Haemophilia Patients Welfare Society - Rawalpindi

Haemophilia Patients Welfare Society - Rawalpindi We treat haemophilia patients and help raise awareness about inherited bleeding disorders Registration was renewed in 2003.

The Pakistan Hemophilia Patients Welfare Society (PHPWS), Rawalpindi/Islamabad Chapter was founded in 1991 as a non- profit organization and registered under the Voluntary Social Welfare Agencies Registered and Control ordinance, 1961 (XLVI of 1961). It is a dynamic voluntary, non- profit philanthropic organization established for people with Hemophilia, supported by the collective efforts of a gr

oup of dedicated and committed volunteers, medical specialists, hemophilia patients and their relatives . The absence of medical treatment, preventive as well as curative causes immense problems, emotional as well as financial, for patients and their families. The PHPWS, Rawalpindi/ Islamabad Chapter was initially setup with the idea of helping Hemophilia patients from Rawalpindi and Islamabad . However, within a short span, patients started coming from surrounding towns and villages, Gilgit , Baltistan, Federally Administered Tribal Areas (FATA) and Azad Jammu and Kashmir (AJK) . The Chapter has developed a network with NGOs and other organizations supporting similar initiatives for the prevention, management and rehabilitation of patients with inherited bleeding disorders. PHPWS Rawalpindi/Islamabad Chapter provides free professional advice and medical assistance at very nominal rates to hemophilia patients. Due to linkages in Rawalpindi and Islamabad our patients get admitted easily in Haemophilia Friendly Hospitals such as Pakistan Institute of Medical Sciences (PIMS) Holy Family Hospital and District Headquarters Hospital. A strong component of the advice given is not only what to do in emergencies and how to prevent complications but also how to reduce the occurrence of Haemophilia in their families. In the process of treatment the Society realized the need for going beyond hemophilia, and an emphasis was also put on community mobilization and awareness raising with enrolment of volunteers so that the community is made aware of all kinds of blood disorders including HIV/AIDS and related health issues included mother and child health . The Chapter also has strong links with other Chapters in the country and with the World Federation of Hemophilia (WFH) based in Montreal, Canada.

Students of CUST University Visit Hemophilia Patient Welfare Society!Today, passionate students from Capital University ...
18/08/2025

Students of CUST University Visit Hemophilia Patient Welfare Society!

Today, passionate students from Capital University of Science and Technology (CUST) visited the Hemophilia Patient Welfare Society to learn how we support patients with bleeding disorders.

They received a detailed briefing on:
🔹 How we provide treatment.
🔹 Our ongoing Welfare projects.
These students learned how they can play an active role:

🤝 Through Awareness.
By Organizing seminars or sessions in their universities

Sharing patient stories and facts on social media
Fundraising.

Together, we can create a more informed and inclusive society. 🌍
We thank these future changemakers for stepping forward in support of the bleeding disorder community.

13/08/2025
Congratulations to Muhammad Ashir Aziz, a resilient patient of Hemophilia B (Factor IX deficiency) and a proud beneficia...
04/08/2025

Congratulations to Muhammad Ashir Aziz, a resilient patient of Hemophilia B (Factor IX deficiency) and a proud beneficiary of Hemophilia Patient Welfare Society, for scoring an impressive 1078 out of 1200 marks!

Ashir's success is a powerful reminder that with the right support, medical care, and determination, nothing is impossible not even for those living with rare bleeding disorders.

We are proud to stand beside Ashir and all our warriors who continue to break barriers every day!

With heartfelt gratitude, HPWS Rawalpindi extends sincere thanks to Ms. Nazia Mushtaq and Mr. Tahir Mushtaq for their ge...
31/07/2025

With heartfelt gratitude, HPWS Rawalpindi extends sincere thanks to Ms. Nazia Mushtaq and Mr. Tahir Mushtaq for their generous donation and continued support. Ms. Nazia beautifully carries forward her father's legacy by standing beside our mission, a true inspiration of compassion and commitment.

Hemophilia Patient Welfare Society,Rawalpindi at Beaconhouse Internship Fair at Margalla Campus .We’re proud to share th...
25/06/2025

Hemophilia Patient Welfare Society,Rawalpindi at Beaconhouse Internship Fair at Margalla Campus .

We’re proud to share that the Hemophilia Patient Welfare Society participated in the Beaconhouse Internship Fair, offering summer internship opportunities to students!

Through this internship, students will:
🔹 Learn about bleeding disorders
🔹 Support awareness campaigns
🔹 Help raise funds for patients in need

We’re excited to engage passionate youth in making a real impact in the lives of those living with bleeding disorders.

07/06/2025
🌍✨ Proud Representation at Global Platform! ✨🌍The World Federation of Hemophilia (WFH) recently organized an impactful 3...
05/06/2025

🌍✨ Proud Representation at Global Platform! ✨🌍

The World Federation of Hemophilia (WFH) recently organized an impactful 3-day workshop in Cambodia, focusing on Inhibitor Management and Novel Therapies. Hematologists and experts from over 10 countries gathered to share knowledge, advancements, and strategies for improving care for people with bleeding disorders.

We are proud to share that Dr. Lubna Zafar represented Hemophilia Patients Welfare Society (HPWS) Rawalpindi, Pakistan, at this prestigious event! 🇵🇰

Her participation highlighted Pakistan’s ongoing efforts in advancing care, raising awareness, and advocating for the rights of individuals living with inherited bleeding disorders.

This global exchange of knowledge is a crucial step towards better treatment options, improved patient outcomes, and a stronger international network of support.
World Federation of Hemophilia

Under the banner of HPWS,RWP , Hifazat Najam is a heartfelt initiative that offers free treatment to individuals with bl...
20/05/2025

Under the banner of HPWS,RWP , Hifazat Najam is a heartfelt initiative that offers free treatment to individuals with bleeding disorders. Our mission is to spread smiles, healing, and light in the lives of those who need it most. Together, we believe every drop matters and every life counts.

Address

Thalassaemia House
Rawalpindi

Opening Hours

Monday 09:00 - 14:30
Tuesday 09:00 - 14:30
Wednesday 09:00 - 14:30
Thursday 09:00 - 14:30
Friday 09:00 - 14:30
Saturday 09:00 - 14:30

Telephone

+92518432751

Website

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The Hemophilia Patients Welfare Society (HPWS) - Rawalpindi was founded in 1991 as a non- profit organization and registered under the Voluntary Social Welfare Agencies Registered and Control ordinance, 1961 (XLVI of 1961) in 2003. It is a dynamic voluntary, non- profit philanthropic organization established for people with Hemophilia, supported by the collective efforts of a group of dedicated and committed volunteers, medical specialists, hemophilia patients and their relatives . The absence of medical treatment, preventive as well as curative causes immense problems, emotional as well as financial, for patients and their families. The HPWS - Rawalpindi was initially setup with the idea of helping Hemophilia patients from Rawalpindi and Islamabad . However, within a short span, patients started coming from surrounding towns and villages, Gilgit , Baltistan, Federally Administered Tribal Areas (FATA) and Azad Jammu and Kashmir (AJK) . The Chapter has developed a network with NGOs and other organizations supporting similar initiatives for the prevention, management and rehabilitation of patients with inherited bleeding disorders. HPWS - Rawalpindiprovides free professional advice and medical assistance at very nominal rates to hemophilia patients. Due to linkages in Rawalpindi and Islamabad our patients get admitted easily in Haemophilia Friendly Hospitals such as Pakistan Institute of Medical Sciences (PIMS) Holy Family Hospital and District Headquarters Hospital. A strong component of the advice given is not only what to do in emergencies and how to prevent complications but also how to reduce the occurrence of Haemophilia in their families. In the process of treatment the Society realized the need for going beyond hemophilia, and an emphasis was also put on community mobilization and awareness raising with enrolment of volunteers so that the community is made aware of all kinds of blood disorders including HIV/AIDS and related health issues included mother and child health . The Chapter also has strong links with other Chapters in the country and with the World Federation of Hemophilia (WFH) based in Montreal, Canada.