As we have lots of new members I thought it might be an idea to post this here, hopefully it will help in some small way. 😊
This was originally written by Christine Miserandino about the way she explained Lupus to her friend and how she struggles on a daily basis. It has since become a disability metaphor.
I found this a while after I was diagnosed with AIH and it helped so much when trying to convey the difficulties on a day to day basis when you're living with fatigue.
Written by
Gemma68
To view profiles and participate in discussions please or .
Just read this now and it’s a clever way of trying to explain my illness. I am always lethargic and no energy feel sick a lot of the time no appetite in pain everyday I have polycystic liver disease and look quite healthy apart from being very thin. I’m am always trying to explain to people why I can’t go out for food or days out now I can show them this.
Glad to help! It's a difficult thing to have an "invisible illness" when it comes to friends and family who don't understand the full extent of our situations. 😊
My friends and family have been great with me but I just feel like I’m letting them down sometimes when I don’t won’t to do anything or go anywhere just because I feel crap. I try my best to join in with everything but it’s getting harder. I’ll stop moaning now there are people a lot worst of them me xx
You're not moaning, yes there are people worse than us but there are a heck of a lot of people that are better than us too! I can understand it's difficult to turn down activities, don't punish yourself by feeling guilty for declining an invitation, you have to make your health and wellbeing a priority and never apologise for it! 😊
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.