"I have been SVR for 2 yrs in October of this yr. Only have known it since October of last yr. because the MD. made a mistake and read the wrong lab results. Idiot.. Anyway, yes there are many of us here. I don't log in much anymore becau..."
agatha56's Profile
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About Me: Female, 66, pASADENA, TX, member since Dec 2008
NEWLY DIAGNOSED WITH HEP C AND AM SCARED SILLY. I AM A HEALTH PROFESSIONAL AND LOVE MY WORK. THIS TIME I AM THE PATIENT AND IT IS NOT A GOOD FEELING TO BE ON THE OTHER SIDE. WILL TRY TO BE POSITIVE. I KNOW ATTITUDE GOES A LONG WAY WITH CHRONIC ILLNESSES.
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Apr 20, 2011
"Carbon dioxide number? Nygirl, are you crazy now. Has nothing to do with Hep c."
Apr 20, 2011
"That is true. I had what they call minimum damage in my left hand and moderate in my right hand. I had the surgery on my right hand in January and now just 3 months later my right hand is waking me up with severe numbness and pain. It wo..."
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06/11
Hey Soul Sister! Trin is ok, trying hard to decide which med to take and what to do. Imagine now the problem for many of the oldies is that are too MANY choices! Certainly wasn;'t that way when we treated right? It's going to be so wonderful to see people getting to UND @ week 1.........winning this battle. Hopefully it will be easier for them cause man it was sure not fun for us! Soooooooooooo great to see your name in my inbox, it's nice when your friends rememember you and pop in. Well back to work for me I hope all is going spendidly for you!!!!!!!
Deb
04/11
Just a quick note to say hi! I am new to this site. Just thought I would say Hello!! This site is so neat because I feel like everything is so open and on the table!!
Thank you Jesus!! Have a great day!!
01/09
Thank you for everything! ps. Thanks for the friendship . I'll help you in any way I can . Kepp your chin up !!
01/09
Thank you for everything!.hi agatha56.yeah you're right about early celebration ! the clinic here told me I have 'zeroed out' (my expression) but must finish the remaining course time and therefore I do not feel well.Figures and numbers are one thing , but until I feel like I'm out of this cloud the fight goes on .
The anemic side effect the docs say is a Ribavirin side effect , which I personally found way tougher than the interferon jabs , the anemia seems to be mellowing now and I haven't yet had any treatment for it from the clinic.That is next week.I will let you know how I get on with it.I would suggest keeping as keen an eye on the Ribavirin as you possibly can.The champagne and fireworks are on ice for the time being ! thankyou again for caring,it means a lot to me . Roger.
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