Way to go Alzheimer’s: It seems to me that... - Cure Parkinson's

Cure Parkinson's

25,518 members26,834 posts

Way to go Alzheimer’s

jeeves19 profile image
10 Replies

It seems to me that are exciting things going with this disease but that PD is trailing. It’s now beginning to be accepted by many that there are distinct protocols that are encouraging recovery in some. One cornerstone to this is their insights into the fact that different Alzheimer’s patients need different protocols depending on their genetic background. For instance, one of these subgroups doesn’t respond well to coconut oil and in fact the latter is claimed to be somewhat inflammatory if the sufferer has a certain gene. Do scientists have such insights for PD yet I.e that your range of symptoms and best treatment would be tailored to genetic background? Maybe this would help us understand why some of us respond to coconut oil and some don’t etc

Written by
jeeves19 profile image
jeeves19
To view profiles and participate in discussions please or .
10 Replies
MBAnderson profile image
MBAnderson

And, perhaps, why some of us respond to any one of many other things, while others don't.

jeeves19 profile image
jeeves19 in reply to MBAnderson

But enlightened clinicians like Bredesen are now genetically showing that one of either 3 genes is present to cause ones Alzheimer’s and treatment is tailored towards each type. I’m just saying I so wish that we had this with PD.

faridaro profile image
faridaro

I preordered book "Dirty Genes" by Ben Lynch, which will be coming out on Amazon on Jan.30 and hope to gain some insights from it. He also has a video on youtube with the statement:

"While genetics play a role, it is more the impact of lifestyle, diet and the environment. Certain genetic polymorphisms can amplify the influence of a harmful environment, lifestyle and diet."

youtube.com/watch?v=yfmbjwe...

I've done genetic testing which revealed certain mutations (like impaired clearance of pesticides among others) may have contributed to PD. Can't wait to get the hold of this book!

jeeves19 profile image
jeeves19 in reply to faridaro

Nor can I! Thanks for a great lead. At the same time I wonder what we’d all do with this information if we’re unsupportre by the conventional medical community? I tried enquiringly about fecal transplants recently as I know they’re available but was told that the ‘practice hasn’t been demonstrated for PD’’. They could have added YET and in 10 years time maybe they’ll get around to thinking outside the box 😕

faridaro profile image
faridaro in reply to jeeves19

I have discovered that for any new or unconventional/alternative treatment you'd need to find a good integrative or functional medicine physician. However, here in the US these kind of practitioners don't accept medical insurance and you have to pay out of pocket significant amounts $$$ .

Astra7 profile image
Astra7 in reply to jeeves19

I read an interesting article about a diy transplant technique! First you need to find a friend....

I have been given Mutaflor by the integrative GP and recently discovered it was made in the 40s using bacteria extracted from someone's faeces. So this idea has been around for quite a while. And I'm eating the descendants of someone's poo!!

NRyan profile image
NRyan in reply to faridaro

Where did you get genetic testing done? I started with 23&me (negative for LRRK2 and GBA) and am doing Invitae PD and dystonia panels soon. What other panels/mutations can be looked at? Thanks!

faridaro profile image
faridaro in reply to NRyan

I did 23&me as well and then found a local integrative MD who went through some training with NutriGenetic Research Institute. Based on their software the MD generated 37 page report of different groups of genetic variants and how they impact various metabolic pathways and detoxification capacity - with supplementation recommendation - most recommended supplements are manufactured by the company which some see as a red flag, but 2 of those supplements greatly helped my son who has Down Syndrome and Lyme - both conditions create excess ammonia. I didn't realize how much they helped until he run out of them and things started getting worse... The report doesn't specifically address diseases except the Lyme study SNPs.

Here is the link:

nutrigeneticresearch.org/?p...

Astra7 profile image
Astra7 in reply to faridaro

Which ones helped? Also what is your sons blood type Rhesus factor?

faridaro profile image
faridaro in reply to Astra7

The supplements which helped are called "Ammonia Scavenger" which is a proprietary blend of of vit. B6 (P5P), arabingalactan, L- Citruline, L-Ornithine, Yucca, Alpha-Ketoglutarate, L-Lysine HCl and another one is "CBS/BHMT Assist" which is a proprietary blend of N-Acetyl Carnitine, Yucca, Lecithin, TMG. My son's blood type is A+.

You may also like...

Exact 40 Hz Gamma Brainwave audio used by MIT to prevent Alzheimer’s

Gamma Brainwave audio used by MIT to prevent Alzheimer’s https://youtu.be/UVne_84qZkA Somebody on...

taking a sleeping pill each night may ward off Alzheimer’s.

Scientists report \\"encouraging\\" results after insomnia drug appears to reduce the build-up of...

Coconut oil vs Olive oil

No one mentions Olive oil The link below concludes Olive oil beats coconut oil hands down...

US doctor discusses ways to prevent PD

of PwP have a genetic cause and 85% is from environmental exposure to chemicals. Some have been...

For Someone Struggling with Being in the Way

hand for the His use. He may use me as a burden in some cases and a boost in others, but in every...