. Pls advise
Your channel is amazing!!!
Glad you like it!