#38 - Roundtable Discussion - Discussion for July 2019

#38 - Roundtable Discussion - Discussion for July 2019

In the latest episode of the SMA News Today Podcast, hosts Kevin Schaefer and Michael Morale discuss updates regarding SMA therapies Spinraza and Reldesemtiv. Also, Kevin and columnist Brianna Albers share their experiences at the 2019 Cure SMA conference. Are you interested in understanding gene therapy? ExploreGeneTherapy.com has helpful information about gene therapy, including its history and how it is being investigated for the treatment of genetic diseases. Visit www.exploregenetherapy.com

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COVID19, Spinraza, Bloating, SPC’s, Being Spontaneous & Transferring Out Of Wheelchair To Take a Nap

COVID19, Spinraza, Bloating, SPC’s, Being Spontaneous & Transferring Out Of Wheelchair To Take a Nap

In the forums a topic of discussion has been the thing that’s on everyone’s mind, the Novel Coronavirus, also known as COVID19. Spinraza has also been discussed. Other topics include bloating, SPC’s...

11 Mars 20205min

Being Spontaneous With SMA & How Body Composition May be a Biomarker of Motor Function in SMA

Being Spontaneous With SMA & How Body Composition May be a Biomarker of Motor Function in SMA

Spontaneity can be difficult when you have SMA. Sometimes it even takes planning. Forums moderator DeAnn Runge shares how she does it and is looking for advice on how to be even more spontaneous. S...

9 Mars 20206min

Maintaining Long-Distance Friendships & MDA Executive’s Discussion of Gene Therapies

Maintaining Long-Distance Friendships & MDA Executive’s Discussion of Gene Therapies

Forums Director Kevin Schaefer talks about maintaining long-distance friendships, particularly with people in the SMA community. SMA News Today’s multimedia associate, Price Wooldridge, details an MD...

6 Mars 20206min

Celebrating Rare Disease Day 2020 with #WhatMakesMeRareSMA & How Music Plays a Big Part in Life

Celebrating Rare Disease Day 2020 with #WhatMakesMeRareSMA & How Music Plays a Big Part in Life

February 29th was recognized as Rare Disease Day across the world. SMA News Today columnists shared what this day meant to them. A social media campaign was also successful in bringing awareness to ...

4 Mars 20206min

#53 - Interview with Alyssa Silva

#53 - Interview with Alyssa Silva

In episode 53, host Kevin Schaefer interviews our very own Alyssa Silva. Alyssa is from Cumberland, Rhode Island, and she is a columnist and forums moderator here at SMA News Today. She’s also the fou...

3 Mars 202044min

Public Interactions with People With Disabilities & Muscular Dystrophy Association Helping Others

Public Interactions with People With Disabilities & Muscular Dystrophy Association Helping Others

When it comes to public interactions with people who have disabilities there are no set rules. As someone who has a disability, DeAnn shares her thoughts on this topic. Also, listen to SMA News Toda...

2 Mars 20207min

Risdiplam Success in Treating SMA Type 1 Babies in FIREFISH Study & Kevin's Spinraza Injection

Risdiplam Success in Treating SMA Type 1 Babies in FIREFISH Study & Kevin's Spinraza Injection

Forums Director Kevin Schaefer talks about his most recent Spinraza injection and SMA News Today’s multimedia associate, Price Wooldridge, discusses the Risdiplam success in treating SMA Type 1 babies...

28 Feb 20205min

Talking About Rare Disease Day & Accessible Parking, Sleepovers with SMA and Product Reviews

Talking About Rare Disease Day & Accessible Parking, Sleepovers with SMA and Product Reviews

Forums Director Kevin Schaefer talks about the upcoming Rare Disease Day, and what it means to him. Also, DeAnn Runge shares the latest activity going on in the forums. Among the topics being discus...

26 Feb 20206min

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