Wylder Nation Foundation

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WARRIORS in the Fight Against Lysosomal Storage Disorders. WARRIORS in the Fight Against Lysosomal Storage Disorders WYLDER NATION FOUNDATION IS DETERMINED TO IMPROVE THE LIVES OF CHILDREN DIAGNOSED WITH LYSOSOMAL STORAGE DISORDERS AND PROVIDE HOPE BY ACCELERATING THE DISCOVERY AND DEVELOPMENT OF TREATMENT OPTIONS.

Founded

2013

Facebook

994

X (Twitter)

146

Address

Scottsdale

Address: 8924 E Pinnacle Peak Rd Ste G5-57, ScottsdaleWeb: Sign in to see organisation websiteFacebook: WylderNationX (Twitter): WylderNationEmployees: 1Volunteers: 8Revenue: 277661ICO: 462849095

Home : Wylder Nation Foundation WARRIORS in the fight Against Niemann Pick Disease Our Mission To improve the lives of children living with a Lysosomal Storage Disease LSD. We remain laser focused on accelerating the discovery and development of treatment options for these diseases with significant unmet medical needs. Our current focus is on Acid Sphingomyelinase Deficiency ASMD also referred to as Niemann Pick Disease Types A B NPA NPB. 48 50 7700 Help advance ASMD research without leaving your house Honor or Remember the WARRIOR in your life Join Us In The FIGHT Get Your Wylder NationHurley Hope Gear Today News Notes Wylder Nation Picnic Health launch ASMD Accelerate study FAAH inhibition to treat ASMD Inhibition of fatty acid amide hydrolase prevents pathology in neurovisceral acid sphingomyelinase deficiency by rescuing defective endocannabinoid signaling Molecular Genetics and Metabolism Reports 24 2020 Clinicopathologic correlations of a case report of a child with NPA Our Warriors Privacy Policy Terms Conditions Donation Refund Policy Automated Recurring Donation Cancellation Powered by Firespring .

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News about from their social media (Facebook and X).

Andrew

๐Ÿ’œ Together, we can make a difference! Honoring all the brave warriors fighting against Lysosomal Storage Disorders. Letโ€™s support Wylder Nation Foundationโ€™s mission to bring hope and healing! #WarriorsInTheFight

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Michelle

๐ŸŒŸ Every small action counts! Whether itโ€™s spreading awareness or donating, we can all play a part in improving the lives of children with Niemann Pick Disease. Join the fight with Wylder Nation Foundation! #HopeForASMD

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Hannah

What innovative fundraising strategies can NGOs like Wylder Nation Foundation implement to raise awareness and support for rare diseases like Niemann-Pick Disease?

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Wylder Nation Foundation

Merry Christmas from our home to yours. Giving gratitude to all of you who are a part of Wylder Nation. Without you, change would not have been โ€ฆ and continue to be possible.

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Wylder Nation Foundation

Wylder Nation WARRIORS donโ€™t miss your chance to join us in San Fransisco for a fun day of golfing. All for one amazing cause in memory of WARRIOR Purnell. Save Purnell Today Early Bird signups are available now for single golfers, twosomes and foursomes.

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Cathy

How can community engagement and volunteerism be fostered to create a strong support network for families affected by Lysosomal Storage Disorders?

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