The works of the World Federation of Hemophilia (WFH) through the Haemophilia Foundation of Nigeria (HFN) has been a glimmer of light for people with haemophilia (PWH) in Nigeria. All we need is your voice to create a flame of hope for PWA ... #wearerarebutwematter
Watching my first son rely on whole blood for the first 8 years of his life was terrifying. Each transfusion brought more fear than relief. Treatment should offer safety and comfort, not added risk. #wearerarebutwematter
💔 Every moment of delay in clearing medication endangers the lives of #Hemophilia patients, increasing the risk of severe complications or even death. @Fmohnigeria@NafdacAgency@CustomsNG@nassnigeria—your action is crucial to ensure timely access to life-saving treatments!
@Kofi_Bartels it's World Haemophilia Day on the 17th of April. Creating awareness through your health program would make the world a better place for people with bleeding disorder.
The WFH is happy to announce that Sobi—a Founding Visionary contributor of the Humanitarian Aid Program —has generously offered to donate 1.3 million IUs of factor for Ukrainians in need. Read more: https://t.co/OZEp0RCqvs
@AOlulesi Good day Sir, trust you are doing great. I would like to connect with you to open up a conversation about the Hygeia Health Insurance plan for Anchor University. A mail has been sent to you, earlier. Hope to hear from you, sir. Regards,
Haemophilia is not a death sentence and it is not contagious... Treatment NOW available at Haemophilia Treatment Centres (HTCs) in most of the teaching hospitals across the country #WHD2021#WorldHaemophiliaDay2021
World Hemophilia Day—will which take place on April 17— is coming up very soon! World Hemophilia Day is about raising the level of awareness of hemophilia and other inherited bleeding disorders.
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He spent 4 days in coma due to an intracranial bleed but with the support of the @wfhemophilia Humanitarian Aid Program we were able to bring him out of coma and prevent permanent paralysis of the right hand #SoroSoke#TreatmentforAll#HFN2020AW
We need people to come out and report these issues so they can get help.
We can be reached at the Haemophilia Foundation via;
☎️;08033206779
Website; https://t.co/M1Yon7YkYj
#DoctorsOnAir
The incidence of Haemophilia is one in every 10,000.
We have less than 400 people in our database in the foundation, this means issues relating to Haemophilia are under reported ~ Mrs Megan Adediran of Haemophilia Foundation.
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