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Edinburgh Live
Edinburgh Live
National
Sian Traynor

Army dad to walk barefoot from Cornwall to Edinburgh to raise funds for daughter's rare disease

An army major is planning to walk barefoot from Cornwall to Edinburgh in a bid to raise funds for his daughter's rare disease.

Major Christopher Brannigan will set off on the 500 mile journey on Monday whilst carrying a 25kg kit to raise awareness for those affected by rare conditions, stating that his daughters life "depends on it".

His daughter Hasti needs treatment for Cornelia de Lange syndrome (CdLS), to ensure she does not end up wheelchair-bound, mute, affected by seizures and requiring round-the-clock care.

The course marked out by the major will run via Downing Street where he plans to deliver a petition and letter to the Prime Minister before continuing on to Edinburgh.

The journey from Land’s End to Edinburgh will attempt to procure research for the first ever gene therapy treatment for CdLS and highlight the plight of all those affected by similar conditions.

Genetic Alliance UK said patients with rare diseases, defined as affecting fewer than one in 2,000 people according to the European Commission, are among the most vulnerable to COVID-19 as well as being hard hit by the measures put in place to contain and deal with the pandemic.

Major Brannigan said: “Hasti’s future depends on her receiving urgent treatment, now, before her condition deteriorates further.

“I have been astonished over the last eight years how little, if at all, rare diseases feature in medical training, how low general awareness is, and how underfunded rare disease care and research are. This needs to change, particularly given Covid.

“I will do everything it takes to improve Hasti’s chances and support the millions of others who share my family’s experiences and aspirations. Children who suffer from rare diseases don’t deserve to be neglected and forgotten.”

Calling all mums, dads and carers - join our friendly Edinburgh Parents group for all the latest family and kids news.

He also plans to launch a parliamentary e-petition and deliver a letter to Downing Street on July 21, where he will meet with Jayne Spink, the chief executive of Genetic Alliance UK.

To donate to the 'Hope for Hasti' fundraiser, you can follow the link here.

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