http://www.ncbi.nlm.nih.gov/pubmed/18364720
Cytoxan info on fertility
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http://www.ncbi.nlm.nih.gov/pubmed/18364720
Cytoxan info on fertility
Sent from my SM-G925V using Tapatalk
Best wishes,
Tom
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2 years untreated. Dx w/ biopsy - 2000
Tx Plan:
NUTRITION
RESTORATIVE SLEEP
RAISE ANABOLISM
REDUCE ALL INT / EXT STRESSORS
Lily, hi. Fertility has been talked about on here, I remember seeing it a few years back. So if u do a search on here. Also I believe Carrie G? Not sure about the g? But she's a member and if u search under her u may get some information... Best of luck to you both!!! Deb.
Found this info regarding fertility and rituximab: Rituximab (Mabthera) | Cancer Research UK
Probably not the news you want, but...
Pete
dx 1/11
"Every day is a good day. Some are better than others." - unknown
"Take your meds as directed and live your life as fully as you can." - Michael Chacey, MD
Lily,hi. I remember I'm pretty sure Carrie C,not G. Dont know how that would effect you're search. Then again,if u just search fertility it would come up,I would imagine... Deb.
Find a rheumatologist that treats people with wegeners. Not all do. I found 3 in a row that had never had a patient before. Finally I found one at a university hospital 2.5 hours away. Don't be afraid to ask them about their experience in treating wegeners. Once you find one, then use them to manage your care. Learn all you can and ask questions. I think it is very likely that you can still be reproductive, it is just a matter of getting the right experts to work on it. So don't despair until you are sure.
I had pneumonia and was suspected of GPA over 2012 Holiday season. I was officially diagnosed and treated Easter of 2013. I had more problems at Easter and went back to hospital now with kidney involvement and lung issues. At least they could do biopsy to make sure it was GPA. I had Rituxin and all the Prednisone etc. to clear it up. I have been using Rituxin for maintenance every 6 months. It is time again but I just don't know what lab work to look at to know if I need to. With 2 major organs already having been involved I am high risk of having more problems. Most of the time I feel fine for my age, 65 with all the normal aches and pains, so I don't know how to tell what counts anymore as symptoms or just normal. Anyone else with similar story?
When i am having a flare up usually it starts with rash on my legs that looks kind of like chicken pox, then comes the joint pain and problems breathing. Best way it to have them do a full panel of blood work when diagnosed they shoild have told you where they prefer your white cell count to be. A higher count usually means trouble is brewing. Hope this helps a little
Loisann, I don't get rashes on my legs and only a few red spots on my arms. Everyone is a little different. For me, the telltale signs of a flare are night sweats, feverish feeling, increased mucus production, rarely joint pain although I did have it before initial treatment. Lily is right about the WBC count, and also in lab work, you need to look at inflammation markers such as CRP and SED rate, and also creatinine level for your kidneys, and protein or blood in urine. If you can get copies of your lab work, you should, and it will tell you what the normal ranges are. Sometimes symptoms and lab results don't coincide perfectly, and docs sometimes let things slide that are just a little off the norm. If you just recently had problems that sent you to the hospital, my intuition would be to go ahead and get another RTX infusion.
Anne, dx'ed April 2011
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