This past week I came into contact with an amazing woman - what an encouragement she has been. Renate Lindeman is the president of the Nova Scotia Down Syndrome Society. Renate has two beautiful daughters who have Down syndrome. Over the years Renate has been speaking out about genetic testing, she has written 8 newspaper articles, she has also done several radio and TV interviews. Unfortunately her initiative has been ignored by many. Recently, Renate put forth a petition entitled "Canada Needs a Prenatal Diagnosed Awareness Act". This act would ensure that when parents receive a prenatal diagnosis, they would also receive balanced and accurate information (you can find a link to sign this petition to the right). Most currently, Renate has started a "Campaign for Down syndrome" with the initiative of bringing awareness to the impact genetic science in having on our society. This campaign aims to ensure that advancing genetic science will be used to help improve the quality of life for people with Down syndrome.
A few interesting facts that I learned from Renate this week:
- approximately 50% of women decline prenatal screening in the Netherlands because they are not pressured, have support and are given a lot of reliable information, also, they have a law proposal that states women need to have 3 weeks of counseling and information before they can decide to terminate
- many European countries as well as the US are preparing legislations on prenatal screening so that it will not lead to discrimination of entire groups. The US has also re-introduced a "prenatal diagnosed condition awareness act"
- The UK has organizations that counsel women who have received a prenatal diagnosis.
1 comments:
I think this is an absolute tragedy. Thanks for your site and post.
Charlene Nelson @ www.cometochrist.ca
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