Published: 12/06/2018 Tags: Ehlers-Danlos in the News

UK Women Build EDS Awareness

Posted by Uckfield News on June 12, 2018

Lara Bloom has walked the London Marathon, carried the torch for the London 2012 Paralympic Games, and is constantly on the move around the world raising awareness of rare and invisible diseases.

If you met her you would have no idea that she lives in constant pain.

She is energetic and articulate and she spoke on Thursday to 18 people who have their own versions of the disease she suffers from, Ehlers Danlos Syndromes.

Those people and their families were thrilled to hear Lara talk. The international director of the Ehlers-Danlos Society came to see them at the Temple Grove Care Home near Uckfield.

They could relate to everything she said about her illness and she understood their frustrations about slow diagnosis and difficulty in getting help they needed, particularly for children.

The reason they were able to get together was because two women who met at Temple Grove decided to raise awareness of the Ehlers Danlos Syndromes.


Both suffer from the disease, which affects connective tissues, and before meeting each other had never previously met anyone locally with it. Now they know many more people affected similarly.

Anita Gallemore said the discovery was overwhelming. She was pleased that she and Emma Woolley were now able to share their camaraderie with others – thanks to support from Temple Grove.

one-off coffee morning for friends and family has grown into a support group with meetings every four to six weeks at the care home for people with Ehlers-Danlos Syndromes.

Support group

The first meeting with Lara Bloom as special guest was held on Thursday and the next meeting of the support group takes place on Thursday, July 19. Anybody interested in attending will be welcome. Please call Kerry, Temple Grove welfare officer, on 01825 714400 to let her know if you would like to go.

Lara was presented with cheques and cash totalling more than £1,300 for the Ehlers-Danlos Society by Anita and Emma during her visit.

Those attending said they were pleased to hear her talk and to meet others with EDS.


Fourteen-year-old Katy Clements, from Heathfield, who attended with her mother Alison, said it was great not having to explain how she felt. “Everyone here automatically understands, they get it completely.”

Most of those in the room had Hypermobility EDS  – which mostly affects the bones and joints – but Sarah Price, 42, from Uckfield, has Vascular EDS which is generally considered the most severe form of the syndromes and which affects internal organs, arteries and muscles.

She told the gathering that she had a heart attack aged just 36 but was only diagnosed with EDS at the end of last year after it was discovered her sister had the vascular form. Her sister’s daughter and her own 16-year-old daughter have since been diagnosed too.

Read the complete original article

Virtual Support Groups

Let’s Chat

Would you like to speak to others living with EDS and HSD but can’t get to any support group meetings, events, or conferences?

Our weekly, monthly, and quarterly virtual support groups for people from all over the world are a chance to come and share your story and chat with others for support.

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