« Reply #9 on: Monday 25 March 13 10:35 GMT (UK) »
Hi
In my Irish emigrant family I have identified 2 generations prior to emigration and another 5/6 since the 1860s.
Death certs can be misleading as although the deceased had been admitted to an Institution suffering from Chorea or St Vitus dance or similar terms the actual cause of death was given as pnemonia or phthisis or even suicide. Coroners Inquests have clarified matters somewhat!
I have medical records for admissions and patient records written over years of "treatment" which clearly describe the symptoms for HD although the actual gene wasn't identified until 1993. This meant that for some families there were beliefs that it was something "caught" from grass or animals or something similar. Unfortunately many myths pervaded and some families were instructed not to talk about it- to the extent that I currently have dealings with a 60 year plus woman who found out in her fifties that she had a brother who had been institutionallised.
If you want to understand more local HD societies have websites and there is quite a lot online (choose a reputable site!)
Briefly if one parent has HD any child has a 1 in 2 chance of inheritance. For example out of a family of 11, 5 girls and one boy inherited HD. The other 5 children did not inherit and neither did their children or grandchildren.
Hope this helps Adie. DID the 37 year old woman have children ? Were any of them affected?
HUNTS: Fairy, Ding, Scotney, Swinton, Burgess, Brace
BEDS: Farey, Fairy, Young, Rootham, Gell, Wildman, Cooper. Deighton, Flavel.
NORTHANTS: Hills, Mobbs, Twelftrees,
DERBY: Fairey,
LONDON: Fairey, Fairy, Burgess, Williams, Tanser, Picknell, Vinall, Plampin, Mullins, Day, Folwell, Bamfield, Brown
WATFORD HERTS; Burgess, Williams
WARKS: Fairy, Ward, Stephens, Reeves, Hodgkiss, Byrne, Hunt, Edgeworth, Harper, Dudley,
WORCS: Callow, Lowe