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Re: Help!! Anyone here also have MS or symptoms of MS?For more information on symptoms and treatment of endometriosis visit www.EndometriosisZONE.org. From: DEENALYN (anonymous@obgyn.net)Fri Apr 13 09:10:36 2007
At Mon, 26 Mar 2007, PennyDoll wrote: > >Not only do I have all the problems of endo, but the past 2 years I've >had flair ups of optical neuritis which can lead to MS and was told that >I may eventually end up getting it. Well the past two days i've had >problems seeing, walking (feels as though someone is draining all my >energy out) and i'm limping or having trouble moving. I went on an MS >early symptoms site and ectually have every one. I can't get an opt for >a neuro until next week. Does anyone here have these problems or have >MS? How does it affect you, and how bad is it when added to all your >endo problems? I just don't know what to do. I feel like i'm at my end. >And all this is just dragging me down. How far can a person be beaton >down? Olease Help > >-- >PennyDoll27@aol.com >Kris > I HAVE MS. I WAS DX IN APRIL 2001. I DO NOT HAVE ON BUT MY EYES DO HURT EVERY NOW AND THEN I GET THIS PAIN IN MY EYES LIKE SOMEONE POKING ME WOITH A NEEDLE. I AM ALSO ON NEURONTIN WHICH HELPS ME ALOT WITH THE ACHES AND PAINS IN MUSCLES. I HAVE MANY LESIONS IN MY BRAIN. THE FIRST NEURO I SEE SAID TO JUST TAKE SOME ASPIRIN AND YOU WILL BE OK. I GOT ANOTHER NEURO WHO DID A SPINAL TAP AND BRAIN MRI WHICH FOUND MS.
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