Since so much has happened since I was posting regularly, I've decided to give updates in small pieces rather than one, long blog novel.
About two years ago I pretty much faded from the blog/vlog world after being
denied disability benefits. From the day of my diagnosis up to that point, my
every waking moment had been spent thinking, talking, writing about and researching Lyme
Disease. Quite honestly, I got sick of it. No pun intended. Even hearing or
seeing the word Lyme brought on a twinge of nausea. The punch-in-the face
reality of how devastated and lonely this illness can leave a person became
all-encompassing, and the more I read about the CDC, Lyme-illiterate doctors,
and the countless people out there struggling to make it
through each day after being tossed aside to suffer and die, the worse I felt. I was
in too deep emotionally. Something had to give. I had started this blog as an
outlet for myself and a source of information to help others understand the
daily challenges a person with this illness faces, but it became such an
emotional drain that I had to walk away and catch my breath. It was definitely the right decision. I’ve returned with a new
approach to daily life. Lyme disease does not define me. I am a human being
who just happens to have an illness and wants to share her joys, struggles and
triumphs with the world. I will focus on what does work, rather than what doesn’t….
what I can do, as opposed to what I can’t.
I think in the long run, that will be far more helpful not only to
myself, but anyone else out there who happens to be reading this.
That’s all for today. Peace out J
Tuesday, October 15, 2013
Thursday, October 10, 2013
I'm back!
Hello everyone! My apologies for being gone so long. I really backed off communication here and on my video blog due to being overwhelmed with this entire situation. Since my last post, I was denied disability benefits despite 3 appeals and appearing in court with a disability lawyer. Very disheartening. I spoke with my lawyer afterward about reapplying... he said it would not be worth it unless my condition worsens drastically or I receive a new diagnosis. Over the next year I struggled quite a lot just to keep my head above water, searching for ways to get my needs met and hitting a lot of dead ends, mostly due to a lack of stamina. I had great ideas, mind you..my body simply could not carry them out. I did learn something about myself, though; that I am capable of handling a lot more than I ever thought I could.
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