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DTSTART;TZID=America/Chicago:20251202T180000
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CREATED:20250605T143721Z
LAST-MODIFIED:20250805T180202Z
UID:10001808-1764698400-1764705600@www.myositis.org
SUMMARY:TMA Minnesota Myositis Support Group Meeting
DESCRIPTION:Register Here \nJoin the TMA Minnesota Myositis Support Group: Connect\, Share\, and Find Support \nThe TMA Minnesota Myositis Support Group offers a welcoming space for individuals living with myositis to connect\, share experiences\, and support one another. Meeting every two months on the first Tuesday at 6:00 PM CT\, this group provides a valuable opportunity to engage with others who truly understand the challenges of living with myositis. \nWhether you’re newly diagnosed or have been managing myositis for years\, this group is here to help reduce isolation\, offer resources\, and build a sense of community. By sharing stories and learning from each other\, you’ll gain valuable insights and feel empowered to navigate your myositis journey with support from others who understand. \nWhen?\nFirst Tuesday of every two months at:\n6:00 PM CT \nJoin us to decrease loneliness\, access helpful resources\, and find strength in the power of community. We look forward to connecting with you! \nRegister Here
URL:https://www.myositis.org/event/tma-minnesota-myositis-support-group-4/2025-12-02/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/jpeg:https://www.myositis.org/wp-content/uploads/2025/06/Minnesota.jpg
ORGANIZER;CN="Lindsay Guentzel":MAILTO:Guentzel@myositis.org
LOCATION:https://www.myositis.org/event/tma-minnesota-myositis-support-group-4/2025-12-02/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20251202T180000
DTEND;TZID=America/Chicago:20251202T200000
DTSTAMP:20251113T233237Z
CREATED:20250605T143721Z
LAST-MODIFIED:20251113T233237Z
UID:10001111-1764698400-1764705600@www.myositis.org
SUMMARY:TMA Minnesota & Wisconsin Myositis Support Group Meeting
DESCRIPTION:Register Here \nJoin the TMA Minnesota & Wisconsin Myositis Support Group: Connect\, Share\, and Find Support \nThe TMA Minnesota & Wisconsin Myositis Support Group offers a welcoming space for individuals living with myositis to connect\, share experiences\, and support one another. Meeting every two months on the first Tuesday at 6:00 PM CT\, this group provides a valuable opportunity to engage with others who truly understand the challenges of living with myositis. \nWhether you’re newly diagnosed or have been managing myositis for years\, this group is here to help reduce isolation\, offer resources\, and build a sense of community. By sharing stories and learning from each other\, you’ll gain valuable insights and feel empowered to navigate your myositis journey with support from others who understand. \nWhen?\nFirst Tuesday of every two months from:\n6:00 – 8:00 PM CT \nJoin us to decrease loneliness\, access helpful resources\, and find strength in the power of community. We look forward to connecting with you! \nAbout the Leaders \n \nLindsay Guentzel is an award-winning journalist\, writer\, producer\, and podcast host whose work has been featured in The New York Times\, CBS Radio\, NPR\, ESPN\, and more. After being diagnosed with ADHD in 2021—an experience she calls the best thing to ever happen to her—she spent two years learning how to navigate life with a neurodivergent brain. Then\, in 2023\, her world shifted again with a diagnosis of Dermatomyositis associated with Anti-Synthetase Syndrome\, a collection of rare\, incurable diseases that drastically changed her daily life. \nJim “Sudz” Szudzik \n \nJames “Sudz” Szudzik  served in the U.S. Army as a Chaplain’s Assistant during the Vietnam conflict. Following his service\, Sudz earned a Bachelor of Arts in Communications from Michigan State University. Over the course of his career\, he held roles with Lansing Probate Court\, Service Beer & Wine\, Miller Brewing Company\, Philip Morris U.S.A.\, Bonanza Beverage\, New Mexico Beverage\, and the Madrigano family. He married Nancy Ann Wygert in August 1985. \nSudz was diagnosed with Inclusion Body Myositis in 2004 and has since dedicated himself to advocating for veterans with IBM and educating others about myositis. His daily life centers on faith\, family\, and friends\, embracing life’s challenges with gratitude and resilience. He also enjoys movies\, reading\, televised sports\, and collecting baseball cards. He lives in Menomonee Falls\, Wisconsin with Nancy and their dog Bodie.
URL:https://www.myositis.org/event/tma-minnesota-wisconsin-myositis-support-group-6/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/jpeg:https://www.myositis.org/wp-content/uploads/2025/06/Minnesota-Wisconsin.jpg
ORGANIZER;CN="Lindsay Guentzel":MAILTO:Guentzel@myositis.org
LOCATION:https://www.myositis.org/event/tma-minnesota-wisconsin-myositis-support-group-6/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251203T200000
DTEND;TZID=America/New_York:20251203T213000
DTSTAMP:20260310T185113Z
CREATED:20250605T143731Z
LAST-MODIFIED:20260310T185113Z
UID:10001330-1764792000-1764797400@www.myositis.org
SUMMARY:TMA Flying Solo Affinity Group Meeting
DESCRIPTION:Register Here \nJoin TMA’s Flying Solo Affinity Group: Support for Those Living with Myositis Without a Live-In Care Partner \nThe TMA Flying Solo Affinity Group is a dedicated space for individuals diagnosed with myositis who do not have a live-in care partner. Whether you live alone\, are married but your spouse is unable to provide care\, or even find yourself as the caregiver for your spouse\, this group is here to offer understanding and support. \nLiving with myositis can be particularly challenging without a live-in care partner\, but Flying Solo offers a community where you can connect with others who truly understand your unique circumstances. Share experiences\, find helpful resources\, and gain insights on managing daily life with myositis while navigating the complexities of independence and self-care. \nWhen?\nFirst Wednesday of each month at:\n8:00 PM ET | 7:00 PM CT | 6:00 PM MT | 5:00 PM PT \nJoin us for this monthly meeting to connect\, find strength\, and support each other in our myositis journeys. You are not alone – come share and learn with others who “fly solo” like you! \nRegister Here \n\n \nAbout the Leader | Rhonda Rogers \nRhonda Rogers\, diagnosed with Inclusion Body Myositis (IBM)\, is a passionate myositis advocate\, also known as “Myositis Warrior”\, who brings connection\, humor\, and heart to everything she does. She co-leads TMA’s Southern California Support Group and facilitates the TMA Flying Solo Affinity Group for people living with myositis who do not have a live-in care partner. Rhonda also administers the popular Myositis Warrior Facebook public group\, known for its upbeat\, candid\, and often humorous take on the unbelievable realities of life with myositis. Whether leading community groups or raising awareness in her signature Myositis Warrior cape at events like Comic-Con\, Rhonda inspires others to meet life with resilience and a smile. \nIn recognition of her outstanding leadership and support for the myositis community\, Rhonda received the Marianne Moyer Myositis Leader Award at MyoCon 2025\, along with her TMA Southern California co-leader\, Nancy Harber. This award honors TMA volunteers who lead the way by helping others and making a lasting impact.
URL:https://www.myositis.org/event/tma-flying-solo-affinity-group-meeting-23/2025-12-03/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/jpeg:https://www.myositis.org/wp-content/uploads/2025/06/flyingsolo-169.jpg
ORGANIZER;CN="Rhonda Rogers":MAILTO:Rogers@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/tZYqc-GsrTksGt3aRRRGipKTWPzy7-n18ME4#/registration
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251204T130000
DTEND;TZID=America/New_York:20251204T140000
DTSTAMP:20251203T161933Z
CREATED:20251030T231809Z
LAST-MODIFIED:20251203T161933Z
UID:10001907-1764853200-1764856800@www.myositis.org
SUMMARY:Myositis Research Insights featuring Dr. Erin Wilfong
DESCRIPTION:Register Here \nJoin TMA for our next Myositis Research Insights webinar\, featuring Dr. Erin Wilfong\, a leading expert in autoimmune muscle disease. Dr. Wilfong will share updates from her latest research and discuss how these findings may impact the understanding and treatment of myositis. Don’t miss this opportunity to hear directly from one of the scientists advancing myositis research and to ask your questions during a live Q&A.
URL:https://www.myositis.org/event/28232/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2025/10/Screenshot-2025-10-30-194158-1.png
LOCATION:https://us02web.zoom.us/webinar/register/WN_869QjHmjQ5esbNbSklDZNw#/registration
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251204T183000
DTEND;TZID=America/New_York:20251204T203000
DTSTAMP:20250904T194239Z
CREATED:20250605T143743Z
LAST-MODIFIED:20250904T194239Z
UID:10001507-1764873000-1764880200@www.myositis.org
SUMMARY:TMA Women Of Color Affinity Group Meeting
DESCRIPTION:Register Here \nJoin TMA’s Women of Color Affinity Group: Empowerment Through Support & Advocacy \nFounded in 2019 by Holly Jones and Kaniah Gunter\, TMA’s Women of Color (WOC) Affinity Group is a vibrant support and advocacy community dedicated to uplifting women of color living with myositis. Through the powerful 3E’s—Encouragement\, Education\, and Empowerment—our mission is to unite and empower women of color affected by myositis and to advocate for their health and well-being. By providing education\, support\, resources\, and the backing of TMA’s expertise\, we are determined to reduce the disparity gap in myositis outcomes for people of color. As we foster a community of strength\, resiliency\, and inspiration; together\, we will break barriers\, challenge inequalities\, and create a future where every woman\, caregiver\, and loved one affected by myositis\, regardless of their race\, can thrive. \nEach month\, WOC come together for impactful workshops and support meetings\, empowering participants to take what they’ve learned and share awareness about myositis within their communities. Whether you’re looking for guidance\, solidarity\, or the opportunity to advocate for others\, this group offers a space for connection\, education\, and positive change. \nWhen?\nFirst Thursday of each month at:\n6:30pm ET | 5:30pm CT | 4:30pm MT | 3:30pm PT \nJoin us and become part of a movement to raise awareness\, educate others\, and empower women of color to take charge of their myositis journey. Visit our group page for more information. \nRegister Here \n\n       \nAbout the Leaders | Holly Jones & Kaniah Gunter \nIn 2003\, at the age of 19 years old Holly Jones was diagnosed with Polymyositis with Interstitial Lung Disease at a CPK level over 20\,000. In 2014\, her lung disease progressed causing her to develop Pulmonary Hypertension that required her to be on oxygen daily. After six years of being in clinical remission\, the Pulmonary Hypertension progressed into Congestive Heart Failure in October 2020. Living with diseases that attack her muscles\, lungs\, and heart; it has not stopped Holly from accomplishing her life goals. A social media entrepreneur\, Holly also serves on TMA’s Board of Directors\, as well as co-leader for TMA’s Women of Color Affinity Group\, and Support Group Leader for the Houston\, Tx regional support group.  Holly lives in Porter\, TX with her husband and children. \nKaniah Gunter\, a Nutrition Health Coach owner of Unique Guidance Nutritional Health Coaching\, LLC\, was diagnosed with dermatomyositis with NXP-2 positive (anti-MJ) and scleroderma in 2007. Kaniah graduated from The Institute for Integrative Nutrition\, one of the largest nutrition schools in the world. \nRecently she completed her certification as a Community Health Worker. She is a strong advocate for the myositis community. At TMA\, she is a regional support group leader for TMA Virginia\, West Virginia and Northwest Carolina as well as co-leader for TMA’s Women of Color affinity group. She has shared her story in many healthcare publications and social media. She serves as an inspiration for others as she demonstrates healing begins within mind\, body and spirit. Kaniah and her two beautiful children live in Norfolk\, Virginia.
URL:https://www.myositis.org/event/tma-women-of-color-affinity-group-meeting-17/2025-12-04/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/jpeg:https://www.myositis.org/wp-content/uploads/2025/06/TMA-WOCAG-WEBSITE-BANNER.jpg
LOCATION:https://www.myositis.org/event/tma-women-of-color-affinity-group-meeting-17/2025-12-04/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251206T130000
DTEND;TZID=America/New_York:20251206T143000
DTSTAMP:20250801T204659Z
CREATED:20250605T143744Z
LAST-MODIFIED:20250801T204659Z
UID:10001751-1765026000-1765031400@www.myositis.org
SUMMARY:TMA Care Partner Affinity Group Meeting
DESCRIPTION:Please note there will be no July meeting to allow our volunteers to celebrate the holiday with their families.\nJoin the TMA Care Partner Affinity Group: A Space Just for You \nBeing a care partner to someone with myositis can be emotionally and physically challenging. Whether it’s dealing with stress\, anxiety\, or the weight of daily caregiving tasks\, it’s easy to feel overwhelmed and burnt out. That’s why the TMA Care Partner Affinity Group\, founded in 2022\, provides a supportive environment specifically for those who care for someone living with myositis. \nThis group meets in its own dedicated breakout room within TMA’s Worldwide Support Group Meeting on the first Saturday of each month. It’s a safe space where you\, the care partner\, are the focus—not the patient. Here\, you can connect with others who understand your unique challenges\, share coping strategies\, and discuss how to navigate the complex healthcare system. Whether it’s accessing resources like home health aides\, meal delivery\, or transportation assistance—or finding the right words to communicate with your loved one or healthcare team—this group is here to help you through it all. \nTo learn more about accessing breakout rooms\, see ACCESSING ZOOM BREAKOUT ROOMS \nWhen?\nFirst Saturday of every month at:\n1:00 PM ET | 12:00 PM CT | 11:00 AM MT | 10:00 AM PT \nThe emotional demands of caregiving are real\, and sometimes\, you just need a place to express frustrations\, share victories\, and lean on others who truly understand. The TMA Care Partner Affinity Group is here to provide the support\, resources\, and community you need to continue on your journey. Join us and find the strength to take care of yourself\, too. \nRegister Here \n 
URL:https://www.myositis.org/event/tma-care-partner-affinity-group-meeting-13/2025-12-06/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/webp:https://www.myositis.org/wp-content/uploads/2025/06/Care-Partner.webp
ORGANIZER;CN="Rachel Bromley":MAILTO:Rachel@myositis.org
LOCATION:https://www.myositis.org/event/tma-care-partner-affinity-group-meeting-13/2025-12-06/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251206T130000
DTEND;TZID=America/New_York:20251206T143000
DTSTAMP:20260413T162341Z
CREATED:20250801T201217Z
LAST-MODIFIED:20260413T162341Z
UID:10001691-1765026000-1765031400@www.myositis.org
SUMMARY:TMA Worldwide Myositis Support by Diagnosis
DESCRIPTION:TMA’s Worldwide Myositis Support by Diagnosis Group is open to all\, especially those without an active support group in their local area. Formally known as Nationwide\, this group has hosted international members since its inception in 2022. The meeting divides into breakout rooms by diagnosis\, and the TMA Care Partner Affinity Group meets in its own room. TMA Worldwide meets on the first Saturday of each month from 1:00 pm – 2:30 pm ET | 12:00 PM – 1:30 PM CT | 11:00 AM – 12:30 PM MT | 10 AM – 11:30 AM PT.  \nRegister here
URL:https://www.myositis.org/event/tma-worldwide-myositis-support-by-diagnosis/2025-12-06/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2025/08/New-Worldwide-2.png
ORGANIZER;CN="Dave Volk":MAILTO:Volk@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/tZMuc-mtqTktHNH_sskpoHflne4zPRAkfS9y
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251209T120000
DTEND;TZID=America/New_York:20251209T130000
DTSTAMP:20251203T154435Z
CREATED:20251120T180929Z
LAST-MODIFIED:20251203T154435Z
UID:10002060-1765281600-1765285200@www.myositis.org
SUMMARY:The JASMINE Clinical Study: An Overview for the Myositis Community
DESCRIPTION:Register Here \nJoin us for a special webinar featuring Dr. Andrew Beaton as he provides a clear and accessible overview of the JASMINE Clinical Study. This session will help members of the myositis community better understand the study’s goals\, design\, and potential impact\, as well as what participation may entail. Whether you’re a patient\, care partner\, or advocate\, this webinar offers an opportunity to learn directly from an expert. Special thanks to AstraZeneca for sponsoring this webinar. \n 
URL:https://www.myositis.org/event/the-jasmine-clinical-study-an-overview-for-the-myositis-community/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2025/11/AstraZeneca-Dec-9-2025-Webinar.png
LOCATION:https://us02web.zoom.us/webinar/register/WN_3JwYkb4BQAOM29q5SbSlMQ
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251209T160000
DTEND;TZID=America/New_York:20251209T180000
DTSTAMP:20251228T231147Z
CREATED:20251105T195356Z
LAST-MODIFIED:20251228T231147Z
UID:10001910-1765296000-1765303200@www.myositis.org
SUMMARY:Hospital of Special Surgery (HSS) New York City Myositis Support Group
DESCRIPTION:The HSS Myositis Support Group is open to people living with myositis\, their families\, and friends. \nIf this is your first time attending the HSS group meeting\, please be sure to contact the group coordinator before the meeting date in order to receive the join link. \nPLEASE RSVP TO SUZAN BEFORE THE MEETING DATE: \nSuzan Fischbein\, LCSW \nSr. Social Work Coordinator II \nemail: fischbeins@hss.edu \nSPONSORED BY \nDepartment of Social Work Programs and The Division of Rheumatology at Hospital for Special Surgery | 535 East 70th Street New York\, NY 10021
URL:https://www.myositis.org/event/hospital-of-special-surgery-hss-new-york-city-myositis-support-group/2025-12-09/
CATEGORIES:Support or Affinity Group Meeting
ORGANIZER;CN="Suzan Fischbein":MAILTO:FischbeinS@HSS.edu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20251210T130000
DTEND;TZID=America/Chicago:20251210T143000
DTSTAMP:20251202T003029Z
CREATED:20250605T143720Z
LAST-MODIFIED:20251202T003029Z
UID:10001105-1765371600-1765377000@www.myositis.org
SUMMARY:TMA Kansas & Western Missouri Myositis Support Group Meeting
DESCRIPTION:Register Here \nJoin the TMA Kansas & Western Missouri Myositis Support Group: A Community for Myositis Warriors \nThe TMA Kansas & Western Missouri Myositis Support Group is a welcoming space for individuals living with myositis. Meeting 3-4 times per year\, this group provides a supportive environment to connect\, share experiences\, and learn from others facing similar challenges. \nWhether you’re newly diagnosed or have been managing myositis for years\, this group is here to help you navigate your journey. Through open discussions and shared stories\, you can find strength\, access valuable resources\, and reduce the isolation that often accompanies chronic illness. \nRegister here to secure your spot and be part of this empowering community. Join us to connect\, find support\, and take the next step in your myositis journey!
URL:https://www.myositis.org/event/tma-kansas-western-missouri-myositis-support-group-meeting-4/
CATEGORIES:Support or Affinity Group Meeting
LOCATION:https://www.myositis.org/event/tma-kansas-western-missouri-myositis-support-group-meeting-4/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251211T120000
DTEND;TZID=America/New_York:20251211T130000
DTSTAMP:20251030T231059Z
CREATED:20251012T044452Z
LAST-MODIFIED:20251030T231059Z
UID:10001897-1765454400-1765458000@www.myositis.org
SUMMARY:Ask the Expert Speech-Language Pathology Edition
DESCRIPTION:Register Here \nJoin TMA for an interactive\, Ask the Expert Q&A with Dr. Kendrea Garand\, a board-certified specialist in swallowing and speech-language pathology.\nThis session will focus entirely on your questions about speech\, voice\, and swallowing challenges in myositis—how to recognize them\, when to ask for an evaluation\, and practical tips that help you eat\, drink\, and communicate more safely and confidently.\nBring your questions live or submit them in advance when you register.
URL:https://www.myositis.org/event/ask-the-expert-speech-language-pathology-edition/
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2025/10/Kendrea-Garand-Dec-2025.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20251213T120000
DTEND;TZID=America/Denver:20251213T133000
DTSTAMP:20251212T162838Z
CREATED:20250605T143707Z
LAST-MODIFIED:20251212T162838Z
UID:10001048-1765627200-1765632600@www.myositis.org
SUMMARY:TMA Colorado Myositis Support Group Meeting
DESCRIPTION:On December 13\, TMA Colorado Support Group call will feature Dr. Richard Nash and Dr. David Korman from the Colorado Blood Cancer Institute.  Their team is now involved in new studies using CAR-T therapy for rheumatologic conditions\, including myositis (IIM). \nDr. Korman\, MD is a rheumatologist in Denver\, Colorado\, and an Associate Clinical Professor of Medicine–Rheumatology at the University of Colorado. His clinical work centers on complex autoimmune and inflammatory diseases\, including myositis and other systemic rheumatologic conditions. He collaborates with the Colorado Blood Cancer Institute on emerging cell-therapy approaches and serves as an investigator for clinical trials evaluating CAR-T cell therapy for autoimmune diseases. \nDr. Nash\, MD is a hematologist / transplant physician at the Colorado Blood Cancer Institute with extensive experience using autologous hematopoietic stem cell transplant (AHSCT) to treat autoimmune neurologic and rheumatologic diseases. He and his team have developed standard-of-care AHSCT treatment guidelines for multiple sclerosis (MS) and systemic sclerosis (SSc). \nHe is also an investigator for clinical trials evaluating CAR-T cell therapy for autoimmune conditions including myositis\, systemic lupus erythematosus (SLE)\, systemic sclerosis\, and rheumatoid arthritis\, and is actively working to expand cell-therapy research for rare autoimmune diseases. \nDuring the call\, they will share recent data on IIM and CAR-T\, provide general education on cell therapy for autoimmune diseases\, and answer any questions we may have. \n  \n \nTMA Colorado Myositis Support Group has reactivated and meets on the second Saturday of each month at noon Mountain Time! \nMeet Jim Milani\, a TMA member who was moved by the efforts of the late Marianne Moyer and the TMA Southwest Florida’s success in organizing a Myositis Symposium for Physical and Occupational Therapists for  Myositis Awareness Month. He called Rachel Bromley\, TMA’s Senior Manager of Patient Education\, Support and Advocacy to offer to organize one in his home state of Colorado. Rachel was ecstatic\, as Marianne’s vision had always been for this event to branch out to other TMA groups! One catch though – TMA Colorado had been dormant for quite some time. So she swung for the fences and said “How about reactivating the Colorado group at the same time? You can connect more PTs and OTs that way\, find a few volunteers to possibly help your efforts\, and provide and receive support for myositis along the way!” \nJim replied with one word “SURE!” And so this journey began. \nFor the past 20 years\, Jim has been a Physical Therapist and is Board Certified as a Geriatric Specialist. After several years of misdiagnoses\, he was correctly diagnosed with IBM in late 2023. Despite this\, Jim continues to pursue his love for activity and sports. He is passionate about sharing his personal and professional “fitness forward” philosophy\, helping people understand how to modify and adapt exercises to their functional level. Jim resides in Colorado with his wife\, Laura. He is a proud father of six adult children and has two grandchildren. Jim says his family and faith help him get through each day. While there is much about IBM that he cannot control\, he focuses on what he can: his attitude and effort. #justkeepswimming \nAnyone can join his meetings\, Colorado resident or not. You can register here! \n 
URL:https://www.myositis.org/event/tma-colorado-myositis-support-group-meeting-15/
LOCATION:https://www.myositis.org/event/tma-colorado-myositis-support-group-meeting-15/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251213T130000
DTEND;TZID=America/New_York:20251213T143000
DTSTAMP:20251119T180316Z
CREATED:20250605T143718Z
LAST-MODIFIED:20251119T180316Z
UID:10001096-1765630800-1765636200@www.myositis.org
SUMMARY:TMA MD\, DE\, DC\, and Northern Virginia Myositis Support Group Meeting
DESCRIPTION:Register Here \nJoin the TMA MD\, DE\, DC\, and Northern Virginia Myositis Support Group: A Community for Myositis Warriors \nThe TMA MD\, DE\, DC\, and Northern Virginia Myositis Support Group is a welcoming space for individuals living with myositis in the Maryland\, Delaware\, District of Columbia\, and Northern Virginia regions. Meeting every two months on the third Saturday at 1:00 PM ET\, this group provides a supportive environment to connect\, share experiences\, and learn from others facing similar challenges. \nWhether you’re newly diagnosed or have been managing myositis for years\, this group is here to help you navigate your journey. Through open discussions and shared stories\, you can find strength\, access valuable resources\, and reduce the isolation that often accompanies chronic illness. \nWhen?\nThird Saturday of every other month at:\n1:00 PM ET \nRegister here to secure your spot and be part of this empowering community. Join us to connect\, find support\, and take the next step in your myositis journey!
URL:https://www.myositis.org/event/tma-md-de-dc-and-northern-virginia-myositis-support-group-meeting-7/
CATEGORIES:Support or Affinity Group Meeting
LOCATION:https://www.myositis.org/event/tma-md-de-dc-and-northern-virginia-myositis-support-group-meeting-7/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20251218T183000
DTEND;TZID=America/Chicago:20251218T200000
DTSTAMP:20251217T201019Z
CREATED:20250605T143655Z
LAST-MODIFIED:20251217T201019Z
UID:10000998-1766082600-1766088000@www.myositis.org
SUMMARY:TMA Missouri and Illinois Group Meeting
DESCRIPTION:Register Today \nJoin the TMA Missouri & Illinois Myositis Support Group: A Community for Myositis Warriors \nThe TMA Missouri & Illinois Myositis Support Group is a welcoming space for individuals living with myositis. Meeting every three months on the third Thursday at 6:30 PM CT\, this group provides a supportive environment to connect\, share experiences\, and learn from others facing similar challenges. \nWhether you’re newly diagnosed or have been managing myositis for years\, this group is here to help you navigate your journey. Through open discussions and shared stories\, you can find strength\, access valuable resources\, and reduce the isolation that often accompanies chronic illness. \nWhen?\nEvery 3 months on the third Thursday at:\n6:30 PM CT \nRegister here to secure your spot and be part of this empowering community. Join us to connect\, find support\, and take the next step in your myositis journey!
URL:https://www.myositis.org/event/tma-missouri-and-illinois-group-meeting-5/
LOCATION:https://www.myositis.org/event/tma-missouri-and-illinois-group-meeting-5/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20251219T170000
DTEND;TZID=America/Los_Angeles:20251219T183000
DTSTAMP:20250731T182943Z
CREATED:20250605T143747Z
LAST-MODIFIED:20250731T182943Z
UID:10001568-1766163600-1766169000@www.myositis.org
SUMMARY:TMA Northern California\, Oregon & Washington IBM Support Group Meeting
DESCRIPTION:Register here! \n\n \nJoin the TMA Northern California\, Oregon & Washington IBM Support Group: Connect\, Learn\, and Find Support\n\nThis group is a welcoming community for individuals living with Inclusion Body Myositis (IBM) in Northern California\, Oregon & Washington\, although all are welcome. Meeting every month on the third Friday at 5:00 PM PT\, this group offers a supportive space to connect with others who understand the unique challenges of living with IBM. \nWhether you’re newly diagnosed or have been living with IBM for some time\, this group is here to help reduce feelings of isolation\, provide valuable resources\, and foster a sense of belonging. Join us to share experiences\, learn about available support services\, and build connections with others in your community who are navigating the same journey. \nWhen?Third Friday of every month at:5:00 PM PT \nAll are welcome to attend—no matter where you are on your myositis journey. This group is a chance to decrease loneliness\, access important resources\, and find strength in the support of others who truly understand what you’re going through. \n\n \n\n 
URL:https://www.myositis.org/event/tma-northern-california-ibm-support-group-meeting-31/2025-12-19/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/jpeg:https://www.myositis.org/wp-content/uploads/2025/06/Northeast-Texas-1.jpg
ORGANIZER;CN="Malati Shinazy":MAILTO:Shinazy@myositis.org
LOCATION:https://www.myositis.org/event/tma-northern-california-ibm-support-group-meeting-31/2025-12-19/
END:VEVENT
END:VCALENDAR