by Chris Morton | Mar 10, 2025 | Blog, Charity news
In this ongoing series of blogs about CIDP, we have already looked at what CIDP is, and CIDP symptoms. Over the next few weeks we will be looking at treatment, living with CIDP, and the impact of CIDP. However, this week we are looking at what is involved in...
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 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...
by Chris Morton | Feb 10, 2025 | Blog, Charity news, uncategorised
Advice on Guillain-Barré Syndrome (GBS) So, you have had a Guillain-Barré Syndrome (GBS) diagnosis, and you are trying to understand what this means. Where do you for advice? This blog looks at who you can speak to, and where to turn for some useful input. If you...
by Chris Morton | Feb 3, 2025 | Blog, Charity news
The Impact of Guillain-Barré Syndrome (GBS) One of the things that we get asked about most is ‘what is the longer term impact of Guillain-Barré Syndrome (GBS).’ This blog looks at what impact actually means, and what a GBS diagnosis may mean for you and your family....
