News & Events

Job Announcement for CEO (2024-06-20)

The Hemophilia Foundation (Pakistan) has decided to hire a Chief Executive Officer (CEO) in order to address the needs of the community.

Job Title: Chief Executive Officer [CEO]
Grade: Senior level management: Managerial position - Upper tier
Job type: Full-time: 48 hours weekly [9 am – 5 pm]

Key Requirements:
− Master's Degree in Management, Business Administration, Finance, Economics or its equivalent
− 8-10 years of successful senior leadership experience at a social impact organization
− Commitment to results; 'can-do" mindset with emphasis on accountability
− Experience in change leadership and change management
− Strong motivational and staff leadership abilities
− Excellent communication and presentation skills
− Sense of humor, integrity, impeccable work ethic
− Knowledge of dynamics related to Hemophilia and other related bleeding disorders
− Preferably an individual from the Bleeding disorders community

Last date to submit CVs: 25th June 2024


Managing Psycho-Social Aspects of Haemophilia (2018-03-17)
Haemophilia, is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.  It is widely accepted that this inherited bleeding disorder can have negative effects on the ability of the PWH to become a productive and participating members of society. 

However the aim of the PHPWS Rwp/Isb Chapter is to combat this notion and help those with Inherited bleeding disorders and lack of clotting Factors to not only cope with normal stress but the extra burden of their disease which can create various types of challenges such as marital problems, school problems, financial problems, and job worries. Women with bleeding disorders have to face even more difficulties as  marriages within families is the norm and they often stay single as no one is willing to take on the responsibility of caring for them , while and at the same time many come from conservative families and  cannot  work and become financially independent. 

Thanks to NNHF Project PK 6 and the generosity of Mr. Zammurad Khan - Patron in Chief, Pakistan Sweet Homes, we held a day-long exercise on stress management for the  registered members  of our Chapter  and their families.  Members of the Peshawar Chapter also attended the session and took active part in Session I.  The first session was for the Haemophilia Community as a whole but knowing how inherited bleeding disorders impact on women, whether they are carriers or “bleeders”, an exclusive session was held for them not only to  reinforce what they had learnt in session I but to allow them to share the problems they face as individuals and help them  can cope with life positively and effectively.

Annual General Meeting 2018 (2018-12-29)

 The Haemophilia Patients Welfare Society (Rawalpindi Chapter) had its Annual General Body Meeting at Pakistan Sweet Homes on the 29th of December 2018. Over 150 members attended making it a very successful meeting. Society’s membership consists of patients suffering from Haemophilia – a medical condition in which the ability of a person’s blood to clot is severely reduced resulting in excessive bleeding even from minor wounds. 

Haemophilia afflicts around twenty thousand people in Pakistan primarily belonging to low income segment of the society. It is causing great hardship to the patients as its treatment is costly and care facilities are very few and far between across the country.  The Haemophilia Patients Welfare Society has been providing the patients’ treatment and care at self-help basis for number of years without any government support. 

The meeting officially started with the recitation of the Holy Quran by a patient, Mr. Sajid Nawaz & a welcome address by a founding member, Dr. Tahira Zafar. She introduced the society to all those attending which included HPWS’s Board of Governers, Medical Advisory Board, Executive Board, Youth Group, Women’s Group, Save One Life beneficiaries, Staff, Patients, Donors & Volunteers. Her welcome address was followed by the passing of the Annual Report 2018 & the society’s 2017/2018 audit done by the President of the Society Dr. Munawar Sher Khan. 

Patient’s also presented their life stories and discussed their hurdles faced and how they overcame them. The first segment was then concluded by a speech from the Chief Guest Maj. General (Retd) Suhaib Ahmed - CEO GRC & a professor at Riphah University & thanking remarks by the Guest of Honor General (Retd) Pervaiz - Consultant Hematologist at Quaid-E-Azam International Hospital and Ex-Comdt AFIP/AFBMTC. They were also presented shields by the Executive Board. The first segment was officially wrapped up with the serving of refreshments for the adults whilst the children participated in drawing/painting competitions hosted by Ms. Abira Maheen. 

The second part of the meeting was patient oriented and had a in depth open panel discussion in which patients discussed their problems with the Medical Advisory Board present. This was followed by Save One Life’s (SOL) sponsorship fund distribution for its beneficiaries. SOL is an international partner of HPWS which provides sponsorship, scholarship and enterprise grant opportunities for people with bleeding disorders in developing countries. 

The meeting was supported by Mr. Zamarud Khan - Patron-In-Chief, Pakistan Sweet Homes & Ex-MD, Pakistan Bait-ul-Mal. HPWS RWP extends its gratitude to all those who attended and especially Pakistan Sweet Homes for always hosting us when needed. 

Open House 2018 (2018-09-29)

 Haemophilia Patients Welfare Society  – Rawalpindi hosted an Open House on Saturday  29th September 2018  to introduce the Society  itself  to   donors, volunteers , well-wishers and to explain to them about Haemophilia   and  what the  Haemophilia Foundation ,  Pakistan (HFP)  which is the  link  not only between the HPWS  Chapters in Karachi. Lahore, Pindi and Peshawar but also with the World Federation of Haemophilia.   

By and large it  was a successful event and  people started dropping in from 12:00 noon onwards and some even stayed  on till 5:00pm  as they  appreciated the general ambience,  met  patients,  staff and members of the Executive  Board  ,  watched a  short video which  was played on loop and  introduced Haemophilia & the Society to its viewers, and also  had interviews of our President – Dr Munawar Sher Khan, HTC Coordinator – Mr. Alamgir Khan Abbasi, patients & a few clips which included cartoons and celebrities talking about Haemophilia. 

Our patients who have their own businesses, two sponsored by Save one Life USA,  set up  stalls to highlight the fact that haemophilia is not a hindrance in any way to  their daily life.


For the first time Hemophilia Foundation-Pakistan [HFP] organized a “National Hemophilia Retreat” for Bleeding Disorder Community of Pakistan. A great opportunity to learn and become a community activist and explore the natural beauty at the same time. A big thank you to HFP-Chapters for their collaboration and facilitation by ROAM AROUND []

Youth Training Session (2018-12-28)
DECEMBER 28th, 2018
1.Recitation of Holy Quran
The session started formally with recitation of Holy Quran that was done by youth group member Mr. Ali Raza.
2.Opening Remarks
For opening remarks Dr. Tahira Zafar from hemophilia patient’s welfare society Rawalpindi formally thanked Mr Masood Fareed for taking out time from his busy schedule and for conducting this capacity building session of youth. She expressed her views and hopes regarding the youth as future leaders who will play their role in hemophilia community.
3. Setting Ground Rules
The opening remarks were followed by setting ground rules for the session that were mutually decided by the participants and the facilitator.
4. Round of Introduction
An ice breaking session of introduction was conducted by Ms. Abira Maheen in which all the members participated and realized their strengths and weaknesses and how they can work on their strengths and overcome their weaknesses.
5. Community Engagement and Empowerment
This session was conducted by Mr. Masood Fareed Malik who paid special emphasis on following;
  1. Time for oneself
  2. Personality development and grooming
  3. Communication skills
  4. Exposure and Learning opportunities
  5. Power of human mind 
  6. Importance of having a clear vision and setting goals and targets along with timeline for making that vision a reality
  7. Social interaction 
  8. Motivational talk to encourage youth for their active participation in welfare of hemophilia community
6.Team Building Exercise
This session was facilitated by Ms. Abira Maheen. Participants were divided into two teams and they were given two different topics i-e Planning for hemophilia day and fund raising. They were given time period of 20 minutes to plan and organize according to their topics and give a presentation. The participants actively participated and at the end of the session they were judged by Dr Munawwar Sher Khan, Dr. Tahira Zafar and Mr. Hassan Raza. Mr. Masood Fareed Malik gave his remarks regarding both presentations and told them how they can improve themselves further.
7.Youth Group Role in Hemophilia Society’s Success
This was a formal presentation by Mr. Masood Fareed Malik in which he shared with the members; the criteria, structure and vison of national youth group and how that can help in local youth group’s activities. He also stated the importance of role of youth in welfare of hemophilia of community.
8. Closing Remarks
Dr Munawwar Sher khan ended the session with closing remarks. She showed her gratitude towards Mr. Masood Fareed for conducting this session and she also showed her hopes regarding youth group as future leaders and volunteers who will play their role in not only spreading awareness regarding the hemophilia and other bleeding disorders but also to play their role for the welfare of this bleeding disorder community and the community as a whole.
Written By: Ms. Abira Maheen


National Patient Registry (2017-08-27)

Data Entry

|Press Release| World Hemophilia Day-2015 [PHPWS-NMO] (2015-04-17)

WORLD HEMOPHILIA DAY 2015::: Building a Family of Support on April 17, World Hemophilia Day PAKISTAN HEMOPHILIA PATIENTS WELFARE SOCIETY [PHPWS] PRESS RELEASE| Islamabad, Pakistan – 17 April 2015: Every year on April 17, World Hemophilia Day is observed around the world to increase awareness of hemophilia and other inherited bleeding disorders. This is a critical effort with an ultimate goal of ensuring better diagnosis and access to care for the millions who have a rare bleeding disorder yet remain without treatment. A significant amount of care, support, and advocacy is done through extended families which come in many forms: medical teams, friends, and colleagues, as well as immediate relatives. These communities share the ability to come together in large numbers and help improve people’s lives. World Hemophilia Day provides an opportunity to talk to your extended family and friends, colleagues, and caregivers to raise awareness and increase support for those living with an inherited bleeding disorder. “We are all working together in the fight to raise awareness and improve care.” said Hassan Raza, President-NMO, PHPWS For World Hemophilia Day 2015, PHPWS through its provincial Chapters will be organizing multiple awareness raising events in various cities across the country. In Pakistan, there are approx. 2600 people diagnosed with hemophilia. These are less than 10% of the total estimated numbers of hemophiliacs who have hemophilia in Pakistan. “We all work together, support one another, and help out when someone needs it. That is what family does for one another.” Says Masood Fareed Malik, Community Activisit, PHPWS “Join the PHPWS family and be a part of our effort to improve the diagnosis and standards of treatment for those who need it.” About hemophilia and other bleeding disorders: Hemophilia, von Willebrand disease, inherited platelet disorders, and other factor deficiencies are lifelong bleeding disorders that prevent blood from clotting properly. People with bleeding disorders do not have enough of a particular clotting factor, a protein in blood that controls bleeding, or else it does not work properly. The severity of a person’s bleeding disorder usually depends on the amount of clotting factor that is missing or not functioning. People with hemophilia can experience uncontrolled bleeding that can result from a seemingly minor injury. Bleeding into joints and muscles causes severe pain and disability while bleeding into major organs, such as the brain, can cause death. About the Pakistan Hemophilia Patients Welfare Society: For two decades, the Pakistan Hemophilia Patients Welfare Society® [PHPWS], a national level not-for-profit organization, has worked to improve the lives of people with hemophilia and other inherited bleeding disorders in Pakistan. Established in 1995, it is a network of patient organizations serving in different parts of the country and has official recognition from the World Federation of Hemophilia [WFH] as National Member Organization [NMO]. Join us on Facebook: Pakistan Hemophilia Patients Welfare Society-NMO. Contact: PHPWS | | |


World Hemophilia Day was observed with more enthusiasm and eagerness as compared to the previous years. It is celebrated to create awareness amongst society regarding Hemophilia and other Inherited Bleeding Disorders. This year, the event focused to encourage and motivate the bleeding disorder community on the theme of: "Get active for haemophilia: Picture the future" Pakistan Hemophilia Patients Welfare Society® [PHPWS] organized a national level celebration of World Hemophilia Day-2015 at Islamabad. The large number of patients in Pakistan on this World Hemophilia Day-2015 were taken to hiking camp on Margalla Hills in support of this year’s theme as it involves teamwork. On the hiking trail, several flag points were established where the patients were given different briefings/informative sessions with regards to their disease. This is a critical effort with an ultimate goal of ensuring better diagnosis and access to care for the millions who have a rare bleeding disorder yet remain without treatment.

Awareness Seminar on Patient’s Outreach - Lahore (2015-02-07)

Pakistan Hemophilia Patient’s Welfare Society® [PHPWS - NMO] has been serving the Hemophilia Community since last decade, and has been infusing all the necessary exertions to reach out, to all the patients in the country. But there is still a large gap between the number of Estimated and Registered Patients. Hence in order to address this issue of gap, this activity was premeditated, and is one of the series of the undertakings which will be apprehended to resolve this issue of gap, sanctioning us to reach out to all the Patients of Hemophilia and Other Inherited Bleeding Disorders with reference to a developing country. This was an initiative to advocate/sensitize the future Doctors and Nurses, ultimately providing them an insight with regards to Hemophilia and Other Inherited Bleeding Disorders in all the facets, with the support from NNHF – Novo Nordisk Hemophilia Foundation under the approved Project.

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