JMHSK - Dedicated to helping those who suffer from hemophilia

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Disclaimer

This agreement governs your use of the JMHSK Website. Additional terms and conditions of use applicable to specific areas of the site may also be posted in such areas and, together with this agreement, govern your use of those areas. This Agreement, together with any such additional term and conditions, are referred to as this "Agreement". JMHSK reserves the right, in its discretion, to change or modify all or any part of this Agreement at any time, effective immediately upon notice published on the Website. Your continued use of the Website constitutes your binding acceptance of these terms and conditions, including any changes or modifications made by JMHSK as permitted above. If at any time the terms and conditions of this Agreement are no longer acceptable to you, you should immediately cease all use of the Website. 

You acknowledge that the Website contains information, photographs, graphics, links and other material (collectively, the "Content") that are protected by copyright, trademark or other proprietary rights of JMHSK or third parties. All Content on the Website is copyrighted as a collective work of JMHSK pursuant to applicable copyright law. You agree to comply with any additional copyright notices, information, or restrictions contained in any Content available on or accessed through the Website. Users of the Service may use the Content only for their personal, non-commercial use. You may not modify, publish, transmit, transfer or sell, reproduce, create derivative works from, distribute, perform, display, or in any way exploit any of the Content, in whole or in part, except as expressly permitted in this Agreement. You shall not store electronically any portion of any Content unless expressly permitted. Except as expressly permitted by the copyright laws, no copying, storage, redistribution or publication of any Content is permitted without the express permission of JMHSK or the owners of such Content or their authorized persons, if other than JMHSK.

The design of this Website is Copyright 2015, Nairobi, Kenya. No part of this web site may be copied reproduced or otherwise used in any form physical or electronic without written permission of the Copyright Owner.

The Website may contain links to sites on the Internet which are owned and operated by third parties (the "External Sites"). You acknowledge that JMHSK is not responsible for the availability of, or the content located on or through, any External Site. You should contact the site administrator for those External Sites if you have any concerns regarding such links or the content located on such External Sites.

Disclaimer of warranties; limitation of liability neither JMHSK nor any provider of third party content or their respective agents warrants that the site will be uninterrupted or error free; nor does JMHSK, any third party content provider, or their respective agents make any warranty as to the results to be obtained from use of the site or the content. The site and the content are distributed on an "as is, as available" basis. None of JMHSK, third party content providers and their respective agents make any warranties of any kind, either express or implied, including, without limitation, warranties of title or implied warranties of merchantability or fitness for a particular purpose, with respect to the site, any content or any products or services sold and/or provided through the service.

On this website the word HAEMOPHILIA includes all types of haemophilia and all associated coagulation deficiencies such as von Willebrand disorder.

The information on the JMHSK website is provided for general information purposes only. JMHSK does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, JMHSK recommends that you contact your Haemophilia Doctor or Nurse or your local treatment centre. Before administering any products, JMHSK urges patients to check dosages with a doctor or hemophilia centre staff, and to consult the pharmaceutical company's printed instructions. 

While every effort has been made to ensure the accuracy of the information on this site, JMHSK does not guarantee the information is accurate, and is not responsible in any way whatsoever for damages arising out of the use of this web site or any of the information contained herein.

About Us


The purpose of the society is to provide service and support to persons with hemophilia or other clotting disorders and their families. Read more

Our Programs


JMHSK runs a number of programs aimed at education; support and offering affordable medical help to those living with hemophilia. Read More

 

Annual Events


17th April: We celebrate World Hemophilia Day

25th April: Family Day as it marks Jose Memorial Day

How you can help


We rely on the generous support of individuals and groups to provide services, education and support for people living with hemophilia and other bleeding disorders. Read More

 

 

 

 

 

 

 

Our Team Our Team

 

Our Vision

Healthy, active and empowered citizens living with Hemophilia

 

Our Mission

To provide comprehensive care, medical support and service to people with Hemophilia through registration, provision of treatment, education and training.

 

Our Programs

Medical Programs


One of the Society’s ultimate goals is to provide comprehensive care meaning that along with factor replacement therapy, patients receive physiotherapy, dental hygiene, genetic counselling, diagnostics, psychosocial therapy, orthopedics and surgical care. 

Organizational Programs


The society was launched on 17th April 2009 during the World Hemophilia Day (WHD) at the MP Shah Hospital to give it credibility and to create awareness on a wider scale. The media was present at the launch in an effort to inform the public of the presence and purpose of the society.

Family Programs


In Kenya, the pressure to provide basic medical care leaves families on the sidelines. Many families are reluctant and afraid to assert their needs and have thus learnt to be helpless and hopeless, and suffer in silence.

Government Lobbying


The society cannot achieve its vision of comprehensive Hemophilia care without the government’s support. Hemophilia is rare and the government faces other urgent medical needs thus our case can get lost in the many voices crying for government attention.

 

Fund Raising & Public Awareness

 

 

As public awareness on the society is raised, more people will contribute to its success. The society will endeavor to run both of these concurrently to ensure success as they are intimately related. We undertake to identify the stakeholders listed below and create linkages.

Funding source include:

  1. The government
  2. Private Individuals
  3. Corporations and Businesses
  4. The General Public

 

 

 

Useful Links

© 2018 Jose Memorial Hemophilia Society. All Rights Reserved.

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