• Autoimmune Abbey : Medical Gaslighting, Religion and Ableism, Keyboard Activist, Chronic migraine, POTS, undifferentiated spondylitis, Mental Health, and IBS

  • 2021/04/05
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Autoimmune Abbey : Medical Gaslighting, Religion and Ableism, Keyboard Activist, Chronic migraine, POTS, undifferentiated spondylitis, Mental Health, and IBS

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  • Medical gaslightingWhat happens when your coping mechanism is removedReligion and Ableismbeing the good friend, daughter, daughter in law, wife.The exodus of family and friendsHow medical gaslighting keeps you from medical care and endangers lives (tiktok nurse)Job impact of chronic illness ADA needsSetting boundaries with family and friends when discussing illnessThe grieving process for chronic illnessThe importance of online advocacy ie keyboard warriorsThe cost of health and life goalsWebsite/Blog, Twitter, & Instagram HandleInstagram: @autoimmuneabbeyName *Autoimmune AbbeyDisorder InfoWhat is your disorder? *Chronic migraine, POTS, undifferentiated spondylitis, generalized anxiety, OCD, gluten intolerance, IBSAt what age did your disorder become a daily issue? *22Who were you before your illness became debilitating? *I was a long-distance runner who loved marathons and ultramarathons and felt completely invincible. Although I was always a bit of a sick kid and teen - I had episodic migraine, a dairy allergy that I eventually started to outgrow at around 12, and a long history of painful periods - I took my health for granted. I was only sick a handful of days each month, and I was ambitious, mentally healthy, and had lots of close friends.What would you do if you were not dealing with your disorder and/or disability? *I would certainly still be a long-distance runner, and I would also be doing triathlons. I would probably not have lost so many friends and would have a better relationship with my parents and in-laws. I experienced the typical quiet mass exodus of friends and family that many other disabled people also experience upon becoming ill. Thankfully my spouse and a few best friends stuck around.What would you like people to know about your daily life? *Chronic illness is isolating, exhausting, and often traumatic. It's really hard to stay mentally healthy when you're fighting daily symptoms but you constantly feel like you have to prove your symptoms to everyone around you. Being gaslighted on such a grand scale, especially by doctors, has a serious impact on a person's health.What would make living and moving in the world easier for you? *The biggest thing that would make the world more accessible to me would be less fluorescent lights. Chronic migraine and POTS make me sensitive to sensory overload, and fluorescent lights are impossible to deal with as a migrainuer. I have turned down jobs simply because of the lighting in the workspace. People think my intolerance for bright lights is just a preference, but it's definitely a non-negotiable accessibility need.Do you have any life hacks? *Write EVERYTHING down in your phone calendar to help compensate for brain fog. It's a game-changer.What kind of support do you get from family or friends? *My spouse and a few of my close friends have been amazing at supporting me through my illness. They are curious about my symptoms and experience with chronic illness, open to learning about ableism and medical gaslighting, and willing to make sure I don't go hungry at social events because of the gluten intolerance. Unfortunately, my family and my spouse's family have not been so supportive. For a while, I tried to be assertive with them about my needs and limitations, but at this point, I'm setting clear boundaries with them - I will not talk to them about my health anymore, beyond just sharing my diagnoses. And of course, like most chronically ill folks, I've lost a few friends since becoming ill.Have you ever had someone, or a medical professional, not believe you have an invisible illness because of your appearance and if so are there any examples that stand out? *YES. This is what I refer to as medical gaslighting. In my experience, the majority of doctors will begin to doubt my symptoms the moment they realize they don't know how to explain my symptoms or treat them. For example, when I asked my OBGYN about Endo, she did an ultrasound and found nothing. Now she blames my pelvic pain on the fact that "redheads have a lower tolerance for pain." My first neurologist told me my chronic migraine was all in my head. And several specialists have blamed all my symptoms on my anxiety disorder.How has your chronic illness affected your relationships? *It has strengthened my relationship with my spouse and a few close friends but has alienated me from most of my family and some friends.Is there anything you are afraid to tell people in your life? *I'm afraid to tell them that I'm still grieving the loss of my health and I badly need their support.What is your best coping mechanism? *My Instagram advocacy work has provided me with so much comfort, community, and a sense of purpose again. I can't imagine dealing with chronic illness without the Instagram community.What are you the most concerned about and the most hopeful for in the future? *I'm most concerned about and hopeful for my future career in therapy. I feel called to the field and I ...
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Medical gaslightingWhat happens when your coping mechanism is removedReligion and Ableismbeing the good friend, daughter, daughter in law, wife.The exodus of family and friendsHow medical gaslighting keeps you from medical care and endangers lives (tiktok nurse)Job impact of chronic illness ADA needsSetting boundaries with family and friends when discussing illnessThe grieving process for chronic illnessThe importance of online advocacy ie keyboard warriorsThe cost of health and life goalsWebsite/Blog, Twitter, & Instagram HandleInstagram: @autoimmuneabbeyName *Autoimmune AbbeyDisorder InfoWhat is your disorder? *Chronic migraine, POTS, undifferentiated spondylitis, generalized anxiety, OCD, gluten intolerance, IBSAt what age did your disorder become a daily issue? *22Who were you before your illness became debilitating? *I was a long-distance runner who loved marathons and ultramarathons and felt completely invincible. Although I was always a bit of a sick kid and teen - I had episodic migraine, a dairy allergy that I eventually started to outgrow at around 12, and a long history of painful periods - I took my health for granted. I was only sick a handful of days each month, and I was ambitious, mentally healthy, and had lots of close friends.What would you do if you were not dealing with your disorder and/or disability? *I would certainly still be a long-distance runner, and I would also be doing triathlons. I would probably not have lost so many friends and would have a better relationship with my parents and in-laws. I experienced the typical quiet mass exodus of friends and family that many other disabled people also experience upon becoming ill. Thankfully my spouse and a few best friends stuck around.What would you like people to know about your daily life? *Chronic illness is isolating, exhausting, and often traumatic. It's really hard to stay mentally healthy when you're fighting daily symptoms but you constantly feel like you have to prove your symptoms to everyone around you. Being gaslighted on such a grand scale, especially by doctors, has a serious impact on a person's health.What would make living and moving in the world easier for you? *The biggest thing that would make the world more accessible to me would be less fluorescent lights. Chronic migraine and POTS make me sensitive to sensory overload, and fluorescent lights are impossible to deal with as a migrainuer. I have turned down jobs simply because of the lighting in the workspace. People think my intolerance for bright lights is just a preference, but it's definitely a non-negotiable accessibility need.Do you have any life hacks? *Write EVERYTHING down in your phone calendar to help compensate for brain fog. It's a game-changer.What kind of support do you get from family or friends? *My spouse and a few of my close friends have been amazing at supporting me through my illness. They are curious about my symptoms and experience with chronic illness, open to learning about ableism and medical gaslighting, and willing to make sure I don't go hungry at social events because of the gluten intolerance. Unfortunately, my family and my spouse's family have not been so supportive. For a while, I tried to be assertive with them about my needs and limitations, but at this point, I'm setting clear boundaries with them - I will not talk to them about my health anymore, beyond just sharing my diagnoses. And of course, like most chronically ill folks, I've lost a few friends since becoming ill.Have you ever had someone, or a medical professional, not believe you have an invisible illness because of your appearance and if so are there any examples that stand out? *YES. This is what I refer to as medical gaslighting. In my experience, the majority of doctors will begin to doubt my symptoms the moment they realize they don't know how to explain my symptoms or treat them. For example, when I asked my OBGYN about Endo, she did an ultrasound and found nothing. Now she blames my pelvic pain on the fact that "redheads have a lower tolerance for pain." My first neurologist told me my chronic migraine was all in my head. And several specialists have blamed all my symptoms on my anxiety disorder.How has your chronic illness affected your relationships? *It has strengthened my relationship with my spouse and a few close friends but has alienated me from most of my family and some friends.Is there anything you are afraid to tell people in your life? *I'm afraid to tell them that I'm still grieving the loss of my health and I badly need their support.What is your best coping mechanism? *My Instagram advocacy work has provided me with so much comfort, community, and a sense of purpose again. I can't imagine dealing with chronic illness without the Instagram community.What are you the most concerned about and the most hopeful for in the future? *I'm most concerned about and hopeful for my future career in therapy. I feel called to the field and I ...
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