So on our weekly illness... the scary part is they keep getting worse and worse... We visited the PEDs Dr. when I first went there I expressed my concerns... I was concerned that the NICU visit with the digestion of her bowel movement caused an infection... that this damaged her immune system and/or intestines. Therefore, I wouldn't feed her wheat because I have no idea what that did to her body... besides processed food is garbage anyhow.
EVERYONE including the Dr thought I was NUTS one of those google crazies who use WebMD as their home page. it's this... no it's that... He said..."You should have been a Dr... you are really smart..."
He came across a disease called IgA or Selective immunoglobulin A deficiency, which is a mild genetic immunodeficiency where you lack immunogobulin A. this is a type of antibody that protects against infection mainly in respiratory and disgestive systems.
There is no treatment for this disorder which has an association with autoimmune disease and this deficiency can compliment diagnoisis of celiacs disease.
I really hope she doesn't have this! We go for more blood work. He was of course curious. I didn't feed her wheat... I chose to delay her shots as I was trying to keep her as healthy as possible as if she would catch every virus they injected her with... which I stated to him... I didn't get her shots, and thank goodness if she does have this things could have been so bad.
He said you did everything right if she does have this. My thoughts were except daycare...
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