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Old 02-10-2015, 05:39 PM #11
MAT52 MAT52 is offline
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Quote:
Originally Posted by mrsD View Post
Never use HOT anything if you have sensory PN. Not steam rooms, not hot baths or hot tubs or heating pads! You will overload the heat sensing nerves, and they are broken and cannot turn off properly.
This does make a lot of sense to me. When my RA flares I crave heat on my joints. However once when I used a padded hot water bottle on my flared wrists the arthritis went crazy and I was up all night with the worst flare I've ever had. My hand has never been the same shape since! Maybe this is because I have small fiber neuropathy alongside RA?
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Old 02-18-2015, 03:14 AM #12
v5118lKftfk v5118lKftfk is offline
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Default Be careful of too hot

Yes, I had to experiment and find the right level of warm water.

I craved hot baths. Since nerve problems can also feel like joint and muscle problems, a hot bath would feel good while I was in it, but then I would have a rebound when I got out and get more problems. However, just the right warmth would relax me. Several doctors really warned me about too hot of baths (which I used to love).

Also, experiment to find the right amount of epsom salts. Some say that people generally don't use enough, however, once I used too much and didn't feel too great. I cut back a little and found the right amount for me. (Sorry can't remember amounts now).

Hope this helps.

Natalie
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Old 02-18-2015, 03:46 AM #13
MAT52 MAT52 is offline
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Quote:
Originally Posted by v5118lKftfk View Post
Yes, I had to experiment and find the right level of warm water.

I craved hot baths. Since nerve problems can also feel like joint and muscle problems, a hot bath would feel good while I was in it, but then I would have a rebound when I got out and get more problems. However, just the right warmth would relax me. Several doctors really warned me about too hot of baths (which I used to love).

Also, experiment to find the right amount of epsom salts. Some say that people generally don't use enough, however, once I used too much and didn't feel too great. I cut back a little and found the right amount for me. (Sorry can't remember amounts now).

Hope this helps.

Natalie
Yes I agree Natalie ive always loved hot baths -especially when the RA was bad as I would get awful chills. Now I have Raynauds in my toes so a warm bath helos but a lovely hot bath has had to become a thing of the past sadly as it acts like a broken thermostat on my small nerve fibers all night.
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Sjögren’s, Hashimoto’s and Systemic Sclerosis with Raynaud’s, Erythromelagia and small fibre polyneuropathy, GI problems top to tail, degenerative disc disease and possible additional autoimmune diseases
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