FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#1 | |||
|
||||
Elder
|
A friend just emailed me and said that the guy she goes to for Watsu (I think that's what it's called) said that "warm water is no longer a no-no for MS patients" and that he "did the research and found that out."
What did I miss? The last I knew, some of us are more sensitive to heat than others, but I don't remember seeing any recent research that changed the basic facts. I wonder if he meant that the symptoms exacerbated by raised body temperature are usually transient? Anybody hear anything I didn't??
__________________
* * * **My flesh and my heart may fail, but God is the strength of my heart and my portion forever. (Psalm 73:26) |
|||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
Cold Water | On the Lighter Side | |||
Under Water? | The Stumble Inn | |||
The benefits of hot water | Peripheral Neuropathy | |||
How much water do you drink ? | Peripheral Neuropathy | |||
Like A Fish Out Of Water | Reflex Sympathetic Dystrophy (RSD and CRPS) |