Diagnosing Oxalate Sensitivity and Lyme Treatment

[Guest guest]

How does one know if you are sensitive to high oxalates? Does the OAT provide

answers? Our doctor said my son did not have high oxalates based on his OAT but

I failed to ask which part of the test said that? Does anyone know how to read

an OAT result?

I am still confused which diet to put my son on. We have been GFCFSCD for 8

years but my son's new diagnosis for Lyme has created more sensory intolerances.

He has become very aggressive which I am sure is due to the infections. But if

it is from oxalates and dumping because I have been giving high Oxalate foods

such as nut breads, some fruits and vegetables, how does one know if there is an

Oxalate issue?

Our doctor recommends the No Amylose Diet to heal the gut but most foods are

high Oxalate and nonSCD compliant. It is so confusing to add the diet into the

mix when the treatment for lyme alone is a challenge.

Today I bravely took my son for a walk and noticed that he at times keeps his

eyes closed or covers his ears. What could this be? Everything seems painful to

him these days. Things seem to subside a little bit with Motrin - proof that he

has severe gut and brain inflammation. He is going to take Calm PRT for

neurotransmitters, Norlox, Avipaxin, Omega3 DHA Select and Resveratrol for

inflammation, K PAX multi-vitamins, S Boulardii and Custom Probiotics DLactate

to strengthen his gut before the course of antibiotics. He also takes Rescue

Remedy and Barberry. Comments?

Also can anyone shed light please on Oxalate diagnosis? Many thanks for any and

all advice. Thank you.

Fransel

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