I was diagnosed with PA & Celiac Disease last October after being sick for more than 6 years. 4 of which I could barely put one foot in front of the other let alone remember why I was trying in the 1st place.
Every doctor I saw immediately prescribed antidepressants, (which I refused to take) stating that my IDA wouldn't cause the symptoms I described, and NEVER testing me for anything else.
It was hell.
Thankfully, I now have a team of doctors who listen.
My question is, will the B12 in my multivitamin make it seem as though I'm getting enough b12 along with my injections? Without intrinsic factor isn't it rendered useless? Should I stop taking the multi & find a different one?
I'm on injections but they're still testing me. I went from weekly to monthly, then bk to weekly, now they've got me trying every other week to see how I do.
My Dr has mentioned that there "seems to be more of an absorption problem" whatever that means. Cellular level??
I don't know, I just don't want the useless B12 in my Vitamin to make it appear as though I'm getting enough if I'm not.
🤔 Does that make sense?
This site has helped me tremendously! Thank you all so much!! 💓