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#1 | |||
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Senior Member
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Today was my 4-month follow-up. The good news, my bloodwork is good. I test regularly because I'm taking Imuran and possible liver problems.
You may have noticed my slowdown in participation. I've been struggling due to the heat/humidity worse then ever. I'm not sleeping, yet exhausted, the hands' hypersensitivity has added the legs/feet now too. So after giving a rundown of new sx, to the NP, the doc comes in to see me. She has been stumped by me since day one (over a decade), my hands have always been a huge issue. Many MS'ers have the legs/feet. Not me, I never could follow the crowd. So, I suggested going back to one of the original meds I dismissed (early in my treatment) immediately due to sleepiness. I've got so many meds that do that, I handle it alot better now. Not working has also made it easier to not have to be at the top of my game constantly. She starts looking through my book of a file and I ask her about upping my Trileptal (anti-siezure) since it helps the tinglies which have worsened too. She's like great, lets do it. So then I ask about going back on Wellbutrin, the only med to give me any real hand relief. I figured (without a medical degree) that since I'm on anti-siezure med and upping it, why not. Backstory, I had a siezure in 2002 while on it. Noone had a reason so Wellbutrin was axed and the search for a replacement began. Since then I've learned via another neuro that siezures seem to be a component of my MS. So my doc says we can do that too. There is a slower acting version available. So they are removing Wellbutrin from my medical no-no record. I've started ramping up, today with the Trileptal. After getting that stable, I can fill and try the Wellbutrin. It's not LDN (she still says no) but maybe I can start feeling better soon. My brain keeps locking up and I'm finding it extremely frustrating to say the least. I've not given up on LDN. I just tabled it until I feel better. That's it from here. I'm going to lie down for a bit and watch the Browns game. ![]()
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-- Beth RRMS -dx 1997 Never doubt that a small group of thoughtfully committed citizens can change the world; indeed, it's the only thing that ever has. - Margaret Mead Breathe In HOPE, Breathe Out DETERMINATION |
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#2 | ||
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Senior Member
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I hope that you feel better.
-Vic |
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"Thanks for this!" says: | MSacorn (08-07-2008) |
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#3 | |||
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Elder Member
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MS I hope you feel better real soon and hope the meds change help you,
__________________
. History doesn't repeat itself, but it does rhyme.............................Mark Twain . ....... . ... . |
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"Thanks for this!" says: | MSacorn (08-07-2008) |
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#4 | |||
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In Remembrance
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Well, Bappy, Darlin, I hope your med changes, bring you much needed and deserved relief. I don't see where adding LDN would do any harm, but keep working on 'em.
![]() I hope you feel better soon.. ![]()
__________________
~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: | MSacorn (08-07-2008) |
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#5 | |||
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Grand Magnate
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i hope you feel better too and that the meds will do their job.
relief is always welcome when you're suffering sx's.
__________________
Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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"Thanks for this!" says: | MSacorn (08-08-2008) |
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#6 | |||
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Elder
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I hope you feel better soon.
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__________________
RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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"Thanks for this!" says: | MSacorn (08-08-2008) |
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#7 | |||
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Senior Member
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I hope you get some relief, Acorn
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__________________
Multiple Sclerosis-Dx May 2007 . |
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"Thanks for this!" says: | MSacorn (08-08-2008) |
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