SAM55
Well-Known Member
Has anyone with experience of ME/Sensory Processing difficulties/Autistic Spectrum found that their sensory processing difficulties have got worse since having WLS?
I noticed my sensory processing was a lot worse after surgery - it started following Swine Flu/ME in 2011 and hoped it would settle down once the trauma was over. It didn't. I have been doing some research on management and came across some dietary info around casein and gluten.
I have had gluten issues both neurological and digestive (but not at the same time) before but eventually became able to manage small amounts with both. I haven't however had any problems ever with dairy and love milk. Since WLS I drink a lot more as there are many other drinks I can no longer tolerate/enjoy.
I am going to try exclusion or at least major cutting back but interested to know if anyone else has had similar experiences, thoughts, info please? Thanks
I noticed my sensory processing was a lot worse after surgery - it started following Swine Flu/ME in 2011 and hoped it would settle down once the trauma was over. It didn't. I have been doing some research on management and came across some dietary info around casein and gluten.
I have had gluten issues both neurological and digestive (but not at the same time) before but eventually became able to manage small amounts with both. I haven't however had any problems ever with dairy and love milk. Since WLS I drink a lot more as there are many other drinks I can no longer tolerate/enjoy.
I am going to try exclusion or at least major cutting back but interested to know if anyone else has had similar experiences, thoughts, info please? Thanks