Swoop
@swoop
AI-Generated Digital Audiences to Enable Precision DTC and HCP Healthcare Marketing that Results in Improved Patient Outcomes
ID: 835068641590689792
http://www.swoop.com 24-02-2017 10:07:33
120 Tweet
202 Followers
1,1K Following
Worldwide Cancer Research
@worldwidecancer
💛 Become a #Curestarter 🌍 Join our united effort to reach a day when no life is cut short by cancer 🕣 Account monitored Mon-Thurs, 9am-5pm
The Stuttering Foundation
@stutteringfdn
A nonprofit organization. Since 1947 — Helping Those Who Stutter
United Cerebral Palsy National
@ucpnational
UCP's is dedicated to promoting the independence and full citizenship of people disabilities. Learn more: linktr.ee/ucpnational
Spondylitis.org
@spondylitis
A Nonprofit Organization dedicated to the quest to cure ankylosing spondylitis & related diseases, and empowering all affected to live life to the fullest.
The Arc of the United States
@thearcus
Working towards respect, dignity, and inclusion for all people with intellectual and developmental disabilities and their families.
United Mitochondrial Disease Foundation
@umdf
UMDF powers the research, education, & support that is advancing treatments for patients and families affected by mitochondrial disorders.
Spina Bifida Association
@spinabifidaassn
Working to build a better and brighter future for all those impacted by Spina Bifida.
Well Spouse® Association
@wellspouseorg
We support the people caring for chronically ill or disabled spouses/partners. Peer support groups, respites, events, advocacy, more. wellspouse.org. 501c3
The Ehlers-Danlos Society
@theedsociety
The global nonprofit organization dedicated to change and progress in the world of Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD).
ThinkFirst Foundation
@thinkfirstfndt
ThinkFirst National Injury Prevention Foundation's mission is to prevent brain, spinal cord and other traumatic injuries through education, research & advocacy.
Solve ME/CFS Initiative
@plzsolvecfs
Making ME/CFS, Long Covid & associated conditions widely understood, diagnosable, & treatable. #SolveME #MECFS #LongCovid Donate @ ow.ly/jQji50Srbuv
XXYY Project
@xxyyproject
XXYY Syndrome is a rare genetic disorder. Our organization serves families affected by this condition. We are a project of @AXYSinfo.
United Spinal
@unitedspinal
Empowering wheelchair users to live independent and authentic lives ♿️
Foundation to Advance Vascular Cures
@vascularcures
Transforming vascular health outcomes for all through patient empowerment, collaboration, and research
Williams Syndrome Association
@thewsa
WSA: research, programming and support for families and caregivers affected by Williams syndrome.
Tufts Medical Center
@tuftsmedicalctr
Tufts Medical Center is an academic teaching hospital in Boston.
Yale Child Study Center
@yalecsc
Official feed of the Yale Child Study Center at @YaleMed @YaleMedicine. Improving the lives of children & families. RTs & follows ≠ endorsement
The Brain Tumour Charity
@braintumourorg
The world’s leading brain tumour charity and the largest dedicated funder of research into brain tumours globally.
TheLAMFoundation
@lamfoundation
Delivering facts about #LAM #RareDisease and The LAM Foundation. We're dedicated to funding research, advocacy and awareness to improve the QoL for all LAM pts.
Team Telomere
@teamtelomereinc
An international community for telomere biology disorders. Facebook: facebook.com/teamtelomere | Instagram: TeamTelomere | Email: [email protected]
The XLH Network, Inc.
@xlh_network
Patient support group w/ 501(c)3 charitable status, representing patients/families with X-Linked Hypophosphatemia (XLH) or related phosphate-wasting disorders
Spinal Cord InjuryAB
@scialberta
Adjust. Adapt. Thrive. Empowering persons w/ spinal cord injuries & other physical disabilities to achieve independence & full community participation. #SCIAB
Vasculitis Foundation
@vasculitisfound
Building on the collective strength of the vasculitis community, the Foundation supports, inspires and empowers individuals with vasculitis and their families
SWAN UK (syndromes without a name)
@swan_uk
SWAN UK (syndromes without a name) is run by @GeneticAll_UK offering support and information to families of children with undiagnosed conditions. #undiagnosed
VHL Alliance
@vhlalliance
We are a non-profit support organization for patients and families affected by von Hippel-Lindau disease (VHL).
Two Rhythms
@two_rhythms
We are an accessible arts charity providing educational and therapeutic programmes for the benefit of people with profound physical and learning disabilities.
XPFamilySupportGroup
@xpfamilysupport
The XP Family Support Group is dedicated to improving the quality of life of those with xeroderma pigmentosum. Visit xpfamilysupport.org for more info!
Vision of Children
@voc_foundation
Dedicated to finding a #cure for childhood #blindness! #FundResearchFindCures
University of Toronto
@uoft
#UofT is Canada's top university, transforming society by challenging the impossible. #UofTDefyGravity Find the latest news & events @UofTNews
Spinal Cord Society
@spinalcordsocty
The Spinal Cord Society is a grassroots organization. Members organize through volunteer chapters.
The Myelin Project
@myelin_project
#Research #Advocacy & #FamilySupport for #Adrenoleukodystrophy (#ALD) & #Adrenomyeloneuropathy (#AMN) since 1989. #SaveTheBoys #NewbornScreening
Wilhelm Foundation
@wilhelmfound
For children with undiagnosed diseases - The #Undiagnosed . Works for World Congresses to start Programs (UDP) around the world to cooperate in Network UDNI
The Snow Foundation
@asnowfoundation
A voice for rare disease, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss neurodegeneration.
Tuberous Sclerosis Association
@uktsa
Support, research and advocacy for the Tuberous Sclerosis Complex (TSC) community. Social media community guidelines: bit.ly/3z4j7hz
The Calliope Joy Foundation
@caljoyfndtion
Cures, community & cupcakes for kids with leukodystrophy. 🧁 Venmo: CalliopeJoy
U. R. Our Hope
@urourhope
Non-profit serving individuals with undiagnosed & rare disorders through education, advocacy, and support in order to bring hope through knowledge, empowerment
ZERO TO THREE
@zerotothree
Translating the science of early childhood development into real impact. 🧠 #LEARNwithZTT and #ThinkBabies to build a better future.
Wolfram Syndrome UK
@wolframsynduk
The official twitter for Wolfram Syndrome UK. We provide support & information for families and people affected by Wolfram Syndrome via website, newsletter etc.
SynGAP Research Fund (SRF)
@curesyngap1
#SYNGAP1 🧬 = 🧠NDD DEE causing #Epilepsy #Autism #ID #Sleep #GI. Incidence = 6️⃣.1️⃣/💯k ICD10 syngap.fund/F78A1 syngap.fund/10 🎙
Tourette's Association of America: Nor Cal/Hawaii
@taanorcal
We are a volunteer led, nonprofit organization supporting the needs of individuals & families affected by Tourette Syndrome & Tic Disorders.
The CGD Association of America
@cgdaofamerica
The CGDAA is committed to advocating on behalf of patients and X-linked carriers by providing news and information about Chronic Granulomatous Disease.
Society of Nuclear Medicine India
@snm_india
Official National Society of Nuclear Medicine Professionals practising in India
Transplant Unwrapped
@txunwrapped
Nonprofit for Intestinal and Multivisceral Transplant Education.
World Federation for Mental Health
@wfmh_official
WFMH is an international membership organization founded in 1948 to promote mental health.
Timothy Syndrome Alliance (TSA)
@tsa_charity
Dedicated to improving the diagnosis, treatment & care of those living with #CACNA1C-related disorders inc. #TimothySyndrome and #LongQT8. @cacna1c.bsky.social
Urea Cycle Disorders Consortium
@ucdconsortium
The UCDC is dedicated to improving the lives of individuals affected by urea cycle disorders. An international collaboration, part of NIH RDCRN @rarediseasesnet
TESS Research Foundation
@tessresearch
We are a 501(c)(3) tax exempt public charity. Our goal is to fund cutting-edge research to find a cure for the genetic disease SLC13A5 Epilepsy.
Xtraordinary Joy
@xtraordinaryjoy
Xtraordinary Joy Inc. is a 501C non-profit providing advocacy and funding for X chromosome deletion research that advances lifelong health, behavior & learning.
TANGO2 Research Foundation
@tango2research
Our mission is to lead the way in finding a cure for TANGO2 related disease. #raredisease
The Avalon Foundation
@kc4ktaf
The Avalon Foundation provides emotional, educational, and mental support to pediatric patients and their families.