PORT CHARITY

Thank You to Our Incredible Supporters Thanks to the generosity of our amazing community, PORT (Pseudo Obstruction Research Trust) is...

Thank you so much to our 3 Brighton Marathon runners who completed the marathon in such amazing times !!, Martin Spurr 3 hours 54 mins,...

Thank you to everyone who came to the Maharaja Benfleet on Wednesday night and to everyone who bought raffle tickets and to all the...

Many thanks to Simon Parton aka the Sheriff of Rodeos Wolverhampton for his continued support of our charity . To date Simon and the...

Please donate to Williams page if you can here I'm raising money for the Pseudo Obstruction Research Trust (PORT) by riding the Fred...

Please save the date . PORT will be attending this PIPO family fun day and would love to meet as many of our families as possible....

Run the Big Half in aid of PORT Charity on Sunday 7th September 2025. Set in the heart of London starting by Tower Bridge and finishing...

The Pseudo-Obstruction Research Trust’s (PORT) Small Grants Round is NOW OPEN! PORT funds research into chronic intestinal...

After years in and out of hospital and increasingly alarming diagnoses, I consider myself lucky to be alive today. I’m a 36-year-old mum,...

PORT are very proud to announce that we have agreed to fund the following project, commencing in September 2023, for an 18 month...

Paediatric intestinal pseudo-obstruction (PIPO) encompasses a group of rare severe disorders affecting the gastrointestinal nerves and...

Our wonderful member Louise Macdonald and her mum managed to get Finn Russel to donate his rugby shirt and sign it to help raise money...

Gastrointestinal dysmotility relates to a spectrum of disorders where there is disruption to the movement of food through the...

The study, funded through PORT ( Pseudo Obstruction Research Trust ), will use human stomach to measure the contractions of the muscle...

We are very sad to share the news that our wonderful patron Sean Lock has passed away. Sean attended our first PORT charity ball, as a...

The Nottingham Gastrointestinal Magnetic Resonance Imaging (GI MRI) group has spent 20 years developing the use of MRI to evaluate the...

The themes of Rare Disease Day 2021 – rare is many, rare is strong, rare is proud. This is our story representing these themes. Pseudo...

Isla is 9 years old and was born with a rare condition that has only been partly diagnosed. Her younger years were mostly spent in...

Ellie-Mai was born in 2011 at 42 weeks. She is my third child and I had an unremarkable pregnancy and straightforward labour. As soon as...

Sadie made a dramatic entrance into the world on the 10th October 2015 and has pretty much turned our world upside down ever since. We...