The tag itself is #millionsmissing and it links to a protest being staged this month for the lives of those with M.E. Lives like mine. The reason I am finding it so moving, is that it articulates a part of my experience that I have never had words for, and it makes me aware of just how many others understand it too.
For years at a time, we went missing completely. Even though we were always in one place; the dark of a room, with only the most vicious dragons for our company. Every sound and beam of light was a knife cutting through us with dreadful accuracy. For thousands, and hundreds of thousands, of minutes we were static and unresponsive and silent but there was no respite for us; not for a moment, because the terrible chaos we were experiencing never needed to stop and take a breath. However much we wanted it to. Existing was so physically excruciating that it seemed impossible to continue doing so. We were in the lands between life and death where there was no one but us, and the dream of being near to other people again. A dream so beautiful and neccessary, it has sustained us.
You will never reconcile to being missing though. You will never wake to find it normal. You are always yourself, displaced, in this terrible new place you have no maps for, waiting for your real life to come back to you. The one where you can run and dance and reach out to put your arms around those who matter.
Perhaps the hardest part is simply the lack of practical help. The doctors are as out of their depth as you are. They can offer you nothing for your pain and, invariably, they cannot treat you. So you are exposed to an illness unchecked. You must face the storm, without a shelter.
You become so very aware of how much pain there is on this planet and that there is no more reason for your miracle to come than anyone elses, and you hope it comes anyway, because this is the only span of time you will ever have.
I do not want to stay missing.
And I do not want other people's lives to go missing too.
But I have no idea how on earth to stop it from happening to someone else, when the voices most raised about it are the ones who are being made to whisper by this disease.
A guest post from Sarah-Louise Jordan for #May12BlogBomb