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DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003732-1920715200-1920718800@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2030-11-12/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20301210T120000
DTEND;TZID=America/Chicago:20301210T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003733-1923134400-1923138000@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2030-12-10/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310114T120000
DTEND;TZID=America/Chicago:20310114T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003734-1926158400-1926162000@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-01-14/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310211T120000
DTEND;TZID=America/Chicago:20310211T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003735-1928577600-1928581200@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-02-11/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310311T120000
DTEND;TZID=America/Chicago:20310311T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003736-1930996800-1931000400@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-03-11/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310408T120000
DTEND;TZID=America/Chicago:20310408T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003737-1933416000-1933419600@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-04-08/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310513T120000
DTEND;TZID=America/Chicago:20310513T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003738-1936440000-1936443600@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-05-13/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310610T120000
DTEND;TZID=America/Chicago:20310610T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003739-1938859200-1938862800@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-06-10/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310708T120000
DTEND;TZID=America/Chicago:20310708T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003740-1941278400-1941282000@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-07-08/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310812T120000
DTEND;TZID=America/Chicago:20310812T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003741-1944302400-1944306000@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-08-12/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20310909T120000
DTEND;TZID=America/Chicago:20310909T130000
DTSTAMP:20261008T203121Z
CREATED:20261008T201100Z
LAST-MODIFIED:20261008T203121Z
UID:10003742-1946721600-1946725200@www.myositis.org
SUMMARY:TMA Arkansas Myositis Support Group Meeting
DESCRIPTION:Join fellow members of the myositis community for the TMA Arkansas Support Group\, a welcoming space to connect\, share\, and learn together. \nWhen: Second Tuesday of every month\, 12:00-1:00 PM CT \nWhy attend: \n\nConnect with others who understand. Share experiences with people who truly know what life with myositis is like\, and leave feeling less alone.\nExchange practical tips. Learn how others manage daily life\, symptoms\, treatments\, and working with their care teams.\nStay informed. Hear about the latest myositis education\, research updates\, and TMA resources and programs.\nBuild a local support network. Meet other members in Arkansas and the surrounding region.\nSupport for caregivers and loved ones. Family members and care partners are welcome and encouraged to attend.\n\nAll are welcome. Come as you are\, listen\, share\, or just be present. \nRegister Here \nAbout the Leaders\n \nMy name is Carol Chavez\, and I live in Huntsville\, Arkansas. I was diagnosed with Inclusion Body Myositis in 2016 after many years of doctors\, tests\, pills\, shots\, and infusions. I was forced to retire after 50 years as a hair stylist and beauty industry educator because of a fall caused by weak muscles. Finding The Myositis Association and its support groups has been life-changing for me. I finally discovered a community of people who truly understand our struggles\, celebrate our successes\, and share everyday tips that make life easier — from the best can openers for weak hands to lightweight rollators and new tools that help us stay independent. I’m excited to help start an Arkansas support group where we can learn from one another\, lift each other up\, and make sure no one in our state faces myositis alone. Whether you’re newly diagnosed or have been living with myositis for years\, you are welcome here\, and you belong with us. \n \nRobin Coggins was diagnosed with DM in May of 2022. Although her father had been diagnosed with IBM fifteen years earlier\, she was not aware of the additional types of myositis. Since diagnosis\, Robin has been honing her skills as an advocate attending multiple Rare Disease weeks on Capitol Hill and attending the MyoCon patient conferences as well as joining TMA to facilitate a new support group for Arkansas.
URL:https://www.myositis.org/event/tma-arkansas-myositis-support-group-meeting/2031-09-09/
CATEGORIES:Support or Affinity Group Meeting
ATTACH;FMTTYPE=image/png:https://www.myositis.org/wp-content/uploads/2026/10/2026.10.08-Arkansas.png
ORGANIZER;CN="Carol Chavez":MAILTO:Chavez@myositis.org
LOCATION:https://us02web.zoom.us/meeting/register/7pl3vk_GQJO3iH92E0Wykg
END:VEVENT
END:VCALENDAR