I know many of you have been waiting for an update since I
had my MRI. I was waiting anxiously,
myself, to find out what the cause is of all this mess. I had the MRI last Thursday and was told my
doctor would receive the report that afternoon or first thing in the
morning. I should expect to hear from
her on Friday or Monday at the latest.
I waited with bated breath, wondering what the answer would
be. Scar tissue? Torn ligaments? Arthritis in the joint? Something worse?
Late Friday evening, just before 8:00, my doctor called with
the news. Or should I say, lack
thereof. The MRI showed nothing. Nothing.
The radiologist indicated it was a normal pelvic MRI. Well, actually, he stated normal pelvic
ultrasound. She thinks that was a typo
and planned to contact him on Monday to confirm that he actually read my MRI
and not the ultrasound I had last month.
She was also hoping to get a copy of the actual MRI, since she knows
something about reading them herself.
She is also going to consult with another internist and the surgeon who
did my hernia surgery.
She’s at a loss. We
all are. Thankfully, she’s not giving up
on looking for an answer but in the meantime, I’m back to waiting. I still can’t move my right leg. I’m still in constant pain, though,
thankfully the severity of that pain varies considerably. And there is no apparent reason why my leg
won’t move or why I’m in pain. I truly
don’t understand that.
I’m back in physical therapy, which is a mixed
blessing. I think it does help to some
degree but it also gets things hurting on a pretty consistent basis. Both my doctor and my PT are leaning toward
that awful prolotherapy as a solution. I’ve
looked into it some more and it sounds even worse than what my doctor first
explained. It involves multiple rounds
of glucose shots into the problem ligament where it attaches to the muscle or
bone. The shots are very painful and the
resulting inflammation is also very painful.
Also, you can’t take anti-inflammatories for relief because the
inflammation is supposed to happen in order for it to heal correctly. You repeat the therapy until the ligament is
healed and doing its job correctly. Oh,
also it’s expensive and not typically covered by insurance. I am absolutely not sold on this idea.
I’m exploring some other options while my doctor also looks
into her side of things. I plan to go
back on a modified anti-inflammatory diet, work with my PT on exercises, as
well as rules I should follow to prevent injury (and I will follow them to a
T), and an essential oil protocol that is supposed to help regenerate damaged
ligaments.
I wish I had some news—I would have taken good or bad. At least,
I would have had a game plan and goal to work toward to get better. This not knowing and thus, not knowing how to
fix it, is the pits! Not to fall into a
pity party but I’m pretty tired of hurting all the time, not being able to move
and do simple tasks (like getting dressed or putting on shoes without
contortions). I won’t go into the amount
of weight I’ve gained this year being totally inactive.
Ok, I’m done with the pity party.
Mostly, I wanted to update you all, since you’ve all been so
caring in messaging me, texting me, and asking me how my test went and what the
results were. I wish I had a good answer
to give you. Thank you for your
continued prayers and love. It is all so
very appreciated.
God is good!