Pam Bertha protocols: Is anyone out there... - My MSAA Community

My MSAA Community

9,678 members21,561 posts

Pam Bertha protocols

Barb_28 profile image
9 Replies

Is anyone out there familiar with the information that Pam Bertha / Live Disease Free recommends and the discussion that MS is being caused by parasites or fungal or other growths in the blood? I have watched many of her u tub videos and am wondering what makes her approach any different than the other "diet / nutritional" suggestions that are out there. I have tried multiple "out of the box" approaches to MS and not sure if this is just another one those.....

Written by
Barb_28 profile image
Barb_28
To view profiles and participate in discussions please or .
9 Replies
jackiesj profile image
jackiesj

Barb_28 Im sure many triggers we don't know can happen.I do watch out for scammers and take all with a grain of salt.Often i ask, diets, suppliments, this year seems to be vinegar cures all and even though we are all different beware of fads.A body in balance as much as it can be is great thought, we do the best we can.I do check out NIH for research stats but genetics play such a role also.Nurture vrs Nature, environment vrs Genetics....After seeing so many ideas, mind is a whirl..i do ask what can i do with the info, will it cost, hurt my body in some way etc...makes it clearer...best wishes...oh i want us ALL healed...Now!

Barb_28 profile image
Barb_28 in reply tojackiesj

Thanks for understanding - my husband says I should give it a try but losing hope on all of the promises out there!

Jazzyinco profile image
Jazzyinco

Hi, Pam, yep i've seen Pam too. I think she's great, she cured her PPMS, just like Dr. Teri Wahls did too, her SPMS, i am following Dr. TERI's diet as much as my $ will allow, & it is starting to wrk. For my PPMS, symptoms aren't as bad as they used to be... So, keep on trucking!💐😍😄

dogdaddy profile image
dogdaddy in reply toJazzyinco

How bad were Pam's symptoms...was she able to walk b4 her supposed cure?

Barb_28 profile image
Barb_28 in reply todogdaddy

From her webinars does sound like it was not as bad as some of us have today. But than I was 50+ when got my DX so I have that frustration of not being able to do what I did all those years.

dogdaddy profile image
dogdaddy in reply toBarb_28

I know I was dx'd in 2011 at 53 when out of the blue with absolutely no warning whatsoever I was suddenly paralyzed (both hand *my dominated hand no less and legs) and lost my speech. I spent 2 months in the Cleveland Clinic and in rehab then they dumped me off in a nursing home. So I had my husband break me out of there (it was a horrible nursing home) and I did my rehab at home. I switched my diet to the Wahl's protocol and started on a new normal but I could still walk with a rollator until this past oct when I had my 1st relapse ...spent a few days again at Cleveland Clinic had to beg them to give me IV steroids as I lost my ability once again to speak really well and taking one or two steps with my husband supporting was all I can muster now but the steroids did help my speech. I've talked to Pam and I don't think she knows anything about severe MS. She had a mild form. And a change of diet and supplements can help but not reverse severe MS no matter what she says...I know...I'm living it !!!!!

Barb_28 profile image
Barb_28 in reply todogdaddy

Thanks for the information. My MS is more similar to what describe. I am insearch for truths before i get my hopes up and energy spent in a direction that only frustrates me and contribute to further anxity.

dogdaddy profile image
dogdaddy

and she charges a small fortune to take her program...which I think is unethical as she's making a living off people desperate for a cure...at least Dr Wahls puts her books out on amazon and they are affordable and you can judge for yourself before investing a large sum of money to get personal coaching!

Kav9 profile image
Kav9

Hiya Barb

Have you had a look at the OMS(overcoming multiple sclerosis) diet?Google it, very informative

Not what you're looking for?

You may also like...

Ocrevus vs Abigio .... more options that aren't so Scary?

Hello!! My Neurologist also sugested that I goon Ocrevus OR Abigio.... Ive tired * MS drugs and...
snakesYuck profile image

Need Pediatric MS Specialist

Ocrevus for 13 year old girl: My daughter, 13 just got out of the hospital on Wednesday. 5 days...

like live FREE yoga?

if you are interested in a zoom chair, yoga class, my teacher is looking for students for a free...
Sandydemop profile image

Hi my name is Kathy. I just joined today. This looks like a great community of supporters.

I was diagnosed in 2005 but had it for several years prior. The neurologist diagnosed me with an...

We are lucky to have MS!

Hello family it is Fancy. After reading a post I thought it was important to put a timely reminder...
Fancy1959 profile image

Moderation team

See all
johnMSAA profile image
johnMSAAPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.