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.