by Chris Morton | Mar 3, 2025 | Blog, Charity news
Last time we gave you an overall idea of what Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is. Over the next few weeks we will dig a bit deeper, looking at diagnosis, treatment, and living with CIDP. But this week, let’s look at the symptoms of CIDP. CIDP...
by Chris Morton | Feb 28, 2025 | uncategorised, Your Stories
I started to suffer with a cold on January 23, which went into a kidney infection then into suspected allergic reaction to my antibiotics. By the 16th of February I was weak, pins and needles in my hands and feet and no taste in my mouth. I was admitted to the RAH...
by Chris Morton | Feb 28, 2025 | Your Stories
We were recently contacted by Pete MacKenzie, who was kind enough to share his story with AMSAN I was diagnosed with Guillain Barré Syndrome (GBS) last May. The 16th to be precise. Since then my life has been split in two… BGB and AGB. Before Guillain Barré and...
by Chris Morton | Feb 24, 2025 | Blog, Charity news
What is Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)? Over the last few months we have written a lot about GBS, but that isn’t the only Inflammatory Neuropathy that we care about. So, lets talk about Chronic Inflammatory Demyelinating...
by Chris Morton | Feb 17, 2025 | Blog, Charity news
The way in which Immunoglobulin (or Ig for short) is purchased and given out in England is changing, and we wanted to make sure that you were aware of what is going on. This doesn’t impact you if you live in Scotland, Wales, Northern Ireland, or the Republic of...
