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April 2010

Young GISTers cross country lines to get together

Written by Stacey McAully

The whole group takes a picture at Edinburgh Castle.My name is Stacey McAully and for those of you who dont know I was the first pediatric diagnosis of GISTs in Scotland. I have had 2 serious surgeries and was on Gleevec for 3 years. Now I am currently GIST free but have many pulmonary chondromas and an esophageal leiomyoma. My family recently got in contact with another GISTer in England and we met up for the first time.

We did some sight-seeing in Edinburgh and enjoyed eating out. Amongst all the fun we knew there was something that brought us all together. GISTs. We spoke about our experiences and what we all knew about this rare cancer. We got on exceptionally well and hope to meet up again soon.

Young GISTers, Pippa & Stacey.We have also started to make plans to raise awareness of GISTs together in the UK. Hopefully some of our plans will work out and soon it will be as well known as other cancers. We hope to raise money for research.


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2 Comments

  1. Great article stace - I am proud of the way you handle all of this in a practical way. I have to say
    It was really helpful meeting other parents who understand what we live with and was our pleasure to
    Help them in any way we can - the positive side to this illness is the start of a 'beautiful friendship'
  2. Well done Taye, what a lovely article! As part of the England GIST group (Pippa's Mum), I can most certainly confirm that the weekend was fantastic! It was a huge relief to finally meet a family going through a similar situation, and what a family! You're all fantastic, we had great fun & are most definately looking forward to meeting up again soon!

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