I have a severe case of sound sensitive myoclonus (exaggerated startle), similar to what others have reported. My startles often trigger painful head spasms, fatigue & disorientation for hours, sometimes days! Been… READ MORE
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Previous Q & A Questions
Now I cannot put any weight on it. I can walk with my walker but it is very painful! Is this related to my MS?
I’d like to know if anybody is using CBD oil and how effective it is and what brand they would recommend? Looking for a good CBD cannabis oil to relive spasm in… READ MORE
I would like to hear others’ stories and effects on who has had HSCT done? I’m tired of them coming out with A NEW DRUG to SLOW MS. I have SPMS and… READ MORE
I am new here and have not been diagnosed with MS as of yet. I have been having a lot of symptoms over the past month or two and my rheumatologist became… READ MORE
Seems that doing simple things such as laundry are just overwhelming for me. I feel as I have become a lazy person as I sit in my apartment. I’ve thought of even… READ MORE
I’m moving to Southern California and want best temperature for MS. Any suggestions?
I’m new to site! Very confused. Dr suggested stopping DMT, said my MS mild but I have deficits on left side which are perm. Not sure stopping DMT right thing to do…. READ MORE
I have been researching CBD for MS symptoms. Seems to be an alternative to taking big pharm medications. Anyone with any information on usage, findings, or opinions I’d appreciate the feedback.
I received my diagnosis this week. I reached out to my sister and mother who were extremely negative. They said it was all in my head (actually it’s all in my spine… READ MORE
After years of wondering what was wrong with me, I was finally diagnosed with MS in January. I am still trying to wrap my head around this – and am surprised at… READ MORE
Hello- I am very new to this so I will attempt to be brief but it won’t be. 8 year ago I believe I had my first major “flare” that was misdiagnosed…. READ MORE
I was first diagnosed when I went to ER with Optic Neuritis. MRI showed a lot of lesions. Neuro and Opthalmologist called in to ER said it WAS Optic Neuritis even tho… READ MORE
I was first diagnosed when I went to ER with Optic Neuritis. MRI showed a lot of lesions but NO oligoclonal bands.
It seems for the past two of these weeks my symptoms are coming and going by the hour. And are worse at night. Numbness tingling face pain bladder walking. My Neuro did… READ MORE
Need recommendations for neutral motion control shoes to fit over a hinged AFO brace wearing as result of foot drop. Researching and more confused than ever. Hv looked at several New Balance… READ MORE
I do not have insurance. I have qualified for low cost or free clinics but no one will test. Can anyone suggest how to get testing done. I am only getting worse… READ MORE
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