Gut health and APS: Hi, I was reading... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,349 members10,537 posts

Gut health and APS

Suejane profile image
5 Replies

Hi,

I was reading an article relating to gut health and APS by a doctor in New York. I contacted his practice and got a reply with this link that you may find useful -

hss.edu/conditions_antiphos...

Sue

Written by
Suejane profile image
Suejane
To view profiles and participate in discussions please or .
5 Replies
Lure2 profile image
Lure2

Thank you for letting us read this!

HollyHeski profile image
HollyHeskiAdministrator

Thanks Sue, interesting - a lot more research needed still though.

bookish profile image
bookish

Thanks for that. I have anticardiolipin antibodies but no other signs (allegedly) and had read that this is believed to be the case for a proportion of those with Small Fibre Neuropathy/Sjogren's/ Dysautonomia. No doubt poor gut health is not the cause for everything but getting it more healthy and diverse can only help. Fortunately it does seem that changing the microbiome positively can be done quite quickly with high polyphenol foods, resistant starches etc. I'll keep working on it! Cheers

new2aps profile image
new2aps

Thank you for sending the article on the gut microbiome. I have taken a probiotic capsule for years...Allign. I probably should have taken different ones and mixed it up a bit. Does anyone else have any positive or negative experiences with taking probiotics, and their effect on APL's?

MaryF profile image
MaryFAdministrator

Thanks, I personally pay a huge amount of attention to my gut health, always have, making sure my diet is excellent but also with pre biotics and probiotics and cider vinegar, but i am not on any Warfarin, so no battles with keeping an INR stable. MaryF

You may also like...

Healthy gut and APS

noticed a swollen, warm right leg. After reading and reading, I suspect it could have been...

APS - Future Health Issues - Am I missing the seriousness?

risk of future PE, strokes etc, but feel like I may be missing something that I should be aware of.

APS

Hi all, new here and glad I ran across site. I've been diagnosed less than a year and don't know...

APS

I got home I looked again and phone up the doctors and told them 4 doctors so fingers crossed I may...

APS

they was ment to know she sed you are on warfin now I sed yes I will see you in a Years time so go...