Gifts

I am often so cautious to add a disclaimer to posts about progress or snippets of positivity. Without one, I have people in my life who assume I am “cured” or that my life is easy. But I am learning that I am not responsible for the ways others interpret me. (And I am also learning to stop making assumptions about what other people might be thinking!)

So today, for me, I just want to share some of the gifts this almost-decade of illness has given me.

  • Patience.
  • Empathy.
  • Gratitude.
  • A bouncebackability.
  • Pride.
  • An ability to laugh with real humour at situations I cannot change.
  • An even-more-wonderful-than-before relationship with my parents.
  • My husband.
  • Strengthened friendships with those special few.
  • Guinea pigs! An excellent selection of only colourful clothes.
  • A chance to try out a pixie cut!
  • Time with my grandparents I wouldn’t have had if I was well and working.
  • Perspective.
  • Increased feistiness over injustice and inequality.
  • Most recently, an increased sense of self worth.
  • A range of novelty slippers.
  • The most supportive people I could ever image who live in my iPad; some of whom I’ve had the pleasure of meeting in real life.
  • Happy tears. So many happy tears.
  • A new definition for what makes a ‘good’ day. A level of appreciation I’d never known.
  • A seemingly unconquerable soul.
  • The knowledge that you can feel more than one feeling at any given time.
  • Time.
  • The opportunity to relearn things or experience things again as if for the first time. (Most people only get that once in their lifetime.)
  • The awareness that I am a work in progress, and should always be one.

No disclaimer.

Paddling in the sea in August 2019.

One response to “Gifts”

  1. marcianapp Avatar

    Thank you Anna, while I would not wish ME/CFS on anyone I also have some lovely things to feel grateful for that have come along for the bumpy ride. I have had some funny looks when I try to explain this, perhaps I should just point people at your blog as you say it so beautifully.

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I’m Anna

Welcome to M.E. myself and I, my tiny little corner of the internet where I share snippets of life in the slow lane. You’ll also find all things Blue Sunday here, the annual fundraising event I started in 2013 to raise awareness of M.E., include people living with the illness, and raise money for the M.E. charities who support us.

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