Circling Over O’Hare

I am in the waiting place. Again. Still. It’s annoying.

I can be patient; I’ve spent hours waiting and watching for things to happen when doing outdoor photography, waiting for the sun to be covered by a cloud so the light is not so contrasty, waiting for the eternal wind to not blow so hard, waiting for an insect to alight somewhere, waiting for it to quit raining, et cetera.

But at the core, I like to operate and make my decisions based upon facts. A lack of (what feels like) sufficient or useful data leads me to milling around, stuck until I can figure out where or how to get the information I need. I also like to know what I’m going to be doing, so I can be prepared and plan around the other things in my life. One of the ways that I reduce stresses in my life is by limiting these free-floating anxieties.

Merely being in the limbo of putting things on hold because I’m stuck waiting is annoying, but I’m an adult. I can deal with feeling like I’m stuck on a dreary flight circling over O’Hare airport, waiting for a runway to free up. There’s no point in having a hissy fit because that won’t change anything. So why am I grousing?

Because my health is suffering from the delays. The arthralgia medication isn’t helping enough lately. Quite possibly because I’ve not had a solid night’s sleep in four months due to hot flashes/night sweats every 30-90 minutes. I got better sleep when I was nursing newborns! (Though frankly I was not sleeping well before the hot flashes.) My joints and muscles ache all over. I get frequent headaches. I have more bruises than ever, and I can’t tell if I’m just being clumsier from the exhaustion & stiffness, bruising more easily, or both. I’m sweating hot and shivering cold and hot and cold and hot and cold, regardless of the time of day or where I am. My stamina is lousy, and I’m mentally mushy half the time (again, good sleep would help). I feel like I’ve had the flu for five months — it’s almost as bad as the summer I had mono and Lyme.

About a year ago, I realised, “Boy, my joints ache a lot …” After a couple months of that, I decided to see my GP. So in March he suggested I see a rheumatologist for the chronic joint pain. I saw her in May, and she put me on better analgesics for the arthralgia. A few months later my GP took me off the HRT, as well as cutting my analgesics in half because he thought they were causing hypertension. (By November I ended up going back to the higher levels of analgesics because not surprisingly, pain makes my blood pressure worse.) My blood pressure has normalised again, but without the HRT I was thrown into menopausal hot flashes. My rheumatologist suggested I see my old OB/GYN about them, which had I not been so bloody tired might have occurred to me — it’s just that I’ve not seen her since the last follow-up after the hysterectomy several years ago. So in November I made an appointment with my OB/GYN, but there wasn’t an opening until December, and then we had to reschedule for January because she was out delivering a baby, as happens with OB/GYNs.

About a year ago, I realised, “Boy, my joints ache a lot …” Now I’ve moved up to “Boy, I can’t sleep and I’m having a lot of headaches and I ache all over.” It takes weeks to see yet another doctor. I sure hope something gets resolved. I’m signed up to take an evening college class next semester, but lately I’m just wiped by the time I get home from the para and tutoring work.

But meanwhile, I have …

to wait.

7 Comments

  1. andrea said,

    23 December 2007 at 14:36

    Amanda:
    positive on the hypermobility issues, which certainly don’t help the osteoarthritis. She didn’t actually count out the Beighton, but I demonstrated enough bendy things for her to say that yes, I am.

  2. Bug Girl said,

    23 December 2007 at 13:26

    All i have to offer is a new thing I just got from my doc–stick on lidocaine patches! It turns the painful spot all numb and tingly, rather than painful.

    I hope you get some answers soon–I remember all the waiting when my sister was getting her cancer diagnosis. They never seem to understand that there might be a sense of urgency on the patient’s part to know WTF is going on :(

  3. amanda said,

    23 December 2007 at 4:19

    And you’ve been checked and/or self-tested for hypermobility, right? (Cause of arthralgia that according to some sources is more common in auties.)

  4. deafmom said,

    23 December 2007 at 0:58

    Going around in circles at O’Hare– been there, done that so many times that I’ve been dizzy!

    Hope you can remedy those joint aches and enjoy the holidays!

  5. David said,

    22 December 2007 at 21:44

    Thank so much Andrea! I just finished my first semester and it went very well! I’ll be getting back to blogging soon. A very merry Christmas to you and yours!

  6. qw88nb88 said,

    22 December 2007 at 14:45

    I don’t think so — that was a few summers ago. I was on antibiotics for a month, too.
    andrea

  7. Club 166 said,

    22 December 2007 at 13:51

    The rheumatologist did check Lyme titers, right?

    Joe


Leave a Reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: