PPMD Supports Secretome Therapeutics with $250,000 for Cardiac Cell Therapy Development Parent Project Muscular Dystrophy has invested $250,000 in Secretome Therapeutics to advance cardiac therapy for Duchenne muscular dystrophy. This funding aims to enhance treatment avenues for a critical health issue.

PPMD Supports Secretome Therapeutics with $250,000 for Cardiac Cell Therapy Development #United_States #Washington #PPMD #Secretome #Cardiac_Therapy

Celebrating the 2026 Advocacy Leadership Awards for Duchenne Research Leaders The 2026 Advocacy Leadership Awards recognize key bipartisan leaders in Congress advocating for Duchenne muscular dystrophy research and care advancements.

Celebrating the 2026 Advocacy Leadership Awards for Duchenne Research Leaders #United_States #Washington #Duchenne #PPMD #FED

Advocates Rally in Washington to Enhance Duchenne and Becker Policy, Celebrating 25 Years of the MD-CARE Act In a momentous gathering, advocates mark 25 years of the MD-CARE Act, pushing for critical Duchenne and Becker policy advancements at the Capitol.

Advocates Rally in Washington to Enhance Duchenne and Becker Policy, Celebrating 25 Years of the MD-CARE Act #United_States #Washington #PPMD #Duchenne_Advocacy #MD-CARE_Act

PPMD Partners with CINRG to Enhance Duchenne Natural History Study PPMD has teamed up with the Cooperative International Neuromuscular Research Group to enrich the Duchenne Natural History Study, driving insights for better care.

PPMD Partners with CINRG to Enhance Duchenne Natural History Study #United_States #Washington #Duchenne #PPMD #CINRG

PPMD Celebrates a Victorious Weekend at the 2026 Disney Marathon in Orlando At the 2026 Walt Disney World® Marathon Weekend, PPMD achieved remarkable success by raising $300,000 and securing two race victories.

PPMD Celebrates a Victorious Weekend at the 2026 Disney Marathon in Orlando #United_States #Orlando #Duchenne #PPMD #Jack_Napoli

U.S. Health Department Includes Duchenne in Newborn Screening Panel for Early Detection The U.S. Department of Health and Human Services has included Duchenne muscular dystrophy in the newborn screening panel, enhancing early care for affected infants.

U.S. Health Department Includes Duchenne in Newborn Screening Panel for Early Detection #United_States #Washington #Duchenne #PPMD #MDA

Duchenne affects more than muscles—it impacts learning, mood, and behavior too.
Prioritizing mental health is essential to whole-person care. 💙
#Duchenne #PPMD #MentalHealth

Celebrating Two Decades of Hope: Sam's Night Marks a Milestone for Duchenne Community The Killian family celebrates 20 years of Sam's Night, an event that has raised over $10 million for Duchenne research and care, showcasing community resilience and hope.

Celebrating Two Decades of Hope: Sam's Night Marks a Milestone for Duchenne Community #United_States #Rockwall #Duchenne #PPMD #Sam's_Night

Preeclampsia - Birth Trauma Resources Between 25 and 34 percent of women report that their births were traumatic.

Women who have endured traumatic pregnancies such as severe #preeclampsia #eclampsia #HELLPsyndrome have a higher incidence of #PTSD #PPMD than women without these complications.

Access our birth trauma resources here: www.preeclampsia.org/birth-trauma-resources

#WorldMentalHealthDay

Celebrating World Duchenne Awareness Day with Bad Shirt Friday and UN Premiere Join Parent Project Muscular Dystrophy in celebrating World Duchenne Awareness Day on September 7, 2025, with events like Bad Shirt Friday and a special UN documentary.

Celebrating World Duchenne Awareness Day with Bad Shirt Friday and UN Premiere #United_States #Washington #Duchenne #PPMD #Bad_Shirt_Friday

Rockford's Mitchell's Run Celebrates 27 Years with a Heartfelt Dedication Ceremony The 27th Annual Mitchell's Run Thru Rockford honors its legacy with a special memorial for Mitchell Peterson, raising funds for Duchenne muscular dystrophy research.

Rockford's Mitchell's Run Celebrates 27 Years with a Heartfelt Dedication Ceremony #USA #Rockford #Duchenne #PPMD #Mitchell's_Run

Parent Project Muscular Dystrophy Bolsters Leadership to Enhance Community Support and Treatment Advancements The Parent Project Muscular Dystrophy (PPMD) is enhancing its leadership team to better serve the Duchenne and Becker muscular dystrophy community, appointing Katherine Beaverson as CEO.

Parent Project Muscular Dystrophy Bolsters Leadership to Enhance Community Support and Treatment Advancements #USA #Washington #Duchenne #PPMD #Muscular_Dystrophy

Several peer-reviewed research studies suggest that women who have endured traumatic pregnancies such as severe #preeclampsia #eclampsia #HELLPsyndrome have a higher incidence of #PTSD and #PPMD than women without these complications

www.preeclampsia.org/birth-trauma...

Several studies suggest that women who have endured traumatic pregnancies have a higher incidence of #PTSD #PPMD than women without #preeclampsia #eclampsia #HELLPsyndrome. Here are 7 tips to help cope.

www.preeclampsia.org/the-news/com...

Unite, Learn, and Inspire: The 2025 Parent Project Muscular Dystrophy Conference in Las Vegas The Parent Project Muscular Dystrophy's Annual Conference in Las Vegas promises connection, knowledge, and innovation to uplift the Duchenne community.

Unite, Learn, and Inspire: The 2025 Parent Project Muscular Dystrophy Conference in Las Vegas #United_States #Las_Vegas #Duchenne #PPMD

Children's Hospital of Philadelphia Celebrated as Pioneer Duchenne Care Center by Parent Project Muscular Dystrophy Parent Project Muscular Dystrophy (PPMD) names Children's Hospital of Philadelphia as a certified Duchenne Care Center, emphasizing its commitment to care and research.

Children's Hospital of Philadelphia Celebrated as Pioneer Duchenne Care Center by Parent Project Muscular Dystrophy #United_States #Philadelphia #CHOP #Duchenne #PPMD

Updated PJ Nicholoff Steroid Protocol Enhances Duchenne Care Standards Parent Project Muscular Dystrophy unveils a vital update to the PJ Nicholoff Steroid Protocol, enhancing care standards for Duchenne patients.

Updated PJ Nicholoff Steroid Protocol Enhances Duchenne Care Standards #United_States #Washington #Duchenne #PPMD #steroid_protocol

I have #ADHD.

I don't have #Autism. Or #dyslexia, or other learning disabilities. Or #CPTSD (not debilitating, anyway). Or #hypermobility. Or crippled by #PPMD today.

Doesn't mean I can't listen to the people who do, stand with them, & advocate for them, when most impacted by policy changes.

Advocacy Rally in Washington D.C. for Duchenne Muscular Dystrophy Reforms More than 150 advocates gather in Washington D.C. for the PPMD Advocacy Conference, pushing for critical Duchenne muscular dystrophy reforms and funding.

Advocacy Rally in Washington D.C. for Duchenne Muscular Dystrophy Reforms #United_States #Washington_D.C. #Advocacy #Duchenne #PPMD

Parent Project Muscular Dystrophy to Host 2025 Summit for Duchenne Healthcare Experts in San Diego, California The 2025 Duchenne Healthcare Professionals Summit hosted by PPMD will unite leading experts to discuss innovations in Duchenne care and research in San Diego.

Parent Project Muscular Dystrophy to Host 2025 Summit for Duchenne Healthcare Experts in San Diego, California #United_States #San_Diego #Duchenne #PPMD #Healthcare_Summit

Celebrating 20 Years of the Race to End Duchenne Program's Impact on Lives The Race to End Duchenne program marks its 20th anniversary with a record of over $18 million raised for Duchenne research, transforming lives.

Celebrating 20 Years of the Race to End Duchenne Program's Impact on Lives #United_States #Orlando #Duchenne #PPMD #Race_to_End_Duchenne

PPMD poster
#smashbros #ssbm #PPMD #melee

A6: #IBCLCs work to support working #parents, reduce incidence of early weaning and #PPMD postpartum mood disorders #NPHWChat