How Long Do Chemotherapy Side Effects Last? All You Need to Know
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- เผยแพร่เมื่อ 6 ต.ค. 2024
- What is the duration of chemotherapy side effects during breast cancer treatment? Can some of these side effects become long-term? How can you effectively manage these side effects, and what factors influence how long they last? In this video, Dr. Jennifer Griggs explains everything you need to know about the duration of side effects from chemotherapy for breast cancer and its treatment
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I had a big operation to remove my reproductive system which was full of stage 4 cancer . Im 46 years old and live in Sydney Australia. I had 6 sessions of chemo ( Paclitaxel and Carboplatin) and only had a bit of occasional pain in my left leg . I was given a new drug called " Akynzeo" prior to each chemo session at the hospital. It is a new capsule designed to help with nausea . I experienced no nausea at all whilst going through treatment. I had a PET dye scan which came back clear of cancer . So I beat stage 4 cancer in 5 months !
Amazing! Well done 👍👍 wish I continued well being
That's incredibly inspiring to hear! Your resilience and positive outcome are truly remarkable. It's great to know that new advancements are making a difference in managing side effects. Your journey serves as a beacon of hope for many others facing similar challenges. Thank you for sharing your story with the Yerbba community!
Fantastic and well done and wish continued recovery and you have just given an inspiration to fight this illness. Thank you!
Aww thats so wonderful and good for you!
A traditional classic formula could solved fatigue issues in chemotherapy.just three ingredients of lamb/ginger and Angelica sinensis, no any side effects. Actually, it could boost your immune system.
The nausea is unbelievable. I find it the worst, then comes fatigue and the inability to sleep. You are a great speaker, thank you for no ums and ahs.
We're truly sorry to hear that you're experiencing such challenging side effects from chemotherapy. It's not uncommon for these side effects to vary in duration and intensity among individuals. It's important to communicate openly with your healthcare team about these symptoms, as they may be able to offer additional support or adjustments to your treatment plan. Thank you for watching.
Have you tried fasting? Apparently that really helps.
I finished my chemotherapy almost 6 weeks ago, and I still have good and bad days. I still have herceptin every 3 weeks until next May. Radiation is next, and praying it will go smoothly. Thank you for all the information and teaching us what to expect!!
Thanks for sharing your experience and taking the time to write.
Have strong faith in lord Jesus Christ beside having medical treatment ,God guides docs as well.
Radiation put me in the hospital last summer.
Radiation is brutal,
I went through it all and my only side affect is fatigue.
During chemo ..the nurse kept my feet and fingers covered with thick Ice pack ..it helped me a lot to avoid the tingling fingers and toes
Thanks for sharing your experience. There is some evidence that cryotherapy, using cold gloves and/or socks, may reduce the risk of neuropathy. Not everyone can tolerate the cold, however. Wishing you the best.
You can also wear too small surgical or nitrile gloves on your hands to achieve the same results as the cold or ice pack therapy during chemo.
@@iabelle85 do we use ice packs with the surgical gloves too or just wear the gloves only?
Thank you for this video, I finished Chemotherapy and Immunotherapy Treatments last November 2023, for Low Grade BCell Non-Hodgkins Lymphoma. I am still having Immunotherapy Treatments every 2 months, for a series of 4 Treatments. Pet Scan has shown Cancer is gone. Thanking Jesus. However, I still have a low endurance level, and have to sit and rest after the simplest of exertion, such as making the bed, or fixing a meal. Also, was diagnosed many years ago with Fibromyalgia, and have found that it has flared up and I am in a lot of pain all over my body. Also experiencing the neuropathy in my feet. Just saying all of this to say that I am encouraged to know that this can be normal after Chemotherapy etc. Thanksgiving you again for the video.
Thanks for sharing your experience. You're still within the window where you can expect to feel better and better each month. The fibromyalgia won't help of course. Hoping you're able to get exercise and good care for that.
I maintained therapeutic ketosis in conjunction with chemotherapy and resolved stage 3c endometrial cancer. As a carnivore, I did not experience any nausea, vomiting, or bowel issues. I am currently NED, with CT scans confirming all internal organs are unremarkable. 👍🤗🥳
Sounds so good. Thanks for sharing your experience.
I was diagnosed with breast cancer and two lymph nodes in Jan of 2022. Got through chemo radiation , immunotherapy and surgery but after stopping chemo, two months later I woke up with severe rheumatoid arthritis. I’m still struggling to walk and am on medication. Will this ever go away but I thank God I am in remission.
Chemo therapy is the Devil! don't do it! It make the Cancer Spread, plus your Dr's get Major Kickbacks for Big Pharma! $9,000/$10,000. per Session!
It's great to hear that you're in remission, but dealing with severe rheumatoid arthritis after your cancer treatment must be incredibly challenging. It is not uncommon for people to have a flare of an underlying, not-yet-diagnosed, inflammatory condition after treatment. It appears that treatment for cancer also treats inflammatory disease. Then when treatment stops, that inflammatory condition become symptomatic. In general, these symptoms do get better with treatment. Wishing you the best.
Men with breast cancer. I went to Stanford for a second opinion regarding my mBC. When I arrived at the department, the signage was "Woman's Breast Cancer Center." I fatuously thought that Stanford is so advanced, there was a "Men's Breast Cancer center." When I asked a passing RN where the men's department was, she looked at me like I was a 51/50. After a endoscopy and a biopsy of the new metz and several scans they showed that the tumor on top of my trachea is expanding at an alarming rate. In 2005 when my doctor ordered a mammogram, my insurance company refused to pay for it because "I was the wrong sex for a mammogram." I paid for it.
It's disheartening when healthcare facilities don't have specialized recognition for male breast cancer. Your perseverance in seeking a second opinion and advocating for necessary tests is commendable. Taking the gender away from cancers traditionally considered specific to any gender is necessary for many reasons. Thank you for sharing your story. Clearly, policy changes are required.
You must be an American .
Sad
A lot of patients hit a problem with the medical profession when they aren't typical for an illness. Like old people with STDs or athletic types with colon cancer. I hope your insurers start backing you in your hour of need with prodding from the doctors treating you. Good luck
Many never go away. I know that as fact. I’m one of the 3% that lived though their barbaric treatment and would never do it again. Trading quality for quantity is cruel. They didn’t tell me that was the deal.
It sounds as if you're having a really tough time with enduring side effects from your treatment. It sounds incredibly tough, and it's deeply unfair that you weren't fully informed about the potential long-term impacts. This situation is undoubtedly difficult, and your feelings of frustration and disappointment are completely valid. It’s important to have open and honest discussions with medical professionals about the expected outcomes and trade-offs of treatments. If there's any way you can seek support-whether through a patient advocate, counselor, or support group-it might help to share your experience and explore ways to improve your quality of life moving forward.
I’m so sorry that happened to you. I had a great doctor, but she didn’t tell me everything. They basically gave me a pamphlet of side effects. Here in the US, health care can be limited. The patient navigator told me about support groups, I went to one, and the women helped me immensely. They told me what to expect, shared their experiences, told me that I wasn’t crazy for feeling certain things, because everyone’s different. I don’t know what I would have done without that support. I do hope you find a group in your area. It’s a very stressful and traumatic to go through cancer treatment. My best to you.
Thank you so much. My nutritionist didn't help to give me the details on why and what. She spent our time giving me complicated recipes for me to stand over a hot stove and prepare which I was not able to do. I had to take matters into my own hands... I ended up with a "joey" bag hung over me injecting directly into my stomach. THAT saved my life. That was for throat cancer. Now that I'm a lot healthier I'm going into lung cancer chemo. Oh boy. I will be using your advice this time. Thank you again.
Thank you so much for sharing your experience. It sounds like you went through a lot, especially having to manage your nutrition on your own. Wishing you strength and health in your upcoming treatment.
Had my first chemo a few days ago. I'm done, not going through hell again.
Thank you for watching. Going through chemo can be an incredibly tough experience. Remember to prioritize your well-being. It is also likely that changes can be made in either the chemotherapy or in the medications used to prevent side effects to make it more tolerable for you. Wishing you the best.
Hey how are you feeling now? My mothers going through the same
Sorry that you have this illness. I have just been diagnosed and getting ready for chemotherapy. I hope you have other options for treatment.
My first week after my first chemo was pure hell. I was so afraid of second infusion. Second infusion (and rest) side effects were way better than first. Hope you can hang in there
My friend refused chemo and is on a keto diet with adding Vit C liposomal and vit D . Probiotics is also à must for immune system
2018 I have breast cancer , confirmed that need operation, Chemo, and radiation almoast 7 months i back to normal this year I’m free , thanks be to God
Congratulations on reaching this milestone! Your strength and faith are inspiring, and we're glad to hear you're doing well after treatment.
Great news for you.
They last for the rest of your life. It's the gift that keeps on giving......😢
Many side effects do last, that's for sure. And yet we're aware of people who are 10 years out from treatment who finally have something resolve that they were told would never resolve. Nonetheless, long term and late side effects of treatment can be so discouraging.
@@yerbba I just leave it here my distress:
I went to consult Geneva geneco and proctologist for anal HPV , i was given 2 cortisone creams - Scheriproct and Procto Synalar N- they knew that I was scared and worried about anal Cancer!!! still they added additional Anal Cancer risk factor to me - when I was already living in anxiety and fear- these creams made me so sick and I am facing huge aftermath of these substances that are highly cancerogenous: huge pelvic , lumbar pains, inability to sleep, agitation, itching, inflamed hemorrhoid ( maybe already cancerous because of these prednisone / cortisone creams ) .. I swear to God - Never ever I will do those barbaric Chemotherapies and Radiotherapies - they are Death therapies and modern medicine does more damage than good !!!! and unfortunately you have to be harmed by medicine - to believe me !!!!!!
I believe that, brain fog is forever. Dry skin, numb hurting feet. After chemo had to have gallbladder remover, complete hysterectomy.
So far side effects are better, still poor taste. 11 yrs.in October.
In our support group, we joked “Chemo, it’s the gift that keeps on giving”. Everyone is different, some people have longer lasting side effects than others. Support groups really help because you don’t feel so alone and sometimes we learn things that help in our recovery.
I would like to add to this topic. Going thru cancer twice, the worst item that comes to mind years later is insomnia, or really thinking that you aren't sleeping at all. I came to the point of begging the hospital EM to put me to sleep. They would only do that if I threatened suicide . My sister looked in on me and observed that I had been sleeping and I swore I hadn't. I went thru HELL. The problems with radiation and Chemo is really it doesn't really take affect until your last treatment. Then it gets worse. If you are treated for any oral or throat cancer, GET a feeding tube before treatment!!!!!!!!! Very important! I had IVa tongue cancer and stage 2Bc T2N1 SCC throat cancer.
Head and neck cancers are well-known for having severe and long-term side effects. Wishing you the best as you move forward.
Sorry friend my family and I are dealing with the big C as well…
When I went on line I found that insomnia is a common problem for cancer patients even after chemo is finished. In my opinion this issue is not taken seriously . None of my work oncology team ever asked if I was able to sleep. My ex primary doctor ridiculed me for having the insomnia" what do you expect?You sleep in a chair". As I said, she is my former primary care.
I'm doing chemo and holistic. I was diagnosed with TNBC in february. No SOC until now. I start chemo tomorrow. Hoping for a good result.
Sending good wishes your way!
I'm now 1 week NED with TNBC (diagnosed in June 2023). I had an amazing result (100%) with chemo. When they start talking about surgery ask about Goldilocks. It is an amazing procedure that is one and done. You are strong you've got this.
@@amyoakes9703 hey how you doing now? Please explain ur treatment?
@amyoakes9703 Hi, I'm tnbc also. Has your onco suggested Zometa infusions every 6 months for 3 years post treatment?
Thank you, Dr. Griggs, for your medical advice (very helpful).
Thank you, as always, for watching!
Very GOOD video. You are great at speaking.
Thank you for your kind words. Your support means a lot to us!
2018: laparoscopic hysterectomy and six rounds of adjuvant chemotherapy for cancer of the endometrium papillary serous (paciltaxel and carboplatin). Experienced nausea, vomiting, extreme fatigue, bone and muscle aches, tachycardia, neuropathy (which I still have in 2024), constipation, blue-black nails, hair loss, mouth sores, rashes and itching.
2023: Recurrence with metastasis to abdomen and abdominal lymph nodes. Twelve rounds of cisplatin and gemcitabine - nausea, vomiting, fatigue, intense itching. Tumors were reduced - am now on maintenance every four weeks with the monoclonal antibody bevacizumab-maly. Side effects of bevacizumab: rhinitis, watery eyes and increased blood pressure, also some stomach upset. Prescribed omeprazole 40mg for stomach upset and low dose hydrochlorothiazide for blood pressure
Just Another Day In Paradise…I’m thankful that last CT scan in November 2023 was clear and CA125 is 22
You have been through so much. Many of the medications you've been on are not familiar to our viewers because they are not used in the treatment of breast cancer. Nonetheless, we at Yerbba are familiar with these drugs and know that they can be difficult. Sounds like your disease is under control. Hoping you continue to recover from the side effects of your treatment.
Hi there,
Were you taking any parp inhibitor, targeted treatment tablet like olaparib after u first completed your chemotherapy treatment in 2018???
What is CA125?
Same.
@@jennycabral7247 It's a marker checked with a blood test to see if someone might need to have other tests to see if they have ovarian cancer. If above 35, that's a concern and other tests should be done, but by itself that's not a test that says for sure someone has ovarian cancer.
When I was70 I got breast cancer I got Chemotherapy and Radiation it will be 5 years in July 2019 I wondered how long does the chemo stay in my body You answered my question very clearly I must say it's great to know you are out there giving advice in layman's terms. I wasnt able to discuss with many people as I felt it was a lonely time but thank God for you
The chemotherapy stays in the body for about 48 hours after each treatment. Its effects obviously last longer. We're glad the information provided was helpful to you and that it helped you feel less alone during your treatment. It’s stories like yours that motivate us to create these videos. Remember, you're not alone, and this community is here for you.
Thank you so very much for your advice. Its all new to me. Looking forward to your support.
We appreciate the kind words. Thank you for watching and being part of our community!
Good day doc I'm from Philippines 🇵🇭 I'm finished my chemotherapy last March 11, 2023 after I finished I feel I'm dying to much pain all my body still pain may feet I feel like a electric in my vains after 7 months still pains I my legs. Stay safe ❤️
We're truly sorry to hear that you're experiencing such discomfort and pain even after completing chemotherapy. It's important to reach out to your healthcare team so they can evaluate your situation and provide you with appropriate guidance and support. They may recommend specific treatments, therapies, or adjustments to help manage your pain and improve your overall well-being. Remember, you're not alone in this, and your health is a top priority.
Stop your chemo and switch to a keto eating therapy ( no sugar at all )
God is good all the time and we will be all healed in mighty name of Jesus.Amen.
I know the pain in the leg. Try Japanese tea and Arnicare cream. Pray for God's help. Panadol for women helps me too.
I always thought chemo was the same for every cancer. But when I had mine I realised its very specific and each person in the chemo room seemed to have a different regime. So the symptoms will vary too. I was very lucky. The drugs I had for ovarian cancer stage 3C made me tired and bald but not nauseous. I still gave a little peripheral neuropathy in my feet 2 years later but I was able to be active quite quickly after my c past chemo op. My memory for names and words sometimes fails me . Interesting to learn here that this was a side effect. Thanks for the language and puzzles tip!
Thank you for sharing your experience with chemotherapy. Treatment regimens are indeed specific to the type and even the stage of cancer, as well as individual patient factors. We're glad to hear that you were able to remain active and that the tips on language and puzzles were helpful.
K ambrose1549 Thank you for your clarification in respect of Chemotherapy. I had not appreciated until recently that it is specific to each patient .
I had a double mastectomy last June, started chemo therapy for Invasive Lobular Carcinoma and On Hodgkin’s lymphoma in my bone marrow, and made it through 4 sessions of two kinds of chemo. Will be starting 30 sessions of radiations… I’m 72 and have been very active until all this. I’ll never again take chemo. It’s been really hard on me. I have the peripheral neuropathy in my fingers and feet.
I'm suffering financially due to paying bills late, suffering layoffs, wrecking my car because my brain doesn't work like it used to. I seriously regret getting chemo a year ago for my early stage cancer.
We're so sorry to hear about your financial and cognitive struggles following treatment. There are programs that can help with cognitive problems that involve getting formal neurocognitive testing. It may also help to connect with a social worker or financial counselor to help you navigate these challenges. There are resources available that might provide some relief. Your health and well-being are paramount, and finding support is key.
@@yerbba Is there anything I can do to heal my brain?
Hi, Iam so thankful to Yerbba for the information . My mum was diagnosed with her+stage 3. She is starting chemo in the 26.09.2023.
my request to you would be to do a her+ treatment video, with trastumab, perjeta.
Thanks so much for talking your time for this educational, much needed videos
Thanks for the suggestion. You may wish to check out our video on HER2-positive breast cancer th-cam.com/video/VeLxQzKuGh0/w-d-xo.html . Thanks for watching!
Thanks
I have just been diagnosed with a rare form of cancer.
I’m 78 with AIDS and a T cell count of below 500…undetectable viral load.
I am Seriously considering NOT going through chemotherapy and radiation therapy.
My concern is that I will endure the horrors of treatment only to find that my cancer hasn’t been treated or that it comes back.
At age 78, what is the point?
I have no family,no partner,no children, no pets.
I have no life’s work I need to complete.
Do I really want to subject myself to this torture for minimal or short term gains?
I am very sorry about the new diagnosis😕 I am a breast cancer survivor! It was rough no doubt.
I was 64 at the time. I could not tolerate the med I was put on after treatment. I stopped it and I put my trust in Jesus🎚♥️. It has not come back….praise to Him🙌🏻
Do you believe in God? I 🙏🏻that you do
Write me back if you need a friend going through this. 😊
Thank you for writing. It is completely understandable that you're questioning the benefit of treatment. Your choices must be aligned with your values and your goals of treatment. For our other viewers, it does not appear that people with AIDS with an undetectable load should not be offered treatment with curative intent. As always, understanding why certain treatments are being offered is essential.
@@yerbba well, I have decided to go ahead with the chemo and radiation.
It’s stage one cancer and the chance of “cure” is high.
I’m still rather daunted by the possibility of long term and profound side effects.
Thanks for replying.
U still have Jesus
Prayers
Uterine cancer survivor 2009. Lymphedema, chemo induced peripheral neuropathy and Levitor Nerve Spasms. Radiation both external and brachytherapy. Open abdominal surgery. Back then no ice packs offered. I am a survivor and grateful, however I am not the same person physically. I have ventral and hiatal hernia too from after surgery effect. Someday we will say “ How barbaric cancer treatments were.” We need more targeted therapies and less broad surgery, radiation and chemo.
We completely agree that we have to do better. Thanks for sharing your experience.
We seem to have same problem. No surgery as yet. Stage 4 endometrial cancer. Only chemo.
2008 breast cancer survivor that I agree no ice packs offered back then and I got neuropathy especially the worst in my right foot. Fast forward to 2024 and I was diagnosed with oral cancer and had a bone, nerve and tissue graft from lower right leg to replace dead bone in my jaw and it's made the neuropathy worse so my balance is affected and I have to be careful if I'm not walking on flat ground or going up and down steps.
Also besides neuropathy was thrown into menopause, had chemo brain, "ALL" hair fell out, and energy never really got back to normal. Some things got even worse with treatments this past year.
many paces don't offer ice packs, you bring them yourself.
Excellent job
We appreciate the positive feedback!
My 77 yr old unkie a smoker got cancer 2 yrs ago. Then he got a port, he was still feeling great n normal. jan 1st chemo feb 2 nd chemo treatment , march 10 hospital n mouth sores bad couldnt eat n drink march 19 died. He was medicine free all life. Doc said he got infection dont know from what meds didnt cure it. I think from port done him in.
We're so sorry to hear about your uncle. It sounds like he went through a lot in a short period of time. Infection can be a severe complication, especially when the immune system is compromised. Sending love to you and your family.
For our other viewers, ports do not cause people to die. Rather, it tends to be the underlying cancer.
What a brutal way to stop a disease. How on earth can they even determine how much and what kind to give you?
Experience and research
Such a great question. Feel free to check out our video about chemotherapy which touches on duration decisions: th-cam.com/video/PgDqTzVovxQ/w-d-xo.html . Please let us know if you have any additional questions!
Very true. I did my best (and I’m good) to avoid RT/chemo for 4 years. I was on a strict Chinese medicine protocol, handfuls of supplements, 4 surgeries, keto etc etc. it has returned every time, within months. I am now starting chemo/rt. Ya gotta do what you gotta do
@thetinmansheart 100% aye! I have been diagnosed with bone cancer and I always every thought that I would rather die than chemo but man when you have to chose between chemo and Death..... chemo is the obvious choice everytime. Hope you are feeling better!
This was very interesting. I went through six rounds of Carboplatin and Taxol for Ovarian and endometrial cancer. That was 9 years ago. I consider myself quite fortunate that I never had any nausea. The fatigue was bad and I had some neuropathy in my toes and fingers. It has mostly gone away it bothers me mostly in the winter months. And Chemo brain bothered me a lot. To me the worst symptoms and some I still struggle with came from the three rounds of High Density Radiation. I would say it took me a good 5 years to say I felt that I had recovered to feel almost normal again. Now close to 10 years post treatment with NED, I am even better then what I was before I was diagnosed. Much healthier all around but it was a long journey. I am still here and watching my granddaughters grow up… that was what I wanted the most. I would not hesitate to have chemo again if it were necessary. I’ve got 10 years of good quality life behind me and I’m still doing great. I am grateful for the treatment I received and the team I worked with.
Chemotherapy can be put into a vein(port), also put into a feeding tube,also put into the spine also put in orally and Chemotherapy creams can be applied to the skin.
I have 4 family members with different kinds and stages of Cancers. So,I have observed these different methods and cleaned up our bodies, clothing , carpets,bedding etc from the vomiting and diarrhea 😢😢😢😢
Thank you for sharing your experience. It sounds like you've been through a lot supporting your family members with different cancers. Your care and dedication in helping your loved ones through such a challenging time are truly admirable.
I hope you are protecting yourself when you are cleaning so as to reduce your exposure to the chemo drugs, including doing their laundry separately.
Definitely realize you might not ever recover after chemo. My wife has Stage 3 Primary Peritoneal Cancer and the chemo nearly killed her. She had horrific bone pain for 6 months. She was a completely healthy 46 year old prior but the chemo has damaged her kidneys, damaged her nerves (she now has fibromyalgia and neuropathy) and damaged her bone marrow so she has chronic fatigue. She has three oncologists and not one told us about 25% of people who have chemo will ever recover.
We're so sorry to hear about your wife’s experience. It's important that her medical team continues to support her in managing these symptoms. For our other viewers, the chemotherapy for primary peritoneal cancer is different from that given to people with breast cancer.
Neuropathy has kicked my butt so far after chemotherapy. I'm staying hopeful.
Mines gradually eased off over 6 months after I finished my treatment …every month it got a bit less. Hope you will be the same 🤞
Good to hear! I am miserable.
@@irene1182 chemotherapy ended in December. I'm taking immune therapy until early November. I will say the vitamins B6,12,3 and 1 have helped. Along with stretching.
@@EdithPleasants-ky9uh it got bad once I started taking the hormone blocker medicine. Definitely add exercise and vitamins. Discuss it with your doctors.
That’s a shame hoping it will ease off..I got Amitriptyline from my doctors ..maybe try that ! Not sure if it helped me or if it would have eased off over time anyway but worth a try
Glad to hesr for my hope
Thank you for watching.
Thank you😢I'm a regrowth ovarian cancer being treated at Princess Margaret Hospital Toronto, and I'm on olaparib pills after finishing my chemotherapy.
Thank you for sharing. We hope your treatment at Princess Margaret Hospital goes smoothly.
Thank you for all your videos..much needed 🙏
We are so glad you found our videos helpful. We appreciate you!
My momhas breast cancer and now she is experiencing after chemotherapy depression as i suspect after 14 sessions of chemotherapy (she has grade 3) now she got more and more not talkative and she cannot move or walk after 2 weeks of vomiting and headaches and now she can’t move her muscles well and she can’t swallow liquids and the problem is every MRI and scans results are good also the blood tests shows a good results. Now we don’t know why she is in this state ? Can you help me please?
Chemo is worse than cancer. People argue on this a lot, but until u see a very close person go thru it, u will never know what that feels. Pleasant death is better than 3-4 years additional life after chemo
_"Chemo is worse than cancer."_
Considering that chemo can help cure cancer, while cancer kills you, that is nonsense.
_"Pleasant death is better than 3-4 years additional life after chemo"_
That's a personal decision everybody has to make for themselves.
I agreement husband died thru having chemo 😢😢
I am so so sorry for your loss Christine
Witnessing a loved one endure such challenges can be incredibly distressing. Thank you for sharing your perspective with the Yerbba community. For our other viewers, talk through the risks and benefits of all the treatments that are offered to you.
I wasnt told anything thank u for the video
We're glad this video could provide you with the information you needed. Thank you for watching, and we're here to help with any more questions you might have!
My niece had hand and foot cramps during 3 years of chemo. Sadly she passed away at age 48.
We're truly sorry to hear about the passing of your niece. Going through cancer and its treatments can be an incredibly challenging journey, and it's heartbreaking to lose someone to this disease. If you ever need support or information, please don't hesitate to reach out. Losing a loved one is never easy, and our thoughts are with you during this difficult time.
So very sorry about your loss. That is a very long time she was on chemotherapy!!!
Excellent information and delivery. I'm only on my first chemo cycle and have already had nausea and vomiting and agree vomiting beats nonstop nausea because at least it makes you feel better afterwards. I already have peripheral neuropathy (non-diabetic, no known cause) so I'm really worried about that getting worse!
Thank you for sharing your experience. It's important to let your medical team know how bad your nausea has been because there are many options to improve your symptoms, including olanzapine, a medication that has been used for many years to treat people with mental illness and happens to work really well in smaller doses to prevent nausea. It’s understandable to worry about peripheral neuropathy worsening with chemotherapy, especially if you already have it. Keep communicating with your healthcare team about your symptoms. You may also want to check out our video on peripheral neuropathy here: th-cam.com/video/weh3SGcWIFQ/w-d-xo.html
RE: Chemo - There is an old saying in medicine: consider when the treatment is worse than the disease. The NCI mentions that the expected survival rate after chemo is 2-3%. Is it really worth the horrid side effects of chemo to gain 2-3 % longer.
For people with low risk cancer, yes, the benefit is very small. For people with high risk disease, the benefit is much much greater. This is why each person is a unique being.
I had the hot flashes over 9 years after my cancer. But my Dr worked with me .
Good to hear that you've found a doctor to help you. Thanks for watching.
Very thorough video -- thank you! You are appreciated.
Thank you for your positive feedback. Yerbba appreciates you!
Thanks for honesty.
Thank you for watching! We appreciate your support.
Please, make a video about aluminium deodorants and breast cancer…it i such a controversial subject. Thanks for all your videos, they are so helpful
Thank you for the suggestion! We will add it to our list!
I have been told to use ice gloves and boots to stop peripheral neuropathy when I start my next course of chemo paclitaxel
They have helped me; I put them on during the pre-med time so that my toes and lower feet area are cold by the time the Taxol is started. Good luck!
I did this. It was tough to cope with for 12 cycles alone (during Covid) with no one to help my get everything iced up when the nurses thought I was crazy I think, but I got through with zero neuropathy.
I used ice on my hands and feet when they started my chemo.. I asked the nurse when to start. Good Luck
Brrr sounds very cold and uncomfortable!!!
There is some evidence that cryotherapy, using cold gloves and/or socks, may reduce the risk of neuropathy. Not everyone can tolerate the cold, however. Wishing you the best.
I take Rso and have not had any nausea or appetite diminished. I sleep well also I’ve had 6 rounds of of rchop.
Thanks for writing. RSO is a processed form of cannabis. (Providing this just for other viewers.
All depends on the type of Cancer, Stage and Grade and how large the tumor is.
Chemotherapy side effects do not depend on the tumor characteristics although a host of other decisions certainly do.
How do you manage chemo sleep disturbance. I've tried everything I know to try.
Sleep problems are so common and can be so difficult to manage. We have a video on managing sleep problems while undergoing or after breast cancer. It's also important to talk with your medical team about your sleep problems.
Hi Susan, my name is Mary Lou. I have Lymphoma & I eat a lot of turkey & it help s me sleep. Prayers
@@maryloutapia315 so long as it isn't processed such as deli meat, which is one of the few foods that is definitely linked to increasing risk of cancer.
Very helpful 😃 I was worried about loosing taste glad to taste does come back because I want to eat food! It has been hard after chemotherapy
Thank you 😊
Losing taste is indeed a challenging side effect of chemotherapy, but we're glad to reassure you that it typically does return. Hang in there, and soon you'll enjoy your meals just as before.
Very helpful ! 🙏🙏🙏
Thank you for watching!
Thank you for such great information, hope to see more of your videos soon!
We appreciate your kind words and support. Stay tuned for more videos, and feel free to drop a comment if you have any specific topics you'd like covered. Make sure to subscribe so you don't miss out on future content! Thank you for watching.
Thank you for doing this.
Thank you for watching!
Taking estradiol for 42 years gave me breast cancer. No one ever told me. 😢Now I’m going through Chemotherapy and Radiation.
❤
Estrogen replacement therapy is associated with a slightly increased risk of breast cancer, particularly with long periods of use. This wasn't known for decades, and many people are still taking estrogen replacement therapy beyond their normal menopause date. Just for clarity for other viewers, estrogen replacement therapy in someone who had their ovaries removed at a younger age is safe and not associated with a higher risk of breast cancer. Estrogen containing birth control pills also do not increase the risk of breast cancer in the present-day formulations.
Hrt replacement therapy have high risks of breast cancer that's what my GP told me when I had my premenopausal syndrome which bothered me..I just have to take supplements and adjusted my diet instead of hrt..
I was so sick with chemo ..I had every side effect.. it put me in hospital for 4 weeks mil by mouth for 3 weeks mouth ulcers throats burns no taste could not eat or drink could not sleep lost weight diarrhea I had neutropienia .. hair loss ..chemo was ceased I have long term damaged eye sight swelling feet stomach problems radiation burns and long term bowel problems vagina
That sounds quite dreadful. A palliative care specialist may be able to help with your symptoms if you're not finding relief with your other medical providers.
After I was diagnosed with BC (male version) in 2005, my wife was diagnosed in 2014. We were Mr. and Mrs. Breast Cancer. Although I declined chemo, she went forward with being urged my her oncologist, that after radiation, it was the next step. My wife and I had a wonderful loving relationship over for over 30 years. After she completed chemo, she seemed to have chemo brain - by the way, is there a medical term for this?- her behavior became odd. She didn't seem to be the person she was prior to chemo. Several years later she locked me out of our home and requested a restraining order against me, saying she was afraid I'd break into her home and attack her. The restraining order was dismissed. She filed for divorce and I haven't seen or spoken to her for over 6 years although we live a miles away from each other. Might this be permanent chemo brain?
What you're describing here and have in your previous comment a while back is not related to chemotherapy-induced cognitive changes.
😊
Breast Cancer chemo, radiation and major surgery. 5 yrs out. The neuropathy is horrid. I will never recommend. Swollen feet, legs. The nerve damage is very painful. Both hands, both feet. And up my legs spasms with turning or twisting. Aches. Pains. No bueno. Prayers for all......
We're truly sorry to hear about the challenges you've faced in your journey with breast cancer treatment. It sounds like you've been through a lot, and your resilience is admirable. Dealing with the aftermath of chemotherapy, radiation, and major surgery can be incredibly challenging, especially when it comes to managing neuropathy and the associated pains. Your willingness to share your experience can be a source of support for others who may be going through similar struggles. Wishing you comfort and healing ahead.
I have just finished my 3rd round of chemo and I have had zero side effects , although I have lost most of my hair. Is this normal? Is there any significance to the fact that I haven’t had any side the effects of nausea, or vomiting?
The chemo doesn’t take effect before 3 weeks and it’s HELL
Some people who have no side effects fear that chemotherapy is not working. This does not appear to be the case. There's no reason to be concerned.
I had 17 rounds of chemo and 25 rounds of radiation. 9 years later my neuropathy has not improved at all section of burning. Pin and needles. Swollen feet. Chronic fatigue where I’ve found myself sleeping and my work desk. On a weekly basis. Arthritic pain becoming more severe and i got diagnosed in 2015. What I’m trying to say pain and discomfort may not go away.
It's true that about 5% of people have long term fatigue and the other side effects you describe. This is one reason we avoid chemotherapy whenever possible. Radiation therapy may also be avoided in some people although most people find that the benefit of treatment outweighs the risks.
Try herbs. Eat cassava or yucca for arthritis. I know the pain. Panadol for women helps me.
I'm sick all the time😢
We're sorry to hear that. Have you discussed your symptoms with your medical team? They might be able to adjust your treatment or provide medications to help manage the side effects. Wishing you some relief soon.
@@yerbba How kind of you to take the time to support me and other sufferers. Today, I took your advice and had my meds changed. Once again, thank you ❤️❤️
Thankyou for you videos
Thank you for watching and being part of the Yerbba community.
You just start to feel a bit better then you have to do it all over again 2 days after chemo was my worst time I couldn’t get out of bed.
It sounds incredibly tough to start feeling a bit better only to face another round of chemotherapy. The recovery rollercoaster can be physically and emotionally draining, especially those days when getting out of bed feels impossible. It's important to discuss these experiences with your healthcare team-they may have suggestions to help manage these lows more effectively, such as adjustments to your post-chemo care or medications to ease the recovery. Thank you for watching and sharing your experience.
Thank you for many informations. God bless.
Your support means a lot to us! Thank you for watching.
The best chemo side effect... remission. I just got my scan results. Last chemo infusion is tomorrow. I am so grateful for this treatment. My tumors are resolved and my DLBCL is in remission.
Great video, do u have videos of taking two different chemo treatments at once. I'm going through this now and its my second round of chemo treatment. Thanks for any information.
Most chemotherapy is a combination of two or more drugs. So everything we share refers to two drugs given at one time. We hope this is helpful.
I was on 3!
Great video doctor. Thank you!! I just finished neoadjuvant AC-T dose dense, got a pCR. SMX is next week. Radiation is next. With a stage 3 multifocal HR+, her2-, grade 1, is recurrence/Mets inevitable? Can they be prevented?
Thanks for writing. Everything you've done has been done to reduce the risk of recurrence. Every oncologist has many patients who are free of disease many many years later. The key is that you've done everything palatable to you.
Chemo......recently had ny first dose.......was fine for 48hrs afterwards but then the pain started. Both legs began tingling at upper thigh then you could feel it travelliing down to both feet. This pain prevented sleep for nearly 6 days then went away but followed by mouth ulcers then hair loss. Each symptom lasted for 3 to 6 days....Hope next course is better.
We're sorry to hear about the challenges you're facing with chemo. It's not uncommon to experience side effects like tingling, mouth ulcers, and hair loss. Remember to communicate any discomfort or side effects with your healthcare team, as they may be able to provide support or adjust your treatment plan to help manage these symptoms. Wishing you a smoother experience with your next course of treatment.
Same with me. Hope you feel better.
I finished my chemotherapy 6 year's ago and I still feel sick and tired most day's.
Thanks for writing. A small but important percentage of people have long-term fatigue. It would be worthwhile to talk with your medical team about being evaluated for the fatigue as there are other medical problems that can cause fatigue.
I had colon cancer stage 3 and they took it out but they found 2 cells in my lump ode so they recommend a chemo theraphy. I finished 3 sessions when I had a seizure and I was in sleep comma for 4 days since then I had arthritis gout and can’t walk sometimes for 1 month or so .
We're sorry to hear about the complications you've experienced during your treatment for colon cancer. It sounds incredibly challenging, especially dealing with seizures and mobility issues. It’s important to discuss these side effects with your medical team to adjust your treatment plan and manage these conditions effectively.
I am receiving chemo every week for 9 weeks and then I change to EC every 3 weeks. At present I have had 5 weeks of paclitaxel. Why do I get it every week? I have cancer in breast and lymph nodes and had lumpectomy and 17 nodes removed.
Thanks for writing. Weekly paclitaxel decreases toxicity and may be more effective than a higher dose given less often.
The Doctor should be able to explain why you are receiving Paclitaxel on a weekly basis . I hope you are coping with this regime and wish you good luck.
Finished my 3rd round of chemo last week and my last round in a couple weeks. Then I start another regimen for 14 rounds.
My wbc was around 700 right after chemo. It comes back up. My main side effects are being breathless and dehydrating. I ended up in the ER this last time because of it. I’ve lost 40 pounds and part of it is because I can’t taste much anymore. I had neuropathy for years so no problem with that or bone pain. I had cyberknife radiation and it was so easy on me. No side effects whatsoever.
Thank you for sharing your experience with the Yerbba community.
My side effects from breast cancer, even after 3 years is still with me and I'm 65...
Thanks for sharing your story. It may be helpful to have your primary doctor look for other causes of your symptoms. Too many times people (including doctors) attribute everything to the cancer and its treatment and don't pick up treatable causes from other conditions.
Please make a video about breast cancer and pregnancy
Check out our video about breast cancer and pregnancy. Feel free to leave a comment with any specific questions you'd like information on. th-cam.com/video/_JCZd4X6mqc/w-d-xo.html
Plz make a video on vmat & ABC ( dibh) radiation , side effects for radiation on left side after mastectomy
We can add that to our list. Thanks for the suggestion.
The brain fog has yet to go away, and the fatigue is never ending it seems. I'm now 5 years clear of colo-rectal cancer.
Congratulations on being five years clear! Brain fog and fatigue can linger long after treatment. We hope you find relief from these lingering side effects soon.
After chemo n a long radiation, it took my body about two years of careful recoup n every healthy diet n supplements to get slowly get back to feeling somewhat what I was! 😕. N the way my body looks after is still monsterous. But the doctors state it Al looks so normal now. But, my body is not their body. Cuz of it was. They wouldn’t have left me like this!
It's tough when the outward "normal" doesn't feel like the normal you know. It's important to have a supportive care team that not only addresses physical recovery but also understands the emotional and psychological impacts. Don't hesitate to express these feelings to your doctors; your perspective is crucial in managing your care.
Thank you so much 🙏🙏😔😔
Thank you for watching. We appreciate you!
My mom after 6 months completed breast cancer treatment; her hair grows around 10 inches now but her body is still weak, sometimes she falls while walking or shower. Anyone has suggestions for her how she can improve her health quickly?..❤❤❤❤
Thanks for writing. Her continued weakness is something worth talking about with her medical team. It is possible that rehabilitation would be helpful for her.
Add more food/calories to her diet. Eating is vital for the body to regain its stamina. I wish your mom the very best. (Ovarian cancer survivor here).
Yes stop the chemo and start à keto food therapy which really works
Eat protein and balanced meals. Dont fall or break bones. Try to sit or hold on to prevent falling.
@@Adèle9988 you don't seem to be reading what people are actually writing before you reply...this is not the only reply you've made where that seems to be the case. While hopefully your intention is to help, you may do more harm than good when people are in a vulnerable state and decide to listen to strangers on the internet.
Unattended depends how long you live my wife took chemotherapy until they totally destroyed her immune system and past away now my question would you take chemotherapy your answer is most likely no I know of several Drs said that they wouldn’t
The decision to undergo chemotherapy is deeply personal and can be influenced by various factors, including the type and stage of cancer, expected benefits, and potential side effects. It's unfortunate to hear about your wife's experience, and it highlights the importance of discussing all possible outcomes and ongoing management strategies with healthcare providers. Thanks for sharing your experience.
Very good 🙏
Your support means a lot to us! Thank you for watching.
My dad is suffering from stage 4 ca gall bladder metastases cancer, they are giving him cisplatin and gemcitabine dose, doctor says we can extend his life only for 1-1&half years, please give me some hope 😭😭😭😭😭😭
We're so sorry to hear about your dad's diagnosis. While it’s so hard to hear about timeframes, there is always hope in how he responds to treatment, and being there for him with love and support is incredibly valuable. There are also people who live beyond what experts estimate. That estimate is an average.
I wish the medical community would be more honest about chemo and especially radiation!!! They never focus on the cause of cancer.
The medical community is searching high and low for the causes of cancer. One thing to remember is that cancer is not one disease but hundreds. It is likely that there are many factors together that cause cancer.
Thank you so much , I'm afraid I have stage four breast cancer and about to start chemo , can I survive this b/c the Dr said it has spread to lungs , neck and shoulder bone . God bless you .
Look up Professor Thomas Seyfried and start your ketogenic diet immediately. The diet alone will be helpful and help your body recover with whatever treatment your Dr recommends. Hopefully your Dr knows a few things here amd there
Facing stage four breast cancer can be incredibly daunting. It's crucial to work closely with your healthcare team to explore all available treatment options and to maintain open communication about your concerns and goals. While the road ahead may be challenging, many people find strength and support in their journey. Remember to lean on your loved ones and medical professionals for support, and take things one step at a time. Sending lots of love your way.
Prayers help you get through this difficult period and Trust in the Lord and Savior.Believe in Him and He the best healer ever. God is Good. Keep on praying and be of positive thoughts and it will help you a lot. Only God can reverse the impossible to possible. I will include on my prayers and others too , I’m also a CA patient and had gone through chemotherapy. ❤❤❤
I would try keto , read so much of it helping to kill cancerI haven't the will power to stick to it but goin to try
@mariedixon6081 Look up: Hippocrates Research Fondation. The people from this channel obviously don't want other information, types of treatment that goes against their standard care, posted here. But cancer is not only a disease, is an industry as well that generates gigantic amounts of money.
Hello Doctor ! During chemo , I lost my hair .But WHY IS IT STRNGE TO ME THAT after my chemo treatment was done afyer a month I Started loosing my eyes brow and eyes lashes
Is this normal even though My chemo treatment was done
That happened to me also but they grew back really fast.
@@donnacampbell6345 you mean eye lashes and brows or hair ..Look my hair is growing after chemo , but at yhe same time is I am loosing my brow and lashes .. dont know why ?? Infact it should be not loosing because my chemo was done
Doctor is the reason for loosing my lashes and brow after chemotherapy Is the cause of RADIATION ? ?? BECAUSE I AM PRESENT ON MY RADIATION FOR 21 SESSIONS
PLEASE REPLY DOCTOR .THANKYOU 🙂
The same thing happened to me. My last infusion was July 12th, but my eyebrows and eyelashes only recently fell out in late August. I was told it was because the eyebrow follicles are not on the same cell cycle as the follicles on the scalp.
I finished my chemo end of April and my eye brows still have not grown back.
Hi doc, thank you so much for all your videos and explanations, I have a request please and I hope you note my comments, Can you please make a video about stage three her2 positive, hormones negative breast Cancer? I find very little information out there on this type, mainly it’s triple positive, or Her2 negative and hormon positive
Thank you for your kind words and suggestion. We have a few videos on HER2-positive breast cancer that might offer some insights here: th-cam.com/video/VeLxQzKuGh0/w-d-xo.html.
I am 20 years out from my mastectomy. I am currently seeking radiation for my second metastasis. I feel like I have an orphan disease because I am a man. I skipped chemotherapy because it seemed worse than the disease. Seven years after my diagnosis, my wife was diagnosed with BC. She had a double. She made light of it by joking, I'm getting breast reduction paid for the insurance company. She underwent chemo and I believe she got chemobrain that I believe she did not recover from as evidenced by divorcing me after being married for 35 years, accusing me of stealing her silver spoon collection, and getting a restraining order against our son stating that she was afraid that he would break into her house and harm her. Our son is like melba toast. Since our divorce she hasn't communicated with him and that's for 5 years, although we live less than a mile away from her. I don't think you addressed permeant chemobrain. Is there any hope that 10 years following chemotherapy she may return from the hateful binge she has been on?
We're sorry to hear about the challenges you and your family have faced. Chemobrain, or cognitive issues following chemotherapy, is a recognized side effect, but the extent can vary. Encouraging her to consult with healthcare professionals and considering support services could be beneficial. However, predicting the future course is challenging. For our other viewers' information, so-called "chemobrain" does not cause the kind of personality and behavioral changes that you described. You may find our video on chemo brain helpful: th-cam.com/video/eUnYrYspVO8/w-d-xo.html
There's no upside to taking chemo only downsides. Would never personally do chemo for any reason to many side effects that lasts forever I'll take my chances with the disease...
Thanks for taking the time to share your thoughts. The benefits of chemotherapy include an improvement in survival, and for many people, the benefits do outweigh the risks. It's important for each person to make an informed decision that is concordant with their values, what's important to them.
Chemo for HER 2 positive breast cancer was not that bad, it saved my life. Tumor was gone after a year of chemo and targeted therapy! Also did 6 weeks of radiation, that was worse than chemo for me. The tumor was the size of a small grape, under the band of my bra just to the left of my left breast.
Thank you for sharing your experience with the Yerbba community. It’s wonderful to hear that chemotherapy and targeted therapy were so effective for you. Everyone's journey is different, and it's helpful to hear that despite the challenges, treatment made such a difference in your life. Wishing you continued health and strength!
As a man living with mBC for 20 years I am so disturbed my the financial priorities in our country. A nuclear air craft carrier cost 10-13 billion dollars, a NASA space probe to study the surface of Pluto cost 1 billion. The most expensive item ever built by man is the ISS - the International Space Station at 150 billion bucks. A B-2 bomber costs 2 billion a copy and we have 16 of them, the budget for NASA is 24 billion a year, the Iraq war cost 2.4 trillion buckeroos. How much is the amount given for the National Cancer Institute .... all of 7 billion. What is wrong with this financial picture?
So much is wrong, isn't it?
What the hell is that all about
I had Colon cancer. And the chemo almost killed me.they should have taken a blood before going through chemo to see if I'm good for having this chemo. So it was like giving me two chemos in one. I was in the hospital for 7 days. I'll never have chemo again. I have been cancer free for 4 years. And still have side effects.i get some good days but more days where I don't feel good at all. I hate it so much.
We're so sorry you had such a tough experience with chemotherapy. For our other viewers, there is a gene variant that can indicate a higher risk of toxicity from a drug called 5-FU or its cousin capecitabine (Xeloda). People with this particular gene mutation can ave a great deal of toxicity. It's a rare mutation, and most people are not tested for it. We are grateful to hear you've been cancer-free for four years, but dealing with long-term side effects is really challenging. Wishing you more good days ahead.
Thank you
Thank you for watching and being part of the Yerbba community!
I have HER2+ IDC in one breast with nothing in lymph nodes. I’m 64. Is there a reason to do more than 4 cycles of chemo? I’ve had some really bad side effects.
It's hard to know what the best treatment for you would be without being part of your care team and having all the information about you and the tumor. Depending on the size of the tumor and the hormone receptor status, less chemotherapy may be as effective as more chemotherapy. Again, we can't offer specific medical advice without being part of your team. All the best as you move forward through your treatment.
@@yerbba yes light chemotherapy is safer and ask a nutruitionist for advice . Sugar is your worst ennemy as well as low carbs. That is NO SUGAR AT ALL
I wish the medical community would be more honest about chemo and especially radiation!!! They never focus on the cause.
The medical community is searching high and low for the causes of cancer. One thing to remember is that cancer is not one disease but hundreds. It is likely that there are many factors together that cause cancer.
Thanks for the video. My blood tests showed my liver was struggling (very high enzyme results). Does the liver return to normal? How long does it take?
If the elevation of the blood tests is due to chemotherapy, these will usually resolve within a few months. If they do not, other causes of the elevation should be looked for so as not to miss something else.
Chemotherapy runs through the whole body and attacks vital organs ( heart, liver, kidneys etc....and finally put your immune system to 0. Any other deseases can kill her . Switch to integrative medecine.
On being a "survivor" of cancer. This is an erroneous term to apply to folks who have cancer. Survivorship is more appropriate to describe a person who has survived a single traumatic event such as a soldier's safe return after 2 stints in the war in Afganistan. Perhaps the term survivor may be more properly applied to describe a person who didn't go down aboard the Titanic. We who live with cancer are much greater than a simple survivor.We are perservers. We who have the beast are always cognizant of harboring a deadly disease that can snap you out of remission on a follow-up CT scan. There is no conclusive proof that whatever the treatments a cancer patient undergoes it may not be sufficient to declare "I'm cured." I believe there is very likelihood that once you have been diagnosed with the "beast" you can not guarantee a life in remission. Cancer cells are minuscule. One of my oncologists explained that "on the average a square centimeter of cancer contains 10 billion cancer cells." Can a cancer patient expect to eradicate all of them to strive for a lifetime of being cancer free?
Many people with a history of cancer live long and full lives and die of natural causes. Your point is well-taken, however. It may be helpful to know that people who survive a traumatic event also experience long term risks given that their life narratives have been interrupted. It may also be helpful to know that one is actually surviving cancer even if one is "living with" cancer.
My doctor said that colon cancer is uncurable , meaning it can always reoccur. Why is that? Looks as if you completely got rid of it , why would it come back? Cant your immune system recognize it if you have had it. Looks like the immune system would be able to detect it if it came back. Makes no sense to me.@@yerbba
Medical industry may have a deferent approach to cure or prevent diseases. Remember "Do NO Harm" doctors moto.
The principle of "Do No Harm" is indeed central to medical practice. It emphasizes the importance of ensuring that any treatment provided does not outweigh the potential benefits. Each treatment approach is carefully considered to align with this principle. Thanks for raising this important topic.
Good to know
Thanks for watching.
I'm on hydroxyurea, 1000 mgs a day.i will be on it for the rest of my life. Can you expand on the side effects of this meds.
Thanks for writing. For our other viewers, hydroxyurea is not used in the treatment of breast cancer. It is used in the treatment of chronic myelogenous leukemia that is refractory (does not respond to treatment), squamous cell carcinoma of the head and neck (excluding the lip) that is locally advanced, used with chemoradiation, in combination with other chemotherapeutic drugs or radiation therapy for the treatment of malignant melanoma, head and neck cancers, and brain tumors.
Side effects of hydroxyurea include the following:
Common Side Effects
Gastrointestinal disturbances like nausea, vomiting, loss of appetite, constipation, diarrhea
Mouth sores
Serious Side Effects
Bone marrow suppression leading to low blood cell counts (anemia, increased infection risk, bleeding/bruising)
Increased risk of developing other cancers like leukemia and skin cancer with long-term use
Lung disease with symptoms like fever, shortness of breath, cough
Blood vessel damage leading to open sores on arms/legs
Patients on hydroxyurea need to be closely monitored for side effects, especially signs of infection, bleeding, or new cancerous growths. Dosage adjustments or discontinuation may be required if serious side effects occur.
Welcome to planet HOPE.
Hope is a wonderful place to live.
I will honestly say that chemotherapy is worse than choosing a natural nutrition therapy such as ketonic mediterranian food therapy . Chemotherapy attacks all your healthy organs and destroys your immune system . Your immune system is paramount when fighting cancer or any other any life-threatening disease . One will live longer and healthier without chemotherapy. Don’t listen to the médical staff who are paid by the pharmaceutical lobbies to encourage you to undergo chemotherapy chemotherapy. That will eventually kill you. My friend who suffers from recurrence breast cancer is going to Germany for an integral therapy. France ( where I live ) has an only one protocole no matter what whoever whatever cancer you suffer from just like you were a number.
It sounds like you had a really rough time with chemotherapy. Just for the sake of clarifying for our viewers, nurses and physicians are rarely paid by pharmaceutical companies to give chemotherapy. Most chemotherapy agents are off-patent and are not marketed by pharmaceutical companies. Nonetheless, a healthy dose of skepticism is appropriate. As another point of clarification, only one part of the immune system is affected by chemotherapy--the part of the immune system that makes the white cells that fight bacteria. For interested viewers, this video may be helpful: th-cam.com/video/zzKCaX8LSok/w-d-xo.html
It’s like slamming your finger tips in a door. It’s very painful. The bottom of my feet feels numb. It’s weird.
Neuropathy, which is most likely accounting for the numbness, is a troublesome side effect. Even after many years, neuropathy can still get better. You may find our video on peripheral neuropathy to be helpful: th-cam.com/video/weh3SGcWIFQ/w-d-xo.html
I’m the same, walking with a walker