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Ok back to thread topic Tecfidera.
Kitty what was/is your WhiteBloodCount? How much did it change from start to end of taking Tecfidera? Mine is now 11 from a constant sky high 15-17. I must say it IS working in that respect thank goodness. |
My neuro never took my blood count. Said it was not necessary. I said I thought it was from everything I had read and from the FDA website and all, and he said no, was not necessary. I stopped because of all the side effects. Even with the preventatives to the side effects, I was still getting some of the side effects, so I said I had enough. It was my second time trying the drug, so it was a mutual NO between me and neuro.
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Ask your regular doc to order a cbc monday. |
I don't have a regular doc. I have no insurance so I don't being able to keep my neuro was a blessing. He only charges 75.00 a visit. Maybe I'll ask him for the blood test. Do you think it would really matter? I was technically on the drug for only a month. I was on for 2 weeks had a bad reaction then he took me off for 3 weeks then back on for 2 weeks and the same reactions even with preventative meds.
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Hi. Well, if it was me i'd want to know because i'm trying hard as I can to hold my MS level where it is for as long as I can, so any little bits of info are welcome. Curious if it effected your blood counts and how. Surprised your neuro wasn't curious as well..and you. I'd go for it if I were you. Test might cost same as a neuro visit. For your own piece of mind/info anyway. Maybe your count was low and made you feel poorly. Nice to know how all them cells are doing once in a while especially if weak, tired ect.
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