7272Re: [huntington's at risk] New member
- Jun 1, 2013Melissa, this is a great place to start. We're sorry for the reason you found us, but glad that you did. Feel free to ask anything you want about HD and we will try to answer your questions. Where do you live? How old is your child? Testing for the HD gene is a huge undertaking. While some want to know their gene status, others do not want to know. I have 4 kids (all adults). My oldest, a son, wanted to know as his wife was beginning to spot some changes in his personality. He has since tested positive for the gene. His 3 younger sisters do NOT want to know and have chosen to live their life one day at a time.Dave
For more information about Huntingtons Disease:
http://www.HDSA.org/il----- Original Message -----From: melly_ajSent: Saturday, June 01, 2013 1:53 AMSubject: [huntington's at risk] New member
My name is Melissa, I am 26 years old and a single mom. My Mother passed away from complications of HD in 2000. I still have a hard time dealing with it all emotionally. I am still at risk of inheriting the gene but have not been tested yet. I am too afraid because I don't think I could handle it if I found out I have the gene. But right now, I think there is still an equal chance of not having HD. I just try ot live my life the best I can because if I do have it, I don't want to be sick and wish I had lived more happily. I go to counseling sometimes but was told maybe I should try to find support groups and others who have been in my situation. It seems alot of people (when I tell them about HD) don'treally understand how bad it is because they haven't been through it....I also am worrying more recently because sometimes my nerves are bad and I am shakey.
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