Thanks so much for reaching out. I sure will follow up!
Thanks for letting me know. I think I'm having similar hot flashes where I don't really sweat much but I do become warm all of a sudden.
Did anyone experience chills/goosebumps on the areas where they had radiation? I finished radiation a month ago but last week I started getting chills only in those spots. My skin also hurts, in the sense that it’s very tender and very sensitive to temperatures. I don’t have any rash or actual bumps but the sensitivity doesn’t go away and I keep getting chills only in those areas.
Hi Emily3,
Sorry to hear about your hurting and chills. I hope your doctors can come up with some answers. Hugging you close in my heart ❤️!
Barbara8
I have read some history posts here and on the internet about how having CA (including Lymphoma) increases the likelihood of getting other CAs. This is with or without getting chemo- or immuno- therapy txs. I know that after my dx, my mammogram came back abnormal with areas that needed to be biopsied and watched. There are more of those areas every 6-month check. My skin CA occurrences which started about 6 years prior to dx have ramped up this last year - with 4 new spots that needed to… read more
I have been thinking about this issue. I finished R-CHOP for follicular lymphoma in January 2023. Since then I have had squamous cell carcinoma on my scalp and am currently scheduling a biopsy for… read more
Yes, I have rashes on and off. Rashes, eczema, hives. The only time I have scabs is when I nearly claw myself to death which I try not to do. I can't take antihistamines ordinarily but found zyzal otc… read more
I had a needle biopsy done in May of 2022,and had one delay after another getting treatment started I have switched to another oncologist but I am really lacking confidence at this point in time.I think the fact that family and friends have pulled away only compounds the problem
Thanks to all you good folks,you are all like a virtual family to me
Relapse B cell. Started with FL, R chop 2014-15, Rituxan 2020, now immunotherapy started 1/3/24
I feel like a kindred spirit.The reoccurrence is inevitable.MCL 2021 original diagnosis,followed by chemo and a stem cell transplant.Ive been on rutuximab bi monthly since.
I am four years post stem cell transplant. The last PT scan was all clear, first clean one since this all started. I have battled swelling in my feet and ankles since the beginning and it is getting tiresome.
Try reducing salt in your diet and taking an over the counter diuretic. But ask your doctor about the diuretic first.
During chemo I always had some numbness in my fingertips and toes. It’s started to go away slowly in my fingers but my toes are actually getting worse and going into the balls of my feet now too. I’ve noticed my toes are also always cold, and the numbness gets more aggravating at night.
Has anyone else experienced anything similar?
My chemo was R-EPOCH
I received RCHOP, and felt that at the end of the treatment, but it went away after the treatment.
Thank goodness!