Safe & Secure Blood Supply
One of the most crucial forms of treatment and cures for sickle cell disease is access to fresh blood. The best way for anyone to support the community is to become a donor.
Safe & Secure Blood Supply
One of the most crucial forms of treatment and cures for sickle cell disease is access to fresh blood. The best way for anyone to support the community is to become a donor.
Safe & Secure Blood Supply
One of the most crucial forms of treatment and cures for sickle cell disease is access to fresh blood. The best way for anyone to support the community is to become a donor.
Be Our Blood Partner
How you can join: 1. Set up an account on blood.ca or on the GiveBlood app for Apple or Android. 2. Select “partners” from the menu. 3. Select “join a team” and search for Sickle Cell Awareness Group of Ontario. 4. Book an appointment to donate blood. Please note: If a member has already donated this year the count will be retroactive to January 1st. Partner ID: SICK327620 (four letters and six numbers) Organization: Sickle Cell Awareness Group of Ontario Thank you for your generosity and commitment to saving lives.
Be Our Blood Partner
How you can join: 1. Set up an account on blood.ca or on the GiveBlood app for Apple or Android. 2. Select “partners” from the menu. 3. Select “join a team” and search for Sickle Cell Awareness Group of Ontario. 4. Book an appointment to donate blood. Please note: If a member has already donated this year the count will be retroactive to January 1st. Partner ID: SICK327620 (four letters and six numbers) Organization: Sickle Cell Awareness Group of Ontario Thank you for your generosity and commitment to saving lives.
Be Our Blood Partner
How you can join: 1. Set up an account on blood.ca or on the GiveBlood app for Apple or Android. 2. Select “partners” from the menu. 3. Select “join a team” and search for Sickle Cell Awareness Group of Ontario. 4. Book an appointment to donate blood. Please note: If a member has already donated this year the count will be retroactive to January 1st. Partner ID: SICK327620 (four letters and six numbers) Organization: Sickle Cell Awareness Group of Ontario Thank you for your generosity and commitment to saving lives.
Blood Donation & Stem Cell Registry Awareness
Mrs. Lanre Tunji-Ajayi,M.S.M. President of the Sickle Cell Awareness Group of Ontario has been advocating for the need to lower the barriers to blood donations, especially for Black and African-Canadian people. “Blood from black communities is like gold to Canadian Blood Service,” she says. However, she notes, it is CBS’ own rules that limit the supply of blood from Black and African-Canadian communities.
Blood Donation & Stem Cell Registry Awareness
Mrs. Lanre Tunji-Ajayi,M.S.M. President of the Sickle Cell Awareness Group of Ontario has been advocating for the need to lower the barriers to blood donations, especially for Black and African-Canadian people. “Blood from black communities is like gold to Canadian Blood Service,” she says. However, she notes, it is CBS’ own rules that limit the supply of blood from Black and African-Canadian communities.
Blood Donation & Stem Cell Registry Awareness
Mrs. Lanre Tunji-Ajayi,M.S.M. President of the Sickle Cell Awareness Group of Ontario has been advocating for the need to lower the barriers to blood donations, especially for Black and African-Canadian people. “Blood from black communities is like gold to Canadian Blood Service,” she says. However, she notes, it is CBS’ own rules that limit the supply of blood from Black and African-Canadian communities.
Blood Donor/Stem Cell Champion
Many individuals living with sickle cell disease require continuous blood transfusion and stem cell transplantation for their care and treatment. Science has proven that those on continuous blood transfusion must receive blood from their community to reduce the chances of developing antibodies. As a result, SCAGO in collaboration with Canadian Blood Services educates and organizes blood donor and stem cell registry drives. Are you attending a post-secondary institution in Ontario? SCAGO is recruiting students as champions to support blood donors and stem cell registry drives. To learn more about/participate in our student championship program, click the below to complete the form below.
Blood Donor/Stem Cell Champion
Many individuals living with sickle cell disease require continuous blood transfusion and stem cell transplantation for their care and treatment. Science has proven that those on continuous blood transfusion must receive blood from their community to reduce the chances of developing antibodies. As a result, SCAGO in collaboration with Canadian Blood Services educates and organizes blood donor and stem cell registry drives. Are you attending a post-secondary institution in Ontario? SCAGO is recruiting students as champions to support blood donors and stem cell registry drives. To learn more about/participate in our student championship program, click the below to complete the form below.
Blood Donor/Stem Cell Champion
Many individuals living with sickle cell disease require continuous blood transfusion and stem cell transplantation for their care and treatment. Science has proven that those on continuous blood transfusion must receive blood from their community to reduce the chances of developing antibodies. As a result, SCAGO in collaboration with Canadian Blood Services educates and organizes blood donor and stem cell registry drives. Are you attending a post-secondary institution in Ontario? SCAGO is recruiting students as champions to support blood donors and stem cell registry drives. To learn more about/participate in our student championship program, click the below to complete the form below.
Advocacy on Blood Deferrals
Advocacy on
Blood Deferrals
À propos du Hub
À propos du Hub
Le Centre d'équité en matière de vaccins sert de plateforme centrale pour les ressources en vaccins et les engagements collaboratifs visant à soutenir le travail en matière d'équité en matière de vaccins pour la communauté de la drépanocytose. Le centre comprend des ressources éducatives et des stratégies visant à améliorer l'équité en matière de vaccins dans la drépanocytose. Le but du centre est de faciliter l'échange de connaissances et de susciter une action collective pour relever les défis de la vaccination auxquels sont confrontées les personnes affectées par la drépanocytose.
Le Centre d'équité en matière de vaccins sert de plateforme centrale pour les ressources en vaccins et les engagements collaboratifs visant à soutenir le travail en matière d'équité en matière de vaccins pour la communauté de la drépanocytose. Le centre comprend des ressources éducatives et des stratégies visant à améliorer l'équité en matière de vaccins dans la drépanocytose. Le but du centre est de faciliter l'échange de connaissances et de susciter une action collective pour relever les défis de la vaccination auxquels sont confrontées les personnes affectées par la drépanocytose.
La stratégie d'équité en matière de vaccinsdans la drépanocytose
La stratégie d'équité en matière de vaccinsdans la drépanocytose
Compte tenu des nombreuses raisons variées de l'hésitation à l'égard des vaccins, il est fortement nécessaire des ressources vaccinales communautaires fondées sur des données probantes, en particulier pour les personnes atteintes de drépanocytose qui sont susceptibles aux infections. Par le biais de son étude sur l'équité vaccinale dans la drépanocytose (EVD), la SCAGO a l'intention de travailler avec les patients atteints de drépanocytose, leurs familles, leurs soignants et les cliniciens afin de co-concevoir et de mettre en œuvre une Stratégie d'équité en matière de vaccination dans la drépanocytose pour soutenir les décideurs politiques, les agences de santé, les hôpitaux, etc., en leur fournissant des informations précieuses pour atteindre l'équité vaccinale (ce qui fonctionne pour la communauté de la drépanocytose) et en soutenant la communauté de la drépanocytose avec des informations factuelles sur la vaccination.
Compte tenu des nombreuses raisons variées de l'hésitation à l'égard des vaccins, il est fortement nécessaire des ressources vaccinales communautaires fondées sur des données probantes, en particulier pour les personnes atteintes de drépanocytose qui sont susceptibles aux infections. Par le biais de son étude sur l'équité vaccinale dans la drépanocytose (EVD), la SCAGO a l'intention de travailler avec les patients atteints de drépanocytose, leurs familles, leurs soignants et les cliniciens afin de co-concevoir et de mettre en œuvre une Stratégie d'équité en matière de vaccination dans la drépanocytose pour soutenir les décideurs politiques, les agences de santé, les hôpitaux, etc., en leur fournissant des informations précieuses pour atteindre l'équité vaccinale (ce qui fonctionne pour la communauté de la drépanocytose) et en soutenant la communauté de la drépanocytose avec des informations factuelles sur la vaccination.
Vidéos VES
Vidéos VES
Quick Links
Location
Address: 235-415 Oakdale Rd. North York, ON M3N 1W7
Phone: GTA: 416-745-4267
Email: info@sicklecellanemia.ca
© SCAGO - All Rights Reserved -Disclaimer - Charitable Registration #: 83332 0872 RR 0001
Quick Links
Location
Address: 235-415 Oakdale Rd.
North York, ON M3N 1W7
Phone: 416-745-4267
Email: info@sicklecellanemia.ca
© SCAGO - All Rights Reserved -Disclaimer - Charitable Registration #: 83332 0872 RR 0001
Quick Links
Location
Address: 235-415 Oakdale Rd. North York, ON M3N 1W7
Phone: 416-745-4267
Email: info@sicklecellanemia.ca
© SCAGO - All Rights Reserved -Disclaimer - Charitable Registration #: 83332 0872 RR 0001