Hi all,
I just wanted to share with you my dramatic improvement returning to Hydroxycobalamin. I was diagnosed with Pernicious Anaemia 10 years ago and received 3 monthly injections from the NHS. After a hospital admission for psychotic depression (long story) I felt I needed more frequent injections and after continually battling with my GP for this I gave up asking and I began to purchase B12 and inject myself. The first time I ordered Hydroxycobalamin and injected once per month, all appeared ok. The second batch I ordered was CYANOCOBALAMIN. I think I ordered it because it was slightly cheaper, I think. I have been injecting this for probably about 8 months, sometimes I would inject twice in a month but it didn't seem to have an affect.
I began to feel very unwell again about 4 months ago and this all came to ahead in the last two months, slowly becoming more tired, vision problems, dizzy, palpitations, depressive symptoms, headaches etc etc. I began to post on this forum as I read, researched and tried to work out what to do in a desperate attempt to regain my health. Why did I have pernicious anaemia symptoms when I was injecting B12 regularly?
I bought some Methycobalamin, thinking this would be better as it is the active form of B12 and doesn't need to go through any changes before having an affect, as I understand it. I began to lift a bit and noticed a slight reduction in my symptoms, I was definitely less tired but I was still very depressed.
Anyway, after having lots of blood tests taken on Monday I decided to inject with Hydroxycobalamin. ( I had also bought this recently). Oh my goodness, I cannot tell you the difference it has made to me. I feel alive again. I have energy again. I am so happy that I can go to work and get through my day with enough energy. All my depressive symptoms have gone, all gone with one tiny injection, I can't believe it. I feel so happy.
Now I just need to work out how frequently I should inject Hydroxycobalamin and I need to speak with my GP to see if they will agree to more frequent injections on the NHS. If they don't I will continue to self inject.
Thanks to everyone who has replied to my post. It is so nice to know there is somewhere you can come to for support and advice. Without this forum I would not have worked out what steps to take.
I hope my story will inspire others to KEEP LOOKING FOR ANSWERS to regain your health.
AutoimmuneAnnie x