DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
Trusted Resources: Community Center
Online groups, photo galleries and blogs
Thalassaemia & Sickle Cell Society of Australia
The Thalassaemia and Sickle Cell Society of Australia is a not-for-profit community organisation that serves as a support and advocacy network for people affected by chronic genetic blood conditions like thalassaemia and sickle cell anaemia.
TASCS Australia is dedicated to: Serving as a support network for Australians affected by chronic genetic blood disorders known as “haemoglobinopathies”, like thalassaemia and sickle cell anaemia, Seeking to educate and raise public awareness of haemoglobinpathies within Australia, and the need to encourage the public to be tested for these conditions, Encouraging healthy members of the public to donate blood to the Australian Red Cross Blood Service, as fellow Australians who are affected by genetic haemoglobinopathies, require regular blood transfusions in order to live and manage their condition.
+myBinderRelated Content
-
videos & visualsSickle Cell Disease: Taking Charge of Your Health Part 1 – Real-World Patient Perspectiveshttps://www.facebook.com/watch/?v=343267...
-
education & researchQualifying for Social Security Disability With Sickle Cell DiseaseIf you or your child has sickle cell ane...
-
people & placesAllan F. Platt, MMSc, PA-C, DFAAPAAllan Platt has served as co-founder and...
-
people & placesSickle Cell Thalassemia Patients NetworkSince April of 1992, the Sickle Cell Tha...
-
people & placesRuth Nankanja, BAForty- three year old Ruth Nankanja is t...
-
news & eventsRare Disease Day at NIH 2023Rare Disease Day® takes place worldwide...
-
education & researchCare Team MembersYour Sickle Cell Care Team Managing you...
send a message
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.