Huntington's disease is a complex condition that demands specialized care. Our team is dedicated to providing comprehensive support, including genetic counseling to educate and support patients and their loved ones navigate the disease.
Designed by a patient for patients, Synapticure is changing the experience and outcomes for the patients we serve, including those with juvenile HD and those who are pre-symptomatic genetic carriers. Covered by most insurance, our telemedicine clinic works with you and your existing care team seamlessly, from the comfort of your own home (or when you’re on the road).
Helping patients and caregivers manage medications, PT, OT, speech therapy and medical equipment, anticipating & coordinating your needs before you need them.
Consult virtually with a HD specialist to talk about your HD care. Discuss trial options, the science of trial drugs, plus your priorities and risk tolerance.
Approximately 75,000 people are carriers of the genetic mutation that causes HD. We coordinate genetic counseling plus testing to help you and your family understand the implications of testing and your results.
Visits from the comfort of home or when traveling—all you need is a phone, tablet or computer.
Expert support when you need it, adjusting medications and helping manage symptoms.
Synapticure is in-network with most major insurers, including Medicare and OptumServe.
We partner with your family doctor, neurologists, movement disorder specialist or HD Clinic and advocate for your needs.
Our growing team of psychiatrists and psychologists are ready to help you or your loved one with HD with issues related to depression, anxiety, apathy, and other psychiatric concerns.
Schedule a consultation with one of our Care Coordinators
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Synapticure itself is a Godsend. They have done more for me through telehealth than the clinic did in a year of in person visits. Synapticure takes care of all the legwork needed to do anything from getting a new powerchair to getting new medication. Actually prescribed me a medicine that I should have been on from my diagnosis. They are amazing.
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Everyone is friendly and caring. The neurologist are great. They listen to what you have to say and help you anyway they can.
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Great people all around. Taking great care of pALS and cALS. Predictable access and patient-centered support using a solid telehealth network.
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Extremely well organized and professional at each step of the process; intake, physician contact, follow up.
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Thank you for the access to genetic testing! It was discovered that I had a mutation of the SOD1 gene which has completely changed my treatment.
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We love the kindness and care from Rebecca and Dr. Jaimie Hatcher-Martin.Great service offered to ALS patients as well as Compassionate, help and understanding!!!
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Those we have worked with are an extremely professional and empathetic group of people.
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I have been more than pleased with the care I have received at Synapticure and am so grateful for the hard work so many have done to bring ALS patients hope.
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The willingness of my neurologist to prescribe off label has given me new hope in my fight with ALS. It allows me to try something new while waiting for a clinical trial. For anyone fighting ALS , time is of the essence and the speed that Synapticure is something other providers should strive for. Thank you for giving me hope!
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Doctor took her time with us and it was a most welcome change to what we have been accustomed to
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We've struggled getting responses and support from other clinics about new drugs; meanwhile, Synapticure has been extremely responsive, and as a result, we have just started on Relyvrio. Additionally, Becky and the Synapticure team have been great! Thanks!
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Crystal has been great and easy to work with. Thanks for offering this service.
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I have a great experience with Synapticure. Michelle and Dr. Faber are wonderful.
Everyone from synapticure has been VERY helpful; from Eva and Dr. Jamie Hatcher. They are so kind and make you feel comfortable. They never rush you and they get things done so quickly.
