Heather MacBeth

Heather & Lachie's RTS fundraising page

Fundraising for Rubinstein-Taybi Syndrome Support Group
£1,584
raised of £1,000 target
Donations cannot currently be made to this page
Event: 2016 Inverness Half Marathon & 5K Fun Run, on 13 March 2016
Participants: Lachie MacBeth
We support families affected by RTS to make sure they know they are not alone.

Story

Our beautiful daughter Eilidh was born with a very rare (1:125,000) genetic condition, Rubinstein-Taybi Syndrome (RTS). RTS affects Eilidh's development in many ways, meaning she has a lot of input from various health professionals, although the rarity of it means that most of them know little or nothing about the condition, so we're all on a learning curve together!

Eilidh has Rubinstein-Taybi Syndrome, but it in no way defines who she is. She is non-verbal, although we hope one day she will learn to speak, but we are able to communicate with her using Makaton signing, and she understands much of what we say to her. She loves her pre-school nursery class and is very popular with staff, her peers and other children in the school. Eilidh has a developmental delay, although she doesn't let that prevent her from trying new things, and is constantly surprising & delighting us with some new found skill! 

We're so blessed to have Eilidh in our lives, she's an absolute joy to have around and her 2 brothers adore her. We're lucky and thankful that she is a healthy, happy, smiley wee girl, who brings sunshine into everyone's life that meets her.

The RTS UK group has been an invaluable lifeline for us as a family, providing us with information and connecting us with other 'RTS' families that we might otherwise never have known existed! 

As with many 'syndromes' there is a wide scale on which those with RTS are placed. Eilidh seems to be on the lower end, having few health issues, but many of those diagnosed with RTS are affected by more serious problems. Some have multiple hospital visits, often for surgery. Most, including Eilidh, have regular appointments to monitor growth and feeding, yearly eye and hearing evaluations, and evaluation for cardiac, dental, and renal abnormalities. Behavioral therapy for many, and special education are a major consideration for most.

RTS UK is a charity based in England, set up to provide help and support to families affected by RTS. Membership is open to individuals with RTS and their parents/carers, and is free of charge. Regular get-togethers and family weekends feature among the group’s activities, and provide families an opportunity to share experiences and friendship. Their twice yearly newsletter ensures that families are kept up to date with current information, events, information and news from other families etc. All of this is financed by voluntary donations and fund-raising.

This is why I want to do something to help them, so me running my longest race yet - the Inverness Half Marathon & Eilidh's big brother, Lachie doing the 5k Fun Run seemed like the best way to do it! Thanks for taking the time to visit my JustGiving page & reading my essay!

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About the charity

We are a small national charity supporting families affected by RTS, a rare chromosome disorder, the main features of which are a learning disability and a high incidence of various physical and behavioural problems. We are entirely dependent on donations and all funds directly benefit families.

Donation summary

Total raised
£1,584.00
+ £315.00 Gift Aid
Online donations
£1,584.00
Offline donations
£0.00

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