The MdDS Foundation is dedicated to finding the cause and cure for Mal de Débarquement Syndrome through educational efforts and research support.
International
Joined February 2011
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🎉The MdDS Patient Registry is in the final stages of preparation for launch! This milestone brings us one step closer to collecting vital patient data that will help advance research into this complex disorder. Find out more on our website at mddsfoundation.org/mdds-pati…
MdDS Foundation retweeted
1/ Experiencing prolonged dizziness after water or air travel? It may be due to Mal de Débarquement Syndrome (MdDS). Follow along this purely educational thread to learn more! 🧵 🌊
#MaldeDebarquement #MdDS #chronicdizziness
MdDS Foundation retweeted
June is also MdDS Awareness Month. I’ve had this since 2019 and it’s so fitting that I’m home today bc my symptoms are too much.
𝗝𝘂𝗻𝗲 is 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵 for #MdDS. While we work hard year-round, focusing efforts to educate the public during June is an effective way to spread awareness and foster understanding of MdDS. Join & add your voice for greater impact! mddsfoundation.org/share-you…
Living with #chronicillness like #MdDS can be a daily challenge. Add highly variable symptom severity to that and it's 🤯. Use our NEW symptom severity scale to help your doctors understand. mddsfoundation.org/introduci…
The #mddsfoundation is dedicated to finding the cure and cause for MdDS. Like and Follow us on Facebook and Instagram. And keep visiting mddsfoundation.org for #MdDS announcements & research updates.
ALT Description of what MdDS is. An image of a brain represents neurological basis. Several award badges are displayed along the bottom with social media locations.
We're proud to be a member of the @AmericanBrainCo!
Tomorrow! Don't miss out on your chance to attend our 2024 Annual Membership Meeting! Register for virtual or in person: bit.ly/3XpCGhR. #AnnualMeeting #BRAIN
The #mddsfoundation is dedicated to finding the cure and cause for MdDS. Like and Follow us on Facebook and Instagram. And keep visiting mddsfoundation.org for #MdDS announcements & project updates.
MdDS Foundation retweeted
🚨 Less than one week left to apply for the 2025 AAN Research Program!
Opportunities are available for different types of research across career levels and discovery stages. Learn more and apply by September 10: bit.ly/3X3hjo3
#ResearchFunding #NeuroTwitter
#AANMember? Interested in #neurologicalresearch? Research Funding is Available through a #ClinicalResearch Training Scholarship. Deadline 9/10. Visit @AANmember site to apply. aan.com/research/clinical-re…
2025 grant apps close on the 10th. Opportunities are available in #ALD, #ALS, #cognitive aging, epilepsy, FTD, #MdDS, #neuromuscular disease, #Parkinsonsdisease… through the @AANmember Research Program. Full listing at aan.com/research/aan-researc…
MdDS Foundation retweeted
🔬🔬🔬 Applications for our 2025 Next Generation Research Grants are now open! americanbrainfoundation.org/…
Over $1.7M total available across 11 awards for early-career clinician-scientists worldwide.
Share with friends & colleagues!
#ResearchFunding #Neuroscience #CureOneCureMany
#AANMember? Interested in #neurologicalresearch? Research Funding is Available through this #ClinicalResearch Training Scholarship. aan.com/research/clinical-re…
#AANMember? Interested in #neurologicalresearch? Research Funding is Available through this #ClinicalResearch Training Scholarship.
🔗 Link to scholarship details on the @AANmember site: aan.com/research/clinical-re…
MdDS Foundation retweeted
NINDS Nonprofit Forum 2024 is underway! Beginning with opening remarks by NINDS Director, Dr. Walter Koroshetz. #NINDS #ABrainCoProud @NINDS
MdDS Foundation retweeted
New findings on the global impact of brain disease make it painfully clear that the work we are doing to support as many brain disease research projects as possible is incredibly critical. Learn more: americanbrainfoundation.org/…
MdDS Foundation retweeted
A donor who believes so strongly in our mission is matching every gift we receive if we can raise $500K by 12/31. Take this chance to double your donation: AmericanBrainFoundation.Org/…
3.4B people live with brain disease. Double your impact with a gift to fund research today!
Can you relate? This story is for everyone who struggles with an #invisibledisability or #invisibledisorder.🧠
#thestruggleisreal #mddsawarenessmonth #ontheblog #mddsjam 🔁PLS RT➡️mddsfoundation.org/2024/06/3…
#PatientAdvocacy is a key component of the MdDS Foundation's Mission. #MdDSFriends is a private, online support group that we provide as a service to over 7,500 members. Here's why it matters! mddsfoundation.org/2024/06/2…
