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It might become very frustrating if the illness prevents me from doing regular day to day activities let alone hobbies and interests. The frustration can easily lead to anger or depression.

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As someone w arthritis and possible fibro

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As someone w arthritis and possible fibro

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Pain like all the time 👍 gets hard when out with people, can really impact how i spend time with people and what we do. It has also lead me to cancel meeting w ppl

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I had glandular fever in the new year, as a result I have chronic fatigue - I've had to drop my hours on the swim team, mental health has deteriorated because I have become unable to carry out day-to-day tasks

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Might have to be very dependent on others which can make it a burden on them and make you feel bad for being that burden

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due to having low mood/feeling sorry for your self you may take your bad mood out on freinds/family

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couldn’t see my family or friends because didn’t want them getting sick felt very lonely and wasn’t able to do every day activities like come to lectures

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Impact on day-to-day tasks, mental health and family

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as someone with a chronic illness, every day is hard because symptoms change all the time. some days i can’t get myself out of bed to eat and have to have a friend come and look after me. my hormones are all over the place because of my condition too so my mental health is through the floor basically every single day.

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Possibly, it takes time to recover psychologically if the illness is severe and it differs to our coping mechanisms

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Changes of routine, feeling like a burden, needing to adapt

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chronic migraines make doing work, leaving the house and going to work difficut

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Feeling bad having to ask house mates for favours all the time, family concerns, change of routine

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Issues surrounding job roles: if there is an unequal job role split due to something such as chronic fatigue from one partner, issues can arise due to a feeling of being without adequate help with household chores and activities.

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with my condition i’m constantly dependent on friends and family when i can’t get out of bed or when i can’t do certain tasks/activities which makes me feel guilty for “using” them