Tag Archives: gait

Tummy Improvement OR Walking Faster?

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I’ve been on the new Zelepar medicine for several days now, and my digestive system is behaving just fine. I don’t seem to be getting quite as much help with my gait as I did with the Requip or Sinemet, however, but I’m still on the samples. When I go back to the Neurologist next Friday, it may be that he will order a prescription for a higher dose or more doses, which might make the difference. Anyway, even if the dose stays where it is now, it seems like a reasonable trade off between stomach problems and balance and walking problems. I’d love to walk better, but I can live with it the way it is now, if I have to. It’s nice not to spend part of every day miserable, with a hot pad on my tummy!

I said at first the Zelepar didn’t taste bitter, however, I’d better amend that evaluation. Yes, it is bitter, but not enough to bother me, anyway. (The trick is to be sure you place it under, not on, the tongue.) It dissolves under my tongue so quickly that it’s just a few seconds, and I can swallow it. You’re not allowed to drink or eat anything for at least 5 minutes before or after taking it, but my saliva quickly washes the taste away.

We’re still staying with my Daddy, which means I spend most of my days and every night in a hot house. We tried to find a compromise temperature for the thermostat, but at 101, he gets too cold, while we’re still sweltering. I have noticed that I’m having more trouble with the heat this week, since I’ve been on the Zelepar, than I was before I started taking it. I’m getting what feels exactly like hot flashes several times a day, and I’ve been past that stage for some time now. I have read that Parkinson’s can mess with the body’s regulation of internal temperature, so I guess that’s what’s happening to me right now. Or is it because of the Zelepar? I really don’t know.

I was on Requip before starting the Zelepar. Requip is a dopamine agonist, but Zelepar is an MAO-inhibitor, so they don’t attack the PD symptoms the same way. There’s big news in the Birmingham News today that a doctor at UAB is close to getting FDA approval for a patch version of a dopamine agonist. That will be good news for me, as the Requip did a better job of improving my balance and walking than it looks like the MAO-inhibitors are going to. I’m all for any PD med that I don’t have to swallow!! So this is something else for me to be hopeful about.

It’s great to see that there is good news on the horizon for the large number of people who really suffer with this disease. My own symptoms and discomfort level are so mild compared to people who have had Parkinson’s for years. I pray that all this new research may bring them relief in the near future, instead of years from now.

Still Increasing Requip Doses

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I’m still increasing the dose size of the Requip very gradually, and this week I’m only taking the half Sinemet and Lodocyn twice a day. I’m not up to a full Requip dose yet, because my walking is not up to normal yet. I can still feel the trembling, particularly on my right side. I can’t balance on my right foot, either, and it’s still difficult to go down steps without holding on and being very careful. But it’s getting there. I see the Neurologist again the first week in November, so he should be able to tell by then just how much more Requip I need. Hopefully, when I get off the Sinemet, my tummy will settle down completely. I sure hope so.

I’m continuing to try to get just as much exercise as I can, and we’re eating as healthy as we possibly can, too. I’ve even started back to putting items on eBay. That’s something I just about had quit doing, while I was so sick with the colitis, and when I was having so much trouble walking. I need to get back to a regular routine, though. We can’t keep going to the estate sales if I don’t start selling some of our purchases, right?

My Arms Were Swinging This Morning!

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Such a little thing, that we take for granted, and don’t even notice … when you walk normally, your arms swing quite naturally at your sides, without any thought on your part. Well, that’s not the case for someone with Parkinson’s, and it hasn’t been that way for me, either. In fact, I have tried to consciously do it, and I couldn’t remember how to coordinate it at all.

Daddy has a long hall at his house, and I noticed for the first time this morning when I walked down it that my arms were swinging again, quite naturally. This is quite an accomplishment, and is sure evidence that the Sinemet is working.

I go to the Neurologist tomorrow, and I’m very excited about seeing him. I’m hoping for a definite diagnosis this time, so I can get down to the business of dealing with handling the meds and my GERD. I’m still having a lot of trouble with that, but I have the Gastroenterologist appointment Friday. It seems to all be coming together.

I’m praying for some definite answers. I realize that Parkinson’s is not something anyone would want to have, but knowing is better than not knowing, any day, IMVHO!

NOT Stupid Walker

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I swallowed my silly pride and used the walker at church this morning. After the first few people stopped me to ask if I was worse, and I assured them I wasn’t, I got used to it, and it wasn’t so bad after all. It really did make the long walk from the car to our Sunday School room soooo much easier. I can walk more naturally with it, too, which should help my muscles get back to a normal gait, I hope.

I realize now that I should have been using a walker for the last few months, but Dr. B is the only medical person who has told me I should have one, so I figured I wasn’t bad off enough to need it. And he didn’t just tell me, he fussed at me big time. Now I’m glad he did!!