@TheAFTD

@TheAFTD has been a member of Linktree for 5 years and joined in February 2021. The social media accounts linked to from @TheAFTD are: Facebook, Instagram, TikTok, YouTube, LinkedIn, Email, Threads, X, Bluesky, Phone, Website. Besides social media accounts, theaftd has populated their site with Navigating Apathy in FTD, Disinhibition in FTD, California Senate Health Committee Unanimously Advances Bipartisan Bill to Add FTD to the State’s Neurodegenerative Disease Registry | AFTD, Running Through It: Mike Brucklier's Marathon Journey, Submit Artwork for FTD in the Arts, Dear HelpLine: The Caregiver Mind, AFTD - The Association for Frontotemporal Degeneration, AFTD - The Association for Frontotemporal Degeneration, When Words Become Hard to Reach: John Corvino's Journey with PPAOS | AFTD, Rev. Jesse Jackson, Diagnosed with PSP, Dies at 84, Introduction to Frontotemporal Dementia (FTD) Biomarkers - Mar 10th, AARP Highlights What FTD Caregivers Need to Know, AFTD's Esther Kane and Volunteer Liz Zadnik Interviewed on Podcast, FTD Call To Action Featured In Canadian Media, The Lived Experience of FTD: FTD in the Arts, AFTD Healthcare Professional Webinar - Feb 12th, With Love 2026, AFTD's 2025 Impact Report, AFTD’s 2025-2028 Strategic Plan, For Health Professionals, For Researchers, FAQs, View all AFTD News, Employment Opportunities, AFTD's Provider Letter, Brain Donation is Final Gift of 24-Year-Old Diagnosed with FTD, Art as Hope: Emma Heming Willis Featured in CNN Segment on FTD In the Arts, Understanding the Path to an FTD Diagnosis, AFTD Blog & Updates, Genetic FTD News Drives an Artist to Pick Up Paintbrush Again, Dignity Care as an Essential Dementia Guidepost, AFTD Advocacy Webinar - January 28, What is FTD?, From Sean 1.0 to Sean 2.0: One Couple's Journey with FTD, FTD & Genetics Overview, Hope on the Horizon: Daniel Barvin's Personal Mission to Transform FTD Treatment, Newly Diagnosed with FTD, Our Deepest Gratitude to Dr. Walter Koroshetz, AFTD Support Groups, AFTD and partners award $2.1 million in first year of new FTD Diagnostic Biomarkers Initiative | AFTD, Comstock Grants, AFTD’s New Genetic Counseling and Testing Recommendation, Helpful Resources, From Caregiver to Advocate: One Woman's Mission to Transform FTD Support, Advocacy Action Center, AFTD's Diagnostic Checklist, Volunteer Opportunities, Recommended Reading, Ways to Participate in Research, Congratulations to AFTD Research Grant Awardees!, AFTD Store, Help & Hope: The Top Articles of 2025, Support AFTD's Mission, Donate to Support Families Like Jennifer and Jim, 'Ask a Genetic Counselor' Webinar on April 14, AFTD Ambassador Carrie Edwards Shares Her Lottery Story on Tamron Hall, Donate to Support AFTD's Mission: 2026 Spring Appeal, The Lived Experience of FTD: “Holiday Hacks” That Can Make the Season More Enjoyable, AFTD 2026 Education Conference, Bobby Kimball, Toto's Original Lead Singer, Living with FTD, Donate to Support AFTD's 2026 Education Conference, AFTD Director of Research Engagement Shana Dodge Presents at 2025 NORD Breakthrough Summit Lightning Round, AFTD Welcomes New AFTD Ambassadors, AFTD 2026 Race Season, AFTD's Awareness Cards, AFTD Independent Events, How to Explain FTD to Kids & Teens, AFTD Insights, AFTD CEO Susan Dickinson Featured on Dementia Untangled Podcast, Dear HelpLine: Sharing the Diagnosis, Love Will End FTD: Katie Brandt on Caregiving, Loss, and Leading Change | AFTD, Finding Your Way Through the Holidays with FTD, The State of FTD Research Featuring AFTD's Shana Dodge, FTD Research 2025: Paving the Path Towards Effective Treatments, Vanity Fair Features Soho Sessions AFTD Benefit in Honor of Bruce Willis, Donate to AFTD Giving Tuesday 2025, Honor Helen-Ann's Legacy Today, AFTD Grantee Leads Basic Science Study Exploring Role of Protein in Tau-Based Disorders like CBD, Amylyx Pharmaceuticals Ends PSP Trial of AMX0035, Rev. Jesse Jackson, Civil Rights Leader, Diagnosed with PSP, National Family Caregivers Month 2025, Ways to Manage Stress of FTD - National Family Caregivers Month 2025, Why Advocacy Matters Featuring AFTD's Meghan B., AFTD and ADDF Award $2.5 million to Vesper Biotechnology for Drug VES001 Clinical Trial in FTD | AFTD, November 2025 Webinar: Supporting FTD Care Partners with Individual Therapy, Dear HelpLine: Find the Helpers, AFTD Ambassador and “Protective Mama Bear” Dawn Kirby Interviewed on Podcast, New Recommendation: Expanding Genetic Counseling and Testing for People Diagnosed with FTD | AFTD, A Rose with Pink Petals: How FTD Revealed Deb Jobe's Hidden Artist | AFTD, Alector Clinical Trial Results Townhall, Tips & Advice: When "I'm Fine" Isn't Fine - Understanding Anosognosia in FTD | AFTD, Alector Therapeutics Announces Results From Their Phase 3 Clinical Trial Evaluating Latozinemab, New York State FTD Registry Bill Signed into Law, Donate to Support AFTD's Mission: 2025 Fall Appeal, AFTD CEO Susan Dickinson to Retire in May 2026; AFTD Board Leading Search for Successor, Epilepsy More Common in FTD than Alzheimer’s, Study Finds, Dr. Laura Podcast Hosts AFTD’s Esther Kane, National Estate Planning Awareness Week 2025, Something went wrong, The Lived Experience of FTD: Anosognosia, The Lived Experience of FTD: The Benefits of Pets, Comedian Shares Her FTD Caregiving Journey on Podcast, October Webinar - Talking to Family About Genetic FTD Risk, Food for Thought 2025, PSP Diagnostic Checklist, Dear HelpLine: What Comes After an FTD Diagnosis, People at Potential Risk of Developing FTD Share Views on Effects of Predictive Biomarker Testing, FTD Science Digest - September 2025, Broadcaster Wendy Williams Diagnosed with FTD, AFTD Ambassador Carrie Edwards donates lottery winnings to AFTD |Lottery Charity Donations, AFTD Ambassador Julia Pierrat featured in Los Angeles Times, Dear HelpLine: AFTD's Awareness Cards, World FTD Awareness Week 2025, Guest Feature: Learning to live with familial FTD, Driving Hope Golf Tournament, What About the Kids?, Living Well with an FTD Diagnosis, Ferrer PSP Drug Receives Fast Track Designation from U.S. FDA, The Lived Experience of FTD: Talk Therapy in FTD - Risks and Benefits, bit.ly, Emma Heming Willis Shares Family Updates on The Oprah Podcast | AFTD, Emma Heming Willis Interviewed by Diane Sawyer in Prime-Time Special, AFTD News - Volume 22 Issue 2: Summer 2025, Leading FTD Expert Dr. Bruce Miller Interviewed on “Big Brains” Podcast, Hope Rising 2025 Keynote Speaker Spencer Cline, AFTD Founder Helen-Ann Comstock, 1933-2025, Honor Helen-Ann's Legacy, Book About Family’s FTD Journey Helps Raise Funds for AFTD’s Mission | AFTD, Altered Production of Certain Protein Groups Identified as Potential Markers of FTLD Severity in Study, AviadoBio and Astellas Senior Staff Discuss ASPIRE-FTD Trial in Interview, Guest Feature: Forget Me Not, AFTD's Provider Letter, Dear HelpLine: Resources for Genetic FTD, Donate to Support AFTD's Mission: 2025 Summer Newsletter, Growing Up with FTD: Young Caregivers on the FTD Journey, From Symptom Onset to Diagnosis: Improving the FTD Diagnostic Journey, In Podcast Interview, AFTD Ambassador Shares How He Found Purpose Amid Grief | AFTD, Genetic Counseling and Testing Should Be Offered to Persons Diagnosed with FTD, Experts Argue | AFTD, PBS Documentary Spotlights FTD Couple to Exemplify U.S. “Caregiving Crisis” | AFTD, Awareness Cards, Sharing Your Story to Make a Difference: How to Connect with Legislators, World Brain Day 2025, Florida Radio Station Spotlights AFTD Ambassador for His Dementia-Care Advocacy | AFTD, Passage Bio Provides Updated Interim Data from UpliFT-D Clinical Trial for FTD-GRN, Brothers Explain in Podcast How They Live With Gene Linked to FTD, Brain Pathology Consistent with FTD Found in Roughly 35% of Motor Neuron Disease Cases in Recent Study, FTD 101: AFTD 2025 Education Conference, Millennial Whose Father Has PSP Explains the Challenges Faced by Millennial Caregivers, Booklets on FTD, Protect Vital Medicaid Programs!, Dear HelpLine: Comstock Grants, Chinese Study Explores the Psychological Well-being and Health of Dementia Caregivers, Promising FTD Gene Therapy from AviadoBio Featured in the UK Guardian | AFTD, Living Well with an FTD Diagnosis, Leonard A. Lauder, 1933-2025, The Lived Experience of FTD: The Challenges of July Fourth | AFTD, Vesper Bio Trial for FTD-GRN Treatment Achieves Enrollment Milestone, Celebrating July 4th with FTD, AFTD Ambassador Shares Husband’s FTD Journey with West Virginia Newspaper | AFTD, AFTD News - Volume 22 Issue 1: Spring 2025, "Alzheimer's & Dementia" Publishes Summary of AFTD's 2022 Holloway Summit, The Critical Role of Biomarkers in Diagnosis and Treatment, Register for the Speech Language Therapy Webinar, British Study Evaluates Ability of Novel Protein Assay to Capture Blood-Based Dementia Biomarkers, Donate to Support AFTD's Mission, Genetic FTD Advocate Linde Jacobs Profiled in CBS Minnesota Segment, Advancing Hope: Blood Test for Diagnosing Alzheimer’s Disease Approved by FDA, Emma Heming Willis Honored with Caregiving Award, AFTD Medical Advisor Emeritus Virginia Lee Elected to National Academy of Sciences | AFTD, Former U.S. Rep. Wexton, Living with PSP, Featured in “Brain & Life” Magazine  | AFTD, The GUIDE Model and FTD, Session Videos Now Available from AFTD's 2025 Education Conference, Study Identifies Profile of Blood-Based Inflammatory Proteins as Potential FTD Biomarker, Coya Therapeutics Reports Positive Interim Results in Clinical Trial for Experimental FTD Therapy | AFTD, Navigating FTD-ALS, Matching Gifts, The Latest in FTD Research, AviadoBio Announces Completion of Second Cohort in ASPIRE-FTD Trial at AFTD Education Conference, Credit for Caring Act of 2025, What is sporadic FTD?, What is familial FTD?, Tips & Advice: Navigating Apathy in FTD, The Lived Experience of FTD: Managing Anxiety, Two Drugs Selected for Evaluation in Platform Trial for PSP, Former Judge Gains Artistic Ability after PPA Diagnosis, FTD and ALS Joint Initiatives, FTD in the Arts, What is apathy?, Genes That Cause FTD, Study Evaluates PET Tracer and Explores How PSP Damages Brain Synapses, Hospice Care for FTD, PPA Telehealth Intervention Gets Positive Results in Phase 2 Clinical Trial, AFTD Webinar - Partners in Drug Development, Planning for Legal, Financial, and Health Insurance Issues, Donate to AFTD's 2025 Education Conference, Register for the AFTD 2025 Education Conference, Speech Therapy CE Course Features AFTD Ambassador Dawn Ducca, Study Evaluates the Efficacy of Nasally Administered Hormone for Apathy in FTD, Hope Rising Benefit Raises Over $1.9 Million for AFTD’s Mission, TD 5 Boro Bike Tour 2025, AFTD Webinar: How to Find a Genetic Counselor, Amplifying AFTD's Advocacy, FTD Science Digest, ABC News Honors AFTD Ambassador Spencer Cline as “Person of the Week”, Review Article Explores Lived Experiences of Ceasing Driving Due to Young-Onset Dementia, Review Article Explores Lived Experiences of Ceasing Driving Due to Young Onset Dementia, Dear HelpLine: Advanced Care Planning, N.Y. Senator Hinchey Reintroduces Bill to Create State FTD Registry | AFTD, “Inside Edition” Highlights Upcoming Documentary About a Family’s FTD Journey, Pair of Studies Make Significant Findings in Search for FTD Biomarkers, Study Examines Nature of Criminal Risk Behaviors in Dementia, Webinar Recording of 'At the Intersection of FTD and the Law', AFTD Joins Nearly 150 Supporters in Letter Urging Congress to Reject Medicaid and SNAP Cuts, TD Bank Five Boro Bike Tour, Passage Bio Announces Interim Data for UpliFT-D Trial for FTD-GRN, Our Journey Through FTD and Why I Wrote “Welcome to the Honey B & B”, Statement from AFTD on the Need for Robust and Consistent Medical Research Funding, National Doctors' Day 2025, AFTD and You: Partners in Drug Development Webinar, FTD Researchers Call for Greater Focus on Diversity to Address Disparities in Care and Research, H&H Advocacy Update: Protect FTD Research, Support the AFTD-Team - Los Angeles Marathon 2025, Submit your Artwork for FTD in the Arts, Statement from the AFTD on Disruption of Scientific Research Funding and Activities, International Women's Day 2025, Vesper Bio Clinical Trial for FTD-GTN Enters Phase Ib/IIa, With Love 2025, FTD Research Roundtable, FTD and Intimacy By Anne Fargusson, RN, Home and Community Care Options, At the Intersection of FTD and the Law Webinar, Upcoming UCSF Trial to Evaluate Effectiveness of Three Drugs for PSP, Managing the Emotional Impact of Job Loss in FTD, AFTD 2025 Education Conference, Recommended Reading/Viewing, AFTD Webinar: Paving the Path Forward -- Advancing AFTD's Public Policy Priorities, Remember Me Podcast Discusses Grief with AFTD Staff in Recent Episode, AFTD's 2025 Policy Priorities, In TEDx Talk, Neuroscientist Shares Her Father’s FTD Story and Her Hope for Dementia Research Breakthroughs, Denali and Takeda Open FTD-GRN Clinical Trial Site at UPenn, Extracellular Vesicles in Plasma Could be FTD-ALS Diagnostic Biomarker, Study Finds, New AFTD Ambassadors, Ohio Care Partner Shares Story to Help Others on the FTD Journey, Paving The Path Forward: Advancing AFTD's Public Policy Priorities, Vesper Bio Clinical Trial for FTD-GTN Enters Phase Ib/IIa, Walking with Grief: Loss & the FTD Journey, Most Asked Areas of Our Website, Become an FTD Research Ambassador, Tips & Advice: Incontinence - A Troubling Symptom | AFTD, Can a Tau PET Tracer Aid FTD Diagnosis? Study Explores How Tracer Performs in Other Tauopathies, Difference Between Clinical Care and Clinical Research, Article Lists Ways Researchers Can Involve People with Dementia in Identifying Research Priorities, Donate to AFTD's Fall Appeal 2024, FTD Research '24 - Where We’ve Come From & Where We’re Headed, Help & Hope: The Top Articles of 2024, Linde Jacobs Shares Her Families FTD Journey with the New York Times, AFTD Research Team: A Year in Review, Types of FTD, AFTD Ambassador Advocates on Behalf of the Older Americans Act, Employer Matching Gifts, Popular FTD Resources, National Virtual Meet & Greet - January 6, 2025, New York Software Company Awards AFTD Gift to Honor Employee's Late Cousin, AFTD Attends 2024 Society for Neuroscience Meeting, Transposon Presents Results from Successful Phase 2 ALS/FTD Clinical Trial, AviadoBio Shares Hopes for FTD Therapeutic Options, AFTD Care Partner Learning Series Webinar: Navigating the Holidays with an FTD Diagnosis, Ferrer Doses First Participant in Phase 2 Study for PSP Treatment, AFTD Develops New Gene Therapy Resource, Sponsored Testing Programs; opportunities for no-cost genetic testing, FTD Research 2024: Where We’ve Come From and Where We’re Headed, AFTD Advocacy: State Resolution Training, Persons with FTD Advisory Council Special Article: Holiday Madness, Denali Therapeutics Shares Insight Into Developing Treatments, All in the Family to end FTD: Colonial Electric’s Food for Thought Event Clears More than $1 Million Since Inception, National Hospice and Palliative Care Month 2024, Young Caregiver Talks About Finding Support Amid FTD Journey on Dementia UK Podcast, Advancing Hope: AFTD Staff Attend NORD Breakthrough Summit in Washington, DC, Thanks to Generosity of AFTD Ambassador, Californians Receive Crucial Financial Help, Impact Report 2024: Empowered Together to End FTD, GemVax & KAEL Announces Results from Phase 2a Clinical Trial for PSP, Dear HelpLine: Navigating Travel During the Holidays, AFTD Webinar: Diagnosing Primary Progressive Aphasia, Care Partner Learning Series: Navigating the Holidays with an FTD Diagnosis, AFTD hosts 2024 FTD Research Roundtable Meeting, Support for Veterans, Emma Heming Willis Shares Her FTD Experience and Advocacy Work in “Town & Country” Magazine, Young Woman Tells Her Family’s FTD Story on Philadelphia News Segment, Understanding Ambiguous Loss and Anticipatory Grief, AFTD Ambassador Shares Her Family’s FTD Story with Massachusetts Newspaper | AFTD, Study Finds That FTD and ALS Have Similar Cellular and Molecular Characteristics, Psilera Announces Positive Preclinical Data for FTD Intervention Candidate, AFTD Advocacy Conversations: Area Agencies on Aging and Older Americans Act, Medical Technology CEO Discusses Using EEG to Differentiate FTD and Alzheimer’s, Guest Feature: One Woman’s Journey - from Getting Diagnosed to Attempting Suicide to Embracing Life, Food for Thought 2024 - Heather Sellers, Food for Thought 2024 - Lindsey Hunt, Food for Thought 2024 - Terry Walters, Food for Thought 2024, Food For Thought 2024 - Big Time's Chili Contest, Food for Thought 2024 - Dawn Kirby, Dear HelpLine: Social Security Benefits for People with FTD, Passage Bio Discusses Hope for FTD Drug Development, Care Partner Learning Series: Navigating Behavioral Variant FTD Symptoms Webinar, Support AFTD’s Mission, World FTD Awareness Week 2024, AFTD's 2024 Driving Hope Golf Tournament (NY), Acurastem Receives CIRM Grant for Targeted Therapeutic Program for ALS/FTD, In Memory of George F. Sidoris: Two Siblings' Labor of Love, FTD Diagnosis and the Hispanic/Latino Community, AviadoBio CMO Discusses ASPIRE-FTD Clinical Trial with Neurology Live, The Lived Experience of FTD: Deb Jobe, AFTD Ambassador Shares Her Story on “All Home Care Matters” Podcast | AFTD, AFTD Events - Colorado, New AFTD Find Support Page Simplifies Search for Help, Study Investigates Incidence Rates of FTD and Other Young-Onset Dementias in Italy, AFTD News - Volume 21 Issue 2: Summer 2024, Spencer & Paul's Bike Across America for AFTD!, Donate to Support AFTD's Mission: 2024 Summer Newsletter, Research FAQ's, Insights on Stigma: Sandy Howe, The Doctor Thinks It’s FTD. Now What?, AFTD Brand Influencer Discusses Commitment to Caring, AFTD Grant Recipient Discuss Gene Therapy for FTD-GRN on Canadian TV, Dear HelpLine: Transitioning to Facility Care, FTD Awareness Week Officially Recognized in Five Additional States, Ways to Participate in FTD Research, Planned Giving Opportunities - Jary Larsen, FTD & Genetics Overview, ASPIRE-FTD Phase 1/2 Clinical Trial Opens First US Site at Ohio State University, AFTD's 2024 Driving Hope Golf Tournament (CO), Philadelphia Marathon 2024, Care Partner Emphasizes the Benefits of Support from Others Who Understand FTD, Finding Answers: FTD Research & You, Get Involved, Opinion Column Highlights Racial Disparities in Dementia Care and Need for Support, Advocate for Awareness: Working with Lawmakers to Highlight FTD, The Lived Experience: Brain Donation, Medical Technology CEO Discusses Using EEG to Differentiate FTD and Alzheimer’s, Volunteer Update: AFTD Welcomes New AFTD Ambassadors, Passage Bio Receives Positive Feedback from FDA on Expanding Gene Therapy to C9orf72, Researcher Explains the Role of Genetics in FTD, Discusses Avenues for Treatment, British/Dutch Study Discovers Role of ANG Gene Mutations in ALS-FTD, AFTD and ALLFTD Collaborate on Brain Donation Video, Dear HelpLine: Support for Familial & Genetic FTD, Vesper Bio Completes Phase 1 Clinical Trial for Potential Disease Modifying Treatment for FTD-GRN, Study Explores Racial Differences in Clinical Presentation of FTD Symptoms, Disease Severity, Advocacy Update: Join AFTD in Advocating for FTD Awareness Week in All 50 States, Delaware Passes Resolution Recognizing FTD Awareness Week 2024, Viewpoints of FTD: Brain Donation, World Brain Day 2024 - Brain Donation Webinar, Newly Diagnosed Checklist, Ways to Give, FTD & Genetics Overview, Insights on Stigma: Seth Stern, AFTD Volunteer Receives “Visionary of the Year 2024” Award for 40 Years of Advocacy, Ways to Give: Recurring Donor Program, AFTD Volunteer Speaks about Trading Career for New “Vocation” as Caregiver, Transposon Therapeutics Receives Fast Track Designation for PSP Treatment, Spring Appeal 2024, Guidance on Brain Donation, Brain Donation Flyer 2024, Aprinoia Therapeutics Receives Fast Track Designation for PET Tracer Used to Diagnose PSP, National Meet & Greet for LGBTQ+ Care Partners, FTD & ALS: A Collaborative Approach to Diagnosis and Care, Biomarkers Consortium Letter of Intent to Qualify FTD Biomarker accepted by FDA, AFTD Board Member Kristin Holloway Tells Her FTD Story to Self Magazine, The new FTD Disorders Registry is Now Live!, Study Discovers How Variations in TMEM106B Gene Influence Risk & Severity of FTD, AFTD Staff and Emma Heming Willis Commemorate FTD Week Resolution in Calif., AFTD Joins National Institutes of Health AMP ALS Initiative as Partner, Passage Bio Highlights Promising Clinical Trial Progress in Quarterly Update, U.K. Researchers to Conduct Nationwide Trial Evaluating Blood Test for Dementia, Case Report Discusses Symptoms & Diagnosis of PSP, Dear HelpLine: Brain Donation, Colfax Marathon 2024, AFTD In-Person Meet & Greet: Bristol, PA, New York State Senator Michelle Hinchey Introduces First-in-the-Nation Legislation to Create FTD Research Registry, AFTD Insights - Spring 2024, Lorenzo’s Worldwide Youth Summit, FTD in the Arts, FTD Advocate Discusses Isolation and Housing Concerns Faced by Family Care Partners, Unidos en el camino: reunión de personas confrontando la DFT, A Fireside Chat with Susan Dickinson & Emma Heming Willis, First Participant Treated in AviadoBio Phase 1/2 Clinical Trial, Tips & Advice: Roaming & Wandering, Not All Forms of PPA Are FTD, as Recent High-Profile Case Highlights, AFTD 2024 Education Conference, Support AFTD's 2024 Education Conference, Perspectives in Research Webinar: Navigating Social and Legal Challenges in Familial FTD, AFTD Ambassador Honors Daughter by Spreading FTD Awareness, Balancing Safety and Autonomy When Persons Diagnosed Leave the Home, Dementia Advocate with FTD Shares Her Perspective on Losing Her Driver's License, Researchers Adapt Digital Intervention for Dementia Care Partners for FTD, Other Dementias, Dear HelpLine: Hyperorality, The Lived Experience of FTD: Driving and FTD, Roaming in FTD Has an Underlying Reason, Report Says, Recent Study Highlights Reliability and Validity of ALLFTD Mobile App for Diagnosis and Research, Noche de Cine y Charla sobre la Demenciade Inicia Temprano, AFTD Partners with ALS Association to Support Advancing Digital Tools, Finding Support and Understanding on the Go with the Hidden Disabilities Sunflower, FTD Care Partner Shares Memories of Her Mother on TikTok, Link Between TAF15 Protein & FTD Discovered in UK Study, High-Profile FTD Diagnoses Boost Public Awareness, AFTD Ambassador Says, Dear HelpLine: Looking for Support Options, A Note to the AFTD Community about Wendy Williams’s FTD Diagnosis, Making a Difference: Become an FTD Advocate Webinar, Magazine Editor Shares Legacy of Beloved Seattle Music Promoter Diagnosed with FTD, #EndDementiaStigma Toolkit, AFTD Launches Social Media Campaign to #EndDementiaStigma, Los Angeles Marathon 2024, Roseville, Calif. Meet & Greet, Advocacy Update: Rare Disease Day and FTD, Guest Feature: Somebody's Sister, AFTD Webinar: The Current State of FTD, Brain Awareness Week 2024, AFTD CEO Discusses Wendy Williams's FTD Diagnosis, AFTD Webinar: The Current State of FTD, AFTD Volunteer Shares Father's FTD Journey to Promote Awareness in News Interviews, Memphis, Tenn. Meet & Greet, With Love 2024, With Love 2024 - Kristen Celusniak, Treat FTD Grant Recipient Discusses FTD-GRN Gene Therapy in Newspaper Interview, Transposon Announces Results from Phase 2 PSP Trial, Interim Results for Phase 2 FTD/ALS Trial, Austin Marathon 2024, With Love 2024 - Michelle Slough, Delray Beach, Flo. Meet & Greet, Addressing Barriers to Diagnosis, FTD Care, and Research Participation Faced by Black/African Americans, FDA Grants Breakthrough Therapy Designation to Experimental FTD Therapy, UK Researchers Discover How to Block Toxic Protein Associated with FTD and ALS, Montana Woman Shares Family's FTD Journey in Interview, Tucson, Ariz. Meet & Greet, Kevin Rhodes Shares His Journey with FTD, Partners in FTD Care - 2023 Winter Issue, Viewpoints of FTD: Addressing Barriers to Diagnosis, FTD Care, and Research Participation Faced by Black/African Americans | AFTD, With Love 2024 - Dianna Smith, Capturing Voices - Considerations When Writing YOUR Book, What to Look for When Considering Facility Care for a Person with FTD, NY State Senator Michelle Hinchey Introduces Bill to Create State FTD Registry, News Report on Tallahassee Couple’s FTD Journey Highlights Challenges of Misdiagnosis, Familial Conference: Uncovering the Genetics of FTD/ALS, With Love 2024, Public Benefits When Notable Names Share Neurological Challenges, UCLA Professor Writes, Dear HelpLine: Dealing With Genetic Uncertainty, Researcher Discusses Integrating Genetic Testing Into Routine FTD/ALS Care in Podcast Interview, AFTD and ADDF Extend Treat FTD Fund Program Through 2035, Become an FTD Research Ambassador, Gene Therapy for FTD: What Do I Need to Know?, The Lived Experience of FTD: Grief on the FTD Journey, “We’re Just Regular People with an Illness,” Dementia Advocate with FTD Writes in Essay, AFTD Ambassadors, Fall Appeal 2023, Tips & Advice: Navigating Apathy in FTD, Passage Bio Announces Hopeful Initial Data from Phase 1/2 Clinical Trial, RedEye Reviews Charity Fundraiser, 2023 Impact Report, AFTD Volunteer Highlights Differences Between FTD and Alzheimer’s in Newspaper Article, U.S. Justice System Stumbles When Faced with FTD and Other Dementias, Article Finds, Volunteer Update: Hosting a Meet & Greet Event, FTD Behavior Tracker, Dear HelpLine: Connecting During Facility Visits, Advocacy Action Center, AFTD News - Volume 20 Issue 3: Fall 2023, Pilot Study Evaluates Virtual Coaching’s Ability to Help FTD Care Partners with Self-Care, Open Hand Foundation Provides AFTD $600K Donation.