Recent Posts

Need Feedback on Hydrogen Peroxide for Ms

Orshi (Exeter, Devon, England) on 01/21/2012

Hi all! I was diagnosed with MS 14 months ago, I had a rubbish year, needed steroid every 3-4 month, havent been able to work as I constatly have problem with fatigue, pins and needles and pretty bad numbness in my feet, bladder dysfunction, constipation, weakness and balance trouble, difficulty with walking, blurry sight with one eye and lots of other symptoms.

Steroid works but every time I get some, by the time I start to get back to normal, the problems slowly come back and I'm going down within two month again. It's very depressing. Now, I'm trying to be positive but right now I can't even walk again for ten minutes without sitting down for a rest. When I was diagnosed I was also told that I have EBV and they couldn't really tell 100% that my symptoms are caused by ms or EBV but most likely ms I guess.

I have been reading about Hydrogen Peroxide therapy for about two weeks and it gave me so much hope that I decided to try it. I am on 14 drops today now, climbing up to 25 and then do the whole protocol as it's in the books... I was wondering if anyone with the same problems has tried HP therapy? Please would you share your experiences with me, and maybe give me a little hope that I will get better one day. I am only 30 but I feel like my life stopped a year ago:-( I know I can't expect anything in a couple of weeks but I believe in this now so much that I tell myself every single day that this stuff will help me and I'm willing to do, even be patient for six months for results as long as I can walk, and after if I get better I am going to drink or inhale hp for the rest of my life.

Please give some good news here dear everyone or Ted! This site is great by the way!

I wish you all good health, and I'm looking forward to some answers. Also here's my email if anyone would share their experience with hp therapy in private orsika(at)hotmail.co.uk

Thank you!

REPLY   1      

Replied by Rsw from Uniontown, Oh on 01/21/2012

I have some good news for you. Please look at this website, www.ldninfo.org. LDN is an inexpensive, FDA approved drug, which when taken in a very small dose can help with many autoimmune diseases, and is usually very effective in stopping progression of MS. Additionally, please join the Yahoo LDN group that has over 10,000 members, at least half of whom have MS. They will help you very willingly and with much understanding and experience. You are not alone and help is as close as your computer. Best wishes!
REPLY   2      

Replied by Bess from Calgary, Alberta, Canada on 01/22/2012

Hi Orshi - I don't know about hydrogen peroxide for MS, but you may find the following TED video very interesting.

TEDxIowaCity - Dr. Terry Wahls - Minding Your Mitochondria

Dr. Terry Wahls learned how to properly fuel her body. Using the lessons she learned at the subcellular level, she used diet to cure her MS and get out of her wheelchair.

http://www.youtube.com/watch?v=KLjgBLwH3Wc

Hope there is some valuable information in it for you. Take care, Bess

REPLY         

Replied by Orshi from Exeter, Devon, England on 01/22/2012

Thank you very much for your help and all the best!

Orshi

REPLY         

Replied by Laura from Denver, Co on 02/01/2012

Hi Orshi, I have MS too, I have found oxygen therapy helpful. Hydrogen peroxide, and also Homozon. I did CCSVI treatment several times but while there were benefits they only last 6 months for me. I had it again and veins were open but symptoms came back. After lots of supplements, and continued progression, I tried stem cell therapy which stopped the progression and with exercise seems to be helping me get better. Went from wheelchair to walker outside the house. It's been 2 months.

Laura laura.laurapino[at]gmail[dot]com

REPLY   2      

Replied by Oscar from Syracuse, New York on 02/01/2012

This is exciting news to me: stem cell therapy. Is it available in the USA at this time ? ...Oscar
REPLY   1      

Replied by Laura from Denver, Co, Usa on 03/03/2012

Hi Oscar, Yes, I know of one place in the US http://www.stem-cell-rejuvenation.com/ the rest are out of the country. I went to Mexico.
REPLY         

Replied by Pete from Vancouver, B.c. on 03/07/2014

Hi,

Just found this site and have been reading all the interesting posts.

My yoga instructor was telling us about Hydrogen Peroxide food grade and how it might be beneficial for people with MS, which I have had for 6/7 years now. Not sure if I can get LDN in Canada but will look into it.

Orshi, if you are still looking at this post every now and then, just wondering how you made out and if you have tried the LDN ??

I am 50 and also have extreme numbness in both legs/feet as well as bladder/bowel/eye problems as well as others.

Anyone in Canada purchasing the LDN? Thanks for any info. Best to everyone, Pete

REPLY         

Replied by Dave from Fountain Inn, Sc on 03/08/2014

Pete, re your MS;

Also look into a substance that Dr Robert Adkins used as his number one go to for his MS patients that he would give to them in IV form, although the oral consumption I have seen is amazingly effective for the symptoms you describe; "Calcium AEP" and the "calcium" part is not the issue...it is the AEP part that is the miracle. You can google "Nutrition Review Calcium AEP" and find an amazing article on the 20 different things AEP can do to help the human body, To deal with leg symptoms, especially when stressed, up to eight tablets of AEP are needed.

Also, I have found Colloidal Silver to be effective in killing viral infections. It is theorized that MS has as a trigger a virus.

REPLY   3      

[YEA]

Replied by Mark from Co on 03/26/2014

I am taking hydrogen peroxide for my MS and find it very beneficial. :)
REPLY   4      

Replied by Don from Melbourne, Australia on 06/09/2020

Oxygenation of blood through any means seems to do the trick with many illnesses. Eg Jim Humbles chlorine dioxide, wim hof breathing method, it all makes sense to me, not withstanding issues with nutrition and over toxicity.
REPLY   1      

Replied by LittleWing from Boston on 05/26/2026

I know this post is super old, but I just read an NHI report that said you cannot get MS if you haven't had the Epstein-Barr virus. So virus-triggered it appears to be.
REPLY   2