ALS: The Disease that Stopped “The Iron Horse,” Lou Gehrig
June 2, 2023
Created by an ALS patient to improve care for everyone facing a neurodegenerative disease, we understand you and your needs. Our virtual clinicians & specialists are ready to make your life easier.
As seen in
Schedule a complimentary intake call here to talk about your diagnosis and current health-related needs.
Each patient is unique. We’ll talk as long as needed to understand your history and to make a plan for you.
Prescription refills, symptom management, insurance navigation, clinical trial guidance, and more—all from your home.
Regular visits with your doctor are important in tracking your progression and regulating medications. We make those check-ins as painless as possible, so that you can get back to living.
Juggling your care is overwhelming. No more scouring the internet to find local resources or new devices; no more researching new clinical trials and off-label therapies on your own. Let someone else do the work for you.
We coordinate genetic testing and counseling in order to place you in the right clinical trials. We navigate insurance for you, to make sure the medication you need is covered. Our list of in-house services is continually growing, with mental health and psychiatry support on the way.
.svg)
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.
.svg)
Everyone is friendly and caring. The neurologist are great. They listen to what you have to say and help you anyway they can.
.svg)
Great people all around. Taking great care of pALS and cALS. Predictable access and patient-centered support using a solid telehealth network.
.svg)
Extremely well organized and professional at each step of the process; intake, physician contact, follow up.
.svg)
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.
.svg)
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!!!
.svg)
Those we have worked with are an extremely professional and empathetic group of people.
.svg)
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.
.svg)
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!
.svg)
Doctor took her time with us and it was a most welcome change to what we have been accustomed to
.svg)
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!
.svg)
Crystal has been great and easy to work with. Thanks for offering this service.
.svg)
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.
You all fill a huge gap in in neurodegenerative disease healthcare. Your support, advice, expertise, referrals and hearts have all been so helpful to our family. I often complained about the healthcare after dad’s diagnosis, essentially harping on all the areas of support you provide as an organization. I literally tell every healthcare professional we meet with to refer their current & future patients to Synapticure.
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.
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 a neuro disease, time is of the essence and the speed that Synapticure is something other providers should strive for. Thank you for giving me hope!
If you are interested in becoming a Synapticure patient, please click here to schedule a call with one of our care coordinators who can answer your questions. If you have other questions, please write to us here and we will get back to you soon.
Please note that Synapticure is only able to serve U.S. based and English speaking patients at this time.
Want to stay up to date on the latest in ALS and Parkinson’s care? Sign up here.
