Maggie

Recently diagnosed


Maggie is a caregiver who has been living with long-COVID for about four months. She has experienced symptoms such as brain fog, fatigue, and a high heart rate when she stands, but the most odd symptom for her was that she has pain in her arms and an inability to lift them. Living with long-COVID has been challenging for many aspects of her life. For example, it is difficult to care for her mother who lives with her and has to rely on family and friends to support her mom’s care. She also has to pace herself with her consulting work and has chosen to work less hours to cope with the fatigue and brain fog. She is also unable to help her children with child care and is unable to play with her grandkids. Maggie is also unable to do many of the things in life that she enjoys, such as socializing and scubadiving. She does hope that her symptoms will improve in time, but it does weigh on her that they may not improve and she may need to consider what adjustments she needs to make in life (e.g., putting plans in place so that her mother is well supported). This experience has made her realize that there is no answer to the question “what happens to the caregiver when the caregiver gets sick” and would like to see resources and services put in place to better support caregivers living with long-COVID.

 

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