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 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 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.

School of Dentistry, in collaboration with PIMS and Hemophilia Patient Welfare Society, Rawalpindi, organized an awarene...
03/12/2025

School of Dentistry, in collaboration with PIMS and Hemophilia Patient Welfare Society, Rawalpindi, organized an awareness seminar on bleeding disorders for dentists.
Grateful to all participants for helping promote safer dental care for patients with inherited bleeding disorders.

09/11/2025
Visit of Punjab Healthcare Commission Team .We were honored to host the Punjab Healthcare Commission Team at HPWS Rawalp...
30/10/2025

Visit of Punjab Healthcare Commission Team .

We were honored to host the Punjab Healthcare Commission Team at HPWS Rawalpindi. This visit marks a significant milestone for our society as we continue working toward improved care and standards for patients with bleeding disorders.
🀝

A Heartfelt Thank You to Miss Fozia Parveen! We are deeply grateful to Miss Fozia Parveen, a continuous donor and true s...
21/10/2025

A Heartfelt Thank You to Miss Fozia Parveen!

We are deeply grateful to Miss Fozia Parveen, a continuous donor and true supporter of the Hemophilia Patient Welfare Society. Her kindness and dedication have brought hope and relief to countless patients and families fighting bleeding disorders.

Your generosity reminds us that real heroes don’t wear capes they extend helping hands.
Thank you, Miss Fozia, for being a symbol of compassion and humanity.

To all our hemophilia warriors and their families: Your resilience inspires us every single day. Facing a bleeding disor...
18/10/2025

To all our hemophilia warriors and their families: Your resilience inspires us every single day.

Facing a bleeding disorder is challenging, but within our society, you will find a network of care, understanding, and shared strength. We are in this together.

Hemophilia Patient Welfare Society, Rawalpindi is here for you.

The Hemophilia Patient Welfare Society extends its heartfelt thanks to Ms. Hajira Binte Sohaib (Volunteer) for her gener...
01/10/2025

The Hemophilia Patient Welfare Society extends its heartfelt thanks to Ms. Hajira Binte Sohaib (Volunteer) for her generous donation of Rs. 100,000.

Her kindness and commitment will directly support the treatment, care, and well-being of patients living with bleeding disorders. Contributions like hers strengthen our mission and bring hope to many families.

Together, we can make a lasting difference.

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:
πŸ”Ή How we provide treatment.
πŸ”Ή 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!

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

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Our Story

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.