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Anyone on here have MS and a lapband?



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Hi, there is a possibility I may have MS and I am scheduled to get my lapband surgery next week. I should find out on Wed. for sure or at least see what my neurologist says. I am just wondering if anyone on here has this and how the lapband has or has not affected your symptoms? Or has not bothered it at all.

I am scared and just wondering what the right thing for me to do is.

Thanks for your help,

Heidi

heidshosh@aol.com

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Sorry can't help you but i just wanted to wish you all the best. Hoping everything goes well.

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I don't, but my sister does. It's really, really difficult (as in impossible!) to predict how MS will progress. There are many good drugs on the market to slow its progression down.

That said, as my sister's disease has progressed, swallowing has been a real issue for her during exacerbations. Being banded would be very uncomfortable for her on days when she can barely get her own saliva down. I am not sure, however, how MUCH harder it would be; maybe a temporary unfill would even the playing field so that she could weather the storm, then pick up where she left off once in remission.

If you are diagnosed, or a diagnosis looks probable, have a talk with your neuro about this. S/he can give you good guidance about the safety and pitfalls of banding. You might be surprised that s/he's very encouraging. As I said, everyone's disease presents a bit differently, and swallowing might never be part of your experience. Attaining a healthy weight, however, might be one of the BEST things you can do to maintain health and mobility. Your doctor will help you weigh these things.

One thing about the band is that, if problems do arise, it can be adjusted; I would think that would help tremendously.

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