WeHaveAFace.org Inc. has created "WeHaveAVoice" Radio for the Huntington's and Juvenile Huntington's disease community. It is time for the community to speak out...speak up! We must openly share what all of us in the Huntington's community experience on a daily basis! Removing the stigmas and broadening social awareness and acceptance is paramount! Visit: www.WeHaveAFace.org/Radio for more information.
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Host, Kevin Jess, talks about Rare Disease Day which is just around the cornerद्वारा WeHaveAVoice
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New Guidelines to Revolutionize Care for Huntington's Disease Patients
13:05
13:05
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13:05
Kevin Jess talks about recent papers published and about to be published concerning changing the diagnostic criteria for HDद्वारा WeHaveAVoice
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Bunny Clark and the 10th Annual Huntington's Heroes Walk
13:38
13:38
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13:38
Bunny Clark talks about The Walk for Huntington's Disease May 28thद्वारा WeHaveAVoice
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Erin Paterson - Huntington's Disease Heroes
22:20
22:20
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22:20
द्वारा WeHaveAVoice
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Kevin Jess announces charity closings and discusses what's next for WeHaveAFace.द्वारा WeHaveAVoice
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Kevin Jess talks about the feeling of worthlessness and how the media may drive this feeling.द्वारा WeHaveAVoice
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Coffee Talk with Kevin and Jen (Chat #7)
38:35
38:35
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38:35
Jen and Kevin discuss possible implications of the overturning of Roe v Wade for the Huntington's Communityद्वारा WeHaveAVoice
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Coffee Talk with Kevin and Jen (Chat #6)
1:00:22
1:00:22
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1:00:22
Jen and Kevin talk about hope, testing and other topicsद्वारा WeHaveAVoice
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Coffee Talk with Jen and Kevin (Chat #5)
44:05
44:05
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44:05
Kevin and Jen talk about a number of things but are focusing on the upcoming International Education Day, June 25द्वारा WeHaveAVoice
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Kevin speaks about memories and nurturing relationships
28:16
28:16
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28:16
Kevin talks about memories of his wife Sheila and how it's important to nurture friendshipsद्वारा WeHaveAVoice
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Coffee Talk with Jen and Kevin (Chat 4)
44:42
44:42
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44:42
Jen gets an unexpected call and discussion ensues.द्वारा WeHaveAVoice
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Coffee Talk with Jen and Kevin (Chat #3)
47:56
47:56
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47:56
Jen and Kevin chat about disappointments over the years in the Huntington's Disease communityद्वारा WeHaveAVoice
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Coffee Talk with Jen and Kevin (Chat #2)
45:24
45:24
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45:24
Jen and Kevin chat about the death of a loved one and strategies leading up to and after death.द्वारा WeHaveAVoice
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Coffee Talk with Jen and Kevin (Chat 1)
39:12
39:12
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39:12
Kevin and Jen kick off a series of coffee talks concerning Huntington's Diseaseद्वारा WeHaveAVoice
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James Valvano and what's next for WeHaveAFace
34:42
34:42
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34:42
James speaks about the Project Change and an array of topicsद्वारा WeHaveAVoice
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Dr. Herwig Lange and James Valvano discuss why it is necessary to change the diagnostic criteria for Huntington's Disease
57:05
57:05
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57:05
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=ZJs8EHEPMagद्वारा WeHaveAVoice
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Louise Vetter concerning support for changes to the current diagnostic criteria for Huntington's Disease
29:56
29:56
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29:56
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 - #PatientsLikeMeद्वारा WeHaveAVoice
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Erin Paterson speaks about having Huntington's Disease and starting a family
44:39
44:39
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44:39
Erin speaks with Kevin about her 5 1/2 year struggle with fertility amidst having a diagnosis of HDद्वारा WeHaveAVoice
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Kevin Jess speaks candidly about the recent death of his wife Sheila
23:52
23:52
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23:52
Kevin Jess speaks about his wife Sheila, how they met up until her recent passing.द्वारा WeHaveAVoice
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WeHaveAVoice: HDSA - HD Parity Act with Jennifer Simpson!
31:16
31:16
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31:16
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!द्वारा WeHaveAVoice
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WeHaveAVoice Radio - HD Warrior, John Howard Poetry!
8:01
8:01
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8:01
#WeHaveAVoice Radio - May is #HuntingtonsDisease and #JuvenileHuntingtonsDisease Awareness Month! Our incredible special guest is John Howard! John recites his powerful poetry! #iHeartRadio #LetsTalkAboutHD #YouAreLovedद्वारा WeHaveAVoice
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WeHaveAFace PSA - HDSA: HD Parity Act with Jennifer Simpson!
3:38
3:38
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3:38
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 …
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Jimmy Pollard - Finding Nana's Smile
33:38
33:38
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33:38
Jimmy Pollard talks about his new children's book, Finding Nana's Smileद्वारा WeHaveAVoice
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James Valvano: Season 1 of WeHaveAFace TV
1:04:31
1:04:31
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1:04:31
Kevin Jess interviews James Valvano about the first season of WeHaveAFace TVद्वारा WeHaveAVoice
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Dr. Finn of the Mayo Clinic: How and when to talk to children about Huntington's disease.
28:00
28:00
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28:00
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 perspective…
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Dr. Bird of the University of Washington speaks about the HDSA Centers of Excellence
54:43
54:43
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54:43
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…
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Grandma has HD and it's okay with Dr. Kelsey Finn
39:22
39:22
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39:22
Dr. Kelsey Finn speaks about when to talk to your children about Huntington's Disease and her new children's book.द्वारा WeHaveAVoice
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HD/JHD Facebook Wish List. What's that about?
43:21
43:21
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43:21
Marie Blankenshop, Jen Almeida and Crystal Zachary speak out their new Facebook Wish List groupद्वारा WeHaveAVoice
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Coping with separation anxiety during Covid-19 pandemic
58:19
58:19
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58:19
Dr. Susan Potter and Dr. Herwig Lange tackle a serious issue concering separation anxiety during the pandemic.द्वारा WeHaveAVoice
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#WeHaveAFace #WeHaveAVoice - Carol Kennedy (President of WHAF England and Wales) HD3 Training Program and COVID-19 Discussion
52:04
52:04
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52:04
#WeHaveAFace #WeHaveAVoice - Carol Kennedy (President of WHAF England and Wales) HD3 Training Program and COVID-19 Discussion.द्वारा WeHaveAVoice
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A trip down memory lane with Mary Etta Robertson
1:00:46
1:00:46
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1:00:46
Mary talks with Leanne and Kevin about yesterday and todayद्वारा WeHaveAVoice
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German Dr. Ansgar Klimke: New approach for hydroxychloroquine in aerosol form for COVID-19
42:08
42:08
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42:08
#WeHaveAVoice Radio! German Doctor: Dr. Ansgar Klimke - New approach for hydroxychloroquine in aerosol form for #COVID19 #Coronavirus #Spreaker #CDC #WHOद्वारा WeHaveAVoice
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WeHaveAVoice: Discussing the Coronavirus (COVID-19)
55:18
55:18
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55:18
#WeHaveAFace #WeHaveAVoice: Discussing the Coronavirus (COVID-19) - #Coronavirus #COVID19 #CDC #HuntingtonsDiseaseद्वारा WeHaveAVoice
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Cherry Chism: When you leave the Roche clinical trial
44:08
44:08
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44:08
Cherry Chism talks about her husband leaving the Roche Trialद्वारा WeHaveAVoice
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Louise Vetter, President and CEO of HDSA: HD Trial Finder
40:14
40:14
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40:14
Louise Vetter, President, and CEO of the Huntington's Disease Society of America (HDSA) speaks with James Valvano about the HD Trial Finder. We must broaden awareness of studies and trials for our Huntington's disease population.द्वारा WeHaveAVoice
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Dr. Peg Nopoulos: KidsHD/ChANGE-HD
35:16
35:16
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35:16
Dr. Peg talks about the ChAND-HD trial.द्वारा WeHaveAVoice
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Jonathan Monkemeyer Rare Disease Day
53:27
53:27
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53:27
Jonathan speaks to us about Rare Disease Day event as well as reusing existing drugs to treat or cure HD/JHDद्वारा WeHaveAVoice
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James Valvano: New Horizons After 2020
1:08:58
1:08:58
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1:08:58
WeHaveAFace founder, James Valvano talks about his upcoming retirement and the future of WeHaveAFace.द्वारा WeHaveAVoice
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Jimmy Pollard of CHDI: HD Education on a Global Scale
58:21
58:21
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58:21
Jimmy Pollard talks about his experiences and imparts lessons to apply to HD caregiving.द्वारा WeHaveAVoice
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Gene Veritas: CHDI Therapeutics Conference
53:48
53:48
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53:48
Gene Veritas talks about his recent attendance at the CHDI Therapeutics Conference.द्वारा WeHaveAVoice
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Karen Marais talks about her relationship with her partner Chris who has Huntington's Diseaseद्वारा WeHaveAVoice
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Advocating in suicide prevention and other topics with Sarah Warehime and Dr. Herwig Lange
57:35
57:35
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57:35
Leanne and Kevin speak with Sarah Warehime, a beginner as a suicide prevention advocate and Dr. Herwig Lange. We talk about a range of topics including suicide prevention and how to get involved.द्वारा WeHaveAVoice
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A caregivers experience with behaviorial issues with Huntington's Disease
57:42
57:42
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57:42
"Kay" talks about her relationship with her best friend who has Huntington's Disease and how her mood swings are affecting important decisions she has to make.द्वारा WeHaveAVoice
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Kevin Jess reads an excerpt from his novel that is still in progress.द्वारा WeHaveAVoice
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One woman's experience with testing for Huntington's Disease
1:10:23
1:10:23
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1:10:23
Kevin Jess talks with his daughter about her recent experience with testing for Huntington's Diseaseद्वारा WeHaveAVoice
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Our panel of speakers for our Convention in November, 2019द्वारा WeHaveAVoice
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James Valvano talks with Kevin about his climb in Scotland
1:10:03
1:10:03
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1:10:03
James Valvano speaks with Kevin about his mountain climb at Ben Nevis, Scotland and a talk about future shows.द्वारा WeHaveAVoice
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Juvenile Huntington's Disease: A Story of Friendship
47:34
47:34
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47:34
Kevin speaks with Rebecca Bratt, Erin Wade's best friendद्वारा WeHaveAVoice
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Kevin and Leanne speak with Cindy Moore, President of WeHaveAFace Canadaद्वारा WeHaveAVoice
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Kevin Jess talks about milestonesद्वारा WeHaveAVoice
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