Latest news and updates from DMD Pathfinders and our members.


Sanjeev watching the Foo Fighters

Monthly Roundup August 2019

Here’s our Monthly Roundup August 2019, better late than never! Summer seems to be winding down and here at DMD Pathfinders we are starting to look at upcoming events we are involved with.  We hope to hold some sessions at the Action Duchenne International conference again this year.  Next month we’ll be heading to Helen House… Read more »

Why slowing down progression of DMD is so important

BY JON REY-HASTIE We recently wrote a letter supporting the extension of ataluren/translarna to people with DMD who are no longer ambulant (with no upper age limit). The letter also has relevance to other treatments being developed to treat Duchenne: Losing the ability to walk is often considered the major milestone of Duchenne Muscular Dystrophy… Read more »

Trip to Majorca

BY MITCH COLES I’ve just got back from a very relaxing 4 night stay in Majorca. I took 2 friends / carers away with me to a pretty posh hotel and we were all well looked after. We stayed at the Ferrer Concord hotel in Can Picafort. It was about an hour from Palma airport… Read more »

social meetup flyer 31/8/19? Come have a drink with us at @No1Harbourside

Monthly Roundup July 2019

We hope you are all enjoying the sunshine and summer in general, this time of year personally makes me want to get out and do more!  First up this month is a catch up from DMD Pathfinders chair, Mark Chapman. Mark’s Catch up (written by Mark Chapman, Chair of DMD Pathfinders) I started this month… Read more »

Working with Hospices: My Visit to Children’s Hospice South West

BY MITCH COLES When I first started in my role as Development Worker at Pathfinders, I was asked to highlight some people and organisations who we could possibly work with in the future. Straight away I thought of a charity that means the world to me, Children’s Hospice South West. From the age of seven,… Read more »

Mark Chapman sitting between Shelley Simmonds CEO of Action Duchenne and their Scottish Advocacy officer, John Miller

Monthly Roundup June 2019

A busy month again for us here at DMD Pathfinders, apologies for not getting this out sooner  but I have had care issues (a common thing for us with Duchenne) and various personal things to deal with.  Enough about me for now though, let’s get on with the roundup. Our games night was great fun… Read more »

Keech Event

On Saturday Jon, Tyran and Mitch headed to Keech Hospice in Luton for our information social day. We were given a warm welcome from Jackie Purdy who works at the hospice and received valuable input from Andrew Rose, a local neuromuscular advisor who helped in putting this event together. We covered a number of topics… Read more »

Sports Night poster - Monday the 8th of July from 7 pm to 9 pm

Monthly Roundup May 2019

Another month already!  Well let’s get started with everything going on here at DMD Pathfinders.  We’ll begin with a few events we have planned. Games Night After the success of our previous games night we are holding another one on the 19th of June at 7 pm, everyone is welcome and we are hoping this… Read more »

Tyran in front of a rally car with two dinosaurs standing near him

Meet Tyran, Our New Development Worker

Meet Tyran, Our New Development Worker Hi, I am Tyran Hawthorn, one of the new Development Workers at DMD Pathfinders.  I currently stay in Clanfield with my parents but have my own critically trained care team which enables me to be self sufficient and live relatively independently. I’ve also been to university where I studied… Read more »

Games Night poster - Monday 6th May 7pm

Games Night Recap

On Monday we held our Games Night. The plan was to play games on Jackbox and Boardgame Arena. In the end we opted to just use Jackbox, though others could still set up games through Boardgame Arena and also play their own console games. We used Discord as our communication hub, that supports text and… Read more »