Pins and needles: All morning til now I... - My MSAA Community

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Pins and needles

dailygrump40 profile image
dailygrump40
โ€ข5 Replies

All morning til now I have had the pins and needles in my hands. First time for my hands. But it made my hands feel froze. I couldn't get them to feel warm to me. My wife was telling me that they were fine. Actually a little to warm. Now I feel like I'm over heated

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dailygrump40 profile image
dailygrump40
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5 Replies
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lbenmaor profile image
lbenmaor

Sorry to hear you're so uncomfortable. Please call your Dr.

Leslie

Jesmcd2 profile image
Jesmcd2CommunityAmbassador

Hard telling dailygrump40 ๐Ÿ˜ž did you sleep wrong? Or pull something? Do you feel like your coming down with something?

Like lbenmaor says call your Dr if it continues! My hands are like ice all the time this time of year. ๐Ÿค—๐Ÿ’•

J๐ŸŒ โ›„

dailygrump40 profile image
dailygrump40โ€ข in reply toJesmcd2

Probably did sleep weird and figured out today I'm also fighting a sinus infection. Mucinex definitely put me on my keyster. Wow!!! I was totally worthless today.

Jazzihorsecat profile image
Jazzihorsecat

Yep, call Dr. Daily, this M.onS.ter in our nerves does that, our wiring is all freakedout, it's like a gremlin is in our CNS= Central Nervous System; messing w/them, Tumeric spic w/ curcumin helps mine....So, does my hemp cream/lotion or a magnesium lotion. Hope U get better!๐Ÿ˜๐ŸŒธ๐ŸŒบ๐ŸŒทBlessings---Jazzy๐ŸŒน๐Ÿ’œ

goatgal profile image
goatgal

dailygrump40 We all know that MS affects the CNS (central nervous system), but research suggests that it does hidden damage to the ANS (autonomic nervous system) which controls such things as breathing, blood pressure, sweating...all those functions that we don't pay much attention to unless they go awry. Many of us with MS have Raynauds syndrome; in Raynaud's exposure to cold causes blood flow to the extremities to shut down, leaving fingers (and sometimes toes) cold, painful, and bloodless. Sometimes in the mornings, when I wake up my palms are red, warm and prickly which I have assumed is related to Raynauds (which I've experienced for 40+ years) and the ANS in some way. So, yes, tell your doctor about your symptoms; if the answer is not to worry, add them to the list of other ways MS manifests itself in you.

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