The Genetics of Huntington's Disease

[@sadiecali7522]

My dad,aunt and grandfather had it....I tested last year negative...so grateful

[@tanyacastruita9429]

glad to hear that👏

[@suppernova1184]

Are you Somali ?

[@sadiecali7522]

No....his family is from Belgium ...is Huntington’s prevelant in Somalia?

[@suppernova1184]

@@sadiecali7522 no

[@nerminc7925]

Benimde babamda vardı ve iki kız kardeşimde ve bir yıgenimde bu hatalık cikti erkek kardeşim yaptırmadı testi korkuyor onun coçuğuda var ama bende yaptırdım bende cıkmadı ama kardeslerimi görünce cok üzülüyorum daha durumları biraz iyi ama ilerde zor durumları benide etkiler. Sizin için sevindim yok diye

[@Moni-ss7gm]

This is scary for me. My Dad had HD. 🙁

[@somadsul1461]

Mine too :-(

[@HDYOFeed]

@@somadsul1461 we are here for you. Please reach out if we can help! www.HDYO.org

[@HDYOFeed]

@monica Gallagher we are here for you! Please reach out if we can help! www.HDYO.org

[@remus907]

And mine, and my cousin. Hope i wont get it kekw

[@mumr4268]

I'm sorry...have you decided to be tested?

[@vinteng825]

Just recently tested positive for HD gene. I'm 25, male with not symptoms whatsoever. My grandmother at 65 started to show symptoms of HD 3 years ago and was ultimately confirmed the following year. Mother already died (not with HD) of cancer when I was a kid so we couldn't tell if she inherited the gene. My brother at 22 tested positive with the gene. While my other 3 siblings refuse to know their status even after having children of their own. With my condition, I decided not to have a kids unless I could afford PGT in the future. I think it's very selfish for someone to conceive if they know that they are at-risk of having the gene.

[@leahcarrier299]

I get my test once this covid-19 settles down. Just waiting now

[@cloroxbleach5159]

I wish you all the best.

[@giselleruvalcaba8330]

i hope everything turns out okay

[@jessbecton9556]

no! dont get tested!!! if you do youll get very depressed. pls research

[@leahcarrier299]

@@jessbecton9556 I'm not worried about it at least I'll know what's wrong with me

[@leahcarrier299]

@@jessbecton9556 oh I'm aware of the s*** show that awaits if I'm diagnosed seeing lots of family members go through it

[@angelc878]

Awesome info! Very informative!! thank you so much😊

[@yeva662]

This wasted a ton of time

[@zbs8334]

Yeah it could have been 2 minutes. Just trying to study for my final tomorrow 🙃

[@omarelwasif9124]

is g silent and not pronunced ?

[@rupalipidurkar6023]

can you described molecular mechanism of HD

[@sggaming4720]

I swear I need to get tested this is making me nervous my grandfather had Hd and my aunt, uncle and my father are passed 50 and show no sights so I guess I’m in the clear but still gets me nervous next time I go to doc I’m asking for a test

[@sadiecali7522]

It’s a huge scary drawn out process of therapy sessions and neurological exams all leading up to a simple blood test ...I did it during summer 2020...thankfully negative for the gene

[@hareecionelson5875]

Considering Huntington's is dominant, if your father has shown no signs, you are (probably) in the clear. Especially since the onset of HD creeps forward over generations due to DNA repeat slippage during replication. Good luck

[@shubhamgiri1926]

I that cross right???

[@gunterliam7411]

All thanks to dr Stanley who cured me from my Huntington’s disease I am forever grateful ..

[@baytimamlakati7013]

وهل كان عندك وشفيت حقا كيف

[@coraldell3091]

Gunterliam hi, how did Mr Stanley cure you of HD ? Or a you just a troll , being annoying.. ??

[@AutoWorldzz]

Huntington, Virginia , 2021 "Nice and creative Videos，I can see A lot of thought has been put into the content and editing of the video， This is really my favorite channel.:) .🌴🌴🌴excellent 👍👌👍👌👍 🌴🌴🌴 🌴🌴🌴 🌴🌴🌴 🌴🌴🌴.

[@bothrealting2598]

😔