Mike Ralls – My CIDP story

Mike Ralls – My CIDP story

Guillain Barré Syndrome …. Chronic Inflammatory Demyelinating Polyneuropathy, two conditions/syndromes/diseases that I had never heard of until Monday 25th June 2018. The week before this date, everything was normal. I was doing Spin classes at my local leisure centre...
CIDP the birth of my princess

CIDP the birth of my princess

My journey began in April 2013. I was a stay at home mummy with two beautiful boys, and William my partner. I was healthy at thirty weeks pregnant, excitedly looking forward to the birth of our daughter who we had already named Kelsey-Mae Patricia. I started with...
My CIDP Adventures

My CIDP Adventures

I have been invited to share with other gain4all readers my experience of CIDP over the past two years. I am in practice, as I recently gave an hour-long telephone interview to a modus researcher who wanted to know about my symptoms and response to IVIG treatment in...
Miller Fisher Four Years On

Miller Fisher Four Years On

My story starts on New Year’s Eve 2011/2012. Since before Christmas, I had a persistent head cold and I didn’t seem to be able to shake it. On this particular Saturday (31st), I had been feeling unwell; feeling that I wanted to topple over. My wife, Mary and I went to...
Mission Accomplished

Mission Accomplished

Jack Robinson had a mission – to donate his hair to the Little Princess Trust, to support his brave cousin Kieran who was diagnosed with Guillain-Barré syndrome and to raise funds for GAIN. Kieran’s mum, Jackie recalls: In September 2008, when Kieran was four we...
A Little Princess – Fundraising report

A Little Princess – Fundraising report

Jasmine Dawood (Age 6) suffered from GBS in November 2013 when she was 3 years old; it was the most frightening time of her life (and her mum’s). What started as a chest infection quickly developed into GBS and she lost all function of her legs and arms for almost...