LymeNet Flash: Anyone doing Hot baths, Peroxide and Epsom?

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Anyone doing Hot baths, Peroxide and Epsom?

UBBFriend: Email this page to someone!

Author

Topic: Anyone doing Hot baths, Peroxide and Epsom?

jenn
LymeNet Contributor
Member # 21687

posted

I have heard a few say that they do
Hot Baths with Epsom salt and Peroxide to open
the skin pores for the toxins to be released.

another method is taking a hot shower or bath then spraying peroxide on skin when the pores are open.

is anyone doing this? and if so how much peroxide do u use?

Posts: 501 | From Hudson Ticky Valley, NY | Registered: Aug 2009 | IP: Logged |

Pinelady
Frequent Contributor (5K+ posts)
Member # 18524

posted

You can search with

peroxide or lemon juice to kill

And find many skin articles. Here are 2.

I do not use peroxide instead I like Lemons and Ginger. But it is worth a try...

http://www.natural-remedies-hiv-aids.com/aidscontroldiet.htm

http://theskinphilosophy.forumotion.net/skin-lightening-f6/lemon-juice-and-hydrogen-peroxide-t223.htm
To me the skin is not philosophy it is a science as our largest organ of the body.

--------------------
Suspected Lyme 07 Test neg One band migrating in IgG region
unable to identify.Igenex Jan.09IFA titer 1:40 IND
IgM neg pos
31 +++ 34 IND 39 IND 41 IND 83-93 +
DX:Neuroborreliosis

Posts: 5850 | From Kentucky | Registered: Dec 2008 | IP: Logged |

sickpuppy
LymeNet Contributor
Member # 23846

posted

I use 2 cups epsom salts and 1 cup baking soda in the bath--not too too hot. Eases the pain. Not sure about detox effects.

Posts: 702 | From North Eastern USA | Registered: Dec 2009 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

I do epsom and peroxide all the time, I always feel better afterward. I also do baking soda, if I have all three in the house.

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

-
Warm is good. However, Hot baths can be very dangerous. Nice and warm is fine but in the hot zone can really cause some major neurological and adrenal set-backs that can last from a day to weeks.

---------

http://cassia.org/essay.htm

When to Suspect Lyme Disease - by John D. Bleiweiss, M.D.

. . . both LD and MS can be aggravated if the patient takes a hot bath. . . .
-

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

WildCondor
Unregistered

posted

The epsom baths help magnesium get absorbed via the skin and is a good way to detox. Far Infrared sauna is very good as well. I never did both epsom and H202 in the same bath, it was usually one of the other. When I did the H202 I used 6 drug store bottles full. I did it IV also but that was a huge waste of $.

IP: Logged |

jenn
LymeNet Contributor
Member # 21687

posted

thanks all!
gonna give it a try!

Posts: 501 | From Hudson Ticky Valley, NY | Registered: Aug 2009 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

Keebler, that's interesting. I swear my husband always makes the bath WAY too hot, and when I get out I have to stand basically in a toe touch position while my heart pounds and I have trouble breathing, and I feel like I'm going to faint. I know I need to be worked up for POTS but I didn't know about what you wrote. Thanks.

How do you hold all this knowledge in your head??

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/