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Monday, November, 30, 2009
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ladygraycloud's SharePosts

TODAY HAS BEEN VERY ENLIGHTING

TODAY HAS BEEN GOOD FOR ME--I HAVEN'T BEEN ON FOR AWHILE AND READING ALOT OF THE QUESTIONS AND SHAREDPOST I HAVE REALIZED HOW VERY HARD THIS IS NOT ONLY ON US BUT OUR DOCTORS TRYING TO HELP AND DO THE RIGHT THING FOR US. WE DON'T ALWAYS SEE IT BUT I FEEL THEY DO THE BEST THEY CAN FOR US AND OF COURSE WE GET IRRATED AND DEPRESSED AND ANXIOUS... Read moreChevron

Well My Appt w/Neuro

Well on monday had my appt with my neuro again and still the same-did find out I don't have menigentis, encyphilisis,or cancer! So thats my good news --for the bad he still says he can't say for sure I have MS either-due to only one (dawsons finger)lession in the brain and only mild relaspes since May. Why do doctors always ask why are you... Read moreChevron

Just Another Wonderful Day in MS limboland

Good Morning to all-hope you all ahve a great day- Is there such a day as a wonderful day-I get up every morning with pain and can't seem to get help for -don't understand- I have a neuro, a psych, and a g.p. but no-one can help me with this pain I constantly live with. They all tell me I should be in a pain management clinic but HELLO, no... Read moreChevron

Well its been hard time lately

It has been hard lately, going to doctors and one want renew script its almost like pass the buck, in turn I running out of meds and back to headaches,pain in limbs and now in the left foot feels like I'm stepping on a knife. I had two more episodes and feel like that land we call limbo is getting bigger and bigger! But I trying to hang in I go... Read moreChevron

Everyday a Different View

You know I go thru the shared post and feel so much emotion for all and I sit with the notion of being told I do have MS and then being told I have an autoimmune disorder but we not sure if it is MS! I don't know somedays if I want to know what this is in my brain or not. Is it fear or just tired of being jumbled around and poked and tested all... Read moreChevron

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