I’m not sure why but I find it incredibly hard to write about my
personal experiences with avascular necrosis. The hardest part is
writing about it without coming off as a negative Nancy or sounding
afraid, and the second hardest part is that not many people know what
the heck avascular necrosis is. It’s bone death caused by poor blood
supply to the area, and in my case it’s in both of my hips. The pain can
be debilitating and sometimes even disabling. My doctor believes that
my necrosis has been linked to my short-term intake of steroids. (I had
severe ulcerative colitis a couple years ago, and needed the ulcerations
to heal quickly so I could get nutrients my body.) And to be completely
honest these past few months have been very scary, and it’s sometimes
challenging for me to be remain positive when I’m experiencing pain
almost every day; I’ve experienced both physical and mental
frustrations. The physical frustrations are my limited range of motion,
limping and leaving school every day with achy bones; which often
triggers my anxiety which makes me feel emotionally drained.
But
I’ve come to conclusion that getting upset over my discomfort only
worsens the pain, and that talking about really does help. As I learn
more about my illness I become a little more comfortable bringing
people’s awareness to it, and proving that underneath all this pain I’m a
joyful young woman. Right now, I’m doing what I love in school, have
passions, goals and dreams just like other people my age. I’m decided to
become my own health advocate and have been researching different
treatment options that aren’t surgical. One procedure that caught my eye
was one that would use my own stem cells from my bone marrow to promote
growth in the diseased area of my hips. It’s recommended for someone
who was recently diagnosed with necrosis, and today my mom is sending in
my x-rays & MRI’s to a doctor who specializes in the stem cell
treatment to see if I’m a candidate… I am praying that I’ll have good
news by next week!
-Jessica
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