MS

[mommaof2princesses]

Hi,

I have a family friend who was diagnosed with MS today. If I remember correctly, I have heard of MS patients being treated with AP and improving. I could be wrong. Have any of you heard of this?

Thank you!!!

[Maz]

[user=944]mommaof2princesses[/user] wrote:

I have a family friend who was diagnosed with MS today. If I remember correctly, I have heard of MS patients being treated with AP and improving. I could be wrong. Have any of you heard of this?

Yup…see the following websites for more info:

http://www.cpnhelp.org

http://www.mssociety.ca/en/releases/nr_20071025_faq.htm

Your friend may also want to look into the following:

http://www.lowdosenaltrexone.org/

http://www.ctv.ca/servlet/ArticleNews/story/CTVNews/20091120/W5_liberation_091121/20091121?s_name=W5

My brother who also lives in Canada has MS and has just signed up for the Liberation Treatment multi-center trials…the one in Toronto, I believe, is at St Michael's Hospital. My best guess about the Liberation treatment for MS is that it is successful at treating vascular insufficiency, but I still wonder what caused the vascular insufficiency in the first place. I think I'd put my money on using minocycline or combination AP and LDN for MS in addition to the Liberation treatment. 😉

Peace, Maz

PS With MS, I'd also get IGeneX labs run.

PPS Momma, just thought to add this link, too. This radio show host is interviewing a woman with MS who got dx'd with Lyme disease (in TX of all places, so she was laughed out of her neuro's office) and, after being on all kinds of MS meds, went on to LDN, which helped for about 5 years, and then she went to have the Liberation treatment done in CA. Very interesting interview and made me wonder how she'd be doing today if she'd got proper antibiotic treatment right from the get-go.

http://www.blogtalkradio.com/elaine-delack/2010/03/02/the-myths-of-ms
 

[casey]

Hi Maz,

By the Liberation treatment, do you mean the one where they put the shunt in the neck vein?

[Trudi]

[user=27]Maz[/user] wrote:

This radio show host is interviewing a woman with MS who got dx'd with Lyme disease (in TX of all places, so she was laughed out of her neuro's office)…

My massage therapist has a client who has MS and was recently diagnosed with Lyme.  Unfortunately, she already has some permanent damage.  I agree with Maz–your friend should be Igenex tested for Lyme–

Trudi

Lyme/RA; AP 4/2008 off and on to 3/2010; past use of quinolones may be the cause of my current problems, (including wheelchair use); all supplements (which can aggravate the condition) were discontinued on 10/14/2012. Am now treating for the homozygous MTHFR 1298 mutation. Off of all pain meds since Spring '14 (was on them for years--doctor is amazed--me too). Back on pain med 1/2017. Reinfected? Frozen shoulder?

[Eva Holloway]

mommaof2,

could you see if your friend can get on LDN, Dr. Berkson in NM has good results with it. Just a thought.

Eva:D

Eva Holloway

[casey]

Maz, Ignore my last post here! It is the same treatment!

[eann]

MS and Lyme Disease cause similar lesions or demyelination in the brain. It would be good to be checked for lyme, to rule it in or out.

[Author]

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