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HDSANational

@hdsanational

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HDSA's mission is to improve the lives of everyone with Huntington's disease and their families.
Supporting youth and young adults @hdsa_nya

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Mariah’s new skates have a very special meaning!

A beautiful blue ribbon on the back honors Kim’s memory and stands for everyone who is fighting, living with, or affected by Huntington’s disease. It’s a little reminder that even when someone is no longer by our side, their love will always be with us.

And of course, she has her number 17 — her moms soccer number.

Every glide and every step forward carries a little extra love, strength, and meaning. So proud of this girl.

Skating with purpose, love, and a piece of Mom always with her.

@hdsanational
#HuntingtonsDiseaseAwareness
#SkateWithPurpose

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I’m thrilled to share that I’ve been featured on FineArtsNews.com!

This amazing opportunity was made possible through Culturale Lab (@culturalelab @culturalelab_art), a platform dedicated to supporting and promoting contemporary artists worldwide.

My story has been published on FineArtsNews.com, a respected international publication covering fine arts, museum exhibitions, and the global art scene. It’s an incredible honor to have my work and artistic journey showcased to art collectors, gallery professionals, museum curators, and fine art lovers worldwide.

This feature explores my creative process, inspirations, and recent works. I’m grateful for this opportunity to connect with art lovers and collectors around the world.

Read the full article: https://fineartsnews.com/2026/10/chelsea-roberts-painting-hope-in-the-face-of-adversity/

#AsSeenOn #FineArtsNews #ArtistFeature #FineArt #ContemporaryArt ArtWorld CulturaleLab

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I’m very grateful to be the 916 Amplified featured artist this month during Hispanic Heritage Month for the @sacramentokings

My girls and their mom really enjoyed the moment while rocking our @hdsanational Team Hope t-shirts during the game this past Wednesday ❤️

For me, the communal aspect of what my art can provide, in the desire to connect us to one another beyond class and status, is what fills my cup. I want to celebrate these instances TOGETHER, as much as is possible for me to.

Thank you so much to Savleen Binning for inviting, planning, and facilitating this spotlight Initiative 🙏🏼

Much love, always

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💙 “I’m Fine. I Don’t Need Help.”

Sometimes a person with HD truly doesn’t recognize changes that others can see.

There’s a name for this: anosognosia, or reduced awareness of symptoms.

Imagine being told you need help when, from your own point of view, nothing is wrong. That can make accepting help really hard.

Understanding this can change how we approach those conversations. 🐤

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💙 Pinch me… I’m going to be in a book!

I’m honored to be featured in 100 World Women in Art 2026. Being included means even more exposure for Huntington’s Disease awareness, and I’m so grateful for the chance to share this cause with a wider audience.

Here’s to hoping that someday, we find a cure. 💙

#HuntingtonsDiseaseAwareness #HDAwareness #WomenInArt #100WorldWomenInArt #ArtistsOfInstagram FindACure

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This crown stands out. 💙

I’ll use that visibility to fight for a cure for Huntington’s Disease.

@hdsanational
@justingraftonstudios
@cesarsolorzano

#internationalms #hopeandimpact #mrspageantry

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💙 A heartfelt thank you to the Huntington's Disease Society of America (HDSA) @hdsa__sf @hdsanational for bringing this incredible community together and allowing JinIX to be part of the Huntington’s Disease Walk as a sponsor.
We had the chance to sit down with patients and families, listen to their stories, and hear firsthand how Huntington’s disease has affected their lives and the people they love. Some of those conversations stayed with us long after the event ended. They reminded us why we started JinIX and strengthened our determination to help patients find more answers, more support, and more hope.
We hope to be part of many more events like this — meeting patients where they are, listening to what they truly need, and finding ways for JinIX to make their journey a little easier.
We are one family. We want JinIX to be more than a technology platform. A companion. A listener. A connection to doctors. And a place patients can always turn to. 💙#JinIX #HDSA #HuntingtonsDisease #HDAwareness #RareDisease #PatientSupport #PatientCommunity

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Photos from the Heroes vs. Villains Team Hope 5K Run & Walk are now available.

Thank you again to everyone who joined us, donated, volunteered, sponsored, and helped make this year’s event such a success.

You can view event photos here:

https://hal.runnertag.site/events/heroesvillains26

Take a look, find your photos, and relive a great day with the Team Hope Denver community.

#TeamHope #HDSA #HuntingtonsDisease #HeroesVsVillains5K #Denver5K

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how blessed are we! today we walked for hope for huntingtons disease. hope that one day there will be a cure and medications to help people. thank you from the bottom of my heart to everyone who came to walk with garrett, and to anyone who donated! our team won the top fundraising award! so proud and honored to have this type of village supporting us for what’s to come 🩵

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Join us for a day of community, connection & hope at the 2026 HD Walk! 💙

Free to register & attend!

🔗 Link in bio

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14 years ago today we watched our Mom take her last breaths on this earth. Our relationship was rocky at times to say the least. She did the best she could! And the more I learn about her past there’s a lot of things that have started to make sense. Huntington’s disease robbed so much of her life. And it continues to rob from ours as well!
If anyone ever wonders why we are so loud about HD, it’s fueled by the ones that didn’t have a voice!
Today we honor our Mom!
#huntingtonsdisease #rip #mom #tillthewheelsfalloff
@tara_cutler_ @boundformisery @hdsanational @hd_genetics @hdreachgameoverhd @help4hdi

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Rob Shaw from our HDSA National Organization is here at our Team Hope Walk along with our social worker Charlotte!

#letstalkaboutHD
#HDSA
#TeamHopeWalk

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