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SummerFest on the Green Fireworks

Posted on : 28-06-2010 | By : Rosalind | In : Entertainment, Photography

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This past Saturday my boyfriend and I attended the city of Morrow’s annual SummerFest on the Green. Starting in the early evening around 6pm, it’s a family/community day kind of thing. There were rides and games for the kids, an open hydrant for anybody who wanted to get wet, food vendors for the hungry, and a pretty good band that played a variety of music. A good time was had by all, and at 10pm, the fireworks show started.

I was really excited about the fireworks, because it’s challenging to get good fireworks photos. I went online before we left, and got a few pointers for photographing fireworks and made a crib sheet from an index card, LOL. Things didn’t go as planned, as I couldn’t use my tripod, which is the best way to take some types of photos like fireworks. I left the tripod’s quick-release plate, that attaches to the bottom of the camera, at home, so I had to hand-hold the camera and do my best to keep as steady as possible and catch the fireworks. I think I did a pretty good job, but you be the judge.

Camera: Pentax K10D, ISO: 100, Shooting Mode: Bulb (B), Lenses: Pentax Takumar (Bayonet) 135mm f2.5 & SMC Pentax-M 50mm f1.7

Click to enlarge

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Time Flies

Posted on : 28-06-2010 | By : Rosalind | In : General, Health

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Wow, time really flies! I just looked at my last post and it’s dated May 26th. I didn’t think I’d been off the blog that long. So, gosh, what’s been going on with me?

Well, I started dating someone, and we’re about 4 months in, now. Things are going very well, and I’m very happy. At the same time, I hadn’t been feeling very well and dreaded going to the doctor, especially now that I don’t have health insurance, anymore. I kept putting off going to the doctor hoping I would get better. I never did, so I broke down and made an appointment.

As far as I know, the lupus is still in remission. But, I also have Fibromyalgia, which is the culprit this time. It’s weird in that most people with lupus also have “fibro”, but most people with fibro don’t have lupus. I don’t know how that works, but it turns out that I was feeling bad because I was having a pretty bad fibro flare. My muscles were really tight all over, and as if that wasn’t enough, all the tendons and soft tissues around my joints (both shoulders, both elbows, both knees, both hands, both ankles, both hips, and my neck) were inflamed, which made them super sore and stiff. And, I had been like that since about March, getting progressively worse, before I finally couldn’t take it anymore.

I was put back on prednisone for a month long high dosage taper, and prescribed a muscle relaxant and a pain reliever. I felt a lot better within 24 hours, and dramatically better within 48 hours. At 72 hours in (3 days), I literally felt like I had a new lease on life. I felt so good! Then I had a very sobering thought… I realized that I had forgotten what it felt like to feel good. Isn’t that a shame? Then, I had another sobering thought: I might be one of the people who can never fully come off of their meds. What made me think of that was when I told my primary care doctor that my (former) rheumatologists had taken me off all meds related to lupus or fibro, he dead-panned that that might be the reason why I was feeling so bad. :eek:

And, y’all, when I say I was feeling bad, I mean I was feeling bad. I scared the poor medical assistant so badly when she put the rubber tourniquet around my arm to draw blood! I hollered, and I couldn’t help it. One of the places I was having severe pain and soreness was in both my elbows. The med assistant tied the tourniquet right around the most tender part of my upper arm, and I was hollering before I could catch myself. End result? A nervous med assistant and the doctor taking the blood samples, himself. He had to put the tourniquet farther up my arm, and it was somewhat of an ordeal to get any blood out of me.

I still feel a lot better than I did, but my body has now adjusted to the prednisone and other meds, so my activity rate is slowing back down to normal. But, I tell ya, those first few days were AWESOME!! So, that’s pretty much been what’s going on with me, and why I haven’t been blogging much. I wasn’t feeling well, and so wasn’t doing anything, and so had nothing to talk about.

Yeah, I got some camera lenses during this time, but I couldn’t really use them since I really wasn’t up to doing too much, physically. But, since I knew there was going to come a time when I would be using them, I bought them anyway. Before I go any further, I just have to say that my boyfriend has been wonderful with all of this. I know he’s nervous about the lupus, fibro, and other issues, but he’s not letting “what if’s” scare him away. He’s the real deal, and I’m glad I met him, and I’m glad he’s a part of my life.

Well, that’s it for the update. Stay tuned for some fireworks pics I took this weekend at the city of Morrow’s annual SummerFest on the Green.