Hi, hope you are ok.. yes you will think always .. I do as my father passed away with this, dad got from grandmother , now brother is showing symptoms so you will always think, check hand is shaking or moving, I can relate. But it doesn’t mean that you got it.. take genome test if you are so worried to know… if not, live your life peacefully.. save money so that if needed, can hire a caretaker later..
Same here. Grandpas got it and not sure about dad but aunt has it as it’s from my dad’s side. Once I turn 18 in a few months going to test for it as I believe I’m mentally capable of the test. I would need to know to plan for the future.
I'm not convinced Huntington disease Can be explained in 6 minutes. It cant be, this is a very very brief explanation. The video is talking about hd, though and thats definitely a bonus, to inform people about the condition.
@coraldell3091 You’re absolutely right-Huntington's disease is incredibly complex, and a six-minute video can only scratch the surface. A brief overview can help raise awareness and introduce people to the basics, but there’s so much more to learn about its symptoms, genetics, and impact on families. Kudos to the video for getting people talking, but deeper dives are definitely needed to do the topic justice!
I'm just wondering whether the HD patients put that much make-up at 1.14 of your video. Try to put some molecular details (like how CAG is repeated, role of glial cells etc.), please.
Im at risk. 44 years old. Not showing strong symptoms yet, still think about it all the time. Very well done video. Thank you.
were your parents carriers?
Hi, hope you are ok.. yes you will think always .. I do as my father passed away with this, dad got from grandmother , now brother is showing symptoms so you will always think, check hand is shaking or moving, I can relate. But it doesn’t mean that you got it.. take genome test if you are so worried to know… if not, live your life peacefully.. save money so that if needed, can hire a caretaker later..
@@anusreetravelAre you saying you have to pay for the test for Huntington's?
Same here. Grandpas got it and not sure about dad but aunt has it as it’s from my dad’s side. Once I turn 18 in a few months going to test for it as I believe I’m mentally capable of the test. I would need to know to plan for the future.
@@katydid1600 it is not an expensive test. In india it costs 5000RS which is ~60USD
Nothing about central neuropathic pain in Huntington's disease again. Believe me. It's hell fire
HD can happen to anybody. Audience wishes hapless victims & grieving survivors all the best. Cheers!
Can hd happen to anybody ? 🤔
To my understanding it's only if one parent has the HD gene.
I'm not convinced Huntington disease Can be explained in 6 minutes. It cant be, this is a very very brief explanation. The video is talking about hd, though and thats definitely a bonus, to inform people about the condition.
@coraldell3091 You’re absolutely right-Huntington's disease is incredibly complex, and a six-minute video can only scratch the surface. A brief overview can help raise awareness and introduce people to the basics, but there’s so much more to learn about its symptoms, genetics, and impact on families. Kudos to the video for getting people talking, but deeper dives are definitely needed to do the topic justice!
What about anxiety medicine and memory medicine?
I'm just wondering whether the HD patients put that much make-up at 1.14 of your video. Try to put some molecular details (like how CAG is repeated, role of glial cells etc.), please.
Where do I send a monthly donation too please😥😔😔
i am 66 years old female
@MsItalianspice Thank you for sharing! If you have any specific questions or need assistance, feel free to ask, and I'll be happy to help!