GAPS diet - has anyone tried it. - PSP Association

PSP Association

9,549 members11,513 posts

GAPS diet - has anyone tried it.

Jane2212 profile image
2 Replies

My Mom Irene, who had PSP, used to say that the problems with her fuzzy head were linked to her stomach ! My husband thought that was a mad thing to say. Mom had an ultrasound on her tum as she was losing weight and they did say she had a leaky gut but no remedial action was ever taken on it.

Last night a former schoolfriend emailed me - she has had ME for some years. She looked up the GAPS diet on the internet and it says that a leaky gut can allow toxins to enter the bloodstream and damage the brain ........ she has been trying the new diet and reported that she is much better lately. I was stunned. She said the diet was developed by a neuro-surgeon for her autistic son who is much better now, and that it also helps ME, MS and other brain-related diseases.

Just wondered if anyone had tried this GAPS diet at all ....... when Mom was here we'd try anything to help her ! My friend describes it as a bit of a 'caveman' diet, very basic. I might try it anyway.

Jane

xxxxxx

Written by
Jane2212 profile image
Jane2212
To view profiles and participate in discussions please or .
2 Replies

By all means try the GAPS diet but also review recent discussions about this topic, and the developer of this diet, as in the following link:

sciencebasedmedicine.org/in...

All the best

Jane2212 profile image
Jane2212

Thanks for this, I hadn't come across this link while I was trawling. I don't think it would suit me but my friend with ME has told me she feels much better already - she wonders if it's a fluke - but she is enjoying it nevertheless. I don't think my Mom could have digested it because of her chewing problems etc but just wondered if anyone with PSP had tried it.

Jane

x

Not what you're looking for?

You may also like...

Suggestion required on liquid diet

My mom is suffering from psp sinsce 2012, now she cant move on her own, she dont speak, and cant...

Increase in crying in Mom with CBD

I am new here. Corticobasal degeneration has effected my family since June of 2015. My mom (57 year...

Keeping it together

It has been great to start reading your blogs - a big step for me as i am inclined to keep...

Try to cough it up Mom ...

So this is what I have been saying to Mom for the last four or five days now, "Try to cough harder...

End stage of PSP

I'm sitting here with my Mom who is in her last days. She was first diagnosed with CBD 2 years ago...