AOFAC Foundation (@aofac) 's Twitter Profile
AOFAC Foundation

@aofac

A patient advocacy group in the areas of Thrombotic Thrombocytopenic Purpura (TTP) with interest in Sickle Cell Disease&Lupus SLE. UK&Wales Regd.Charity

ID: 2311906891

linkhttp://aofacfoundation.org calendar_today26-01-2014 13:58:52

431 Tweet

94 Followers

207 Following

AOFAC Foundation (@aofac) 's Twitter Profile Photo

At our Annual #TTP Awareness last Friday - 12th September at Francia Marion University - South Carolina 🇺🇸 A big thank you to our lead and our volunteers and everyone that made it possible. We are grateful for all your supports. #TTPAwarenesseverywhere #AOFACFOUNDATION

At our Annual #TTP Awareness last Friday - 12th September at Francia Marion University - South Carolina 🇺🇸
A big thank you to our lead and our volunteers and everyone that made it possible. 
We are grateful for all your supports.
#TTPAwarenesseverywhere #AOFACFOUNDATION
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Earlier this month (3rd Sept) at our annual USP (Palmer’s College) Educational Prize giving; We awards the best student that performed excellently in their education among all odds - a Health and Social care student Congratulations to our winner for her well-deserved recognition.

Earlier this month (3rd Sept) at our annual USP (Palmer’s College) Educational Prize giving; We awards the best student that performed excellently in their education among all odds - a Health and Social care student
Congratulations to our winner
for her well-deserved recognition.
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Have your say on sickle cell & genomics research! 🧬 Help shape the Top 10 priorities by sharing what matters most to you, your family & community. Survey closes Oct 14, 2025 👉 surveymonkey.com/r/YVHCF5Q #PSP #SickleCell #Genomics #PatientVoice #ResearchMatters

Have your say on sickle cell & genomics research! 🧬
Help shape the Top 10 priorities by sharing what matters most to you, your family & community.

Survey closes Oct 14, 2025 👉 surveymonkey.com/r/YVHCF5Q

#PSP #SickleCell #Genomics #PatientVoice #ResearchMatters
Genetic Alliance UK (@geneticall_uk) 's Twitter Profile Photo

The new EURORDIS-Rare Diseases Europe Rare Barometer survey is live. Share your experience of living with a rare or undiagnosed condition, from coping with stress to support and community life. Open worldwide in 25 languages until 14 Dec 2025. Take part here: tiny.cc/RB-MH

The new <a href="/eurordis/">EURORDIS-Rare Diseases Europe</a> Rare Barometer survey is live. Share your experience of living with a rare or undiagnosed condition, from coping with stress to support and community life. Open worldwide in 25 languages until 14 Dec 2025. Take part here: tiny.cc/RB-MH
AOFAC Foundation (@aofac) 's Twitter Profile Photo

At our awareness event earlier this month at South Carolina USA 🇺🇸 A big thank you to our lead at -Florence SC USA and everyone that participated; We are grateful for all your supports. #TTPAwarenesseverywhere #AOFACFOUNDATION #TTP Meeting Point: Myrtle beach

At our awareness event earlier this month  at South Carolina USA 🇺🇸 
A big thank you to our lead at -Florence SC USA and everyone that participated;
We are grateful for all your supports.

#TTPAwarenesseverywhere #AOFACFOUNDATION #TTP
Meeting Point: Myrtle beach
AOFAC Foundation (@aofac) 's Twitter Profile Photo

At our awareness event earlier this month ( 25th October) at Florence South Carolina USA 🇺🇸 A big thank you to everyone that participated; We are grateful for all your supports. #TTPAwarenessEveryWhere #TTP #aofacfoundation2025walk #KickCancer #KickTTP Meeting Point: Florence

At our awareness event earlier this month ( 25th October) at Florence South Carolina USA 🇺🇸 
A big thank you to everyone that participated;
We are grateful for all your supports.
#TTPAwarenessEveryWhere #TTP
#aofacfoundation2025walk
#KickCancer #KickTTP
Meeting Point: Florence
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Due to unforeseen priorities, the AOFAC Foundation will pause our Annual Charity Ball this year. We will, however, gather on a smaller scale to honor our community and mission. Please consider donating at aofacfoundation.org. #TTPAWARENESSEVERYWHERE

Due to unforeseen priorities, the AOFAC Foundation will pause our Annual Charity Ball this year. We will, however, gather on a smaller scale to honor our community and mission. Please consider donating at aofacfoundation.org. #TTPAWARENESSEVERYWHERE
AOFAC Foundation (@aofac) 's Twitter Profile Photo

📣 Our “What is TTP?” poster is now up at Broomfield Hospital in the Haematology Day Unit and MAU! 🙌 Huge thanks to the teams for helping raise awareness. 💛 #TTP #BroomfieldHospital #Awareness #PatientSupport

AOFAC Foundation (@aofac) 's Twitter Profile Photo

📣 Our “What is TTP?” poster is now up at Orsett Hospital in the Haematology Day Unit and MAU! 🙌 Huge thanks to the teams for helping raise awareness. 💛 #TTP #OrsettHospital #Awareness #PatientSupport

AOFAC Foundation (@aofac) 's Twitter Profile Photo

🎄 Season’s Greetings from AOFAC Foundation! This Christmas, we celebrate the strength and unity of our TTP community and thank everyone who continues to support and inspire positive change. Wishing you peace, joy, and a hopeful New Year. ✨

🎄 Season’s Greetings from AOFAC Foundation!
This Christmas, we celebrate the strength and unity of our TTP community and thank everyone who continues to support and inspire positive change.
Wishing you peace, joy, and a hopeful New Year. ✨
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Happy New Year from AOFAC Foundation We honour our TTP survivors, patients, carers, and families. Your strength inspires us, and we remain committed to supporting you. Wishing you a healthy, peaceful year ahead. #TTPAwarenessEverywhere #TTP #Healthy #2026

Happy New Year from AOFAC Foundation
We honour our TTP survivors, patients, carers, and families. Your strength inspires us, and we remain committed to supporting you. Wishing you a healthy, peaceful year ahead.

#TTPAwarenessEverywhere #TTP #Healthy #2026
AOFAC Foundation (@aofac) 's Twitter Profile Photo

At our TTP awareness event in Chelmsford, Essex, we learned that many people—including some medical professionals—have never heard of TTP. That’s why awareness matters. Awareness saves lives. #TTPAwarenessEverywhere #TTP #AOFACFoundation

At our TTP awareness event in Chelmsford, Essex, we learned that many people—including some medical professionals—have never heard of TTP. That’s why awareness matters. Awareness saves lives.
#TTPAwarenessEverywhere #TTP #AOFACFoundation
AOFAC Foundation (@aofac) 's Twitter Profile Photo

TTP patients & survivors — your NHS experience matters. Please take 10 minutes to complete this Patient Experience Survey and help improve care for the TTP community. Share your voice here: patients-association.org.uk/share-your-exp…

TTP patients &amp; survivors — your NHS experience matters.

Please take 10 minutes to complete this Patient Experience Survey and help improve care for the TTP community.

Share your voice here:
patients-association.org.uk/share-your-exp…
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Today is Rare Disease Day focusing on #EquityforRare, we envision a world where every person affected by TTP receives equitable, timely, and accurate diagnoses, compassionate care, and an improved quality of life. Equity in care, awareness, and support is the path forward.

Today is Rare Disease Day focusing on #EquityforRare, we envision a world where every person affected by TTP receives equitable, timely, and accurate diagnoses, compassionate care, and an improved quality of life.

Equity in care, awareness, and support is the path forward.
AOFAC Foundation (@aofac) 's Twitter Profile Photo

Rare Disease Day 2026 reminds us that rare diseases affect 1 in 17 people in the UK. TTP is rare, life-threatening, and often misunderstood. Rare can mean delayed or missed diagnosis. Awareness save lives. Equity in diagnosis, specialist care and treatment must be the standard

Rare Disease Day 2026 reminds us that rare diseases affect 1 in 17 people in the UK.

TTP is rare, life-threatening, and often misunderstood.

Rare can mean delayed or missed diagnosis.
Awareness save lives.

Equity in diagnosis, specialist care and treatment must be the standard
ISTH (@isth) 's Twitter Profile Photo

📅 It’s almost time! Join us March 12 at 16:00 UTC for our TTP Guidelines Webinar on the management of congenital TTP (cTTP). Spots are filling quickly, register today: bit.ly/4bSObr8

📅 It’s almost time! Join us March 12 at 16:00 UTC for our TTP Guidelines Webinar on the management of congenital TTP (cTTP).

Spots are filling quickly, register today: bit.ly/4bSObr8
AOFAC Foundation (@aofac) 's Twitter Profile Photo

We are here for you — and with you. If you have questions about TTP or need support, please reach out. Together, we raise awareness and support those affected. #AskMeAboutTTP #TTPAwarenessEverywhere #TTP #AOFACFoundation #AwarenessIsKey #AwarenessSavesLives

We are here for you — and with you.
If you have questions about TTP or need support, please reach out. Together, we raise awareness and support those affected.

#AskMeAboutTTP
#TTPAwarenessEverywhere
#TTP
#AOFACFoundation
#AwarenessIsKey
#AwarenessSavesLives
AOFAC Foundation (@aofac) 's Twitter Profile Photo

“TTP may be rare, but awareness can save lives. Early recognition, timely diagnosis, and prompt treatment make all the difference.” Help us spread the word — awareness is key. #TTPAwarenessEverywhere #TTP #TTPSurvivors #AOFACFoundation #AwarenessMatters #AskMeAboutTTP

“TTP may be rare, but awareness can save lives. Early recognition, timely diagnosis, and prompt treatment make all the difference.”

Help us spread the word — awareness is key.

#TTPAwarenessEverywhere #TTP #TTPSurvivors #AOFACFoundation #AwarenessMatters #AskMeAboutTTP