#HighRiskCOVID19: Reality Check from the Immunocompromised Community


COVID-19 & AiArthritis: Special Series, Episode 3

Air Date: March 29, 2020

Welcome to AiArthritis Voices 360. This episode join your hosts Kelly Conway and Charis Hill to discuss COVID-19 and the potential impact on the AiArthritis Community. This is the third episode in a breakout series on COVID-19 and what you can do to protect yourself during the pandemic. They will discuss raising awareness for the risks experienced by disabled and chronically ill people during the pandemic and what you can do to join the movement. They also dive into being discriminating about the reliability of sources when reading about COVID-19 and prioritizing your mental and emotional wellness during social isolation.


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Show Notes: Episode 21 - "COVID-19 &AiArthritis: High Risk COVID-19"

00:52 - Kelly welcomes listeners

02:23 - Kelly lives with Rheumatoid Arthritis

02:37 - Today’s topic is the high risk community of AiArthritis patients living during a COVID-19 outbreak

02:45 - Kelly welcomes patient co-host, Charis, who lives with Ankylosing Spondylitis 

03:19 - In the beginning of the outbreak, the messaging focused mostly on the fact that children were not at risk and the elderly and people with compromised immune systems were in the most danger

05:50 - Charis drafted language in a social media post that was adopted by their local mayor to communicate to the public that individuals at increased risk from COVID-19 needed others to practice socially responsible behaviors to help thwart the spread of the virus

06:50 - Charis has been spreading the message that it is everyone’s job to stay home so that everyone doesn’t get sick instead of the idea that immunocompromised people should self-isolate if they want to be safe

07:44 - All people need to stay home as much as possible to prevent asymptomatic carriers from spreading the virus to vulnerable members of our society without knowing it

08:51 - Charis explains the origin of #HighRiskCOVID19

12:34 - It’s important to put a face to the category of “high risk people” so that the public understands who all they are protecting when they are practicing social distancing

14:57 - Before her workplace closed, Kelly was approached by multiple people concerned about whether she was at risk, but she didn’t know the answer

16:12 - CreakyJoints is a great resource for reliable information and support during the COVID-19 pandemic

16:36 - If you are concerned about conflicting information, you should consult with your personal physician who is familiar with your condition about the best way to proceed

16:58 - The Spondylitis Association has also issued a resource document for Spondyloarthritis patients about COVID-19

17:11 - Check sources on any articles you find online because there is a lot of misinformation floating around the internet

17:26 - Patients living with chronic illness and disabilities may be more prepared than the general population to avoid infection during a pandemic

18:16 - We know what to do to protect ourselves, but we are also relying on the community to keep us safe because this virus is so dangerous for disabled and chronically ill people

18:28 - Charis and Kelly share the end of life plans they have made in case they contract a fatal case of COVID-19. These plans allow them to live without anxiety, NOT because they are being pessimists 

20:40 - It’s important that everyone be patient and kind with people who are still working - especially healthcare professionals

21:22 - If you are healthy and have been stockpiling medical supplies, please consider sharing them with people who need them now 

26:05 - Everyone knows someone who works in the healthcare, service, or food industry putting themselves at risk, and the least we can all do is to avoid unnecessary trips out

27:04 - You can be a superhero right now by doing nothing and staying at home

27:46 - People probably need to take breaks from COVID-19 news to preserve their mental health

30:43 - People need to prioritize social connections (while social distancing) to preserve their emotional wellness

32:05 - People who deny the seriousness of this virus may be clinging to that belief to manage their own anxiety

33:08 - Schools and employers have been claiming for years that remote work or remote learning is not possible, but now it is suddenly possible when able-bodied people need it 

33:58 - Follow #Accessibilityforableds to see how frustrated disabled people are that the accommodations they’ve been told were impossible are now available to everyone

34:18 - Disabled people hope that these distance policies will remain possible after the virus 

36:42 - This is the first time in a long time that teachers have had the freedom to educate their students without having materials forced on them by publishers, politicians, and administrators. Kelly hopes that will be a catalyst for change in public schools after the virus

38:40 - There is no one look for being high risk or vulnerable

39:29 - Many of the symptoms that people with AiArthritis diseases live with every day are documented COVID-19 symptoms, and that can cause anxiety for people who are trying to decide if they are flaring or sick

40:12 - Get in touch with your doctor if you think you need to be seen because any trip to urgent care or the ER is likely to expose you to the virus

44:04 - We probably won’t know much conclusively about the virus for several years because researchers will need to repeat experiments multiple times and have research peer reviewed before it will be accepted as fact

45:29 - Kelly thanks Charis for taking the time to do this episode despite being ill

45:54 - The COVID-19 special episodes are currently airing during the regular AiArthritis Voices 360 dates and times, but they will soon branch out into their own series so that patients wishing to take a break from COVID-19 news can listen to our regular show

46:35 - For more information on COVID-19, you can join our organization’s COVID-19 group on Facebook by connecting to our page @IFAiArthritis

47:09 - We will also have many COVID-19 resources available @ aiarthritis.org/COVID19

47:19 - If you would like to take a seat at the table, visit us on the web at aiarthritis.org/podcast, on social medias @IfAiArthritis on all platforms, or email us @ podcast@aiarthritis.org



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If you are a patient, a parent of a juvenile patient, or any other stakeholder (doctor, nurse, researcher, industry representative, or other health services person) - are you ready to join the conversation? It's your turn to pull up a seat. Join our new AiArthritis Voices program, where people living with AiArthritis diseases and other stakeholders who we need 'at the table' to solve problems that impact education, advocacy, and research sign up to have a voice in our initiatives. By signing up, you’ll get notified of opportunities to be more involved with this show - including submitting post-episode comments and gaining insider information on future show topics. Patients and all other stakeholders are encouraged to join so we can match you with opportunities to pull up a seat and TOGETHER - as equals - solve the problems of today and tomorrow.


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AiArthritis Voices 360 is produced by the International Foundation for Autoimmune and Autoinflammatory Arthritis. Visit us on the web at www.aiarthritis.org/talkshow. Find us on Twitter, Instagram, TikTok, or Facebook (@ifAiArthritis) or email us (podcast@aiarthritis.org).

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Your Co-Hosts & Guests: Who is at the table this episode?

Kelly Conway
Kelly is a speech-language pathologist, author/blogger, and a patient advocate. She has been living with autoimmune arthritis since age 14 but wasn’t formally diagnosed until age 32. That diagnosis has changed more than 5 times over the past 18 years. Through social media, she connected with fellow patients and co-founded the International Foundation for
Autoimmune and Autoinflammatory Arthritis. She has represented her state of Pennsylvania on Capitol Hill for the American College of Rheumatology multiples times, and speaks of the patient perspective at medical/pharmaceutical conferences. Kelly believes in the power of the patient voice and sharing our stories to raise awareness, education, and advocacy.

Follow Kelly: Check out Kelly’s blog is “As My Joints Turn: My Autoimmune Soap Opera” at www.asmyjointsturn.com. Visit her facebook page https://www.facebook.com/Lolabellaquin/ and twitter twitter.com/lolabellaquin. She has also authored a book about her chronically ill dog, called, “Making Lemonade with Georgia Grace.” Visit the facebook page about Georgia at https://www.facebook.com/georgiathecavalier. 
Charis Hill
Charis is an unstoppable, award-winning advocate since 2013, professionally disabled writer, speaker and model living with Ankylosing Spondylitis (AS), Major Depressive Disorder, Anxiety and Post-Traumatic Stress Disorder. Charis has been instrumental in creating spondyloarthritis disease treatment guidelines, designing and conducting patient-centered rheumatological research, forming international criteria for disease treatment outcomes, and is consistently involved in nationwide/international advocacy, awareness, and legislative campaigns to improve spondylitis education, funding, and access to treatment. They have modeled in Los Angeles Style Fashion Week and New York Fashion Week; and have been on the cover of Féroce magazine, Arthritis Today, and Spondylitis Plus magazine.

You can find Charis at www.BeingCharis.com, Twitter & Instagram: @BeingCharisBlog

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