I have a Cystic Hygroma.
Never heard of it, have you. I'm not surprised. Very few people have - and I include the medical community in that.
Apparently, I've been lucky with mine. They are a catch all phrase for a malformation in the lymph system localised around the neck area (normally) so, ok, a way to understand this is - when you get swollen glands, or the flu - what swells up? Your neck 'glands' and sometimes ones under your arm pits, right? It's the same thing here, except, uh, chronic growth patterns, basically.
Many people have them in the womb, and are the aborted. The first time I heard that, I wept for all the children who could have been me. I felt like shouting "No, you stupid people, give them a fucking chance to prove they can live with it!" But in reality, many of the cases of it are worse than mine by a long way.
The teeth grindingly sickening thing is that it was only after I started working here and did a web search that I found out about a support group in the UK. After 16 years of living being a freak, I found I wasn't alone on here. The support group is run by a great lady called Pearl Fowler, and the thing is, she hasn't even been on the Internet. Wry irony r us. I promised then to help out with a web solution, but didn't know my arse from my elbow at that stage. Instead a lovely man in Ireland, Tony Scott, set up a page, and I bought www.cystic-hygroma.org. We're working out a way to hoik over the content and develop CGI's on the Flirble server at the moment. The most important thing is to let people know they're not alone.
|