SICKLE CELL ASSOCIATION OF BC
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  • Research Links
    • About Sickle Cell >
      • About Sickle Cell Hb SC Disease
      • Sickle Cell and Malaria
      • Creating Your Own Sickle Cell Self Care Program
    • Medical Research
    • Integrative / Holistic Research
    • Pain Management >
      • Preventative Measures for Sickle Cell
      • Before a Painful Episode >
        • Medical Research for Health Care Professionals >
          • New Theraputic Approaches for Sickle Cell Disease - slide presentation
      • During a Painful Sickle Cell Crisis
      • Emergency Room for the Sickle Cell Patient
      • After a Sickle Cell Crisis
      • Awareness of Sickle Cell Triggers
      • When No One Beleives You
    • Diet, Nutrition, & Home Remedies >
      • Unique Ways for Keeping Hydrated for the Sickle Cell Patient
      • Cold & Flu Season for the Sickle Cell Patient
    • Lifestyle, Self Care, and Children >
      • Children with Sickle Cell
      • Parents with Children with Sickle Cell
      • Parents with Sickle Cell
    • Personal Stories of Healing >
      • Storma's Story: We're Just Like You
      • Bev's Story
  • Lectures
    • Sickle Cell, Covid-19 & Cold/Flu Season: How to protect ourselves - Sept 2020
    • Voices: National Conversation without Boarders June 19/2020
    • The Hopes & Realities of Bone Marrow Transplantation as a Curative Therapy for Sickle Cell Disease - June 17, 2020
    • Sickle Cell: Are we doing enough? with Dr. Hatoon Ezzat. Nov 15, 2018
    • Bodywork for Sickle Cell Disease
    • 2019 Sickle Cell Information Session on New Therapies
    • Pain Management Lecture Sept 21, 2018
  • Donate
  • Services

Welcome to Sickle Cell Association of BC

We are a registered charity committed to enhancing the quality of life for people living with Sickle Cell Disease. Upon your donation a tax deductible receipt will be provided. 


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Mission:
  • To provide current information (both medical and holistic / integrative), resources, support groups, and        online events for Sickle Cell patients, their families, friends, and health care professions in order to empower and enhance quality of life.

Home Page:
The Sickle Cell Association of BC is always looking for members and volunteers. Please contact the [email protected]
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            The Sickle Cell Association of BC is dedicated to providing families with the information they need to make educated
            and informed decisions to improve the quality of life for those suffering from Sickle Cell Disease and their families. 

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SCDABC is a member in good standing with the Sickle Cell Disease Association of Canada/ Association d’Anémie Falciforme du Canada  (SCDAC/AAFC)

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We would like to thank ApoPharma for the support they gave so that we may share lectures on Sickle Cell research.

Disclaimer: 
Information or materials on this website or in any event the Sickle Cell Association of BC creates are not intended to treat or replace your doctor’s advice nor do we endorse any particular product, technique, or idea. 
It is highly recommended that patients contact their haematologists or health care provider for adequate care and treatment. 

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