Hot baths,hot tubs,sauna,hot sun -UC

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Old Mike
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Date Joined Jan 2007
Total Posts : 2348
   Posted 4/1/2013 1:08 PM (GMT -6)   
Anyone see any improvement in your UC after prolonged stay in heat,even al little bit.
I seem to feel generally better after a real hot bath,not that I have noticed anything with the UC don't take many baths,usually shower.
Might be interesting to try if you have a hot tub.
Has a lot to do with HO-1 may start a thread on HO-1.
Old Mike
http://www.ncbi.nlm.nih.gov/pubmed/17575720

Post Edited (Old Mike) : 4/1/2013 12:15:16 PM (GMT-6)


Michelejc
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Date Joined Jan 2011
Total Posts : 1197
   Posted 4/1/2013 1:16 PM (GMT -6)   
I love the beach and tanning. I don't see any drastic changes after a day at the beach. I do feel more relaxed, which is good.
MODERATOR-UC FORUM
54, female - diagnosed with ulcerated proctitis/mild colitis
Canasa - once a day
Lialda - once a day
VSL#3 DS - 1/2 pack a day
Zocor - 40 mg
Boniva - once a month
Calcium with Vitamin D
Glucosamine
Magnesium
Herbs -
Valerian - when needed for sleep
St. John's Wort, Black Cohosh, ginger

Levi
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Date Joined Nov 2009
Total Posts : 1537
   Posted 4/1/2013 1:19 PM (GMT -6)   
Hmmm...When I do my DMSO I get in the tub and have hot water around me because it sometimes gets cold doing it on the bed after I clean my body very well for it. Maybe they are both working together on the OH-1?
29 years old
Diagnosed 2009 proctosigmoiditis, 2010 Crohn's colitis, 2011 ileocolitis
Symptoms since 10.2007
Pentasa, four grams/day, 6mp 50 mg/day
Rowasa enema, 3 grams every other night
VSL#3 DS one packet/day and VSL#3 yogurt
Turmeric, digestive enzymes, boswellia, propolis, cat's claw, l-glutamine, fish oil, vitamin D, kefir, blueberries
Liver-Milk Thistle; Heart-Hawthorn, sometimes

bananagirl
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Date Joined May 2011
Total Posts : 4317
   Posted 4/1/2013 2:56 PM (GMT -6)   
i don't think anyone can deny that a hot bath feels amazing. same with sunbathing- the heat feels good against our skin. i don't think it's done anything for my UC, just my general well-being.
Joanna 23
Current: 2-4 bms/day- very anemic/low hemoglobin
Supps: vit C/D, CLO, astaxanthin, b12 shots, colostrum, dig. enz, l-glut, serrapeptase, culturelle, prescript assist, sacro b., scdophilus, molasses, liver
Diet: SCD/paleo
Tried: canasa, rowasa, entocort, pred, 6mp, remicade, humira, lialda, welchol, bentyl, LDN, cipro, flagyl, VSL, Vit E, 8 FT, clay, aloe, slip. elm, vanco for c diff

Canada Mark
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Date Joined Jan 2013
Total Posts : 2005
   Posted 4/1/2013 3:02 PM (GMT -6)   
I'm always drawn to the heat. Be it a hot bath or a dip in the hot tub. Always feel 100% better after, but it's very short lived unfortunately. While I'm in it though - it's always as if the disease went away for that time period.
Diagnosed Crohns-Colitis about 8 years ago - Past Meds: Antibiotics, Prednisone, Methotrexate, Remicade - Current Meds: Prednisone 30 mg/Daily, Immuran (Jan 21, 2012) 150 mg daily. Actually achieved full clinical remission for about 2 years using Remicade, Diet (SCD) and Exercise

“An expert is a person who has made all the mistakes which can be made, in a very narrow field.” - Niels Bohr

Probiotic
Veteran Member


Date Joined Mar 2007
Total Posts : 2731
   Posted 4/1/2013 3:57 PM (GMT -6)   
I agree with the other responders- nice soothing heat of bath can soothe the body temporarily, but it never had any actial impact on my IBD. In bad flares I would have hot baths quite iften for that temporary relief though.
"In order to save the village organ, we had to destroy remove it" -- Doctor's Prescriber's proverb.

uc-logic
Regular Member


Date Joined Oct 2010
Total Posts : 147
   Posted 4/1/2013 4:05 PM (GMT -6)   
I mostly flare during the winter, I feel better any time I can get warmer whether it's a shower, bath, standing by the wood stove, but nothing beats summer sun/heat!

I think a big part of UC is general well being/comfort, when I am happy, warm and worry free even for a short time I generally feel better and my UC is noticeably less if bothersome at all.
Diagnosed Feb 2010
Started Remicade March 5th 2012
Multi Vitamins

Been on: Asacol, Sulfasalazine, Prednisone, Imuran

katarzyna
Regular Member


Date Joined Dec 2012
Total Posts : 329
   Posted 4/1/2013 4:26 PM (GMT -6)   
The warm to hot water helps with the pain just like a heating pad would. But it doesn't improve it or anything.
Currently in "remission"; no pain, D, mucous, etc. 21 year old female diagnosed with UC August 2011.
Asacol EC 400mg, Centrum multivitamin, Iron 65mg.

Diet of mainly vegetables, fruits, fish, and poultry. Minimum ingestion of red meats, oranges, and soda. Distilled water, lemon water, or organic green tea for drinking.

Old Mike
Veteran Member


Date Joined Jan 2007
Total Posts : 2348
   Posted 4/1/2013 4:48 PM (GMT -6)   
I guess this is really talking about hyperthermia,where you would stay in a hot hot tub,for say 1/2 an hour or more,they do hypothermia treatments but they raise the body temp to 104 F,a little dangerou if you dont watch it. They do this for 4 or so hours with infrared heat in german spas,then you need a 4 hour recovery period,this is not for UC but what I found on hyperthermia treatment.
Old Mike

TheAnswersYouSeek
Veteran Member


Date Joined Jan 2013
Total Posts : 2543
   Posted 4/1/2013 5:30 PM (GMT -6)   
I feel better in all of those situations because my detox pathways open and I sweat.
Current: No Dairy, Sugar, Wheat or Soy.. Olive leaf (20% Oleuoropein), Lauricidin/monolaurin, NA-Cysteine, CoQ10, Psyllium/Apple pectin, Ferula, Triphalia, methylation pathway support, sodium butyrate, anantamul, Blis K12, VSL#3, PB8, Proteolytic enzymes, Proferrin
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