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Blogs
The latest news and opinions from the Inflammatory Neuropathies UK team.
We also have a blog series where we take an accessible look at the conditions we support. These started last year with GBS, and our CIDP blog series came to an end in April 2025. Filter the blogs via:
GBS Blog Series
CIDP Blog Series


IN UK at the ABN
This year, we made the decision to attend the Association of British Neurologists Conference. On paper, it’s a professional gathering of experts. But for us at Inflammatory Neuropathies UK, it’s something much more human than that. It’s all about people, and more specifically our Community. People who are living with rare, often misunderstood conditions. People who may still be searching for a diagnosis. People who don’t yet know that support, information and community exist


Why GBS and CIDP Awareness Month matters, and why I’m asking you to get involved
Every May, something powerful happens. Across the UK and beyond, people impacted by Inflammatory Neuropathies all look to raise awareness and talk about their condition. GBS and CIDP Awareness Month isn’t just a date in the calendar for us at Inflammatory Neuropathies UK. It’s one of the few moments in the year where our whole community (people living with conditions like Guillain-Barré syndrome (GBS), CIDP, and other Inflammatory Neuropathies, along with their families, cli


MMN - How is Multifocal Motor Neuropathy Treated?
You join us for the fourth in our weekly blogs dedicated to taking an accessible look at Multifocal Motor Neuropathy - or MMN. In previous editions, we've looked at what MMN is, the common MMN symptoms, and how you might expect MMN to be diagnosed. So what happens when someone finally gets a diagnosis of MMN? What does treatment look like? Can it be treated? Can it be cured? Let's start with - can it be cured? The short answer is, no. There is no current cure for MMN at the


MMN - How is Multifocal Motor Neuropathy diagnosed?
You join us for our third in our series of accessible, bite sized blogs all about MMN. In week one, we took a general overview of the condition, and last week we investigated some of MMN's classic symptoms and warning signs. This week, let's look at what happens next. Misdiagnosis and Timeline We'll be honest, this part is hard. Officially, your time to diagnosis should be around one to two years. However - and it's important we say this is anecdotal from conversations with


MMN - What are the symptoms of Multifocal Motor Neuropathy?
Last week we took a look into MMN as a whole - what is this rare condition? What does diagnosis and treatment look like? And of course, what are the symptoms of MMN? This week, we're diving into that last question in a little more detail. We'll look at some of the early signs, and key symptoms you should look out for. Early Signs of MMN MMN often starts subtly, which makes it easy to miss in the early stages. Many people later diagnosed with the condition noticed a weakness


MMN - Doing more for you
As February is MMN Awareness Month, it is time to not just shine a light on MMN, but also on ourselves about how we support people impacted by MMN.
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