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#1 | |||
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I posted another post earlier about my neuro and dh on my case about getting the jc-virus test, well, I DID IT!! Now everyone can get the heck off my back about it!! Positive or negative results, no matter to me because Im never doing tysabri. DH tried to talk me into trying it today if the test is negative, and I had to put my foot down again. Man, will he NEVER get the hint!! I did the test, and the phlebotomist botched it. I told her my only good vein is in my right arm, so what does she do
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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#2 | ||
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"Thanks for this!" says: | SallyC (09-22-2012) |
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#3 | ||
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n/a
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Reps aren't even allowed to leave pens or pads of paper with the drug name printed on them anymore. Which is nice for me since DH doesn't bring them home anymore to clutter up the house! |
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"Thanks for this!" says: | SallyC (09-22-2012) |
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#4 | |||
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In Remembrance
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I think some Neuros are convinced that Tysabri is their MS patients best bet, right now. They could be right....just not good enough for me. My old Neuro thought so and just laughed at me and my LDN. NOT my Doc anymore..
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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"Thanks for this!" says: | ANNagain (09-25-2012) |
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#5 | |||
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Senior Member
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Glad you did the test, B2Y! And glad it is negative!
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RRMS, diagnosed '00 Everything will be alright in the end. If it's not alright, it's not yet the end. |
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