MY new NEUROLOGIST DIAGNOSED IT AFTER A CO,PLTE EXAMINATION... I HAD EVERY PROBLEM THAT SAID ..MSA MULTIPLE SYSTEM ATROPHY . IN IT'S FULL STAGE.. MY REWARD FOR CARING FOR MY DIABETIES FOR 63 YEARS..... HE WAS IMPRESSED THAT I WAS A TYPE 1 FOR SUCH A LONG TIME.......... I AM GOING TO SEE IF I CAN TRY TO GET MY IMMUNE SYSTEM BUILT UP. THAT'S THE CAUSE OF MY BODY ORGANS FAILNG. EES, SKIN, BP. DIGESTION, MUSCLES, GAIT, BLADDER NYTHING ELSE,
Does any one have MSA???????? IT IS a cous... - PSP Association
Does any one have MSA???????? IT IS a cousin of PSP & PD.... YET MORE PROGRESIVE ,,,,,,,,,,,
My husband has been diagnosed with PSP/MSA/Lewey bodies dementia with Parkinson's, yet although his symptoms match some of these he does not fit exactly into any. I think it is because the symptoms are similar and overlap that the doctors/neurologists cannot be certain.
We are awaiting the results of a second MRI scan in 16 months but I am not expecting anything new.
Well done you for managing Type 1 diabetes for so long, my husband has been Type 2 for 20 years and has not always managed as well as he does now - because I make sure he has his medication regularly !
Keep trying any therapies etc that you think may help. We have not ruled out trying anything !
NanBabs
My brother has MSA and Amantadine seems to help him the most. We are also trying certain supplements such as cinnamon and coconut oil as well as A&D ointment for skin issues.
Keep an open mind and try anything you feel will help!
Hi GenaBenedict
Sorry to hear about your diagnosis. There is a charity that supports people with MSA You may wish to visit their website msatrust.org.uk/