Research-based Treatment of Tics, OCD, and Depression
04/23/24 • 32 min
In this episode, I had a compelling conversation with Dr. Angie Landeros-Weisenberger, an Associate Research Scientist at the Yale Child Study Center. We discuss the current state of research and the latest breakthroughs in treating tics and co-occurring conditions such as OCD and depression. Dr. Angie's expertise and passion for research left me both inspired and hopeful for what's on the horizon in patient care.
Episode Highlights:
[01:30] - Dr. Angie’s history of research.
[02:39] - Innovative treatments on the horizon.
[06:10] - Exploring genetic mysteries of tics.
[09:37] - Breaking the habit loop.
[13:33] - The future of wearables.
[16:18] - Trichotillomania research and why it’s not a tic disorder.
[18:48] - Gender bias in tic diagnosis.
[20:46] - A lifetime with OCD and tics.
[24:33] - Selective serotonin reuptake inhibitors (SSRIs) treatment for OCD.
[27:09] - Science is not set in stone, changes will occur with more research.
[27:25] - Advances in research of tools, such as ketamine, for treatment-resistant depression.
[31:34] - Very promising things are coming through research and studies.
Links & Resources:
Yale Child Study Center: https://medicine.yale.edu/childstudy/
New Jersey Center for Tourette Syndrome and Associated Disorders (NJCTS): https://njcts.org/
I want to remind all our listeners that each episode we share is a stepping stone to better understanding the intricate world of Tourette Syndrome and related disorders. If you've enjoyed today's episode, rate us and leave a review. Your feedback not only supports the show but also helps us reach and educate more people like you.
In this episode, I had a compelling conversation with Dr. Angie Landeros-Weisenberger, an Associate Research Scientist at the Yale Child Study Center. We discuss the current state of research and the latest breakthroughs in treating tics and co-occurring conditions such as OCD and depression. Dr. Angie's expertise and passion for research left me both inspired and hopeful for what's on the horizon in patient care.
Episode Highlights:
[01:30] - Dr. Angie’s history of research.
[02:39] - Innovative treatments on the horizon.
[06:10] - Exploring genetic mysteries of tics.
[09:37] - Breaking the habit loop.
[13:33] - The future of wearables.
[16:18] - Trichotillomania research and why it’s not a tic disorder.
[18:48] - Gender bias in tic diagnosis.
[20:46] - A lifetime with OCD and tics.
[24:33] - Selective serotonin reuptake inhibitors (SSRIs) treatment for OCD.
[27:09] - Science is not set in stone, changes will occur with more research.
[27:25] - Advances in research of tools, such as ketamine, for treatment-resistant depression.
[31:34] - Very promising things are coming through research and studies.
Links & Resources:
Yale Child Study Center: https://medicine.yale.edu/childstudy/
New Jersey Center for Tourette Syndrome and Associated Disorders (NJCTS): https://njcts.org/
I want to remind all our listeners that each episode we share is a stepping stone to better understanding the intricate world of Tourette Syndrome and related disorders. If you've enjoyed today's episode, rate us and leave a review. Your feedback not only supports the show but also helps us reach and educate more people like you.
Previous Episode
Advocating for Neurodiversity with Slayton Cooper
Today I am joined by Slayton Cooper, a high school senior valedictorian and youth ambassador for the Tourette Association of America. Slayton is a passionate advocate for Tourette Syndrome, neurodiversity, and related conditions. We explore what it means to truly embrace our unique neural landscapes in school and at work.
We explore the positives and negatives of labels, the importance of advocating for your needs, and finding your most authentic self. Slayton offers profound wisdom well beyond his years on self-acceptance, resisting judgments, and seeing the beauty in our differences. His message of empowerment for those with Tourette Syndrome and similar conditions is truly uplifting.
From personal struggles to triumphant advocacy, this conversation unveils the importance of understanding, acceptance, and empowerment within the neurodiverse community and beyond. Don't miss this insightful journey into the heart of neurodiversity.
Timeline Highlights:
[01:20] What does neurodiversity mean?
[04:29] Advocating for inclusion.
[07:39] Challenges in employment.
[11:30] Stigmas in the workplace.
[16:43] Navigating standardized tests.
[20:23] Balancing goals and ambitions with neurodiversity.
[23:00] Tools and resources
[31:54] Suppressing tics.
Links & Resources:
New Jersey Center for Tourette Syndrome and Associated Disorders (NJCTS): https://njcts.org/
Thank you for tuning into this enlightening conversation on neurodiversity. If you've found resonance or inspiration in our discussion, I encourage you to rate, follow, share, and review our podcast. Your support helps us bring more stories like this to light, empowering others to embrace their unique selves fully.
This episode is dedicated to and in memory of, Patricia Phillips. Rest in peace, Pat. May your memory be a blessing, always.
Next Episode
Diagnosed in the 1970s by Dr. Shapiro with Daniel Ferron
If you're looking to be inspired, you're in for a treat with today's episode of our podcast. I had the privilege of speaking with Daniel Ferron, an extraordinary individual whose journey with Tourette Syndrome is nothing short of incredible. Daniel has navigated life's highs and lows with a condition that was scarcely understood when he was diagnosed in the 1970s. His story is a testament to the power of perseverance and the importance of support. Daniel Ferron is an entertainer, actor, and filmmaker.
Episode Highlights:
[01:20] - Daniel Ferron’s diagnosis in the 1970s by Tourette pioneer Dr. Arthur K. Shapiro.
[04:06] - Early treatment and studying with Daniel’s documentary.
[06:13] - Removed all treatment in his adolescence and had 10 years of tic remission.
[07:30] - Embracing Tourette Syndrome with humor.
[08:27] - When the tics returned.
[10:04] - Daniel’s experience with school in New Jersey.
[11:09] - Family support was paramount to his success.
[13:27] - Finding his calling in entertainment.
[15:45] - The advancement of Tourette advocacy leading to understanding.
[17:30] - Going to the movies and getting into the entertainment business.
[20:05] - Daniel’s documentary “My Life, My Story, My Tourette’s”.
[23:40] - Advice for the younger Tourette community.
[27:03] - Advice to disconnect.
[28:50] - Clarity and sense of self naturally improves as you age.
Links & Resources:
Daniel Ferron's Documentary: "My Life, My Story, My Tourette's"
New Jersey Center for Tourette Syndrome and Associated Disorders (NJCTS): https://njcts.org/
Remember, each story shared on this podcast brings light and understanding to the diverse experiences within the Tourette's community. Your journey is your own, and it's filled with potential and promise. If Daniel's story resonated with you, I encourage you to like, share, and leave a review to help us connect with more listeners.
The UpTic - Research-based Treatment of Tics, OCD, and Depression
Transcript
Angie 00:00
We think that Tourette's definitely has a genetic composition to it. So we know from studies being done, for example, at Yale, we have a Dr. Fernandez that has been working with the genetics and they've actually been working closely with Rutgers and other groups around the world, actually. So we know that that genetics play a role in Tourette's, and tics in general, his line of work has been focused specifically on rare variants. So looking at people that don't have a family his
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