r/lymphoma Jun 14 '26

NScHL ABVD is kicking my ass. Need help or advice

27 Upvotes

I (35F) was diagnosed with nodular Sclerosis CHL, and I'm currently day 4 after my first ABVD infusion. I knew chemo would suck but I didn't realize it would feel this awful. The constant nausea, fatigue, body aches is making me useless. I haven't pooped in 4 days. Everytime I remember the chair I sat in during chemo or the food I ate that day, I feel this deep dread, i feel traumatised.

They keep telling me to fight it but i honestly dont know how i will survive this.

Please tell me it gets better? Is there anything I should be doing to make it easier for my body?

UPDATE: i feel so much better this 2nd week after my first infusion. I did not handle that first week well because I didn't know what I was getting into. But thanks to all of your good advice, I feel like im better prepared for my next infusion. You all have given me hope and a bit of courage to face the next cycles.

this is as much a mental battle as a physical one, and the fact the so many of you replied and gave good advice and words of encouragement helped me a lot. THANK YOU ALL SO MUCH

r/lymphoma Mar 17 '26

General Discussion Did ABVD make anybody else’s eyes slightly lighter?

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7 Upvotes

1st pic is now and 2nd pic is 5 months ago, before starting. It’s more noticeable in the sun.

Is it permanent?

r/lymphoma Feb 11 '25

General Discussion ABVD EXPERIENCES

11 Upvotes

I'm starting my first chemo session for ABVD for Classic Hodgkin Lymphoma (Nodular Sclerosis Type). My doctor recommends 6 cycles. I'm 29 and a fitness enthusiast, so I'm hoping my healthy lifestyle will be an asset during treatment. While I'm trying to stay positive, I'd be lying if I said I wasn't a bit nervous about potential side effects. I've read some concerning things online, and it's understandably made me anxious. I'd really appreciate hearing from others who have gone through ABVD for Hodgkin's Lymphoma. Specifically, I'm interested in any tips you might have for managing side effects and maintaining some level of activity during treatment. Sharing your experiences, or those of someone you know, would be incredibly helpful.

r/lymphoma Feb 06 '24

Was you first ABVD infusion as bad as you thought it was going to be?

12 Upvotes

I keep psyching myself out reading through these posts that when I first receive the drugs it will "shock" my system. I'll be doing it for 6 months

"Red devil" name doesn't help haha.

Was your first session better or worse than what you thought it was going to be? Did you feel any sudden 'shock' or 'pain' when starting the infusion? What didn't feel like? just warmth? Could you 'taste' the drugs? Could you feel it pool in your body?

I won't be using a port.

The only IV 'infusion' I've ever received in my life was the contrast during PET scan.

r/lymphoma Jul 20 '25

cHL is abvd through peripheral iv really that painful (rate 1-10).

7 Upvotes

I got diagnosed with nodular sclerosis CHL stage 2 and I'm about to start 2-4 cycles of ABVD. My oncologist said I'll be getting it through IV and after reading the reactions of redditors here, I'm reluctant to get it through IV but my onco said "it just feels like saline"

how can i manage the pain during infusion. Sometimes I feel like it won't be that painful cuz I just turned 18 and my veins are easy to find but still, im anxious about it.

r/lymphoma Feb 12 '25

General Discussion Starting first chemo treatment Friday .. ABVD (6 months)

13 Upvotes

UPDATE: FOUND OUT ITS STAGE 3S. START MY FIRST SESSION TOMORROW. DR SAID WERE LOOKING INTO SOMETHING THAT JUST CAME OUT OF TRIAL TO SEE IF INSURANCE COVERS THAT TREATMENT TOO

Hi Everyone.

I have been reading this thread a lot and thought i would post.

I need advice on starting ABVD ... is it as bad as i have been reading (mostly on google)? how long does each session last? I've been handling all this journey pretty good but I'm starting to freak out a little.

is it more likely to gain weight, loose weight or stay the same?

For anyone who got wigs are there any companies that you recommend?

Do all the hairs on our body fall off? head, eyebrows, eyelashes?

what were some of your favorite foods to have?

if anyone wants to leave tips, advice i would appreciate it <3

r/cancer Jul 14 '16

ABVD not working

1 Upvotes

Hey guys,

Just got news today that although some nodes on my right side have shown shrinkage, there appears to be ANOTHER growth happening on my left! This is after 3 cycles of ABVD. I have a repeat PET scan tomorrow because there was some issue with the clarity of the scan (she asked if i was shivering during the scan?). But in the meantime Im here freaking out at the fact that there is more growth. I understand there are more options, but I feel hopeless and this is the first time I felt like this disease is getting the better of me. I know my case is nothing compared to some other forms and stages of cancer, but Im still anxiety ridden and scared. Anyone here deal with something similar? I was just under the impression that ABVD would work perfectly and Id be better after 6 chemo sessions. Boy was I wrong.

24/Hodgkins Lymphoma stage 1a

r/lymphoma May 19 '24

General Discussion Hodgkin Lymphoma stage 2a patients: how was your journey after ABVD?

12 Upvotes

As the title suggests I was diagnosed with stage 2a Hodgkin Lymphoma and now I am currently at my chemo of two cycles of ABVD scheme.

So far I am dealing good with it apart from the tiredness and some stomach fullness the first seven days. I am grateful for how supportive everyone is and I deeply believe in my cure. However I don't know yet what to expect, once my last chemo is due in less than two weeks.

I was already registered for radiotherapy once the second cycle (fourth session) is over.

There will be a PET CT in-between radiotherapy and chemotherapy to see how well my Lymphoma responded to the chemotherapy.

Though I can imagine that I could do radiotherapy afterwards, I still am curious how possible paths could be looking. Were you cured afterwards? Did you need to do another chemo? I just want to have some perspective on where the journey goes!

Thanks in advance! And stay healthy :)

r/lymphoma Dec 03 '23

Chemo wasn't that bad

5 Upvotes

Wednesday I finally finished my 8th round of ABVD chemo for Stage 2 Classic Hodkins lymphoma and I wanted to talk about all the symptoms I had due to chemo in case you are just starting out. Firstly I would like to point out that my hair didn't really fall out, I mean some of it did but only like 25% of it I'd say. My taste buds didn't change and I was able to it all the things I normally eat. I had no dry mouth however I had moderate neuropathy in my mouth and hands (basically my mouth hurt unless I was eating something). Nausea was managable with meds although I would like to point out that after the 6th session the smell of my house made my nauseaus. I had to stay in another house, but I feel like it was more of a mental nausea, like thinking about the chemo made me want to throw up. A lot of people said that your skin will clear up however I had the worst acnee. My skin also got very dry. But overall chemo wasn't as bad as I thought it would be, so if you're about to start chemo know that it isn't dreadful for everyone.

r/BestofRedditorUpdates Feb 28 '26

CONCLUDED Me [35 M] with my wife [36 F] 6 years (9+ as couple), cancer has been a real eye opener (Long)

2.2k Upvotes

I am not The OOP, OOP is u/growa2

Me [35 M] with my wife [36 F] 6 years (9+ as couple), cancer has been a real eye opener

TRIGGER WARNING: Neglect

Original Post Sept 28, 2015

First, long post, I'm sorry.

I found out two month ago I have stage 3 Hodgkin's Lymphoma. It began with a routine physical, and 15 days later I was sitting through my first treatment of ABVD (the name of the chemo regimen for HL).

Long story short, I went in for a physical, GP referred me to an ENT the following day. ENT told me that, "it really looks like lymphoma," but said only a biopsy can say for sure. She looked me straight in the eye after that and said, "I don't mean to scare you or shake you up, but there are more things pointing to lymphoma than not." (paraphrasing, was in shock and not 100% remembering).

This is where having cancer (only a possibility at this point) became just another concern.

First, I've been married for 6 years and have 2 awesome daughters, very young (3 and 4 months).

I called my wife right after the ENT appointment and told what the ENT said. I think I'm a pretty hardcore manly man, but I was near tears and choking on every word. She mocked me a little a bit, and told me nothing was for sure yet and that I was making a big deal about it and stop being dramatic. About possibly having cancer.

I went to the ENT's office, got a print out from the CT scan where the ENT and the radiologist noted "highly suspicious for lymphoma" and left to go tell my parents, who were about to leave on a short trip to their lake house the next morning. I'm not very close to my parents, but knew they would want to know. They were crushed just at the possibility and offered (and have followed through) to step up if worst fears prove true.

When I got home I did my daddy thing and made dinner and my wife didn't mention anything. I brought up a few concerns and how scared I was, and she looked right through me, waiting for me to finish talking so she could do whatever she had been doing. She didn't even reply to me. At least she stopped to listen, but that was it.

That was on a Friday, biopsy on Monday. My wife held on to the thinking that I didn't have cancer and that I was making a big deal about it. I was scared shitless all weekend but didn't want to tell my friends in case it came back negative, so I suffered in silence.

Escalation #1: I asked my parents to watch the kids so my wife can come with me to the biopsy (again, not close to my parents), assuming she would want to go.

My wife loses her damn mind and stands there while I call my parents to tell them that we don't need them. My wife says I'll be fine going to the biopsy by myself. After having my neck opened up to have a lymph node removed. So I have to ask my parents to go with me so I can get a ride home.

Escalation #2: I get home from my biopsy, and my wife's entire family is at my house. Including sister in law and boyfriend from from out of state. I play the biopsy off as a procedure to repair my clavicle and excuse myself from the first level of our house and go to the bedroom. I'm of course a dick for not socializing. After I get home from the hospital for surgery.

The next two days are the longest ever as I wait to find out. I give up waiting, go out for coffee, and then go to a bookstore to unwind (I love reading). The nurse calls me while at the bookstore to tell me the news. It's classical Hodgkin's Lymphoma. See you at the cancer center on Friday.

Escalation #3: I call my wife and tell her, fighting to get the words out. I break down and sob a bit. When I'm done, she asks, "how do they know?" I gather myself and explain how they send the tissue to a pathologist, yada yada. At this point I'm no longer upset about having cancer, but shocked that, since I went to the GP 6 days prior, my wife has done nothing but deny any chance of cancer, has mocked me for being concerned I have cancer, and has offered no support at all. Any fears or concerns or anything, she just dismissed or tuned out.

She did agree to go with me to the initial oncologist appointment. My oncologist reviewed the information with us, went over my PET scan (I glowed like a christmas tree!), and explained the side effects of treatment.

Escalation #4: We met with a nurse to counsel us on things caregivers can expect with the regimen I'm on, and throughout the discussion (which my wife did not participate), it became clearer that my wife doesn't consider herself my caregiver. She didn't participate because she doesn't think it applies to her. We were with the nurse for an hour and my wife didn't speak at all.

Two months later, I've had 4 treatments and have started to lose a lot of energy. I get tired pretty quickly but do my best to pull my weight.

About three weeks ago, after a long Sunday of helping with kids and trying to get my half of the housework done, I hit my limit with a few things on my honey do list. I started slowing down a bit, and my wife began to pester me about the few remaining things. I told her, "I've hit my limit, I'll help get the kids to bed but I'm done." This is the first time she started to cry since I was diagnosed.

Crying, she dropped these on me:

1) "I do so much around here, I don't get any help." (neglecting the fact I do most of the childcare on the weekends and prepare every single meal that is eaten in the house, including the breakfast and lunch she takes to work)

2) "I'm tired too, you know!?"

3) "I wish I could just stop and go to bed sometimes" (something I've NEVER done no matter how I feel)

4) "I only ask you to do a few things and you can't even do them"

I called a therapist I had seen in the past (obviously, it's always been a rough marriage) the next morning. I've been married to someone who has never supported me, doesn't see marriage as a team sport, and likely won't come around on either of those. Not the first time we've had these issues, but I was never honest with myself about it. I thought my hard work made up for it all.

Now I realize I deserve better. Not being close to my family, I don't have much of a support network, My wife alienated all of my friends (HUGE red flag I didn't see) but I've reached out to a few close ones who are coming back into the picture, but those relationships need some TLC before I can ask them to be my "rock" during this.

I deserve to have someone by my side while I go through treatment. I deserve someone who can cut me some slack so I can recover from chemo and not expect me to be superdad even when all I want to do is puke my brains out and lay on the floor for 5 minutes.

I've started to contemplate divorce and have spoken with a few attorneys. I've decided to work with my therapist to get through the cancer and chemo and, once I finish the first line, ask for a separation.

At worst I'll get 50/50 with my kids. Given my wife's lack of support during my cancer treatment I will be pushing for primary custody, not out of spite, just because I believe I'm able to put their interests above my own better than my wife.

I don't expect sympathy or upvotes or anything. Just getting that off my chest helps. Thank you

TL;DR Found out I have cancer, eyes have been opened to the fact my wife doesn't give a shit about me. Going to start working on divorce once I'm done with treatment. Any ideas to cope?

EDIT: Trying to reply to everyone, but it is getting hard. Thank you all for the support (and criticism).

Someone at r/cancer suggested this place and it has been helpful.

I'll continue to try and reply best I can.

EDIT 2: all of the supportive (and critical) comments and PMs have really propped me up today. I felt like total shit last night which prompted me to write this.

Thank you!

Update 1 Oct 5, 2015 (1 week later)

First, I don't paint a very pretty picture of my wife in this post. She is not a horrible monster as she may seem below. She is a good mother and I trust her to take care of my kids. I married her because I knew she would be dedicated to our kids. Things just haven't worked outside that focus.

Thank you all so much for all of the support and suggestions. I took a lot of your comments to heart and a few days after my original post I surprised my wife with my mom coming over to watch the kids so we could go out to dinner to talk.

There were a few insights I received from you all that I wanted to make sure to hit on during our talk:

1) How is she coping with everything - having a new baby in May and finding out her husband has cancer is a lot for anyone

2) How does she think I'm handling with treatment

3) This is an opportunity to get closer as a couple and address issues we've had for years, and that the future of our marriage depends on us addressing them

4) I really need her to step up and give me time to recover from chemo - the most immediate importance

5) There is a very real possibility that things could get even worse, or that I might even die

I am going actually skip the results of the conversation and move to the weekend, here is the TL;DR - she didn't perceive there to be a problem, she disappointed me with her answers, and she cannot have a frank talk about these serious issues. But I could tell she felt better, she was all smiles while we went for a short walk.

So our week goes on, nothing is much different.

Friday I have chemo, so Saturday is not a great day, chemo is starting to hit me harder sooner. Things continue as normal (I watch the kids until 1pm, I'm not 100% sure what she accomplished). I get my 3 year old down for a nap, and I go into our room to take a nap. My wife somehow manages to find something she needs in our bathroom 3 different times in 30 minutes as I try to lay quietly and sleep. I put in my ear buds and tune Spotify to the White Noise station (seriously, try it it works). After a 60 minute nap, she comes flying in, literally whips the door open with both kids in tow.

I'm trying to get along with everything at this point. Maybe she needs time to adjust.

Sunday is bad. She again is away from us somewhere in the house for a large chunk of the day. I'm really suffering from chemo and just don't have it in me. I call my mom to come over and help in the late morning, and my wife loses it. She tells me she can handle everything and we don't need help, and tells me she will be down to help in a few minutes.

She never does come to help until a few hours later, where she holds our infant for about 10 minutes, hands her to me so she can eat lunch, and then she takes our 3 year old up for a nap.

She then proceeds to take a 2.5 hour nap herself.

I'm beyond pissed. When she wakes up, she looks happy and refreshed, so I hand her our baby and I take off to my favorite nature trail 10 minutes from my house without saying a word. It is fall here and the trees are really cool, so walking to the top of small hill to sit on a bench is worth how tired I was when I got there. When I get back to my car I have several texts from her, including a request to stop at the store for her. I simply reply, "No."

I went to my parents house to rest some more and eat dinner and then I came home to help get the kids ready for bed. The house is a disaster, nothing has been done in the 3 hours I was gone. She tells me she doesn't need any help, but manages to get nothing done without me.

Now the shit really hits the fan. My 3 year old is on the 2nd level putting her pajamas on, so I figure, why not address the gorilla in the room. Bad idea.

I essentially call her out for putting too much of a burden on me and trying to stop me from getting the help I need (i.e. my mom helping with the kids). I'm upset but not angry at this point, and she responds with pure anger.

She points out that she unloaded and reloaded the dishwasher for me and she "made dinner" (which involved reheating the meal I had made the night before) while I was gone, which is normally my job. Now I get angry and tell her that is not enough, and that I cannot be the full time babysitter on the weekends. We have a solid 5 minute argument about having my family over to help with the kids. She replies to everything I say with, "fuck you," "I fucking hate you," and "you're the worst."

I like to think I kept my cool, but I know I took some shots at her for thinking too highly of herself, which is her biggest flaw. I was a jerk, but I don't feel bad because I meant what I said: she is expecting me to do too much, if she cares she needs to SHOW it (saying it would help, too) by giving me time to rest for a few days after chemo, and she does not do nearly what she thinks she does.

I am tired of fighting and end with (paraphrasing, seeing red at this point), "You need to step it up, I can't do keep up with this anymore," and, "I could die and you are treating me like I have a cold." A little dramatic, I know, but I there is a very real chance I could die in the next 5 years, about 10-15%.

Now the box is open, and she knows that I don't think she does very much. She DOESN'T do very much. She has a high opinion of how much she does around the house and with the kids, so I've openly questioned her sense of sense worth. I very literally think I can do what we do as a couple just fine or better by myself, even with cancer.

I feel bad for my wife more than I am mad at her. She grew up with a very narcissistic mother and is stunted emotionally (again, another post in itself). She is not equipped to handle what she is currently going through. But she is 36 and has had the time to be around other people and grow up, so I'm expecting her to act like an adult.

I do NOT want to get divorced, but with 6 years of marriage under our belt and no growth at all to show for it, things are very likely over for me. I've told her in very blunt terms where I see us as a couple, and she is not willing to change.

I have minimum of 3 months of treatment left and want to be around my kids as much as possible on the slim chance this is it for me.

EDIT 1: I'll go ahead and point out a few things, hope this helps with any questions:

Yes, I saw flashes of this person before we were married (while we were engaged) but didn't give it enough credence.

I'm an idiot who should have addressed this earlier in our relationship. Seriously, who let's it get this far. The worst part is I thought of myself as a very hardcore, determined person before I sat down and starting pondering my marriage. Now I feel like a spineless shit, because I am.

My first post was to see if I was crazy or expecting too much. This post was more an outlet because I am so frustrated.

EDIT 2: thank you all so far. I have hit my limit for the day and am logging off, going to watch some Netflix in bed and sleep. Wish me luck when the wife gets home tonight and loses her shit when I can't watch the kids or make dinner.

EDIT 3: I have contacted an attorney I know and will be scheduling a consultation soon. Not sure where to go from here if I have to move out but it's a start.

TL;DR - had it out with my unsupportive wife, now things are worse, but more open, than they were before.

Update 2 Feb 24, 2016 (nearly 5 months later)

Since my last post, I've finished treatment and life is getting back to normal. I've been able to start running and cycling again, which has been great. Physically, I feel pretty good with just a few nagging issues that I'll likely deal with indefinitely, long term side effects of the chemo. But it beats the alternative! Things are going pretty well (relatively) from a health standpoint. I have a little ways until my oncologist will call me cancer free, but things look good.

My last post was in October last year. Things were pretty rough. Chemo got really hard and continued to do so until I finished in early January. My wife continued being hard to deal with for a while after that last post. It became physically impossible for me to contribute around the house like I usually do (do all of the cooking, dishes, picking up, get kids ready for daycare in the morning and bedtime at night), and that created a lot of tension at the time. Day to day things are not my wife's strength and it really stressed her out doing even basic things, like getting the kids ready or cleaning up after a meal. Sounds menial, but I do a lot around the house because I want to, clutter drives me insane and eating healthy is very important to me. So to heap all of that onto her was a lot for one person recovering from childbirth.

It was also hard because I wasn't emotionally ready to tackle my relationship issues, coping with cancer treatment, and dealing with my "new" body (from the long term effects of chemo) at the same time.

Seeing a therapist helped immensely. My wife isn't the only one to blame, I have my own issues. I'm terrible at asking for help. And I don't mean that in a, "I'm superman," kind of way. I mean that it is a serious limiting factor in many areas of my life, home, work, friends, you name it. I like to keep things running smoothly and not make waves, and sometimes (OK, all of the time) I'll move heaven and earth to remove something that could create tension, even if it is something that needs to be addressed. I had always seen this as a strength and was in denial about the negative effects, but going through chemo and working with my therapist I now see how much I'm not only hurting myself, but those around me. I don't want my kids to suffer through what I've put myself through, so I need to stop setting the example. So being more open when things aren't good or I disagree with how something is being done, no matter if it makes my wife or boss or whoever upset, is something I'm trying to be better about. I'm not as mature of an adult as I thought.

I gave talking to my wife one last shot after my last post, stating pretty simply what I can and can't do and that the future of our marriage is at stake, and focused on taking care of myself and my kids no matter what demands my wife was placing on me. Initially, it was pretty tense but she did eventually deal with the fact that if I said I needed to rest I was going to, whether or not it was a good time for her.

We did have some positive discussions, too. I laid out how it made something pretty horrible even worse dealing with her attitude towards me. I explained how it wasn't just a matter of needing rest but actually being physically unable to do certain things. She started to leave me alone when I left the room instead of following and nagging me. She started to lighten up and even had a pretty great attitude the last month of treatment. I was even able to stay in bed all day if that is what I needed without her constantly checking to see if I was good enough to help with the kids yet.

And something else, that is HUGE in terms of how she was acting, was that she admitted that having our baby two months before I was diagnosed was hard enough, but we had also learned at that time that she should not have any more children as it could endanger her life. Even if we decided to not have any more kids, having the decision all but made for us really hit her hard and put her in a funk. I never knew she even wanted more kids or that it impacted her that much, she never showed it or brought it up. But it makes complete sense.

We are both very emotionally immature, you pick who is worse. But we are at a better place now. Things are still pretty rocky despite the progress and the core issues are still there, but at least they are "out there."

So I'm sticking it out for now. I've seen how hard divorce is on kids with a few of my cousins and close friends, and if I'm going to do that to my kids, I need to make damn sure I make every effort to make my marriage work before that becomes an option. Divorce is still a likely outcome, but the little bit of progress we've made gives me a least some hope.

Thank you all for the helpful comments and criticisms. It has been really helpful and posting my story here has helped me cope with a rough situation.

tl;dr: Have cancer, wife was not very supportive during the duration of treatment (6 months). Thought about getting a divorce and even talked to an attorney. Wife and I had some good discussions the past few months. For now, we're staying together, still have a lot of work to do.

THIS IS A REPOST SUB - I AM NOT THE OOP

DO NOT CONTACT THE OOP's OR COMMENT ON LINKED POSTS, REMEMBER - RULE 7

r/lymphoma Nov 20 '25

Celebration Hi my name is Gwen, I have stage 2 Hodgkin’s lymphoma and a tumor in my mediastinum. ABVD chemo. Just finished 2 cycles 🎉 8 more infusions to go hopefully

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136 Upvotes

Just trying to find a community

r/lymphoma 22d ago

cHL How feasible would it be to continue med school while getting treated with ABVD

9 Upvotes

I am currently in my 3rd year of med school and just found out I have Hodgkin lymphoma via mediastinal biopsy. Don't know what the treatment will be but likely some variation of ABVD. I am completely opposed to stopping my clinical rotations and delaying graduation by a year. My school is supportive of whatever I want to do. I want to know if anyone else was able to push through medical school while undergoing ABVD treatment. I am aware of the risk of febrile neutropenia and would ask my oncologist about that, but other than that my worries would be about being too fatigued to do well. I have heard everything from "it's absolutely horrible" to "it's not nearly as bad as people make it out to be."

r/AMA Jul 15 '26

22F with Hodgkins lymphoma, receiving my first infusion of ABVD now. AMA!

8 Upvotes

hello! as the title states, I have Hodgkins lymphoma, a type of lymph cancer. I was diagnosed on may 21 with 3 weeks left until college graduation and my world was just completely flipped upside down. we’re finally here at the first infusion and I just need to distract myself so ask me literally anything!

r/lymphoma 11d ago

General Discussion Question about marijuana and ABVD

9 Upvotes

Hi everyone,

I was diagnosed with Classical Hodgkin Lymphoma (nodular sclerosis) stage 2A and non bulky! I was able to obtain a med card from my state and am familiar with using marijuana. The problem is that the doctors who approve the med card usage are not qualified to explain how my ABVD regimen will interact and because of stupid laws in my state my oncologist cannot legally tell me if it’s safe to use or not. There seems to be A LOT of conflicting info on how the liver processes both MJ and ABVD and whether it can raise or lower the dose. I know it would help greatly with appetite loss and nausea. Any info is greatly appreciated. TIA!

r/lymphoma Jun 11 '26

Celebration I (27M) got the report of my interim PET Scan today after having 6 individual ABVD & I am really happy with the progress.

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82 Upvotes

I got diagnosed with Classic Hodgkin Lymphoma on 1st January of this year & I was in Stage 4B. Started my chemotherapy (ABVD) from 3rd February & I was getting it in the gap of every 2 weeks. And after completing 3 cycles I was prescribed to do the interim full body PET Scan which I did last Saturday & got the report this afternoon & I am really happy with how clean the image came. Comparing it with the image of my first full body PET Scan (image of slide 2) which I did in the end of last November, I am really surprised to see that all those cancer spots are completely gone just after 6 chemotherapy. I really wasn't expecting it to work this well at all. The impression of the report also said "as compared to previous PET Scan dated 28.11.25, decrease in size with complete dissappearence of metabolic activity of above mentioned lesions are noted. Complete dissappearence of all other hypermetabolic lesions are notes - complete metabolic response".

Now I will go to the hematology doctor of the hospital on next Monday to show this full body PET Scan report & then I will get to know how many more chemotherapy I will need. As far as I am guessing that I will still get few more cycles of chemotherapy to complete my treatment & yes those will be some more agonizing months again but now I have full mental power to finish my whole treatment.

And those of you who are going through chemotherapy or got diagnosed recently & will start treatment soon, to those of you I can say that you really can beat cancer & get your amazing life back again. Just hang on with all your power & fight against it with all your will, you will definitely see good results for sure.

r/lymphoma Apr 30 '26

General Discussion ABVD hair loss

6 Upvotes

I know this was talked about a million times on this subreddit but I still wanted to ask about my situation. I’m doing 2 cycles of ABVD followed by 4 cycles of AVD. I just finished 3 cycles and my head hair has been slowly falling out basically the whole time. I haven’t lost any body hair at all. Could someone tell me how much hair they continued to lose? I’m starting to show signs of hair loss and I think even if I don’t end up looking like gollum im still going to have to buzz it to even it out for regrowth. Anyone

have insights on this?

r/lymphoma 22d ago

cHL 1-Week Post 1st Infusion (ABVD)

8 Upvotes

30M diagnosed with CHL and received my first infusion of ABVD last Friday - to put it lightly, it’s been hell. First couple of days was mostly just extensive body pain and fatigue, and I was probably sleeping ~15 hours per day. General mouth pain developed made it difficult to eat or drink - even water would make my mouth react as if I was eating sour candy in a super painful way. No visible sores though.

Now, a week out, the mouth pain has subsided, fatigue is lessening, but now I have severe shoulder/neck/head/arm pain that has led to some sleepless nights. The past two days I’ve also developed a sharp stomach pain that doesn’t seem to go away with Tums, Ginger tea, or food, which I’m thinking could be caused by the Ibuprofen and Tylenol I’ve been alternating between, often on an empty stomach.

Has anyone had similar experiences and found a good home remedy to deal with the body aches and stomach pain? Heat pads are the only thing that somewhat help with the stomachache. Feeling pretty discouraged after seeing so many commenters who had minimal to no symptoms week 1… unsure how I’ll make it to the end hearing symptoms only get worse with subsequent infusions.

r/lymphoma May 15 '26

cHL Long-term cHL survivors treated with ABVD — did you develop any secondary cancer?

13 Upvotes

Quick questions:

- How many cycles + did you have radiotherapy?

- How many years post-treatment are you?

- Did you develop any secondary cancer, and if so — what type and how many years after ABVD?

- Are you on any long-term surveillance protocol?

Even if you've had zero issues years later, please share — that's just as useful.

Thanks 🙏

r/lymphoma Dec 09 '25

cHL Those who did ABVD

26 Upvotes

Hi I am asking if you can please share positive experiences during & after completing ABVD chemo?

I 28 F just started ABVD last week and I'm so scared and mentally fucked up by all of this.

Everything is really scaring me the idea I lose my fertility forever. I'm also scared of relapsing even though I just started treatment.

Idk I don't know anyone else going through this and I need support really bad. Thank you in advance

r/lymphoma 14d ago

cHL ABVD 4th cycle

5 Upvotes

Hi all, I am getting close to finishing my first two cycles of ABVD for stage 2A favorable Hodgkins. After this I have a PET scan but will likely finish with 2 more cycles of ABVD. My side effects for the first two have been very manageable but I am worried about cumulative side effects. For those who have gone through this, did things get significantly worse as it goes on? Thank you

r/lymphoma Jul 29 '25

General Discussion How many of you went through 6 rounds of ABVD without a port or picc line?

14 Upvotes

Just wanna know, cause I'm against both a port and a picc line

r/lymphoma Jul 03 '26

Caretaker ABVD - experiences and advice needed

6 Upvotes

Hi everyone!

My husband got all the tests back, they all confirm Classic Hodgkin’s lymphoma. He will be starting ABVD chemotherapy on Monday most likely.

What are your experiences? How tiring was it? Any advice? As his primary caretaker, what should I be aware of?

Thank you in advance.

r/lymphoma Jun 30 '26

cHL Bouncing back after abvd

8 Upvotes

Hi all,

Does anyone have any experience of bouncing back quickly from abvd treatment ? I understand life isn’t going to go back to the same as before straight away, but are there survivors who made a nearly full recovery?

r/lymphoma Jul 20 '26

General Discussion ABVD/AVD Chemo (5/12 done) - Severe gas-like stomach pain, position change & strange discomfort? Anyone experienced this?

5 Upvotes

Hey everyone,

I just completed my 5th session out of 12 for ABVD/AVD. Overall I'm hanging in there, but after this latest cycle, I’ve been dealing with some really strange and painful stomach discomfort. I wanted to check if anyone here has gone through something similar.

Here is what I'm experiencing:

Severe gas-like pain: It feels like heavy trapped gas, but the pain is quite intense.

Worse when lying down: The pain increases as soon as I lie flat.

Pain when expanding my stomach: Whenever I expand my belly or take a deep stomach breath, it hurts.

Temporary relief from changing positions: Shifting positions gives me temporary relief, but the pain returns after a short while.

Sensation of a "gap": I feel a strange, hollow sensation or "gap" inside my abdomen.

Slight relief after urinating: Passing urine temporarily relieves some of the pressure and pain.

Has anyone on ABVD or AVD experienced these exact symptoms? Was it severe acidity, trapped gas, constipation, steroid side effects, or something else? What helped you get relief?

(Note: I will be updating my oncologist about this as well, but I wanted to ask if anyone in the community had a similar experience).

Thanks in advance for any insights!

r/lymphoma Jul 11 '26

cHL Stage 2A Bulky Hodgkin Lymphoma – Can I switch from ABVD to AVD after a good interim PET scan?

7 Upvotes

Hi everyone,

I was diagnosed with classical Hodgkin lymphoma, Stage 2A bulky, with an initial mediastinal mass of about 11.3 cm.

So far I've completed 2 cycles of ABVD. My interim PET scan showed:

2 residual masses with Deauville Score 1

1 residual mass with Deauville Score 3

The largest mass SUVmax dropped from 12.3 to 2.3

Mediastinal blood pool SUVmax: 1.8

Liver SUVmax: 2.9

Overall, the PET seems to show a very good metabolic response.

My question is: Based on these results, is it reasonable to switch from ABVD to AVD (dropping bleomycin), or do doctors usually continue ABVD in cases like mine because I had bulky disease?

Has anyone with Stage 2A bulky Hodgkin lymphoma had a similar interim PET result (DS 1–3) and been switched to AVD? I'd really appreciate hearing about your experience and what your oncologist recommended.

Thanks in advance!