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Down Syndrome & Adoption as an Option

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Manage episode 310287081 series 3051496
Contenu fourni par Grey Genetics. Tout le contenu du podcast, y compris les épisodes, les graphiques et les descriptions de podcast, est téléchargé et fourni directement par Grey Genetics ou son partenaire de plateforme de podcast. Si vous pensez que quelqu'un utilise votre œuvre protégée sans votre autorisation, vous pouvez suivre le processus décrit ici https://fr.player.fm/legal.

Stephanie Thompson still vividly remembers when her son Christopher, now 27 years old, received a diagnosis of Down syndrome. As a young woman and a first time mother, the diagnosis came as a shock. What she wishes her younger self knew? That it would be okay. Stephanie worked for eleven years in many different roles within the Down Syndrome Association of Greater Cincinnati and has deep insights into when, where and how a diagnosis of Down syndrome is given to parents and how this can be handled better. Today, Stephanie is the Director of the National Down Syndrome Network (NDSAN), whose mission is to ensure that every child born with Down syndrome has the opportunity to grow up in a loving family.

Have thoughts or a related story you’d like to share? Leave us a short voice message here! We may use your message on a future show.

Links and Resources

National Down Syndrome Adoption Network

Resources for Patients

Resources for Medical Professionals

Stephanie’s blog post on the Grey Genetics News Corner: Adoption as an Option: The National Down Syndrome Adoption Network

Stephanie’s interview on The Lucky Few podcast: Adoption & Down Syndrome w/Stephanie Thompson from the NDSAN

Connect with NDSAN on Social Media:

NDSAN on Instagram: @ndsan321

NDSAN on Twitter: @dsadoption

NDSAN on Facebook

NDSAN on LinkedIn

National Council on Disability Recommends More Regulation of NIPT.” Genome Web, October 23, 2019.

Genetic Testing and the Rush to Perfection, National Council on Disability, October 23, 2019.

Donate to Patient Stories

Leave us a review on iTunes

Patient Stories on Twitter: @GreyGeneticsPod

Patient Stories on Instagram: @patientstoriespodcast

Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.

  continue reading

94 episodes

Artwork
iconPartager
 
Manage episode 310287081 series 3051496
Contenu fourni par Grey Genetics. Tout le contenu du podcast, y compris les épisodes, les graphiques et les descriptions de podcast, est téléchargé et fourni directement par Grey Genetics ou son partenaire de plateforme de podcast. Si vous pensez que quelqu'un utilise votre œuvre protégée sans votre autorisation, vous pouvez suivre le processus décrit ici https://fr.player.fm/legal.

Stephanie Thompson still vividly remembers when her son Christopher, now 27 years old, received a diagnosis of Down syndrome. As a young woman and a first time mother, the diagnosis came as a shock. What she wishes her younger self knew? That it would be okay. Stephanie worked for eleven years in many different roles within the Down Syndrome Association of Greater Cincinnati and has deep insights into when, where and how a diagnosis of Down syndrome is given to parents and how this can be handled better. Today, Stephanie is the Director of the National Down Syndrome Network (NDSAN), whose mission is to ensure that every child born with Down syndrome has the opportunity to grow up in a loving family.

Have thoughts or a related story you’d like to share? Leave us a short voice message here! We may use your message on a future show.

Links and Resources

National Down Syndrome Adoption Network

Resources for Patients

Resources for Medical Professionals

Stephanie’s blog post on the Grey Genetics News Corner: Adoption as an Option: The National Down Syndrome Adoption Network

Stephanie’s interview on The Lucky Few podcast: Adoption & Down Syndrome w/Stephanie Thompson from the NDSAN

Connect with NDSAN on Social Media:

NDSAN on Instagram: @ndsan321

NDSAN on Twitter: @dsadoption

NDSAN on Facebook

NDSAN on LinkedIn

National Council on Disability Recommends More Regulation of NIPT.” Genome Web, October 23, 2019.

Genetic Testing and the Rush to Perfection, National Council on Disability, October 23, 2019.

Donate to Patient Stories

Leave us a review on iTunes

Patient Stories on Twitter: @GreyGeneticsPod

Patient Stories on Instagram: @patientstoriespodcast

Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.

  continue reading

94 episodes

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