Update on the PPI Med

I called the pharmacy yesterday to ask about the ppi med. I’m on. I told them about the pain it was causing me and how it’s also causing flu like symptoms.

She told me in no uncertain terms to get off the med. It shouldn’t be doing that. I can’t tell you how relieved I was. Well I can, but I’m sure you already know.

So I had some other ppi’s here from when my Internist had me on them to protect my stomach from anti-inflamatories which I can no longer take.

I asked the pharmacist about taking them. I told her they didn’t make me sick last I was on them. She said they’re in the same family, take them instead. So I’m using up the old script.

The jury’s out on how I’m doing with them. When I took the pill this morning I felt okay. Now I’m hurting. I don’t know if that’s the med or the ulcers. I’m at least not running to the washroom so that’s something.

It’s always a guessing game with autoimmune disease. Is the illness making me sick or the meds, or both?! It’s such a mind game. A roller coaster ride I’d really like to get off.

I wish the medications didn’t cause issues as serious as the diseases. Gotta wonder what pharma companies are up too.

Anyway, I hope that you’re all having a low pain day.

Don’t forget I have a FB support group for those suffering with autoimmune disease! I’d love to see you there!  https://www.facebook.com/groups/crankypantsautoimmunediseaesupport/

Stop the snow & Bring back the Sun,

CrankyPants