@Helen I am in the UK and diagnosed with Pernicious Anemia, so I am given a hydroxycbl injection every 6/8 weeks. (for past 6 months) this has helped but is not enough. I have tried self injectin (3 times a week) but get an allergic reaction (possibly a nickel allergy) which is bearable but not great. The reaction is why I have switched to Fredds protocol. I cant say that I am better (yet) than I was taking hydroxy, but will give it a while longer.
Symptoms I am left with are fatigue and general malaise!
I see you are in Sweden - could I ask where you get your injectable methyl? and why do you use methyl rather than hydroxy?
Thanks
I get them from one of the few doctors who from experience know that some patients need injections even every second day. Authorities have been after some of them, but now they should have mutations from gene tests as a proof for this. But I also had a doctor that recommended me to buy MCbl in Spain without prescription. I don´t know if this is possible any longer, but before friends travelling bought MCbl for me.
Have you had a 23andme test? What ingredients are there in the HydroxyCbl as you get an allergic reaction? Are you convinced that the diagnose pernicious anemia is correct? Do you get intrinsic factor as a supplement?