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    Lovely here today. 80 and sunny out but with the windows and doors closed the house is staying at a nice 72 degrees. All the leaves are finally out and flowers are blooming and color is taking over the yard. I think all of the birdhouses have nests active and birdsong is plentiful. Got out briefly today to trim last year's growth off the Lace Hydrangea but it was too warm to be out for long. The pool is back up and running and I've done a 35 minute workout each of the last two days. I really had gotten stiff being out of it for so long.

    Comment


      Originally posted by agate View Post
      Being disabled isn't for sissies, no doubt about it.

      P.S. I'm guessing here: WPB = West Palm Beach?
      My guess is WPB = Wide Pudgy Bottom.
      "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

      Albert Einstein

      Comment


        Originally posted by Howie View Post
        My guess is WPB = Wide Pudgy Bottom.
        Will Punish Buffoon?


        Whatever happens around you, don't take it personally. Nothing other people do is because of you. It is because of themselves. -- Miguel Ruiz

        Comment


          Hi Suze Q-
          I became a paraplegic immediately during my first exascerbation due to transverse myelitis.
          The dime size lesion is a tad lopsided so atrophy has occurred more so in my left leg.

          Lefty is skeeeny but not entirely without peripheral nerve activity so it isn't a boney stick.
          My right leg has shrunk a bit but is short skirt worthy…..CHUCKLE.

          I had mighty legs, rock hard calves from love of walking.

          Early on I decided I needed to love my body regardless of what
          shape it took. I have a special fondness for my scars which make me
          a candidate for a biker gang.

          Hmmm, leather jackets and fast rides.

          WPB, got to think about that one.
          Last edited by renee; 05-17-2015, 10:58 PM. Reason: cuz.

          Comment


            Well, I made it through another whole week, without having any kind of
            emergency, power outage, flare, or other crappy mishap...Hoot Hoot!!
            However....,I have noticed my age and weaknesses, a bit more, lately.

            I wonder, how long I will be able to do it, at home, on my own?? Everything
            is getting harder and harder to do, but I'm doing my best to keep it moving.
            Doing my PT and OT each morning and afternoon. Standing and walking
            in place....etc.... I sure hope n pray, I'm good for the next 10 or 20 years.

            Praying, also, that this is a good week for you all!!

            WPB = Won't Pop Bubble..
            Love, Sally


            "The best way out is always through". Robert Frost






            Comment


              Ooh I just thought of another one:

              With Perfect Balance!


              Whatever happens around you, don't take it personally. Nothing other people do is because of you. It is because of themselves. -- Miguel Ruiz

              Comment


                Sally you will be around for a long time....someone needs to keep an eye on Howie.

                We had rain yesterday!!! .37 inches in a couple hours. A downpour of Biblical proportions....for us anyway. Along with hail that was 1/4 inch and covered the ground. I haven't had the nerve to go check the garden or the new fruit trees.

                Comment


                  :) Hi everyone. WPB is where I live, West Palm Beach. The guesses were funny.

                  I slept until 4 PM today from 11:30 last night. Lacy got up on the bed and onto my chest and pawed me on the cheek to wake me.

                  No call from Andy yesterday or today. He will call when Jamie is going to be released from the hospital. He will be by here tomorrow to put out my trash and recycle.

                  Sally I wonder the same thing. Everything I have to do uses energy and I have only a little of that. I hope to be able to stay in my house until I die. The weaker I get the more I worry. Take care everyone. Jeanie :)

                  Comment


                    Thanks all for muscle atrophy experiences. I suspect mine is related to CNS nerve damage too, unfortunately.

                    Renee, do you do physio to lessen muscle loss, or it wouldn't help, given nerve damage? Agate do you? Howie?

                    Sally, avail yourself of all resources in your area that assist people to remain independent and in their own homes. It saves the system money to keep people in their homes, where possible, bringing in ancillary resources or making minor retrofits to help out. Chat with a social worker, they can assess and find resources to makes it more comfortable and easier for you to live at home, they are a goldmine of information.

                    Jeanie, I'm so sorry about the difficulties that Jamie is going through. A real challenge and emotional toll for everyone who loves her. I hope this latest hospital stay will put her on an easier path. Glad you made it out to visit your friend and pushed yourself a bit. I now have b12 and will start the shots myself, hoping for a bit more energy too.

                    WPB: women's profound brilliance?
                    WPB: way past bedtime?
                    Please Note that my posts may have been arbitrarily altered by a Moderator and may not reflect my original content.

                    Per Mike Weins: "...the admin/mod team doesn't have to provide a forewarning/warning/mention about altering a members post. It doesn't matter if they fix a link, remove a link, fix a typo, or whatever...."

                    Comment


                      I don't, and never even considered it. Taking care of me, and two cats is enough for me!
                      "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

                      Albert Einstein

                      Comment


                        I've had several courses of PT and still do the exercises I was told to do. I try to get some exercise in every day, up to half an hour a day.

                        With diabetes (Type 2) I understand that diet can control it but not without daily exercise.

                        The importance of exercise is made clear to me every time I skip a day of it.
                        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

                        Comment


                          Originally posted by agate View Post
                          The importance of exercise is made clear to me every time I skip a day of it.
                          AM E N Joan. Thanks all for your cheerleading me forward.
                          I love you!!
                          Love, Sally


                          "The best way out is always through". Robert Frost






                          Comment


                            Suze-

                            I don't do any kind of PT to pump up leg muscles.
                            Muscle building has to come from work that I make my legs do.
                            Since legs don't listen to me there are as they will be-
                            any musculature I have is related to involuntary muscle movement.

                            I asked one doc about it and he replied that yes, atrophy can be reversed but
                            your muscles need to be able to respond to the direction from your head.

                            That's that.

                            Comment


                              Originally posted by renee View Post
                              Suze-

                              I don't do any kind of PT to pump up leg muscles.
                              Muscle building has to come from work that I make my legs do.
                              Since legs don't listen to me there are as they will be-
                              any musculature I have is related to involuntary muscle movement.

                              I asked one doc about it and he replied that yes, atrophy can be reversed but
                              your muscles need to be able to respond to the direction from your head.

                              That's that.
                              I thought that sometimes they can strap our legs to a cycling machine when they don't work on their own, and in that way, move legs and build muscle. Not sure, but I think I saw that on tv for people with spinal cord injuries?
                              Please Note that my posts may have been arbitrarily altered by a Moderator and may not reflect my original content.

                              Per Mike Weins: "...the admin/mod team doesn't have to provide a forewarning/warning/mention about altering a members post. It doesn't matter if they fix a link, remove a link, fix a typo, or whatever...."

                              Comment


                                Yes Suz, I sometimes have to grab my left leg or foot and
                                move them manually. Then, usually, they will start to move
                                on their own as my brain insists...LOL.
                                Love, Sally


                                "The best way out is always through". Robert Frost






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