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AllStripes Profile
AllStripes

@_allstripes

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Following
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693
Statuses
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Our mission is to unlock new treatments for people affected by rare disease.🚀

San Francisco
Joined July 2017
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@_allstripes
AllStripes
2 years
By joining forces, we’ll continue the work of harnessing the power of patient data to shape the future of evidence generation.
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@_allstripes
AllStripes
2 years
PicnicHealth and AllStripes’ patient-centric model enables a deeper view of each patient's health while reducing the challenges of traditional site-based studies.
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@_allstripes
AllStripes
2 years
From the bottom of our hearts; thank you to all our partners and supporters for being a part of our journey and our important mission. We are excited to continue our work within PicnicHealth to put patients at the center of research.
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@_allstripes
AllStripes
2 years
Today we are excited to announce that we are joining forces with PicnicHealth, a company that shares our vision of putting patients at the core of research. Read the full announcement here:
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@_allstripes
AllStripes
3 years
Thank you to the patient advocacy organizations who helped make this work possible: @CLOVESSyndrome, @GoPI3Ks, @WonderFILsmiles & @LGDAlliance. 3/3
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@_allstripes
AllStripes
3 years
This data which covers demographics, diagnosis, symptoms and more was collected from 123 CLA and PROS patients and analyzed by the AllStripes Research Team. 2/3
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@_allstripes
AllStripes
3 years
Today is #LGDAwarenessDay, a day to raise awareness of lymphangiomatosis (complex lymphatic anomalies) and Gorham's disease. To help in these efforts, we are excited to share the final round of data insights from our CLA and PROS research cohort! 1/3
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@ChildrensTumor
Children's Tumor Fdn
3 years
#FACT: Tumors from schwannomatosis may cause pain that can be extremely difficult to manage. More NF Facts at https://t.co/DCE6afd6ye. More ways to #MakeNFVisible at https://t.co/nmJuZ2yKET. #endnf #schwannomatosis #swn
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@_allstripes
AllStripes
3 years
GM1 is an inherited lysosomal storage disorder that destroys nerve cells in the brain & spinal cord. Researchers have classified the condition into 3 major types: infantile (type 1), juvenile (type 2) and adult onset or chronic (type 3).
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@_allstripes
AllStripes
3 years
Today, May 23rd, is International GM1 Gangliosidosis Awareness Day! We want to share some information about this rare condition to help in the community’s awareness raising efforts.
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@_allstripes
AllStripes
3 years
Two of the rare conditions for which we have research programs, Morquio A & propionic acidemia (PCCB subtype), have been selected by the FNIH to be part of its Accelerating Medicines Partnership® Bespoke Gene Therapy Consortium clinical trial portfolio.
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@ehlersdanlosuk
Ehlers-Danlos Support UK
3 years
Today is #REDS4VEDS Day. Put on the red and let the whole world know to help raise awareness of vascular Ehlers-Danlos syndrome (vEDS).⁠ Wear something red, take a selfie & share it with #REDS4VEDS.⁠ Learn more about vEDS here: https://t.co/OVMdkIWE54 #vEDS #VascularEDS
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@ChildrensTumor
Children's Tumor Fdn
3 years
🌍💙Today is World NF Awareness Day!💙🌍 NF is a group of genetic disorders that cause tumors to grow on nerves. It affects millions of people worldwide, and today is about shining a spotlight on this important cause. https://t.co/nmJuZ2yKET #makenfvisible #endnf #iknowafighter
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@_allstripes
AllStripes
3 years
Today is #WorldNFDay. NF refers to neurofibromatosis type 1 and type 2, genetic conditions that cause tumors to grow on nerves throughout the body. @ChildrensTumor is working on their awareness campaign to ‘Make NF Visible.’ Learn more here:
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@CurePSP
CurePSP
3 years
Join us on 5/17 for Community Conversations - Legislative Advocacy for PSP, CBD and MSA. Our guest speakers will share their experiences and insights on creating change in our community. Let's make a difference together! Register today! https://t.co/g1AdQbXGNp #HopeInAction
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@_allstripes
AllStripes
3 years
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@_allstripes
AllStripes
3 years
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@_allstripes
AllStripes
3 years
May is @CurePSP Month of Awareness. We asked our PSP Ambassadors to share what they wish more people knew about #ProgressiveSupranuclearPalsy. #HopeInAction #BecauseHopeMatters (1/3)
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@RaremindsUK
Rareminds
3 years
Sadly this is not surprisingly - the interim results for our #Rare Mental Health Survey 2023 show that 76.3% of respondents report never having #MentalHealth support or signposting offered by their health care providers. #MentalHealth #MentalHealthAwareness #RareMindsMatter
@_allstripes
AllStripes
3 years
It’s #MentalHealthAwarenessWeek. A study by BCM Health Services Research found that out of 1,800 rare patients & caregivers living in the UK, less than 50% were asked by healthcare professionals about their mental health or emotional well-being.
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