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Remicade Treatment

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I hope that your infusion is gentle, and that you have an easy time. I know that it's scary to go into uncharted territory.

From what I've read in the Remicade trials it does look like it is a good choice for us. I know I was glad to see that. Now, if I can just get my insurance to say yes.

Compassionately,

Tracie

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Tomorrow is the day. I start my Remicade Infusions. I'm not sure

what to expect, I've heard all kinds of things about the drug and

the infusion itself. The RN at the Infusion Clinic said I don't

need anyone to go with me and it will go great. I hope she's right.

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Hi. Christy I think it was? Good luck to you today. Im starting my Remicade infusions next Thurs. Im kinda nervous about it too. They told me the same thing, that I could drive myself in & out and the infusion itself would be no problem. So at least we're on the same page there... Let me know how it goes for you. I will be thinking of you today.

Good luck. Luv, Debbie T.

bengel@...> wrote:

Tomorrow is the day. I start my Remicade Infusions. I'm not sure what to expect, I've heard all kinds of things about the drug and the infusion itself. The RN at the Infusion Clinic said I don't need anyone to go with me and it will go great. I hope she's right.~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database

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Hello everyone, I finally found a key to make the letters bigger but I can't find a way to make the letters bigger on mail I receive or does that have to be done on the end of the sender. I hope everyone has a good day. I go to see the neurosurgeon today, and hopefully will have some answers about the MS/NS thing and if this thing with my eyes can be dealt with non-invasive. The prisms helped and from what I have been told that shows that it could be that nerve thing the opthamologist told me about so we may be back to the MS thing, hopefully, we will be able to just up the methotrexate and get things back on track. I will let you all. Take care and I will be thinking of you. Your friend in Texas, Jeanna

-- Re: Remicade Treatment

I hope that your infusion is gentle, and that you have an easy time. I know that it's scary to go into uncharted territory. From what I've read in the Remicade trials it does look like it is a good choice for us. I know I was glad to see that. Now, if I can just get my insurance to say yes.Compassionately,Tracie ~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database

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