Wehaveavoice

Kevin and Jen talk about a number of things but are focusing on the upcoming International Education Day, June 25

Kevin talks about memories of his wife Sheila and how it's important to nurture friendships

Jen gets an unexpected call and discussion ensues.

Jen and Kevin chat about disappointments over the years in the Huntington's Disease community

Jen and Kevin chat about the death of a loved one and strategies leading up to and after death.

Kevin and Jen kick off a series of coffee talks concerning Huntington's Disease

James speaks about the Project Change and an array of topics

Dr. Herwig Lange and James Valvano discuss why it is necessary to change the diagnostic criteria for Huntington's Disease. To watch this episode with video, please go to https://www.youtube.com/watch?v=ZJs8EHEPMag

Louise Vetter (President and CEO of HDSA) underscores her support for the initiative to change the current diagnostic criteria and introduces the new Huntington's disease support platform - #PatientsLikeMe

Erin speaks with Kevin about her 5 1/2 year struggle with fertility amidst having a diagnosis of HD

Kevin Jess speaks about his wife Sheila, how they met up until her recent passing.

Please listen to James Valvano interview Jennifer Simpson HDSA on the HDParityAct! It's time to pass the HD Parity Act and remove the two-year waiting period for Medicare and SSDI! We must communicate the dire need of these medical supports and services to the US Congress!

#WeHaveAVoice Radio - May is #HuntingtonsDisease and #JuvenileHuntingtonsDisease Awareness Month! Our incredible special guest is John Howard! John recites his powerful poetry! #iHeartRadio #LetsTalkAboutHD #YouAreLoved

On May 11, 2021, James Valvano will interview Jennifer Simpson (HDSA Assistant Director, Youth & Community Services), to discuss the HD Parity Act! ALS just recently made drastic changes to the description of what ALS is. They furthered their efforts by having unanimous consent by Congress to pass their bill for patients to obtain immediate access to benefits. The HDSA wishes to have the HD Parity Act pass by unanimous consent by Congress for individuals with Huntington's disease to receive the same benefits as our friends with ALS. Act today! - Join the HD Acvocacy Act: https://cqrcengage.com/hdsa/Caucus

Jimmy Pollard talks about his new children's book, Finding Nana's Smile

Kevin Jess interviews James Valvano about the first season of WeHaveAFace TV

Dr. Kelsey M. Finn is a geneticist, bioethicist, and empathy enthusiast. Dr. Finn has devoted a large part of her career to researching whether, when, and how to communicate about genetic conditions and health information with children. She has interviewed countless parents, kids, and health providers to learn from their experiences and perspectives on how best to communicate with kids. A current anonymous survey is available for parents and guardians to help Dr. Finn with her research. www.WeHaveAFace.org/survey2

Dr. Bird of the University of Washington speaks about the HDSA Centers of Excellence. Dr. Herwig Lange of the George Huntington Institute of Germany joins the conversation. Topics: What is a Center of Excellence (CoE)? How does a facility become a Center of Excellence? Should doctors diagnose patients earlier so a treatment plan can be put in place? How can environmental factors affect Huntington's disease patients regarding the onset of symptoms? Update from Louise Vetter (CEO/President) of the HDSA regarding Centers of Excellence using telemedicine during these trying times with COVID-19.

Dr. Kelsey Finn speaks about when to talk to your children about Huntington's Disease and her new children's book.

Marie Blankenshop, Jen Almeida and Crystal Zachary speak out their new Facebook Wish List group