Hiya my original Fibro family. I have not posted for a long time. This post is addressed for my friends here as I share much love for u. I am posting from my own experience so I ask that I get no hecklers from the wings.
My Doctors turned around some months back n informed me that my B12 injections would be stopped. I felt lost as I can just function on these 12 weekly jabs! So I made a plea for help on a Pernicious Anemia forum. They were so kind n u can read the post on my profile. They taught me more than any of the doctors I have seen. They introduced me to self injecting, the Myelin sheath n finally Dr Klein.
I discovered that a lot of my weird fibro symptoms were signs of a B12 deficiency. So I commenced my first injection on May 1st. Then I injected every other day. It didn’t take long for me to notice small changes. Please read my second post I put on the Pernicious Anemia forum also on my profile n u can see after a time I lost over half of my severe fibro pain!
As well as this the next thing I was told shocked me. I had two friends with fibro who were told by Dr Klein that their ‘fibro’ seemed to be a severe B12 deficiency n just like me after starting to SI they started to improve too! I can’t believe that I can actually walk now?! Before I could just about walk around my flat. So I urge my closest friends to ask ur Dr for a B12 test. It must be an Active B12 test. Before I started my injections I was blacking out, falling, getting dizzy, weeing for England, run down n struggling to open my eyes at times. Now I’ve not had falls, blackouts or struggle to open my eyes. No more weeing for England either lol! This is my journey which will take time to repair the damage done to my Myelin sheath. I hope it can help others. I don’t want any unkind replies on my post, this is for my good friends. If it can help just one of u I’ve done my duty 😊🤗💜