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Sharing my story of Huntington She can go to the toilet for herself, so we can take mum out of the aged care facility anymore.
She is becoming a stranger and the worst part is mum is only 50 years old. It louis vuitton bags england so hard to be with her but I don have a choice. As I watching my mother become this stranger and can do anything about it. My children will never know who their nanny was and what an amazing person she was. I miss my old mum louis vuitton ipad 2 case amazon so much and every time I go to see her I cry afterwards. It hard being in a daughter/carer relationship and sometimes I feel like I fail her. It was hard being her carer because not many people knew what Huntington disease is and what she needed. I had to fight for all the services that she had, with the help of Huntington Qld. And even still fighting to keep her guardianship because no one understands the needs of people with Huntington disease and how it affects them. I don want my children to have to go through what I going through with mum and being her carer. I 28 years old and still don understand the full effect of Huntington until mum goes through them and I see it with my own eyes. I wouldn have been able to get through caring for mum without louis vuitton briefcase cost the support of Huntington Qld. After I got the test results and saw that they were positive for HD, I had a very dark period in my life and thought what have I done to my children. Without the support of a very special lady at Huntington Qld, I wouldn have been able to get through it all. She made me see there is hope for my children future. I wouldn be where I am at in this part of my life and fighting for Huntington awareness without her. She listened to me when I had no one else and pushed me when I needed it. Thank you C. Here the link for Huntington Qld, without them Queensland families with HD would be lost. This is my life and I trying to bring Huntington disease out of the darkness and into the light by using my voice to make the world aware of Huntington disease which is a terrible and painful disease for everyone involved. Huntington disease (HD) is an inherited neurological condition. This means that it is a disease of the brain which affects the nervous system and is passed down through a family line. Huntington affects men and women as well as all races and ethnicities HD symptoms will not usually appear until a person is between 35 and 45 years of age and can include impaired movements, mood, speech and memory. As the disease progresses, symptoms worsen. There is no cure. I inherited Huntington disease from my mother and she inherited from her mother and my children have a 50% chance of inheriting this horrible disease. For me to spread the awareness about Huntington disease, I need you to help me and pass the message along. So please help me get and keep Huntington out of the darkness by making the world aware of Huntington disease and help find a cure, so the next generation is HD free. I have a Facebook page if you would like to join, Huntington Dis AC. Thank you for reading my story. Toowoomba Newspapers Pty Ltd 2017.
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