Tysabri Recovery Series - Summer heat and MS
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Uploader Comments (vbeachy)
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One of my first symptoms was when I went for a hot tub bath - I could not even walk at all
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Thanks Steve! I hope you enjoy my website too!
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hi Vern, please stay cool and keep up the great pioneering work .... I must check out your web-site next...
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Thanks James...I, too, am looking for more QOL improvements. :)
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I am sorry to say that mine is awake 24/7. Heat really exacerbate my problems.
Hugs,
Sefardisafran
LuisM
Hoboken NJ
Sefardisafran 3 years ago
Thanks Luis!
Yes...summer heat USED to paralyze me, but it is much better with Tysabri.
vbeachy 3 years ago
1/2 mile walk at 90F? you don't have MS my friend. Just came back from hospital after visiting an MSer with an exacerbation due to heat.
Wish you good.
Sefardisafran
Sefardisafran 3 years ago
Ha! Sometimes I like to thing I don't have it anymore, but then I get a rude awakening of fatigue.
vbeachy 3 years ago
Keep up the good work Steve. Thanks! I think I'm the only person with MS that actually benefits from the heat. The cold gives me that "paralysis" feeling. Anyway, stay blessed----Pat.
SAS4 3 years ago
Thanks!
Vern
vbeachy 3 years ago