PVNH Support

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PVNH Support

PVNH Support

@PVNHsupport

International community for Periventricular Nodular Heterotopia(PVNH),GMH,SBH disorders. Unite.Educate.Research. Find a cure. #PVNH #FLNA #MarchOnPVNH @PVNHday

Vancouver 가입일 Ocak 2012
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PVNH Support
PVNH Support@PVNHsupport·
Super excited to release a new episode of our #podcast Misplaced Neurons, featuring Sarah Ayala and her daughter Elani, on this #MarchOnPVNH Monday. Thank you Sarah for your advocacy, your raw honesty and for being the wonderful mom you are! youtu.be/L-2obfjRi98?si… #PVNH
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PVNH Support
PVNH Support@PVNHsupport·
Thank you to International League Against Epilepsy (@IlaeWeb) for the update!
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PVNH Support
PVNH Support@PVNHsupport·
There are still too many babies affected by PVNH / FLNA deficiency lung disease that do not survive. It breaks our hearts. Hopefully, the parents got the support they need. We are so sorry for their immense loss. We'll always be there for support. #FLNAlungdisease
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PVNH Support
PVNH Support@PVNHsupport·
@MarkELindsay Thank you for helping to bring awareness to X-linked PVNH/ FLNA deficiency lung disease! 🩷💛🩷
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Ismail A. Ibrahim
Ismail A. Ibrahim@ismailamehesen·
Big thanks to my amazing Global Alliance of Young Researchers team members and supporters! 👏 - Milad Shenno - Almonzer Al-Qiami - Lojin Elhaw - Abdulqadir Nashwan You can access the publication here: doi.org/10.1016/j.inat…
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Ismail A. Ibrahim
Ismail A. Ibrahim@ismailamehesen·
Thrilled to share that our manuscript, "A Rare Presentation of Bilateral Periventricular Nodular Heterotopia with Intra-axial Pontine Lesion: A Case Report and Treatment Approach," has been accepted and PUBLISHED! ❤️ ✨
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UNE COM
UNE COM@com_at_une·
Last month student doctor Sarah Khan, OMS 2, presented her abstract, "Potential New Genetic Variant in Periventricular Nodular Heterotopia," at the Massachusetts Neurologic Association Conference in Waltham, MA under the mentorship of Dr. Alexandra Filippakis.
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PVNH Support
PVNH Support@PVNHsupport·
Will you join in and wear pink and/or yellow in support of impacted families, and ask us about World PVNH Day, PVNH, GMH, and SBH? 🩷💛🩷 #BecauseWeCan
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PVNH Support
PVNH Support@PVNHsupport·
2/2 impacted your view on the PVNH, GMH, or SBH diagnosis you or your loved one lives with? #PVNH #GMH #SBH #Hope
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PVNH Support
PVNH Support@PVNHsupport·
1/2 #MarchOnPVNH It is fitting we end this month on hope. Hope is the one thing we all have that carries us through the hard days. Hope of relief for our afflicted loved ones, hope for greater research and answers, and hope for an eventual cure. How has hope for the future
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PVNH Support
PVNH Support@PVNHsupport·
3/3 brings comfort and greater resources for others struggling and their families. Share your experiences in advocating for yourself or your loved one with PVNH, GMH or SBH and how you bring awareness! #PVNH #GMH #SBH #Awareness #Advocacy
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PVNH Support
PVNH Support@PVNHsupport·
2/3 we constantly advocate for ourselves and our children, whether for recognition of symptoms, care solutions, or for therapy, services, medical needs and more. We raise awareness to tese disorders so others don’t have to start from square one like many families do. It also
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PVNH Support
PVNH Support@PVNHsupport·
1/3 #MarchOnPVNH Awareness & Advocacy Raising awareness for PVNH, GMH and SBH is critical for a number of reasons : 1) quicker diagnosis 2) improved care and 3) the ultimate goal of funding research for a cure! As adults affected or parents of children affected by the disorder,
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