Posted by Lory
on September 23, 2000 at 10:21:11:
In Reply to: Re: Which choice would you choose? posted by Bruce on September 06, 2000 at 01:39:42:
: : : : : : : I am sure there are many people reading this board that have occasionally been told you "can't" do something because you have pd. Well, I have just been forced to use a walker, and I got to thinking how do I know I can't push a vacuum cleaner unless I tried it. Moping the kitchen wasn't dificult. I just kept moving around in my scooter. Today I vacuumed the living room keeping the walker in front of me. This was a little harder, because the legs were causing some problems, but I would stop and take a short break and then get up and push that sweeper again. This may not be much to some people, but it did give my morale a big boost. BBruce
: : : : : : Bruce you proved that you can.What is the saying,I can,I can,I can !!!!.
: Betty H, Googy and Lory, I just returned from my a
: : : : : Bruce
: : : : : You are such a wonderful role model, but how do you do it? Where do you get so much strength & courage? I have had P.D. over 5 yrs. & I know it's here to stay, along with Psoriatic Arthritis and other aggravating problems, but I haven't accepted it. I didn't ask for all this in my life and I hate it & it can just go away. Right! Like all of you I'm sure, you hope you'll wake up & find it was just a nightmare. I realize this sounds stupid & I'm thinking like a child, but how do you make yourself go every day with such a load to carry. I consider myself to be a religious person, but I must admit, my faith is dwindling, I use to pride myself in being the ideal patient and being in control, but not any more. You are never away from it. Just all the pills alone, you feel like you should explode any min. The first thing that came to mind when I was diagnosed was, "what a burden I'm going to be on my famly". and that is in my mind almost constantly. They are wonderful & supportive, but that doesn't make it any easier.
: : : : : I'm sorry, I guess I've gotten off track. I know you all have this to deal with and more, but thanks for listening. And Bruce, "way to go", if anyone can do something, I think you can.
: : : : : Thanks for motivaing us!
: : : : : Betty H.
: : : : Betty H: I don't want to mislead anyone, in that I don't feel courages but just an ordinary guy trying to cope with this diswase. I was hoping to motivate someone when I wrote the message,This is what I truly believe that helps cope with it all. It is importent to accept the problem and try to adjust to the changes in our health as time goes by. When I was concerned about not being able to walk again, I thought about it for a long time and decided I would fight it anyway I could think of. Also, having pd has really made me appreciate the little things in life that many people are not aware of in there high pressured jobs. The next thing Betty is just take it one day at a time and live tthat day the best that you can and try to enjoy life and I never wish for something I can't possibly attain. Today was even more rewarding then yesterday. My great neighbors offered to do my grocery shopping for me, but even though they mean well, that is not good for my mental health. Today I finaly had to get over this barrrier and decided to try it. I had no idea how far I could walk with the walker. To my surprise, it was an easy walk. I told my neighbor what I did and he said "you should have called." Do you see the significace of thst shopping trip? That was a fantastic "high" because it showed I am still a healthy person and can still do most things everyone else does from day to day. I know it is harder the sicker you are, but try not to punish yourself and think of the things you can still do well. Happiness amd attitude are dependent upon how hard we have to fight for it. If we choose to be sad we probably will be sad. There are a lot of beautiful and fascinating things to see and experience in the world. All we have to do is open our eyes and our hearts to discover it. This is my challenge to you Betty. Try some of those things I talked about and see what a difference it will make in your life. Bruce
: : : Bruce,
: : : Thank you, you are amazing.
: : : I guess my problem lies, at least partly to the fact,that soon after the PD arrived, then I was diagnosed with the arthritis. The arthriris wrecked my feet in short order and I have spent the entire summer in a foot & leg cast, following surgery on my left foot & in lots of pain. The metatarsal joints had to be fused & with a bone graft, bunionectomy & shorten & reposition 4 toes. It has really gotten me down, mentally & physically. (That 4 day hospital stay was a nightmare in spite of my planning. I think you are familiar with that kind of situation.) Unfortunately I am a #1 worrier, but fortunately I'm married to an optimist. I spent the better part of 35 yrs. working as a nurse, caring for other people, and with my husband's help, have raised 4 children. As you all know, it's very difficult being on the other side of the fence, when you have been the care giver for so long. I still want to do things myself & my way, but I guess as hard as it is, I'm going to have to relinquish that role. I did learn, long ago, to stop & smell the roses. It seems I've opened my eyes to some degree, but need to open my heart & stop dreaming for what was & will never be again. (It looks so good on paper, but so hard to carry out.) I have 2 "sayings" on my refrig. you will probably like, author unknown.
: : : "I TRY TO TAKE JUST ONE DAY AT A TIME... BUT LATELY SEVERAL DAYS HAVE ATTACKED ME AT ONCE."
: : : (There is a picture of a very frazzled looking person.)
: : : "ALWAYS REMEMBER THAT WHAT HAPPENS AROUND US IS LARGELY OUTSIDE OUR CONTROL, BUT THE WAY WE CHOOSE TO REACT TO IT IS INSIDE OUR CONTROL." I guess I should read the latter more often. I made a copy of HAPPINESS IS NOW that Carole posted last month, which is so true. It seems I better do my best to work on a few things or this journey of life, such that it is, but the only one I have,is going to pass me by. I'm sure you've heard, LIVE THIS DAY AS IF IT WERE YOUR LAST, AS SOME DAY IT WILL BE.
: : : Bruce, thanks for caring & thanks for sharing.
: : : Betty H.
: : What you all write is so very meaningful to me. I work in a nursing home, and by regulation we have to let folks do as much for themselves as they can to increase their independence, maintain their dignity and respect, and give them a mental and physical sense of well-beiing. And it is so hard NOT to do for them -- to allow them 20 minutes to button their shirt, etc. Then, when I am all thumbs, it is so HARD for ME to ask someone in a meeting to take minutes because my hand and leg shake so much. Or to allow myself to fix a frozen pizza for my husband after a day at work, instead of fixing him a "nice" meal (he LOVES pizza, but I still feel guilty). Keep up the nice motivational aura -- it's good for all of us here. Lory
: Betty H, Googy and Lory, I just returned from an appointment with Dr. Hubble at Ohio Stateand yes, we got lost again. She has got to be my all time favorite doctor. She had a very sophisticated walker in her office and I immediately saw a lot of benefits using it. This is what I wanted to share with you. Since my sister doesn't have a computer, hopefully she won't read this message. She is having pain in one knee and now has developed back pain. All she would talk about is the things she cann't do, her aches and pains, and makes herself miserable by thinking about wanting to get outside and doing yard work. She had told me in the past that she gave up on using a walker, because she said it was to "heavy" to lift and it strained her back. So after I got home I immediately called her about this great walker which most of it would be paid by medicare. Then came the excusses: cost to much, wasn't sure it would work for her and finally she said I should try it first. She finally started crying and said she just wasn't as strong as I am. In other words, it was begining to sound like she was giving in to her problem and was really into self pity. I told her those same words just take it one day at a time and try to be more patient. Also, I reminded her I can't walk without a walker, but I am doing better walking with the walker. Also, I am really excited about getting the high tech model, because it is all on wheels and their is no danger of walking to far, because it has a small seat to sit and rest. I feel so strongly about regaining my mobility that I am determined to walk every day. We all have choices, my sister chooses to sit and brood all day and I choose to fight it and continue to enjoy life. Which choice would you choose? Bruce
Bruce - Re: your walker -- I just found/was turned on to a walker that was designed for Parkinson's folks like us. Go to NPF site, then click on Products of Interest . It is a U-Step Walking Stabilizer. As of 10-99, Medicare has agreed to fully reimburse those with PD. Let me know if this is what you have. I printed the info to show the PT/OT folks at work. Lory