Top Tweets for #Synapticure
Doubting the credibility and effectiveness of @synapticure?? This should put your mind at ease and inspire you to give it a chance. #ALS #Synapticure
This makes me really happy:
9.5 out of 10 @synapticure patients would enthusiastically recommend their Synapticure doctor to others.
If you are living with Parkinson’s, ALS or PLS, I hope you will enroll and experience the difference for yourself.
https://t.co/2U8D2kVmQp
At #Synapticure, we are committed to providing compassionate, personalized care for those living with neurodegenerative diseases.
Read about why one of our amazing nurses, Crystal, joined Synapticure and is changing care as we know it.
https://t.co/fBR6KPv1mQ
This #NurseAppreciationWeek, we're especially thankful for the incredible #Synapticure nurses that support our patients & care partners every day.
If you're fighting #Parkinsons, #ALS, or #PLS, reach out today and see for yourself how amazing they are!♥️
https://t.co/irjZtz0cBY
Let the games begin! @AANmember #AAN2023 Help me help my @synapticure patient
@LahainaLaura #LauraTriplett raise #ALSAwareness! Let’s take a pic and post!
When #Synapticure launched, we focused on exclusively supporting #ALS patients and care partners.
Our co-founders (@bsw5020 & @sabrevaya) are fighting ALS, so we knew the ALS community's needs and felt confident we could help meet them.
But the plan was always to expand.
One last reminder: Tune in tonight at 7p ET to hear two incredible #ALS physicians discuss available treatments, clinical trials, clinic/#Synapticure partnerships, and more.
We can't wait.
https://t.co/gRLlj68Sl9
We're excited about this one(!)...
On Monday, tune in to hear Dr. Jinsy Andrews and Dr. Danielle Geraldi discuss ALS care today. They'll cover promising treatments in the pipeline, limitations of ALS care today, and how Synapticure partners with clinics.
https://t.co/gRLlj68Sl9
Join us Monday for an FB Live with Synapticure's Dr. Geraldi (@DGeeEss1) and Columbia's Dr. Jinsy Andrews (@JinsyMd).
They'll discuss ALS care today, treatments in the pipeline, and how #synapticure partners with clinics to support patients.
RSVP today! https://t.co/gRLlj68Sl9
We're excited about this one(!)...
On Monday, tune in to hear Dr. Jinsy Andrews and Dr. Danielle Geraldi discuss ALS care today. They'll cover promising treatments in the pipeline, limitations of ALS care today, and how Synapticure partners with clinics.
https://t.co/gRLlj68Sl9
Comment below with questions or topics you'd like them to cover--we'll be addressing audience questions throughout, so be sure to post them here!
#als #telemedicine #neurology #neurodegenerative #neurodegenerativedisease #clinicaltrials #synapticure
If you or a loved one is fighting #als, #pls, or #parkinsons, would you reach out today? We'd love to connect you with Jean to see how she can help you.
We're in this, together❤️
#ssdi #insurance #disability #caregivers #caregiver #neurodegenerative #telemedicine #synapticure
Did you know that National Caregivers Day is this week? ❤️🤲
At Synapticure, we're celebrating the best way we know: We're hosting a live panel with incredible caregivers to #Synapticure patients. RSVP using the link below to join us on Thursday at 7p!
https://t.co/9xjyyoe7Yf
Our dream world🌎 looks a lot like what @kimfrench0405 describes--every patient feeling like they're the #1 priority.
RSVP to join us live tomorrow, where Kim will share how #synapticure changes the #ALS care journey. We're so excited to hear from her.
https://t.co/VkZjfAbj4j
My experience with @synapticure has been nothing but pure excellence. My care coordinator, Crystal has always made me feel # 1 priority. If you have #ALS you need @synapticure and follow @bsw5020 #EndALS
Help us out, team--what do you most want to hear Dr. Geraldi discuss on tomorrow night's ALS-focused "Ask Me Anything"?
Comment here and we'll cover as many questions as we can!
#ALS #neurodegenerative #telemedicine #startup #startups #webinar #facebooklive #synapticure
Wanna know the best part of our Monday?
Hands down, today's highlight was watching Carla and Denby's amazing video about their experience with #Synapticure 😍
We're honored to support their #ALS journey and we'd love to do the same for you. Enroll today: https://t.co/irjZtz0Krw
@DrJaimeMartin is back to share with you about Sinemet, one treatment for Parkinson's, and the truth behind how it works. View the full video here: https://t.co/5v4xTkwJTq
From prescription navigation to virtual visits and insurance approvals, #Synapticure is here to help.
@synapticure 🤸♀️🤸🤸♂️🤸🤸♀️👏🏼👏🏼👏🏼 Exciting news for those of us in the PLS Club. Thank you Synapticure, @bsw5020 and @sabrevaya for listening and stepping up to the plate. #pls #synapticure #als
I could not be more pleased to be invited to join the Expert Advisory board for this startup, which aims to transform #ALS care- including basic no cost genetic testing. #ALS has changed again! https://t.co/wBz0vxFO0H
#synapticure #ALS #ENDALS @RepMullin @JimInhofe @krhern
NME
Honored to be on #Synapticure's Expert Advisory Bd.
It will help patients access:
▪️Genetic testing & counseling
▪️Telehealth w leading #ALS docs
▪️Info on ALS trials
▪️Quality care regardless of where you live
▪️Personalized Care Services
⬇️INFO⬇️
https://t.co/1U14iazUMr
1st @bsw5020 & @sabrevaya changed #ALS advocacy w @iamalsorg. Now they are changing ALS care w an innovative new company called #SYNAPTICURE.
ALS is a heterogeneous disease.
It's time your care is personalized for you & your ALS.
LEARN MORE:
https://t.co/1U14iazUMr
@nytimes
We are so excited to publicly launch with this story by @maureenmfarrell in @nytimes. This telemedicine company will bring personalized care to all living with ALS. Together, we'll leave behind the era of, "I'm sorry, but I can't help you." #NewEraOfHope
https://t.co/AUebrm9Jbw
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