The Diabetes Research Team here at Barts Health / QMUL have teamed up with the Gastroenterology group for this study. We are keen to let people who have diabetic gastroparesis know about ongoing research
The reason we exist is to help each other. Our Group and Charity can only function with and for you.
We are delighted to continue our awareness campaign with something very special from Gift Member Jackie. When we asked what Gift UK means to her we didn't expect such a heartfelt response. We won't say anymore we'll let Jackie do the talking.
Super exciting day today, after 6 months of hard work, we can finally release our awareness film.
Big thanks to Gift UK members; Natalie, Rachael, Jackie, Sophie, Sue, Becky, Becky, Ashely and Tom for taking part in the film, being brave and telling it as it is.
The idea is super simple, for anyone who knows someone affected by Gastroparesis and related disorders, to donate the price of one plate of Christmas dinner to Gift UK, to continue to provide support, information, and fund research.
So lets begin with a simple question? Do you remember the last time you had a stomach bug? The last time you had food poisoning? Or the time where you could not stop vomiting? Maybe the time you had the flu? Where you lacked energy unable to do anything? All of theses are what patients with gastroparesis live with daily. It is like a stomach bug, food poising or the flu that never goes away.
I have had a feeding tube for over three years. Gastroparesis and intestinal dysmotility mean my stomach no longer functions and my small intestine does not absorb nutrients well. Having a feeding tube that bypasses my stomach and delivers a partially digested solution into my small intestine ensures my body can still get essential nutrients, calories and fluid. Without my feeding tube I would not be alive.
Hello,
Welcome, come in and make yourself at home.
If you type Gastroparesis into Google, you will get a whole list of different websites all with similar brief pages. Most of them will tell you what GP is, what the symptoms are and the very limited treatments that are available.
True self-love is hard to achieve in the world that we live in and we forget that as humans we are not perfect we have flaws, tonnes of them in fact. However you also have so much that is amazing about you, nobody does you like you do.
We aim to provide reliable information and resources to all our members. We write from the heart, and tell our own personal stories. We want the world to know what it's really like to live with Gastroparesis, to help others know they are not alone. In hope of changing some of the common misconceptions in health care today.
We are still a small organisation and our running costs are low. This allows us to donate a large proportion of our fundraising directly to research into gastric motility disorders at the Wingate Institute, London and similar projects throughout the UK.
Founded in 2012 by Natalie Roux-Bean and Rachel Stott, after their own battles with Gastroparesis. GIFT was created when the girls met through the American support group G-Pact. After years of feeling alone, they shared their experiences.
Knowing someone else understood was half the battle, but that was not enough! Understanding that there must be others living with the condition in the UK, they decided to do something to help. GIFT was born! An online support group and educational resource for anyone, be it patient, carer or professional.
Through online resources and social media the group has helped hundreds of people find support, information and understanding from those who really know.