OUR TIMINGS

Pakistan Thalassemia Welfare Society remains open from:

OPD : 8:00 to 4:00PM

DAYCARE: 8:00 to 8:00 PM

Emergency: 24Hrs

You are welcome to visit us at your convenience. You can meet the patients and the caregivers. You may donate blood for the children with thalassemia. Your blood donation will be a wonderful gift to keep them alive.

 

 

Location

Thalassaemia House
Opposite Rawalpindi Medical University
Tipu Road
Rawalpindi

 

Email

pakthalassaemia@hotmail.com
info@pathwel.org.pk

 

Phone

+92 51-5706551
+92 51-5706515

Don’t Hesitate to Contact us for any Information.

Call us for immediate support to this number

+92 51-5706515

 

Cover for Pakistan Thalassaemia Welfare Society - Regd

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Pakistan Thalassaemia Welfare Society - Regd

Pakistan Thalassaemia Welfare Society – Regd

PATHWEL is a registered society working for the welfare of Thalassaemic Patients since 1991.We have over 2000 registered patients of Thalassaemia.We provide them good quality blood Transfusion Services free of cost.


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The 5th International Meeting for People with Thalassemia will take place on May 17th at 9 P.M. (India time) and is organized by Abrasta – Brazilian Thalassemia Association, with institutional support from TIF – Thalassemia International Federation.Through an online platform segmented by age group and topics of interest, with simultaneous translation into Portuguese, English, and Spanish, the event will bring together thalassemia patients from around the world to exchange experiences.We need the support of as many patient-focused associations as possible to reach as many people as we can, so we ask for your help in sharing the following post in your social media tagging @abrasta @tif.Don’t forget to register on Abrasta’s website

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The 5th International Meeting for People with Thalassemia will take place on May 17th at 9 P.M. (India time) and is organized by Abrasta – Brazilian Thalassemia Association, with institutional support from TIF – Thalassemia International Federation.Through an online platform segmented by age group and topics of interest, with simultaneous translation into Portuguese, English, and Spanish, the event will bring together thalassemia patients from around the world to exchange experiences.We need the support of as many patient-focused associations as possible to reach as many people as we can, so we ask for your help in sharing the following post in your social media tagging @abrasta @tif.Don’t forget to register on Abrasta’s website!

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Here’s a suggested caption for an Instagram or Facebook post:“Check out 5️⃣ reasons to join the 5th International Meeting for People with Thalassemia! Share with friends and check out the details:📅 May 17th💻 Online event🕑 Starting at 9:00 P.M. (India standard time) / 12:00 P.M. (New York Time)📲 Register at: (copy the website link)The event is completely free.Be part of this amazing experience! 🌟”The image for the feed or stories post is attached.

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The event will be held online on May 17th, lasting 4 hours, starting at 9:00 p.m. (India standard time). The schedule includes welcome remarks, a chat with multidisciplinary specialists on overall well-being, followed by themed discussion groups based on age groups. The event will close with a special masterclass on new drug technologies and integrated care, presented by experts who will take a multidisciplinary approach to ensure the best outcomes and quality of life for people with thalassemia.The 5th International Meeting for People with Thalassemia will offer simultaneous translation into Portuguese, Spanish and English, so all participants can interact and enjoy the full content.Access the website of Abrasta for more details and to register.

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