First on the Detrol LA, I've had similar bladder challenges, and have
just finished with a fairly completely assessment with a urologist.
Bottom line is that Ditrapan is better than Detrol. Better yet is
Oxytrol, which is a transdermal patch. This is new on the market, and
most insurance won't cover it. I won an appeal because I have long
documented swallowing problems, which the dry mouth side effect makes
worse. The Oxytrol makes a big difference. I have no idea why.
Another thing, just for the record: using a catheter is absolutely no big
deal and can be very liberating.
As to the Antegren, I know nothing about it, but I do know that current
thinking is that anyone with MS should be on one of the ABC drugs.
Copaxone is easy to do and has no side effects for me.
I'd say kimberly has given detrol a long enough time to work and now something else should be tried! Ask your doctor. Ruth...
zoee15
Jan 24, 2004 3:07 pm
First on the Detrol LA, I've had similar bladder challenges, and have just finished with a fairly completely assessment with a urologist. Bottom line is that...
Personally I have no experience with rebif. I do think however there was a recent study that said temporarily stopping has no effect on how the medicin works....
Hello, To get more information about M.S.therapies go to http://www.MSWatch.com and http://www.MSuniversity.com If someone is on Copaxone Therapy, then call...
As most newly diagnosed MS patients I tried everything, including Bee Venom Therapy. BVT is exactly what is says, therapy via the induced venom of Bees. You...
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I, too, have terrible veins; so bad that I was told not to come back for IV treatments without a portacath. This is implanted high on my chest and has worked...
Hello everyone. I am hoping by joining this group I may get some suggestions for when those "weird" symptoms occur. I was diagnosed about three years ago. I...
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My experience with both ditrapan and Detrol LA is not the same. Ditrapan did work fine for what it was taken for, but made me very groggy and sleepy. I get...
Hi all, I'm new to this group too and will introduce myself but I wanted to say to Robyn that it does sound like what is happening in your arm and hand is...
lemon_drops1 wrote: << snip>>...I am hoping by joining this group I may get some suggestions for when those "weird" symptoms occur. I was diagnosed about...
One thing about ms is that you can't put it in a box and say "these are the symptoms." We're all as different as snowflakes so we all end up with a different...
Thanks for the ideas and the support. Right now that problem has been moved to the back burner. I went through the steriod injections and had a bad reaction so...
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JTsRetreat
Jan 31, 2004 10:48 pm
gail_demaine wrote: <SNIP>I, too, have terrible veins; so bad that I was told not to come back for IV treatments without a portacath. This is implanted high ...
Thanks for the input. I have recently moved and am looking for a new neurologist in the area. My second episode that you referred to that masked the symptoms...
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Hi everyone, I've had RRMS for the past 10 years and have my good days and bad. My main problem is balance, not vertigo (dizziness) but just totally losing my...
I was diagnosed w/ R/R MS in 1999 and my sister was diagnosed in 2003. (I gained a huge amount of weight while on Rebif but am now doing very well on ...
KR Pace
Feb 3, 2004 12:12 am
Hi, I got bee venom therapy last year (6 bites in every 2 days), and since I didn't have to go to steroid treatment since then (usually I have to go twice a...
Copaxone I recently chatted with my Dr about Copaxone. He said it wasn't that effective. Obviously you like it. Is anyone else on it? Dr told me today he has...
Jack Notarangelo is planning on running the Boston Marathon this year for Multiple Sclerosis which has affected multiple people in his family. To run the...