Nigeria's only awareness walkathon for Pulmonary Hypertension. A program of @Cardiaccomm #PHNOBEJOKE #YouSabiPH #Walk4PH
Lagos, Nigeria
Joined March 2021
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Walk4PH retweeted
Hello lagos , join @Walk4ph first physical PHabulous Meetup happening in Lagos! On
Fri, December 4th 2026 🤲 location is at
SICKLE CELL CENTRE, Idi-Araba
People living with pulmonary hypertension, caregivers and families, come connect, learn and be supported ❤️
Register for free via : tinyurl.com/MeetPHabulous
Walk4PH retweeted
🌍 Across continents, the PH community deserves to be seen, heard and supported.
This November, PHAEUROPE & Global stands with PHA USA! 🤝 “Pieces of Hope” and “Living Under Pressure” unite us in turning awareness into understanding and hope. 💙
#PHAwarenessMonth #PHCommunity
Walk4PH retweeted
🫁💙 5 GROUPS OF PH. INFINITE PIECES OF HOPE.
Different challenges. Shared hope.
🧩 Group 1: Targeted therapies transform PAH care.
🧩 Group 2: Heart failure and valve care address underlying causes.
🧩 Group 3: PH-ILD therapy has shown gains in exercise capacity.
1/2⤵️
Walk4PH retweeted
“My piece of hope came from someone I never knew.” 🫁💙
After 7 years living with PAH, Natalia received a life-saving double lung transplant in Vienna. A decade later, she is breathing freely and advocating for patients globally as a board member of @PHAEurope.⤵️
Walk4PH retweeted
🇭🇺💙 #goodPHnews from Hungary!
At Budapest’s 2nd Hungarian Health Picnic, Tüdőér Egylet PH raised awareness through interactive breathing activities and powerful patient stories. 🫁
👏 Congratulations to our Hungarian colleagues for making every breath and every voice count!
Walk4PH retweeted
Pulmonary Hypertension (PH) isn’t always visible. 💙
This Invisible Disabilities Week, let’s listen, believe, and support without judgment.
Join our PHabulous community and get updates about our first meetup in Lagos.
#InvisibleDisabilitiesWeek #PulmonaryHypertension
Walk4PH retweeted
🧠 What stands between a happy face and a sad face? 😊😔
For many living with pulmonary hypertension (PH), it’s an invisible burden. Research suggests 37% experience anxiety and 28% depression.
💙 On #WorldMentalHealthDay, let’s care for the mind as well as the heart and lungs.
Walk4PH retweeted
World Heart Day ❤️
PH doesn't only affect the lungs. It can place significant strain on the heart, making timely diagnosis and access to appropriate care essential.
This #WorldHeartDay, we're supporting the theme "Don't Miss a Beat" by raising awareness of PH and encouraging people to learn more about the condition.
Whether you're newly diagnosed, supporting a loved one, or looking for trusted information, our PH resources can help.
📚 Learn about PH: pvrinstitute.org/living-ph/w…
🤝 Explore patient resources: pvrinstitute.org/PH-patient-…
🌍 Find support locally: pvrinstitute.org/living-ph/f…
Walk4PH retweeted
Europe needs a stronger, shared commitment to lung health. 🫁
A European Lung Health Plan can bring prevention, early diagnosis, access to care and investment together — while tackling stigma and protecting future generations.
Our policy is to #KeepBreathing.
#ELHG #PHAEurope
Walk4PH retweeted
❤️ 29 September – World Heart Day | #DontMissABeat
Every heartbeat matters — and so does the circulation that connects the heart and lungs.
Cardiovascular disease remains the world’s leading cause of death, but many risk factors can be prevented or managed through awareness, ⤵️
Walk4PH retweeted
What barriers limit cardiopulmonary rehab in Africa? Join us to explore practical solutions with experts from Nigeria, Malawi & DRC.
📅 25 Sept | 4 PM WAT 🔗 bit.ly/CPRehabAfrica2026📌 Members: This webinar serves as our Sept MGM!
#HeartHealth #CardioTwitter
Walk4PH retweeted
❓️ Why do clinical trials matter for patients?
Clinical trials help improve treatments, advance research, and improve care for people living with PH.
In the second video of our 'Understanding clinical trials' PH patient resource collection, Louise Bouman from Alliance for PH explains why clinical trials matter and how research helps shape the future of PH care.
🎥 Watch the full series: pvrinstitute.org/PH-patient-…
Developed by PVRI's Patient Engagement & Empowerment Workstream.
Walk4PH retweeted
Raising awareness on Pulmonary Hypertension in Nigeria via @walk4ph >>>
Walk4PH retweeted
Your 5h, 1k or or any amount could help a pulmonary hypertension patient survive
Account Name: Cardiac Community Advocacy Support
Account Number: 1017538126
Bank: Zenith Bank
Walk4PH retweeted
Brooke │ Hungary
#HopeInEveryTrial
“ I am a pulmonary arterial hypertension patient from Canada, diagnosed in 2014. Living with PAH means facing uncertainty every day. For me, advocating for clinical research was never only about new treatments. It was about being part of ⤵️
Walk4PH retweeted
WHY I CAME BACK HOME
After almost 30 years in the United States working as an Interventional Cardiologist, people still ask me why I returned to Nigeria.
Every day at Tristate Hospital, Lekki, I am reminded that my return to Nigeria was not just a career decision. 1/8
Walk4PH retweeted
Natalia │ Argentina
#HopeInEveryTrial
“I live in Córdoba, Argentina, and 10 years ago I was diagnosed with Pulmonary Hypertension. When my doctor invited me to join a clinical trial, I accepted immediately — for myself, my children, and patients worldwide. I didn’t know if⤵️
Walk4PH retweeted
S/O to everyone who made it possible , #walk4ph2026 is definitely gonna be remembered! One more thing , y’all should help us keep spreading the word about PULMONARY HYPERTENSION . #PHNOBEJOKE
We'd like to thank all the organizations who made walk4PH 2026 possible. Thank you for the unwavering support and your invaluable contributions toward the success of Walk4PH 2026. 💙
This event would not have been possible without organizations and brands who believed in our mission, stood with the Pulmonary Hypertension community In Nigeria, and chose to be part of something bigger than themselves. Your generosity, commitment and selfless support helped us create a meaningful day of awareness, advocacy, hope, and impact.
Because of your support, more conversations were started, more lives were touched, and more people now know that pulmonary hypertension deserves attention, care, and action.
Thank you for walking with us, believing in us, and helping make Walk4PH 2026 a success.
Walk4PH retweeted
Dora │ Hungary
#HopeInEveryTrial
“My name is Dora, and I live in Hungary with pulmonary hypertension. When existing treatments no longer worked well for me, joining a clinical trial became a new direction — and a new hope. It required time, tests, and commitment, but it also⤵️
