Ayrshire PBC Suffers: Is there anyone out... - PBC Foundation

PBC Foundation

9,404 members8,054 posts

Ayrshire PBC Suffers

JaniceK profile image
6 Replies

Is there anyone out there from Ayrshire or surrounding areas. I did have contact with a lovely lady from Ayr and one from Millport, however, I have not been on for some time.

Jan

Written by
JaniceK profile image
JaniceK
To view profiles and participate in discussions please or .
6 Replies

Have you tried contacting the PBC Foundation, they may have volunteers in that or the nearby area, it’s worth a try.

millieja profile image
millieja

On the emails from HealthUnlocked at the bottom there are 4 circles click on the circle that says `Meet Others`

CatGus profile image
CatGus

Hi Janice, I'm Heather from North Ayrshire and diagnosed with PBC on 08 03 2020, then lockdown

JaniceK profile image
JaniceK in reply to CatGus

Hi CatGus I was diagnosed in 2004 with PBC and was put on the Urso immediately, and still on them, not as high a dose now. When I was diagnosed like everyone you panic, however I have been carrying on my life up until about two years ago, when on holiday I was really unwell with indigestion pains in my stomach, when I came home I contacted my GP who got me an urgent referral for a scope to discover that I have varices on my oesophagus and had to have them banded which is the first sign of anything to do with this illness in all these years. I have been under constant review since then having lots of scopes and at one point I was banded as a 4 in the scope level which is very high they have up to 5 levels. I was seeing my consultant every year, then when this happened it was every 6 months. However, when I last saw him he didn't want to see me for a year and reduced my doze of Urso, but was still getting scopes, due to lockdown I have not had one since January and was due one in March.

Like most people are saying you can get different symptoms, I also had the itch but didn't take anything, I get very fatigued, tired and cold which the symptoms are of CFS which I was diagnosed with in 2002.

I live in Heathfield area in Ayr and maybe once lockdown is open we could meet and attend the meeting that they have in Glasgow and sometimes they try and have a meeting in Ayr.

Let me know how you are getting on.

Janice

CatGus profile image
CatGus

Thanks Janice yes I wouldlike to attend meeting when lockdown eases. I will let you know how I get on when I write to my GP for some answers.

JaniceK profile image
JaniceK

Hi Heather, write down what questions you want answers too thats what I did especially when I went to see my consultant, as he specialises in PBC thankfully when first diagnosed my GP is a liver consultant and he was really good, he has since retired and now i deal with the other GPs who are not so much up to answering questions, so that was why I had went to the consultant. Heather do you attend UHC and who is your consultant? Stay in touch keep me posted with updates.

Best wishes

Janice

You may also like...

PBC and also suffering with Pancreatitis

take it. Since then, I have been prescribed Ocaliva(Obetecholic acid), has anyone had great...

Surgery in PBC Sufferers

replacement but have been told that having PBC increases the risks in surgery. Has anyone else been...

Advice for a \"young\" PBC sufferer?

Hi All, I have recently been diagnosed with PBC and all the doctors and consultants kept saying that

Australian pbc sufferers?

Travel Insurance for PBC sufferers

I have just taken out insurance for myself and husband (who has PBC) for two weeks to Tenerife for...