First off my Great GM, GM, Mother , Aunt and Uncle all had it… However some choose not to be tested knowing the history. Living… Continue reading Huntingtons to know or not to know is the question
First off my Great GM, GM, Mother , Aunt and Uncle all had it… However some choose not to be tested knowing the history. Living… Continue reading Huntingtons to know or not to know is the question
I was diagnosed with Huntington Chorea a month ago. I also have a son named Max who the Neurologist said has a 50 percent chance of inheriting Huntington… Continue reading Huntington’s Korea
I’m 18 years old and I’ve been diagnosed with Huntingtons since October. There’s no cure, it’s basically Alzheimer’s, Parkinson’s and MS in one disease.
hello i am melissa, february is rare disease month let me tell you about my rare fatal brain disease. huntington’s disease is a rare neurodegenerative… Continue reading my fatal rare disease
Sou o José Miguel Abrantes Figueiredo 39 anos de idade sou de Portugal vivo perto de Lisboa.Desde que me lembro sempre tive pequenas dificuldades na… Continue reading A coreia que é minha vida
Growing up in a family impacted by Huntington’s Disease – a rare and incurable genetic disorder, I feel compelled to share my exceptional life experiences… Continue reading Love Isn’t Rare
I have Huntington disease
Maddox is a 14 yo boy who was diagnosed with Juvenile Huntingtons Disease 4 years ago. He suffer from Epilepsy as part of the disease… Continue reading Maddox
Me, part 1 I don’t know about you but for me, I connect with people most when I know their story, and when I share… Continue reading My HD journey