Recently diagnosed with PA although have had symptoms for 10 years, thought being given a name for it was the answer I needed to get the treatment I required! B12 level 99 March 14, 85 Sept 14, 3 loading doses later 300. My body continuously produces milk as a result of a hormone imbalance which is a result of PA, I also take a tablet every day for over active blabber again as a result of PA, I still display pins and needles, brain fog, memory loss, hair loss, insomnia, exhaustion, lack of concentration, dramatic weight loss, crippling stomach spasms as well as constant muscle aches, the list goes yet my GP insists I must wait until March 31st for my 3 monthly injection. I continue to be a single parent to a teenager and a 10 year old, work as a child minder as well as run a family home because I refuse to give to this even if I am in daily pain, shattered and most days are a struggle I cannot afford mentally or physically to give in. My main reason in reaching out to people in the same boat is to try to find anyone from my area to either chat with or that can recommend health professionals for me to approach as I feel my situation is quite desperate. I live in the Glasgow area and am able to travel to meet with doctors that have been recommended.