Excessive Sweating When Glutened anyone else?
#1
Posted 06 September 2004 - 07:52 PM
#2
Posted 07 September 2004 - 08:20 AM
I have lupus and have night sweats related to that autoimmune disease off and on for years. I also had terrible night sweats just before I got my gall bladder removed (turns out it was inflamed).
If you have night sweats, but don't think you were 'glutened', I would be sure to mention it to your doctor, as they can be a symptom of many things....
Good Luck,
Pam
#3
Posted 27 February 2005 - 10:29 AM
Ian
What does not kill you makes you stronger.
Nobody cares about losers and quitters never win. If you fail with the cowards then what's the message you send?
Can't get it right, no matter what I do. Might as well be me and keep fu@$ing up for you. - Brian Thomas (Halloween, the greatest metal band ever!)
Ian Moore. Self diagnosed at 36 because the doctors were clueless.
Started low-carb diet early 2004, felt better but not totally gluten-free. Went 100% gluten-free early 2005 and life has never been better.
#4
Posted 27 February 2005 - 11:56 AM
mstone@ups(dot)edu
#5
Posted 27 February 2005 - 08:24 PM
#6
Posted 27 February 2005 - 09:46 PM
South Georgia
9 yrs gluten-free
...also DH, fibromyalgia, neuropathy, osteopenia, hypothyroid...
After almost 10 years, I am doing soooo much better!
#7
Posted 14 January 2006 - 08:51 AM
pamelaD, on Sep 7 2004, 09:20 AM, said:
I have lupus and have night sweats related to that autoimmune disease off and on for years. I also had terrible night sweats just before I got my gall bladder removed (turns out it was inflamed).
If you have night sweats, but don't think you were 'glutened', I would be sure to mention it to your doctor, as they can be a symptom of many things....
Good Luck,
Pam
PAM...
This was a great Post here, & very informative! I have the "night-sweats" really bad as well, but have attributed it to MENOPAUSE. I noticed only a slight change since I went "gluten-free," but am still wondering if maybe some of mine might be related to an autoimmune reaction/inflamation too? I have an Aunt who has Lupus, and Lordy, I'm sure this stuff runs in the Family!!! When my tests results came back, I was told I had alot of antibodies in my system, so your post here was most interesting! I still have my Gall Bladder tho....... many of my Family members have had theirs removed.
This is a very interesting subject to think about, and thanks for Posting! Regards!
Quote
#8
Posted 14 January 2006 - 10:29 AM
Mballerina, on Sep 6 2004, 07:52 PM, said:
This is my husbands only symptom to being glutened.
Before being dx he suffered from them really bad!
Nikki
Husband diagnosed with Coeliac Disease 2004 by biopsy
Son diagnosed with Coeliac Disease Oct 2006 by biopsy (at age 13yrs)
#9
Posted 14 January 2006 - 10:45 AM
"Life is what happens while you're busy making other plans"
"When people show you who they are, believe them"--Maya Angelou
"Bloom where you are planted"--Bev
Celiac.com - Celiac Disease Board Moderator
#10
Posted 14 January 2006 - 12:51 PM
#11
Posted 18 January 2006 - 07:10 PM
#12
Posted 02 March 2006 - 02:52 PM
Gluten Free since 4/05 - adult onset
Symptoms for 4+ years prior
Immediate family tests negative
No Known family members w/ celiac disease
#13
Posted 02 March 2006 - 03:53 PM
Gluten Free - August 15, 2004
"Not all who wander are lost" - JRR Tolkien
Celiac.com - Celiac Disease Board Moderator
#14 Guest_Robbin_*
Posted 02 March 2006 - 06:32 PM
#15
Posted 02 March 2006 - 06:40 PM
Since gluten free, my hands shake. When I drink water out of a bottle, I can see the water vibrate. Don't know about that either.
If anyone can explain, please post.
Gluten Free - August 15, 2004
"Not all who wander are lost" - JRR Tolkien
Celiac.com - Celiac Disease Board Moderator

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