How Long Do Chemotherapy Side Effects Last? All You Need to Know

[@yerbba]

Get your Yerbba Report Here: www.yerbba.com/ Take control of your breast cancer treatment with personalized insights.

[@janewilliams2352]

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 !

[@ggunga7764]

Amazing! Well done 👍👍 wish I continued well being

[@yerbba]

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!

[@ggunga7764]

Fantastic and well done and wish continued recovery and you have just given an inspiration to fight this illness. Thank you!

[@donnaatienza8001]

Aww thats so wonderful and good for you!

[@名氏无-j5g]

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.

[@nora768]

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.

[@yerbba]

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.

[@pankajrohaj]

Have you tried fasting? Apparently that really helps.

[@renzo6490]

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?

[@joanquigley6363]

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. 😊

[@yerbba]

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.

[@renzo6490]

@@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.

[@anniekormah1139]

U still have Jesus

[@jobowman3144]

Prayers

[@cynthiayee5116]

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

[@yerbba]

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.

[@iabelle85]

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.

[@nature942]

@@iabelle85 do we use ice packs with the surgical gloves too or just wear the gloves only?

[@sue-lanvermaak8505]

With my treatment, I have to avoid anything cold. I am not able to open a fridge or touch metal for 5 days after my treatment.

[@jocelyncabilan3603]

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

[@yerbba]

Congratulations on reaching this milestone! Your strength and faith are inspiring, and we're glad to hear you're doing well after treatment.

[@paulachin9130]

Great news for you.

[@carolbraswell4488]

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!!

[@yerbba]

Thanks for sharing your experience and taking the time to write.

[@promillakandhari9450]

Have strong faith in lord Jesus Christ beside having medical treatment ,God guides docs as well.

[@johnkrieger185]

Radiation put me in the hospital last summer.

[@TraceyMella]

Radiation is brutal,

[@816Lynnie]

I went through it all and my only side affect is fatigue.

[@vernawalzak969]

I'm praying all of us here get relief and healing. I was diagnosed with breast and lymphnod cancer on 9/30/24. Still waiting on details, staging and grading. I'm in a lot of pain and hoping to get my port tomorrow and chemo soon.

[@yerbba]

We wish you weren't going through this. This is a life-altering diagnosis, and waiting for details can be one of the hardest parts, especially when you're in pain. We hope you get your port soon and can start your treatment.

[@CarrieNoble-j4q]

Oh , so sorry that you have to go through this pain and struggle. 🙏🙏🙏

[@SlotstheMetaphysicalwa]

Hi shoot me an email found out in July 2024 breast stage 4 lymphnodes and lungs. I'm still testing in NJ, but I'm also using RSO oil it's nasty if ur a non cannabis user. It does help with pain also been using castor oil packs since day 1 of diagnosis on breast and lymphnodes.😢😢😢🙏🙏🙏

[@DALDO135]

May I pray for and heal you, AMEN 🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏

[@DALDO135]

*Jesus

[@evankopald8737]

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.

[@yerbba]

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.

[@Michelle-yw1lv]

You must be an American .

[@kathysteiner9468]

Sad

[@kambrose1549]

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

[@mrsz1988]

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.

[@yerbba]

Sending good wishes your way!

[@amyoakes9703]

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.

[@foodybabes9272]

​@@amyoakes9703 hey how you doing now? Please explain ur treatment?

[@michelegray9007]

​@amyoakes9703 Hi, I'm tnbc also. Has your onco suggested Zometa infusions every 6 months for 3 years post treatment?

[@ritaterry4284]

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.

[@yerbba]

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.

[@disellin4871]

They last for the rest of your life. It's the gift that keeps on giving......😢

[@yerbba]

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.

[@evefairy7740]

@@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 !!!!!!

[@angelslove58dr]

I believe that, brain fog is forever. Dry skin, numb hurting feet. After chemo had to have gallbladder remover, complete hysterectomy.

[@carolbaughan8768]

So far side effects are better, still poor taste. 11 yrs.in October.

[@alineanderson4320]

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.

[@martdod]

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.

[@yerbba]

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.

[@alineanderson4320]

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.

[@philipcondenzio5987]

I’d rather leave this earth than have that sinister crap coursing through my body.

[@NappturallyTrendy]

​@alineanderson4320 my nurse navigator just signed me up for survivorship group. I'm having a hard time dealing with chemo side effects. Telling us everything will return to normal after chemo is the furthest thing from the truth. Thank you for letting me know the group does work❤

[@TrangNguyen-ns2uo]

​@philipcondenzio5987 quote from an actor" your love one will miss u if your gone"

[@yacaattwood2421]

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

[@yerbba]

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.

[@navbharat1443]

Hi there, Were you taking any parp inhibitor, targeted treatment tablet like olaparib after u first completed your chemotherapy treatment in 2018???

[@jennycabral7247]

What is CA125?

[@Lisa-io6pr]

Same.

[@ChooseForToday]

@@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.

[@johngrafton6868]

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.

[@yerbba]

Head and neck cancers are well-known for having severe and long-term side effects. Wishing you the best as you move forward.

[@cherylcosgrove511]

Sorry friend my family and I are dealing with the big C as well…

[@lindajones4849]

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.

[@annmcnamara8]

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

[@yerbba]

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.

[@patmolnar8810]

Very GOOD video. You are great at speaking.

[@yerbba]

Thank you for your kind words. Your support means a lot to us!

[@bobbipetty7411]

Had my first chemo a few days ago. I'm done, not going through hell again.

[@yerbba]

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.

[@aminatakunda3674]

Hey how are you feeling now? My mothers going through the same

[@yogi8284]

Sorry that you have this illness. I have just been diagnosed and getting ready for chemotherapy. I hope you have other options for treatment.

[@judybee6698]

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

[@Adèle9988]

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

[@aliciaforte60]

Thank you all for prayers. I’m sending prayers back.

[@yerbba]

Your gratitude and prayers are so touching; sending them right back to you.

[@kurtiswichmann4699]

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.

[@yerbba]

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.

[@kambrose1549]

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!

[@yerbba]

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.

[@annewalden3795]

K ambrose1549 Thank you for your clarification in respect of Chemotherapy. I had not appreciated until recently that it is specific to each patient .

[@lj9524]

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.

[@yerbba]

We completely agree that we have to do better. Thanks for sharing your experience.

[@amelapapan6625]

We seem to have same problem. No surgery as yet. Stage 4 endometrial cancer. Only chemo.

[@melissaliles965]

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.

[@melissaliles965]

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.

[@ChooseForToday]

many paces don't offer ice packs, you bring them yourself.

[@24carrotgold8]

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. 👍🤗🥳

[@yerbba]

Sounds so good. Thanks for sharing your experience.

[@afsanakhan9592]

Please share your diet

[@jamaaznyaboke9434]

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

[@yerbba]

Thanks for the suggestion. You may wish to check out our video on HER2-positive breast cancer kzbin.info/www/bejne/jJavqYSwgNp6npI . Thanks for watching!

[@jamaaznyaboke9434]

Thanks

[@Nasha.Ahsan.1]

My father 76 was diagnosed with stage 4 lung cancer, he's just had this 3rd session of chemo (and 2nd session of immunotherapy), his body weight is going down because he can't/won't eat anything. His energy levels are extremely low and after this session he's had Nausea, Vomiting and diarrhoea. We're seriously considering proceeding with it for the 4th session.

[@naththomas9946]

Thank you, Dr. Griggs, for your medical advice (very helpful).

[@yerbba]

Thank you, as always, for watching!

[@eileenenriquez7894]

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 ❤️

[@yerbba]

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.

[@Adèle9988]

Stop your chemo and switch to a keto eating therapy ( no sugar at all )

[@LitaSantos-gd3cr]

God is good all the time and we will be all healed in mighty name of Jesus.Amen.

[@amelapapan6625]

I know the pain in the leg. Try Japanese tea and Arnicare cream. Pray for God's help. Panadol for women helps me too.

[@susanstrong9218]

How do you manage chemo sleep disturbance. I've tried everything I know to try.

[@yerbba]

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.

[@maryloutapia315]

Hi Susan, my name is Mary Lou. I have Lymphoma & I eat a lot of turkey & it help s me sleep. Prayers

[@ChooseForToday]

@@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.

[@discospiders]

Cannabis edibles are the only thing that let me sleep all night.

[@evankopald8737]

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.

[@yerbba]

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.

[@judithmargret5972]

No, it is not worth it.

[@discospiders]

@@evankopald8737 the expected survival rate for all humans is 0%. We are all going to die eventually. You’ve left out the most important part of the equation- remission times. These vary greatly, depending on the person and the type of cancer.

[@Rosie-wj1le]

My niece had hand and foot cramps during 3 years of chemo. Sadly she passed away at age 48.

[@yerbba]

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.

[@louiseamrhein7408]

So very sorry about your loss. That is a very long time she was on chemotherapy!!!

[@GladstoneGander33]

What a brutal way to stop a disease. How on earth can they even determine how much and what kind to give you?

[@hmgrraarrpffrzz9763]

Experience and research

[@yerbba]

Such a great question. Feel free to check out our video about chemotherapy which touches on duration decisions: kzbin.info/www/bejne/hpinooewi9SprrM . Please let us know if you have any additional questions!

[@thetinmansheart]

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

[@pankajrohaj]

​@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!

[@susanlanglo-killian7096]

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.

[@namiesnaturals3557]

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.

[@yerbba]

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.

[@marniebrindley]

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?

[@Adèle9988]

The chemo doesn’t take effect before 3 weeks and it’s HELL

[@yerbba]

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.

[@discospiders]

@@marniebrindley I haven’t experienced any nausea or vomiting, after 4 rounds of carboplatin/paclitaxel

[@discospiders]

@@Adèle9988 that’s not true at all. The chemo takes effect immediately. Some cocktails have cumulative effects, some do not.

[@richardcooper3360]

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 😢😢😢😢

[@yerbba]

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.

[@ChooseForToday]

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.

[@roselucht4583]

I had a double mastectomy last June, and started chemo therapy for Invasive Lobular Carcinoma and Non Hodgkin’s lymphoma in my bone marrow, and made it through 4 sessions of two kinds of chemo. I 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 lower legs and feet… the peripheral neuropathy is starting to go away in my fingers. It’s been almost 4 weeks since I had my last chemo. I started doing water aerobics several times a week which feels wonderful, I sleep better at night now. I have fatigue in that I can’t walk as fast as I used to and I have to sit more… I want to get more active and wonder how long chemo drugs actually stay in the cells in our body.

[@yerbba]

It sounds like you've been through so much with both the double mastectomy and chemotherapy for invasive lobular carcinoma and lymphoma. Chemotherapy can be extremely hard as you know, and it’s understandable that you wouldn’t want to go through it again, especially with the peripheral neuropathy you're experiencing. Make sure to talk to your care team about ways to manage those symptoms and take care of yourself as you prepare for radiation. Wishing you strength and comfort through this part of your journey.

[@robertsiefman7543]

I take Rso and have not had any nausea or appetite diminished. I sleep well also I’ve had 6 rounds of of rchop.

[@yerbba]

Thanks for writing. RSO is a processed form of cannabis. (Providing this just for other viewers.

[@jaypalnitkar4400]

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

[@hmgrraarrpffrzz9763]

_"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.

[@christineholley9593]

I agreement husband died thru having chemo 😢😢

[@jaypalnitkar4400]

I am so so sorry for your loss Christine

[@yerbba]

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.

[@ameliagoodlyfe3633]

My dad's death was peaceful no chemo. My brother has stage 4 stomach cancer and just had chemo. He's a terrible mess 😢

[@amelapapan6625]

Thank you so very much for your advice. Its all new to me. Looking forward to your support.

[@yerbba]

We appreciate the kind words. Thank you for watching and being part of our community!

[@deschelbutler4859]

Neuropathy has kicked my butt so far after chemotherapy. I'm staying hopeful.

[@irene1182]

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 🤞

[@EdithPleasants-ky9uh]

Good to hear! I am miserable.

[@deschelbutler4859]

@@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.

[@deschelbutler4859]

@@EdithPleasants-ky9uh it got bad once I started taking the hormone blocker medicine. Definitely add exercise and vitamins. Discuss it with your doctors.

[@irene1182]

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

[@evankopald8737]

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?

[@yerbba]

What you're describing here and have in your previous comment a while back is not related to chemotherapy-induced cognitive changes.

[@JoanVBruce]

😊

[@rindarossouw1725]

So sorry for your loss. ❤

[@thelmaallen2446]

I'm so sorry to hear about that I have a friend that's fighting cancer too she just got done with chemo

[@yerbba]

It’s incredibly tough to see someone you care about fighting cancer. Your friend is fortunate to have your support-it makes such a difference. Encouraging words, a listening ear, and small gestures of care go a long way.

[@lasurfette7830]

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.

[@yerbba]

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.

[@lasurfette7830]

@@yerbba Is there anything I can do to heal my brain?

[@adel4717]

Thank you for all your videos..much needed 🙏

[@yerbba]

We are so glad you found our videos helpful. We appreciate you!

[@tnach1341]

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?

[@dreileenmillerministriesfo9328]

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.

[@yerbba]

Thanks for writing. Weekly paclitaxel decreases toxicity and may be more effective than a higher dose given less often.

[@annewalden3795]

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.

[@vilmavelazquez1979]

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?

[@yerbba]

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.

[@julieocampo5493]

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.

[@yerbba]

Thank you for sharing. We hope your treatment at Princess Margaret Hospital goes smoothly.

[@kathleenalexis7636]

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.

[@yerbba]

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.

[@amelapapan6625]

Try herbs. Eat cassava or yucca for arthritis. I know the pain. Panadol for women helps me.

[@wannettahoskins4812]

I had the hot flashes over 9 years after my cancer. But my Dr worked with me .

[@yerbba]

Good to hear that you've found a doctor to help you. Thanks for watching.

[@terrimccarthy2253]

All depends on the type of Cancer, Stage and Grade and how large the tumor is.

[@yerbba]

Chemotherapy side effects do not depend on the tumor characteristics although a host of other decisions certainly do.

[@cynthiayee5116]

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

[@donnacampbell6345]

That happened to me also but they grew back really fast.

[@cynthiayee5116]

@@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

[@cynthiayee5116]

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 🙂

[@SheonaThomson]

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.

[@shenanigans8799]

I finished my chemo end of April and my eye brows still have not grown back.

[@tinakersey3813]

I have been told to use ice gloves and boots to stop peripheral neuropathy when I start my next course of chemo paclitaxel

[@joyrisher8841]

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!

[@donnacampbell6345]

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.

[@lisawilliams359]

I used ice on my hands and feet when they started my chemo.. I asked the nurse when to start. Good Luck

[@jillmeader5882]

Brrr sounds very cold and uncomfortable!!!

[@yerbba]

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.

[@emmazoenoellescornerofcuri7904]

I just began my 4th cycle, halfway there. Side-effects are like Forrest Gump's box of chocolates. It's horrific, but I'll gladly go through this as many times as needed if it means I'll be here for my little girl for as many years as possible.

[@EdithIjeomah]

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 .

[@Eddu13]

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

[@yerbba]

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.

[@myrnajoven9339]

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. ❤❤❤

[@mariedixon6081]

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

[@Eddu13]

@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.

[@accodianali]

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.

[@yerbba]

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.

[@amelapapan6625]

Same with me. Hope you feel better.

[@Kathy17]

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.

[@yerbba]

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.

[@Adèle9988]

​@@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

[@Mia444]

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!

[@yerbba]

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: kzbin.info/www/bejne/rZbLZIZ9mLx8fLM

[@blueanna26]

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.

[@yerbba]

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.

[@leighdevault9371]

I was on 3!

[@christinan005]

I wasnt told anything thank u for the video

[@yerbba]

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!

[@Shainnelle]

I finished my chemotherapy 6 year's ago and I still feel sick and tired most day's.

[@yerbba]

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.

[@susanyeserski5389]

Excellent job

[@yerbba]

We appreciate the positive feedback!

[@montecorley3998]

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.

[@yerbba]

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.

[@carineccarinem5857]

Very helpful ! 🙏🙏🙏

[@yerbba]

Thank you for watching!

[@ggunga7764]

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 😊

[@yerbba]

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.

[@dianesmith6745]

Taking estradiol for 42 years gave me breast cancer. No one ever told me. 😢Now I’m going through Chemotherapy and Radiation.

[@melhepburn4095]

❤

[@yerbba]

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.

[@marizcampolet2729]

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..

[@discospiders]

I’m midway through 6 chemo sessions of carboplatin and taxol, for stage 3 Ovarian Cancer. I have had zero nausea or vomiting. I have 3 days of severe bone pain, on the 3rd day after treatment. I get a shot the day after chemo, to help my bone marrow make more wbc. The worst side effect I have is neuropathy. My toes and fingers are completely numb. My feet are starting to get worse. I will try ice pack next treatment.

[@yerbba]

It’s great to hear you’ve managed to avoid nausea and vomiting so far, but we’re so sorry to hear about the neuropathy and bone pain you’re experiencing. Ice packs can definitely help some people during chemo. Be sure to talk to your care team about other ways to manage these symptoms. Know that you’re doing an amazing job advocating for yourself. The bone pain is likely from the shots you receive afterwards. Consider talking with your doctor about managing this pain.

[@discospiders]

@ thank you!

[@CecMorris]

Long term side effect - took me 17 months to get tastse buds back after completion of chemo. Sure was great when food taste came back!

[@yerbba]

Seventeen months is a long time, but how amazing it must have felt to enjoy the full taste of food again! Thank you for sharing this-it’s a reminder that recovery takes time but can bring small victories along the way.

[@americafirst6628]

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......

[@yerbba]

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.

[@angiem2832]

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 .

[@yerbba]

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.

[@dewarb8311]

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

[@yerbba]

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.

[@judithmargret5972]

dewars, Sad to hear about all your side effects. What's happening with cancer, are you having any other treatment?

[@mjflorida1335]

i completed chemo in March of 2022. after one year of treatment for BC (stage 2 grade 3 Her2+HR+). The nails on my toes and hands have not recovered. My nails are not completely attached to the nailbed and sometimes my toenails will just fall off. They look terrible and I need to keep them painted. My hair completely fell out and grew back somwhat. To this day my hair is not the same. My hair is very fine and thin, especially in front and on top of my head. I need to cover my head in this area because it looks like I'm balding. I take 1mg Anastrozole every day. I'm wondering if this drug is contributing to the baldness. Will my hair ever grow back and will my nails ever recover.

[@yerbba]

It is possible that the aromatase inhibitor is affecting your hair and your nails. If that is the case, these changes should be reversed when you stop the aromatase inhibitor. These sound like frustrating side effects.

[@WendyMurray-hm4tz]

I am current in going through chemotherapy it is pretty tough..1st day okay but up to 6 days after I'm extremely sick...before treatment I've lost 9 of my fingernails..I know how embarrassing and ugly that looks..but thank God one lady at nail salon creatively build fake nails and nail bed for me.I don't know when my nails will come back and my hair is now balded too...I'm 33 started chemo inJan.2024...it is not easy may God heal us and carry us through...MY smell and taste o my God,terrible mouth sores too and rashes

[@tiny_tots2950]

​@@WendyMurray-hm4tzsending you prayers and good wishes my sister just started 2 weeks ago and is struggling.thank you for sharing

[@WendyMurray-hm4tz]

@@tiny_tots2950 same to you..now on my 3rd cycle today March 4th,will have to do blood infusion because my number is low...something new again I never had before

[@WendyMurray-hm4tz]

@@yerbba ok

[@martinsmith439]

I’ve had two sessions of doxatosel chemo for prostate cancer and I have had no side effects whatsoever .?yet, maybe that will change after my third session,

[@yerbba]

Thanks for writing, and we're happy to hear that you're doing well with chemotherapy. You are correct that side effects can be cumulative, but starting off this way bodes well.

[@tnach1341]

My mom is experiencing after chemotherapy depression as i suspected because 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?

[@yerbba]

It is hard to know what is causing your mother symptoms without being able to see her. Given how severely she is affected, calling her medical team would be important.

[@tnach1341]

⁠@@yerbba we found out sadly the cancer was mitastasis and it moved to her brain causing her to stop moving and talking and controlling her muscles. And it was too late for radiotherapy and unfortunately i lost her this month. 💔😔

[@gemagomez7606]

I’m sorry for your lose

[@tnach1341]

@@gemagomez7606thank you 🥺🙏🏻

[@peter58peter]

Thanks for honesty.

[@yerbba]

Thank you for watching! We appreciate your support.

[@kathleenrau2079]

Thank you for doing this.

[@yerbba]

Thank you for watching!

[@cherylcosgrove511]

Is this info the same for a lung cancer patient ?

[@yerbba]

Good question. This is generally the case, yes. People with lung cancer, however, have a more difficult surgery and furthermore, the radiation therapy includes the esophagus (swallowing tube) and thus can have more side effects that may last a little longer.

[@marivicchansing4717]

Today my 3rd day of capecitabine my side effect are my hands cramps does not hurt but my fingers are twisting is that something to worry about?

[@yerbba]

Thanks for writing. For a symptom like this on a new medication, it would be prudent to contact your medical team.

[@rejakoye1620]

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

[@yerbba]

Thank you for your kind words and suggestion. We have a few videos on HER2-positive breast cancer that might offer some insights here: kzbin.info/www/bejne/jJavqYSwgNp6npI.

[@Barbara-ex3ge]

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?

[@yerbba]

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.

[@Adèle9988]

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.

[@John-ms1sz]

How about Prof Valter Longo's research on 72 hours of fasting prior to chemo and radiation? Ir prevents most side effects.

[@yerbba]

The scientific understanding of fasting before chemotherapy has evolved. While early studies by Professor Longo showed promise, larger reviews of hundreds of studies haven’t found strong evidence that fasting significantly reduces chemotherapy side effects compared to regular nutrition. Small studies suggested benefits like less fatigue and fewer digestive issues, but larger trials have shown no meaningful differences. Many patients also find fasting difficult, with only about 20% able to stick to the protocols. More importantly, fasting during treatment can pose safety risks, including malnutrition, weight loss, and slower healing. Most cancer centers now prioritize maintaining adequate nutrition over fasting. Research into alternatives like fasting-mimicking diets continues, but for now, the best approach is to discuss any dietary changes with your oncology team, who can tailor recommendations to your specific needs.

[@sointu123]

Is peripheral neuropathy only affecting sensory/pain neurons or also motor neurons? If someone already has prior nerve damage (e.g. drop foot) can chemo make it worse?

[@yerbba]

Peripheral neuropathy primarily affects sensory neurons, causing symptoms like pain, tingling, and numbness. However, in some cases, it can also impact motor neurons, leading to weakness or difficulty with movement. If someone already has nerve damage, such as drop foot, it is not clear that chemotherapy will make it worse unless the neuropathy is due to a "toxic" neuropathy (alcohol exposure, diabetes, etc.)

[@sointu123]

@@yerbba Thank you for your detailed reply. That is one of my greatest fears in terms of side effects. Mine is due to nerve damage that happened during surgery because of a lack of turning.

[@isimotmuheeb4024]

Thank you for sharing this video

[@yerbba]

Thanks for watching!

[@dragoftw5910]

I have been diagnosed with Ewing sarcoma in my pelvis and it also spread in femur and tibia bone also lungs the pain in my leg is feels like hell from the Saturday onwards chemo starts and im scared to know about the side effects 😢

[@yerbba]

We're sorry to hear about your diagnosis and the intense pain you're experiencing. It’s completely normal to feel scared, especially with chemotherapy starting soon. The side effects can be daunting, but your medical team will be there to support you every step of the way. We’re here for you too, and we hope you found the video on chemo side effects helpful in preparing for what’s ahead.

[@mercysanchez3012]

Thank you for many informations. God bless.

[@yerbba]

Your support means a lot to us! Thank you for watching.

[@cja398]

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.

[@jeannie_enilno]

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.

[@yerbba]

Thank you for sharing your experience with the Yerbba community.

[@pritisinha3404]

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 😭😭😭😭😭😭

[@yerbba]

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.

[@juneachempong726]

My side effects from breast cancer, even after 3 years is still with me and I'm 65...

[@yerbba]

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.

[@LovTheNose]

It’s like slamming your finger tips in a door. It’s very painful. The bottom of my feet feels numb. It’s weird.

[@yerbba]

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: kzbin.info/www/bejne/rZbLZIZ9mLx8fLM

[@gemagomez7606]

I’m the same, walking with a walker

[@joyrisher8841]

Very thorough video -- thank you! You are appreciated.

[@yerbba]

Thank you for your positive feedback. Yerbba appreciates you!

[@martinsmith439]

Thankyou for you videos

[@yerbba]

Thank you for watching and being part of the Yerbba community.

[@salas831]

How long can they keep you on chemo on 1 sitting?

[@yerbba]

The time that a person is sitting depends on the treatment. For the very first treatment with chemotherapy and, for people getting targeted therapy, the time spent sitting can be up to 6 hours. The following treatments will be much shorter as long as there are no reactions to treatment. It is also possible to get up and walk to the restroom for example.

[@salas831]

​@@yerbbabeing on chemo for 2 days straight isnt normal?

[@dorothywells-wz5nr]

About 2 hrs per session. I found it helped to think of it as a beauty treatment. I finished Chemo and am now on Radiation. God Bless D

[@mariaiosif741]

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

[@yerbba]

Thank you for the suggestion! We will add it to our list!

[@Qghostz]

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?..❤❤❤❤

[@yerbba]

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.

[@amandabsmith11]

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).

[@Adèle9988]

Yes stop the chemo and start à keto food therapy which really works

[@amelapapan6625]

Eat protein and balanced meals. Dont fall or break bones. Try to sit or hold on to prevent falling.

[@ChooseForToday]

@@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.

[@JudyGyles]

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.

[@yerbba]

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.

[@VJLB]

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.

[@yerbba]

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!

[@HareKrishna3760]

Plz make a video on vmat & ABC ( dibh) radiation , side effects for radiation on left side after mastectomy

[@yerbba]

We can add that to our list. Thanks for the suggestion.

[@sarvjeetkaur8965]

After 1month of chemo some red spots on the body is normal in aml luekemia plz reply ..mam

[@yerbba]

Red spots can sometimes occur during chemotherapy for AML leukemia, but it's important to have any new symptoms checked by your medical team. The key concern would be that you have low platelets. Wishing you the best in your treatment.

[@amysizemore4750]

I have stage 3 tnbc. Finished my chemo still have two months radiation and immune therapy and surgery. I have the chemo brain really bad bad it’s constant Ed everyday I am depressed now. And I been on my depression medicine seens I was 40 I am 48 now but now it’s worse and my neuropathy is really bad. The struggle is real and I wish I had my life back before this wht makes it worse I got denied for ssi cause my age I have fatigue bad now I had some on chemo I had setback on the red devil but I made it three finally

[@yerbba]

It’s clear how much this journey is taking a toll on you. Chemo brain and neuropathy can feel overwhelming especially when paired with depression and fatigue. Please know that these side effects are common and may improve with time, but managing them often requires a team approach. Consider asking your doctor about physical therapy for neuropathy and cognitive exercises for chemo brain. It's important to know that some of the very medications used to treat neuropathy can cause cognitive problems, so run those by your doctors. Also, appealing your SSI decision with the help of an advocate could be worth exploring. You’re doing so much just by pushing forward. We also have a videos on how to manage chemo brain and fatigue you may want to explore: kzbin.info/www/bejne/m4bRiqWPqNWJhZo kzbin.info/www/bejne/f6Tch36Dg7h2idU

[@GladstoneGander33]

I believe that chemo has induced a low heart rate and afib. Is this possible? Does anyone have any advice on this as I have been experiencing both since starting chemo. The doctor says that it probably isnt the chemo. Something sure has set it off.

[@yerbba]

These would be highly unusual from chemotherapy. One thing that has been written/published about is the higher rate of detection of any medical problem because of more frequent medical visits. Each person is different, however, and it may be the case that they are related despite the lack of evidence that this is related to breast cancer treatment.

[@jayoopatwardhan4040]

Very good 🙏

[@yerbba]

Your support means a lot to us! Thank you for watching.

[@sheilarennie2636]

I'm sick all the time😢

[@yerbba]

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.

[@sheilarennie2636]

@@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 ❤️❤️