Hannah was diagnosed with HMS aged 24, having been symptomatic all her life. She did well in school and university, but a year after starting work as an Environmental Health Officer her symptoms reached a disabling level and her Postural Orthostatic Tachycardia (POTS) became severe.
After working part time and flexible hours for a while she was medically retired in 2010 – age 28. By this point, while in hospital and unable to put a sentence together, she had discovered a talent for stickman cartoons. What started out as a way to tell others about her condition in a fun and stylish way naturally grew into a business – communicating about disability with charm, humour, and unerring accuracy. Read More
The Hypermobility Syndromes Association (HMSA)is a UK charity but we are happy to support people with Hypermobility syndromes worldwide
The Hypermobility Syndromes Association is a charity registered in England and Wales (1011063) and in Scotland (SC037916)
