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Big news! Synapticure is a Best in Class Finalist for Caregiving, Aging & Care Navigation at the 2026 @DigiHlthHubFdn Awards!

We're proud to help expand access to specialized neurological care.

Heading to #HLTH2026? Connect with us in Las Vegas!

#digitalhealth
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Specialized neurological care should be easier to access.

Synapticure now offers virtual MG care with neuromuscular specialists, personalized treatment, and ongoing support.

Read the full press release:
vist.ly/5pgim

#MyastheniaGravis #DigitalHealth
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Proud to be a Quarterfinalist in the @digitalhealthhubawards HLTH 2026 Awards for Best in Class: Caregiving, Aging & Care Navigation! 🏆 Thanks to our partners & the families we proudly support through Alzheimer's, Parkinson's, ALS, FTD, Ataxia & Huntington's.
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The ALL ALS study is enrolling participants living with ALS nationwide to take part in remote research. Contact us at assess-als@synapticure.com or 708-507-9691 to learn more!
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A future without ALS starts with research. Learn more by reaching out to us at assess-als@synapticure.com or 708-507-9691.
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Synapticure retweeted
Eight years with ALS has taught me a lot.
Some things have changed. Others stay the same. Joy looks different now, but it's still there. In my girls. In Sandra. In a great pair of socks and a mountain I wasn't supposed to be able to ski.
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Replying to @synapticure
If you or a loved one is living with Parkinson's, you deserve a specialist who understands the full picture. Synapticure connects patients with Movement Disorders Specialists in weeks, not months. 🔗 synapticure.com/?utm_source=ra…
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Replying to @synapticure
🎥 Watch the full conversation: youtube.com/watch?v=eqbjlu…
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Your brain doesn't rest while you sleep. It cleans itself. 🧠
For people with Parkinson's, sleep quality may be one of the most powerful ways to support your brain.

We sat down with @RayDorseyMD and Dr. Liz Ferluga to talk about living well with Parkinson's. 💙
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Replying to @synapticure
Talk to a Synapticure physician virtually to discuss trials and expanded access programs: synapticure.com
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ALS took @Telepath_8 s arm mobility. With his @neuralink device, he regained a level of independence he thought he'd lost forever.

His BCI (Brain-Computer Interface) connects his brain to a robotic arm that allows him to gesture, microwave food, and grab a cup of water again.
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Replying to @synapticure
Talk to a Synapticure physician virtually to discuss trials and expanded access programs: synapticure.com
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Meet Brad @ALScyborg, the third person in the world to receive a @neuralink brain implant. Brad lost his voice to ALS. Neuralink has given that back, and with it, the ability to reconnect with his loved ones.
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Replying to @synapticure
Talk to a Synapticure physician virtually to discuss trials and expanded access programs: synapticure.com
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Jake @PairedWith_P7 is an ALS patient and @neuralink clinical trial participant, helping develop new ways to type for others that have lost mobility in their arms.

He’s in the process of writing a book about his story – using just his thoughts.
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Replying to @synapticure
Watch the full event recording here: youtu.be/pKYCGbGCb-E?si…

Talk to a Synapticure physician virtually to discuss trials and expanded access programs: synapticure.com
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Recently, we hosted a webinar with @neuralink , and interviewed three ALS patients actively participating in Neuralink clinical trials. @ALScyborg @PairedWith_P7 @Telepath_8 walk us through some common misconceptions people have around BCI (Brain-Computer Interface) technology.
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When co-founders @sabrevaya and @bsw5020 received a life-altering diagnosis, they built a cost-effective, accessible neurology care network across the U.S. Thanks to @melindagates @PivotalVentures for supporting our vision.
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Look forward to seeing everyone shortly to meet with ALS patients who in @neuralink's BCI study and learn how they're using it to today.

Register here to join or receive the video. vist.ly/4b2p7
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Replying to @synapticure
@neuralink BCI has the chance to restore the little things we take for granted as healthy adults every day -- communication, moving a mouse, and hopefully someday replacing lost control of movement. We're grateful for the chance to build awareness for these and other programs in ALS.
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