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We are taking a little break this week after a crazy long Rett Syndrome Awareness Month. We will talk with you next week!
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
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For our top three this week we talk about some incredible updates that have come to Rett research as well as our recap of Rett Syndrome Awareness month. If you would like to look at the articles for this week's top three you can find them here:
Taysha Gene Therapies receives a $50 million investment from Astellas
Report from the Externally-Led Patient-Focused Drug Development Meeting
On this week’s episode we sat down with Kevin Pierce the Chief Operating Officer for Girl Power 2 Cure. Kevin shares with us how he got started with the organization and how the organization itself has grown since it’s inception. As a grandparent of an individual with Rett he brings understanding and personal passion to his position. We learned not only about Girl Power 2 Cure but also about their connection to Rett University and how the organizations support one another.
If you would like to learn more about Girl Power 2 Cure you can find them on their website, www.gp2c.org or on Facebook and Instagram.
If you would like to learn more about the services offered by Rett University you can find them at their website, www.rettuniversity.org or on Facebook and Instagram.
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
----------
Social Media, Podcast Platforms, & more! - https://drum.io/prettyhappypodRe
Send us a voice message - https://anchor.fm/prettyhappypod
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Wow, these last two weeks have been an absolute whirlwind when it comes to Rett syndrome research. To start with, Neurogene announced on January 23, 2023 that they had received approval from the Food and Drug Administration (FDA) in the United States to begin human clinical trials of their gene therapy drug, NGN-401. This was an absolute shock to the community considering that it's been less than a year since Neurogene announced plans to begin developing a drug.
Neurogene Initial Announcement (May 18, 2022) - https://www.neurogene.com/press-releases/neurogene-announces-new-development-program-in-rett-syndrome-utilizing-novel-exact-technology-platform/
Neurogene EXACT Technology Explained - https://www.neurogene.com/our-technology/
Rett Syndrome Research Trust sits down with Neurogene - https://youtu.be/QuTu_zLcVoI
We also continue our conversation with Dionne Snyders by discussing more specifics of what it's like running a school with such a diverse student population. To learn more about Nova School, visit their website.
https://www.nova-school.co.za/
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
----------
Social Media, Podcast Platforms, & more! - https://hopp.bio/prettyhappyplaceSend us a voice message - https://anchor.fm/prettyhappypod
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On this weeks episode we chat about three businesses that were started because of individuals with Rett syndrome. The first is Eye Designs by Emily. Emily, who has Rett, shares her talent to create works of art using an eye gaze device. She donates all of her proceeds to Rett syndrome research. You can find her on her website, Instagram and Facebook. The second business that we looked at is Blüm and Bee. They had their soft opening at the end of 2022. Blüm and Bee's online store only employs those with disabilities and even provide a training program to help those individuals succeed. Blüm and Bee was started by Anna Cate's mother. Anna Cate has Rett and when she finished school they knew she would need something fulfilling and worthwhile to fill her time and Blüm and Bee was born. You can support them by following them on Instagram. The third business that we talked about is West Coast Door Mats. Ebony (who has Rett) and her mom Allie create custom designed door mats. They work together to design and paint every door mat by hand. While they are located in Australia, they ship world wide. Find them on Facebook and Instagram.
If you have ever wondered how the Rett Clinic at Children's Hospital Colorado functions, this is the episode for you! Tristen Dinkel an RN and coordinator extraordinaire for the clinic. We chat with Tristen about everything from how she got involved with the clinic, to the function of a Rett clinic and how you can prepare for your visit. You can find more information about the Rett Clinic at Children's Hospital Colorado at their website and you can find more information about other clinics at on IRSF's website.
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
----------
Social Media, Podcast Platforms, & more! - https://hopp.bio/prettyhappyplace
Send us a voice message - https://anchor.fm/prettyhappypod
--- Send in a voice message: https://podcasters.spotify.com/pod/show/prettyhappypod/message -
On today's top three, we looked at the headlines to see what was new for Rett syndrome. We found great information on the history of Trofinetide as well as information about the end of the clinic trial. If you haven't heard about Trofinetide yet, it is the first drug that potentially will soon be on the market to treat symptoms of Rett. You can read more about that here. Second, China was sharing the love and sharing information about Rett syndrome on one of their biggest news outlets. That's pretty exciting when you think about all the good it can do to spread awareness. Clink here to read the article. Third is two big donations to Rett syndrome research! One donation went to the Rett Syndrome Research Trust (RSRT) specifically for the development and testing of a product called Emerald. Its a device designed to monitor vitals from a distance. Learn more about Emerald here. The other donation was given to the International Rett Syndrome Foundation for the purpose of furthering the research of Rett in males. This was donated by a family in honor of their son Otis who as Rett syndrome. You can learn more about their story here.
When you have a medically complex child finding the right equipment can be difficult. And when you do find equipment that works, there's no guarantee it will continue to work as your loved one ages or their diagnosis progresses. We haven't been on this journey long but we have learned about some things that help and some that we thought might but in the end weren't the right fit. Today we're talking about 3 pieces of equipment that didn't work out and 3 that we really love.
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
----------
Social Media, Podcast Platforms, & more! - https://hopp.bio/prettyhappyplace
Send us a voice message - https://anchor.fm/prettyhappypod
--- Send in a voice message: https://podcasters.spotify.com/pod/show/prettyhappypod/message -
Welcome back to the podcast everyone! Glad to be back after our end of year break. To start this episode we are going to be talking about Rett in the news. There was a new MECP2 gene mutation found and connected to Rett Syndrome. Is that a good thing? In short, yes! That means that we are learning and research is progressing. If you want to learn more by reading the article you can find it by clicking here. We also share about an app developer that donated to IRSF. While we love that there is more money going to Rett research make sure you do your research when choosing what apps to use. Sam did a deep dive into this one and didn't find much. You can read more about their donation here. For our final top three, we talk about a study that looks at Rett affecting sleep....well duh! It looks at sleep structure abnormalities and you can find more information about that article here. BONUS: We need to correct something that we've said in the past. There have in fact been other gene therapy trials in the US. We're sorry for the confusion. We won't go into all the details but if you'd like to learn more about the history of gene therapy in the US you can find it on this website.
On this week's episode, we welcome Dionne Snyders to the podcast. Dionne is from South Africa and is very active in the Rett community and with Rett SA. Dionne joins us to talk about her daughter who has Rett as well as her response to inadequate schooling for her daughter. Dionne along with another parent and an SLP started a school! Nova School is specifically for learners using AAC. They currently even have some students that do satellite schooling and use zoom to access the classes. Every learner has a communication partner who makes sure all the environmental and personal needs are met so the teachers can focus on what they do best...teaching! If you would like to learn more about Nova School you can visit their website or follow them on Instagram and Facebook.
If you are a newly diagnosed family, you can find loads of information regarding Rett Syndrome on our website (linked below), including links to various foundations and support groups worldwide. And, of course, feel free to reach out to us; we love connecting with new families!
Subscribe today so that you never miss an episode. And we'll see you next time!
----------
Social Media, Podcast Platforms, & more! - https://hopp.bio/prettyhappyplace
Send us a voice message - https://anchor.fm/prettyhappypod
--- Send in a voice message: https://podcasters.spotify.com/pod/show/prettyhappypod/message -
Episode 16. Author, political commentator, and Bravo super fan S.E. Cupp joins Kristen & Luke this week to talk about the #Scandoval that has rocked our worlds. Kristen lays down the actual truth of how Ariana found out about Tom’s affair and how she’s been doing in the days that have followed. They are #TeamAriana (as we all are). Also, get to know S.E. on a personal level as she discusses balancing her work/home life, and gives us her advice on what keeps her marriage alive and thriving!
Follow us: @kristendoute @luke__broderick
Email us: [email protected]
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