MPend2009.wmv

[joysworld61]

What is mp

[seanlane1]

I have been on the MP for 2.6 years and have lost reversed all of my neuropathy,which the neurologist was quick to point out that it was "the kind that does not go away" CFS is nearly gone as well as bipolar disorder and food sensitivities. Maybe it's that the immune system's generation of antibodies in response to the die off of bacteria varies from person to person,and for some it may be intolerable  to stimulate the dysfunctional immune system...it's hard to say. Praying for new insights.

[Claggy]

After watching one of your videos from around a year ago, watching this one made me smile a lot! :D Thank you for all of these videos... and I do hope many people that do not have or are not aware of CFIDS/ME watch your videos!

[Claironess]

I've had CFS for 45+ years. I didn't become totally disabled until 6 yrs ago, but should have stopped work 2 years before. At my worst, my life was like Natalie's. Been on the MP for 3 yrs. now. I'm not improving at the rate that Natalie has (b/c I've been sick for so long), but I am making significant gains. 1st 2 years on the MP were TOTAL HELL & had I stopped, I may have thought it made me worse & may have been worse as a result of stopping it in that condition. Glad to be here now.

[flymo42]

I do agree that the MP is a challenge and not for all. I take my strength from those that didn't waiver, the alumni that had their lifes returned and the fact the minds far superior to ours are tackling this in China and the MP is gaining ground with more and more practiioners. Time wil determine the reality.

Glad to see you full of life Natalie!

[fatlion12]

I'm really happy for you but don't assume that everyone will have this reaction to the MP. That protocol essentially crippled me and even after discontinuing it I am constantly bed bound and in non stop pain. I know others who have been hospitalised and have a host of new problems as a result of the MP. So while I am glad for you, please don't start peddling the MP as assuming everyone will improve on it. Very few people have.

[obscenely]

I would never assume the MP is for everyone - it's not, and I firmly believe it's not. But for me, it's working.

[flymo42]

fatlion

Dont assume that because you did not deal with the MP that others cant...If you had such a strong reaction, you and/or your doc did not address it, you were not following the MP Plain and simple.

Sorry to hear that you are still very ill, I hope you find a way through.

I'm 15 months into the MP and it does what it says on the label.

Way to go Nat!!!!

[flymo42]

"peddling the MP as assuming everyone will improve on it. Very few people have". ....you base that on.....? From your description I would still argue that you did not follow the protocol.

Please dont scaremonger or patronise those who have the right to make their own choices.

What "host of new problems".....? Health?

For those who are following the protocol...Nat being one, has improved their lives by following the MP. If you don't subscribe, there are many other outlets. your choice.

[SharkBateNait]

Wow that's amazing! Good for you!!! :) That's such fantastic news, it's so nice to see you so happy! You may actually be the happiest person I've ever seen, lol

congrats!

[obscenely]

Haha, thank you =)

[WackyLisa]

Congratulations on your success on the MP.

Best wishes on your plans for the next year. :)

[obscenely]

Thank you!

[killandra23]

Awesome video! Glad to hear MP is working for you! Nice to see you in the sunlight. :)

[obscenely]

Nice to be able to BE in some sunlight. Thank you x