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09-30-2006, 07:09 AM | #1 | ||
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Junior Member
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Good to see some familiar faces. Its been a rather rough year. My dd is sick-something neurological/psychiatric and scaring us half to death. Waiting for an appt at sick kids beginning of Nov witht he pediatric ms specialist.
I'm on no meds right now. Not much for me as i am in category limbo. Am i rrms or spms or rpms..the debate goes on. It makes little difference on my day to day life-but whoah, the labels make or break a drug deal. |
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09-30-2006, 08:44 AM | #2 | ||
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Member
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Hi Dale, welcome back.
Funny you should be here at this moment. I had just posted on the thread about the autologous stem cell transplant and said sometihng to the effect that you had considered it, or had actually tried it. |
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09-30-2006, 10:14 AM | #3 | |||
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Welcome home, my friend! I wish you had the options for meds in Canada that we tend to have here.
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09-30-2006, 10:58 AM | #4 | ||
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Junior Member
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Hi Dayle, great to see you and sorry about your daughter having medical problems! How long has it been going on, all summer? I cannot imagine your worry and I hope for the best possible outcome to this.
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09-30-2006, 10:59 AM | #5 | ||
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Junior Member
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09-30-2006, 11:03 AM | #6 | |||
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Grand Magnate
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Quote:
I was going to ask the same question of Cherie, endure . . . I think we have the same options here as in the US. Cherie |
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09-30-2006, 11:07 AM | #7 | ||
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Junior Member
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I think Cherie is likely thinking about availablity of IVIG (which she and I have discussed). It is not available for Canadians with ms. Also tysabri has been held up with health canada and hospital ethics committees..i know a friend who was in the trial is just getting back on the program this week. It will be more limited here at least for now.
But we do have access to the MPB8298 trial..which is not available in the US yet. |
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