Yesterday was ME/CFS awareness day. It shows really hope much this condition is a spectrum. Some people are mild can work etc, some are moderate can do little things but crash often, others are severe can’t even get out of bed at all.
It’s sad to see and a lot of posts can be relatable. But for me I can’t let myself sit in the sadness. I’m not going to be an advocate for chronic fatigue/ ME. I don’t want to give that much attention and stress to tell people about my condition.
Ever since Covid there’s so many more people who are getting ME/CFS and or POTS. Which is good for research and treatment…bad for those people. You have to be REALLY strong to handle this. I know. And you need God.
I’m done with that. If I’m using a mobility aid, I’m not going to explain to the person what my conditions are. I’m just going to enjoy my day.
I have some friends that focus on advocacy and I swear the stress and fear surrounding those conversations makes them more exhausted especially mentally.
I’m focusing on me. My health. My mind. My peace. Giving it to God. Letting go letting God.
T
Teresa Love 
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