How to Register

How to Register

Introduction

The Hemophilia Treatment Center looks after patients with Inherited bleeding disorders. These are diseases which are due to an inherited (passed on from parents to their children) deficiency of coagulation factors. This results in prolonged bleeding after cuts / injury. The commonest disorder is Hemophilia which is X-linked (mostly males are affected).  Von Willebrand’s Disease (VWD) is the next common and has autosomal inheritance (both males and females are affected).

Registration at UWF

New Patients with Inherited Bleeding disorders are required following steps / documents for registration. 
 
Blood test Requirement 
Complete Coagulation Profile
Factor level
HBs Ag
HCV
Other tests like Blood CP, LFTs, etc if required.
 
Document Requirement:
B- Form / CNIC of Patient
Parents CNICs
2 passport size pictures of Patient
Home address or (Proof of residential documents if the patient is foreign national)
Phone No. / Email
 
Advantages of registration:
Free check up by the MO
Free consultation & check up by the consultants at HTC ,if required
Free / subsidized treatment (as per Policy)
Free Referrals to & consultations by our Medical Advisory Board (MAB) &relevant Doctors at Haemophilia Friendly Hospitals (HFH) ,if required
Admission in HFH if required
24 hr on call service for emergencies
Subsidized emergency care per policy
Free physiotherapy sessions
Free counseling
Free training to prepare factors
Free training to infuse factors
 
Access and invitation to Awareness activities, Seminars , workshops , picnics etc with free refreshments.
 

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