Scotland Online Support Group Meeting
22
May
2026
7:00 pm - 8:30 pm
Topic: Patient Advocacy, information and tips on dealing with your doctors
PAS support group meetings are an excellent way to meet other members of the society, share experiences, learn of how PA has impacted on their lives and how they have developed coping strategies to deal with the ongoing symptoms in a welcoming and friendly environment.
Our Support Group Coordinator, Karen, will be holding an online Support Group Meeting on the 22nd May.
Whilst Karen is based in Scotland, you don’t have to live in that area to attend. It doesn’t matter where you live as this is a Zoom meeting and all members are welcome to attend.
Hope you can make it!
Find the link to register for this meeting on your membership homepage. (login here)
I have pa would like more support undstanding it
I have low b12, starting injections on 27th April. I only got here by organising privately an active b12 test. I have peripheral neuropathy. Getting worse, ice cold or burning left foot the worst part. My gp did an antibody test. Said all normal, no more required. Don’t have pernicious anaemia. I’m overseas but on return will argue I might still have PA. How do GPs not know this? My understanding is that with neurological issues I need help. If need be I can get private help but need to be clear. I’ve so far discovered a cousin who had b12 deficiency and gets injections every so often.
I’d welcome comments as to how to proceed.
Oh and I’ve discovered I have tubular adenomas.