My adopted daughter had symptom onset at 3, and was finally diagnosed, once she started having seizures, a few months after her fifth birthday. Her repeat count was 141. Disease progression has been rapid. She can no longer stand or walk, and has almost no comprehensible speech. Two months ago she turned six. She will probably not see seven. This disease is monstrous and it should be getting much more research support and funding than it is actually getting.

My 26 year grandson just diagnosed. 55 repeats. My heart breaks for all those...prayers

To everyone saying that you shouldn't have kids if you have HD, I agree. But if it happens to you like it did in my family, we only found out we had HD on my grandfathers side when everybody was already born. Back in the day it was a very taboo subject... until one of my granddads brothers got diagnosed and everybody got scared. Of couse my great grandfather also had it, but we were never told

My niece 28 , just diagnosed. 51 repeat .. we are all heart broken

Jasmine, having gotten to meet you and your dad through the HD support group in Tucson, and a supporter of my family member with HD, I found this so touching, so real, and feel this documentary is so special. Thank you for sharing it publicly.

I'm so sorry that you tested positive. I hope the trials of pridopidine are helping people now and that (or another drug) will be able to prevent symptoms in young people who aren't symptomatic yet. With IVF, Huntington's could end within a few generations. Thanks to you and your family for sharing your stories and helping to educate the public on a disease most people have never heard of.

What a beautiful family. I pray that a cure is just around the corner. It should be a top priority to get rid of this terrible disease.

I am so very sorry you’ve tested positive. Holding out hope there will be a treatment soon for HD.

Jasmine, you are brave and strong. You have hope. And there will be a treatment someday. God bless you and your family. Prayers said for all of you.

I’m so so sorry. You are so brave to video while you got the results. Sending you lots of love and hugs beautiful lady ❤️💞❤️

Bless you Jasmine. Praying for you and your family 🙏

Heart breaking. Beautiful family. Praying for a cure. Praying for all who carry this gene. Thank you to this family for courageously educating us all. WE MUST HOPE FOR A CURE.

Hi, just wanted to share that you're not alone. My mom is the oldest of 9 kids, and I'm the youngest of 7 kids. With so many age groups between me and my mom, I'm seeing this disease tear apart my family as we speak. You're lucky however, to have such a supportive husband.

Omg, how heartbreaking. That was so sad to watch. I hope you’re living your best life and know we care about you ❤

This was so beautifully done. I was a SW intern in an HD clinic- you captured the devastation and the hope. I am rooting for you on this journey that I so wish was not so rough.

My dad was diagnosed 5 years ago and this video really hits home. It’s a horrible disease. Just like the other neurodegenerative diseases, it starts taking your loved one away piece-wise. There’s no other way to describe it. It makes family members feel absolutely powerless which has compounding effects psychologically. I used to be the most upbeat, positive person but I feel like a shell of my former self. I just don’t know what to do.

I have never heard of Huntington disease until I came across someone 19 yrs old with it. Thanks

My thoughts are with you and your family. I tested negative. I lost my father to HD.

I’m so sorry. I pray to God that he can help us find a cure soon

I wish you all the best, for you and your whole family. Love from Germany, Andrea

Oh how sorry I feel for you wonderful family. I hope we can choke this terrible disease. Please people we need to not put more people in the tragic line of getting this monster.

I am So sorry Jasmine. xx from Australia God will take care of you xx

I’m so sorry. It’s in my Fathers family but it has skipped me, for which I am very grateful. I have other things I’ve inherited from my moms side. But none as bad as that. Mrs. S.

Thankyou for sharing. Your so brave.

On March 15 2021 I tested positive for Huntington’s disease I am 44 years old and my cag is 45 I have swallowing problems and walking balance issues.

I'm sorry, sweet girl. 😞 And like you said all the wonderful things you inherited from them. That's so relevant. We carry on both these wonderful loved ones beautiful genes & the genes that hurt us all so much. 2 brothers just 11 months apart in age I met by chance as a teen & hung out w/until we were in our prime adults. They lost their dad to suicide when they were toddler's. He just wasn't feeling right but nobody knew why & they didn't remember him all that well. At about age 29- 30 one of the 2 brothers started acting funny, getting up once at a restaurant just punching another customer, landing him in jail. It just wasnt him. When he came home from jail it was observed he was symptomatic w/ chorea. Nobody knew what was going on, he kept getting arrested & accused of being drunk in public or while. Finally he was diagnosed. He eventually died & his brother & I have since veered away from our old friendship group in our 40s now & maintained friendship getting together once in awhile but considering ourselves a bit of social phobes. Lol. 2 years ago I saw him & he was fine & we had so much fun. Since then we've been texting, usually several times per week, mostly venting about life & just being each other's friend. A family member of theirs s died in August so when everyone saw him at the funeral at (now at age 44 & hadnt seen anyone much in 2 years) he was obviously visibly symptomatic of HD & rigid. 2 years ago no symptoms that I could see. He went & got tested in Oct & has seemed weirdly happier since finding out, because he's felt like something has been wrong for awhile didn't think it could be Huntingtons since the brother developed symptoms, between 28 & 30. I think he's glad he knows what's wrong now but he'll text in the middle of the night really scared sometimes. Which makes me sad. Sometimes I'll bring bailey's & his favorite cheesecake & we'll do a movie. I'm really sad about the diagnoses, especially after we lost his brother/who was my other good friend to this & him & I have stayed in touch this whole time w/my friend all through his brothers death, through it all & the years following. 2 good hearted brothers, my friends- following the same fate, same cross to bear. I watched your video in full. My advice to your pre-existingknowledge: hit that bucket list now & live it ALL up! Do everything you always wanted to do. Go everywhere you always wanted to go. We're all gonna get something. May you be blessed w/peace, good times & longstanding health! 💜

This is a heart wrenching video and very informative and well made. I am sending love and support. I hope you will keep your viewers updated on your precious life. I am telling people about this disease and hoping the research will produce a cure or good treatment soon.

I'm sorry you and your family are dealing with this. My family is affected by autosomal dominantly inherited (familial) ALS. A lot of the same struggles and stigma.

I am so very sorry. Life can be cruel.

I lost my husband to HD in June last summer. I pray for a cure.

Jasmine, I'm crying with you.

Sorry for the positive results! You did a tremendous job on this film!

this was so sad but beautifully presented if that makes any sense God bless thanks for sharing

Chke this disease..many ways to have children, just don't pass on this monster.

Let's all hope for a cure, or at least a treatment that meaningfully slows the progression of this horrendous disease.

Smiles, I wonder if you are a journalist now sharing amazing stories ❤❤

So sad what a shame. Really hope they find a cure or really good treatment to stop it.

This is called the "Devil's Disease " for a good reason. God be with all those who are affected. If anyone is interested, Chris Furbee has a story over 18 years in the making on HD. Called The Huntington's Dance

God bless this family.

It is not over kiddo. You can brake the cycle. In vitro children and a surrogate to have HD free family. Good that you got tested. Prayers and Blessings. Amen.

I’m So so sorry

beautifully done video, very touching. though i will never understand why people with HD have children without testing in ivf!!

beautifully tragic, really appreciated your video. thank you so much for sharing your family's bravery. my granny had 42 repeats, my dad has 42 and i do not yet know my fate (neither do my two siblings) but i'm now a mom of three young kids. curious if you have any follow up, ivf? children? how are you doing now? how's your dad? i hope you are all doing as well as you can xo

Heartbreaking having to face that in a young life when you have already seen what it has done to other members of your family.Please pray that a cure or a good treatment is found soon 🙏🙏🙏

Can't help but wonder why any loving couple would risk passing on this life/death sentence to future generations. Until a cure is found there is only one way to stop it.

This was a great documentary and I am moved by your situation. The good news is you can stop the gene from continuing by not having children the normal way. There are other options thankfully. And of course they are working hard to find a treatment. All the best to you and your future.

There are two diseases that I pray for a cure for. Huntington’s and Cystic Fibrosis. I’m optimistic, because there are so many bright young people in the world today.

So sorry

The neurologist lady with the severely chapped lips was painful to watch & distracting. Thank you for shining light on the hope for genetic assistance. What a frightening diagnosis to have to face.

Why keep having kids

I'm trying to be kind, her life

My mother had 42 repeats and became symptomatic in her late 50s and died when she was 72. My brother also had the disease but became symptomatic in his 40s. He opted for doctor assisted suicide at the age of 54. None of the rest of us 3 other kids has HD but my brother has 2 kids whose status is unknown.

Im so sorry Jasmine. This is really rough. My dad has Parkinsons.

🙏🙏🙏

So sorry.

We all have our struggles , may god bless you all. Your not alone god just wants you to ask.

I'm curious, since they figured out how to deal with SMA via gene therapy, why not see if they have testing on for something similar? I know trinucleotide repeats are especially tricky (lost a friend of mine from childhood due to DRPLA so that's how I got interested in all this) but it might be worth a try.

If you search online for her name, you will find an article from April 2023 in a publication called, "The Cut." Jasmine elaborates on her thoughts and plans regarding Huntington's Disease.

My brother has his first appointment tomorrow. Im so scared.

Darling live everyday and don't let this steal your healthy years remember you could have been negative and get hit by a bus in your thirty's we never know what is a head of us and kick the hell out of the next twenty years and have double the fun ❤️

Keep having kids - brilliant .

My name is Irma I have a sick sister and my mother died of that my aunt uncle many members of my family I would like to know if there is something to help my sister is 46 years old

😢

They didn't say the father was only 47? That can't be right...

A good friend lost his wife, son & daughter. What upsets me is...as a young couple when his wife was diagnosed with HD and told by all the medical professionals not to have children, they both ignored all the advise & had three children, the first child doesn't have HD but the other son was dead by age 19, the daughter by age 27 both dead. People listen to the professionals do not pro created! Get tested if either of your parent's have HD!!!

So why did your father decide to have two children?

Ever thougt of praenatal testing?

One might not have but their offspring can? I mean can it skips generations?

Huntington's Disease can happen to anybody at any time. Audience wishes hapless victims all the best. Cheers!

Then WHY are these people pros creating more people w/ this horrible disease ????? Want a kid ? ADOPT. But to push forward having children is just keeping this death sentence alive and well.......ADOPT, there are plenty out there that were given up.

Anyone who has it just shouldn't have kids. Not just to not pass it to the next generation but don't put your kids knowingly into a situation where they will see you ill and suffer and maybe even have to be your caretaker at a young age. Don't be selfish.

I don't think her husband understood about having children..unless he understood they would be using a donor egg and not hers..he kind of said well decide if we will do it natural or through IVF..SO IM hoping he knows it would have to someone else's egg and not hers.

Easy for the husband to say...it means nothing, boo hoo life goes on, that is very cold, seems they are trying to act like this means nothing either way & that is not true.

even using an egg donor...if you have a baby at 30, become symptomatic around 40, the child could lose the parent around age 20, before they are independent....unless a treatment is found...

Q