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    OT November Chit Chat

    Hello everyone,, and I really feel for the folks out east, what a way to start the winter months,,

    Iowa is still enjoying some awesome weather, but alas , all good things eventually come to a end,, we have winter projects done already,, this is a first,,, but Joe will find more,, trust me,, he always does,,

    Nothing to report,, I am feeling really good,,I eventually would like to get back in the pool,, and educate the new excercise teacher, who says people with MS, does not belong in the water,, her mother has MS, and she relapses being in the water,, ok,, thats one person, I will be nice,, my friends all called me, said get over here ! hahaha !

    Halloween,, two adorable grandkids,, Thain was a military man,,Eleanore {Nora} was a angel..

    later then,,
    " Don't outsmart your common sense"

    Peg

    #2
    You sound good, Ms Peg.
    Welcome to november.

    I hid in a restaurant and ate too much this evening.

    Split pea soup and low budget meals for the next two weeks.
    Ohhhhh, that butternut squash gnocchi was fiiiine.
    Hear that all you vege-vegans... fiiiiiine.

    As a lifelong northeasterner, I can't live here and not expect my buns to get kicked
    with an extreme geo-meteorological boot every few years.
    My burg is less than an hour's drive from a line over which tornados and many
    catastrophic storms don't cross.
    It is a small pocket where more times than I can remember, everyone surrounding us
    got nailed and we had nothing to bellow about. But we get our share.

    November is when I count up my accumulated part-timer vacation hours and divide it
    among holidays (and runaways) through december. And start thinking about next year.
    To live among swine or move?
    What a hard decision.

    Comment


      #3
      Here goes my usual comment........... What November already!

      Not working is not all that its cracked up to be. case in point: last night my renters were doing the evening milking and the wind was blowing spitting ice as I watched out the kitchen window and while I don't miss doing chores in bad weather NOT being able to do it is different than not HAVING to do it. Sigh..........

      This oral surgery is for the birds. It still hurts ALOT. Waaaaa I know. To be honest until I had MS I never had tooth problems so as a result for some 40 years I never went to a dentist. No cavities now no (almost) teeth. Good thing I have happy pills. Not to sure about the happy part.

      Weather is typical windy and cold, of course not windy enough to blow the leaves into the empty fields. What is happening as I look out the living room window is the leaves that fell on the empty field are blowing onto the yard! There is only 32 acres in our front field to collect them. Good thing I have a riding lawn mower. I reinvented some lawn mower blades that blow like a jet engine. So its not to hard to fight mother nature.

      Check in time everyone.

      Comment


        #4
        Peg, the exercise teacher whose mother with MS relapses when she's in the water for swimming must be the first time I've heard anything negative about swimming and MS. I'm wondering if anyone checked the water temperature when this woman was having her relapses?

        Busy here catching up on appointments that I put off during the summer months. I've been to the podiatrist. He says I have a cyst on one foot, but no problem unless I'd like surgery which I wouldn't like. The bunions are doing OK (no worse, no better), and new diabetic shoes are going to be ready soon. Tomorrow it's a trip for some fasting blood work I have to have done periodically, plus a flu shot.

        Later there will need to be a hearing test and a hearing aid checkup. I've had these aids for 8 years now and don't seem to be hearing so well lately.

        Somebody called me from school the other day--a total surprise as I'd lost touch with her since we were about 13! She was never a loud person, and I couldn't understand half of what she was saying but was so astonished by her call that I didn't think to tell her I couldn't hear well.

        If your hearing hasn't been great for quite a while, you get in the habit of letting things that are said go by you. You assume you probably heard right, and if you didn't, you don't want to keep saying "What?" all the time.

        I go through the alphabet sometimes trying to figure out what word a person actually said. Was that "bell" or "dell" or "fell"?

        I hope nobody has been hit by the snowstorms.

        renee, for instance?

        When I lived in Massachusetts, there was a fierce ice storm on May 9 one year. No power for 4 days, and it was still quite cold out. The lack of heat had some of us scurrying to motels and burning furniture in our fireplaces. New England isn't for sissies. (Being a sissy, I left after only a couple of years.)
        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

        Comment


          #5
          Happy November Everyone.

          This is beautiful, with Floyd Kramer on the piano....
          Enjoy, SallyOnly registered and activated users can see links., Click Here To Register...

          It takes awhile to load...sorry.



          .
          Last edited by SalpalSally; 11-02-2011, 05:29 AM.
          Love, Sally


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






          Comment


            #6
            I live in MA and there are still folks without power to the west of me. Some friends to the south just got theirs back last night.

            Ours stayed on thank goodness. We only lost internet and cable for a few hours Sunday! :)


            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


              #7
              We had no power for 52 hours. We got it back yesterday. Linda is still without power. I had/have a cold which would have been gone except for freezing cold house. Typically setting off MS crap-vertigo, exhaustion.

              Thankfully we had a snow day today. I started a new teaching job last week. I couldn't have called in sick. It's only two afternoons a week. I am trusting I'll be better tomorrow.

              First time teaching in 5 years. I figured if I didn't take the risk I'd never know if I can do it. Thanks to Ampyra, I can.

              ~Susan (whose husband is skiing at Killington today. He couldn't resist.)
              Be the person your dog thinks you are

              Comment


                #8
                Susan- that is a long time. Many are still w/o power. If you are speaking (smoke signals?) w Linda give her my best wishes. I hope she is warm.

                ANN
                There comes a time when silence is betrayal.- MLK

                Comment


                  #9
                  Hi Ann,
                  I spoke with her this afternoon. Her phone is working intermittently. They have heat a part of the house from the greenhouse generator. Their power may be out for another week. Yikes! She is in good spirits though. I'll pass on your regards.
                  ~Susan
                  Attached Files
                  Be the person your dog thinks you are

                  Comment


                    #10
                    We had snow but only a little under an inch. Took three days to have it melt though as it's staying in the 30s during the day. Went to Boston yesterday to meet an old boyfriend that I had not seen in 37 years...since he came to visit during the time I had brought David home from Houston to introduce my future husband to friends and family. Mike (old BF) is now one of the world's leading stem cell researchers. He is going tomorrow to a conference in Miami with the company that did Peg's therapy although he has principally worked with ES (Embryonic Stem Cells). We had a delightful visit.

                    To the MS Dream Center here this morning for Bible Study, Financial planning seminar and a story teller telling haunted tales of our area. Now we have a houseguest from ME who just came to the door as I was writing this and dinner is almost ready to go on the table.

                    Later...

                    Comment


                      #11
                      What did Stem Cell Researcher have to say about adipose cells? It's like a plum fell in your lap! Do tell.
                      ANN
                      There comes a time when silence is betrayal.- MLK

                      Comment


                        #12
                        Ann, I was thinking the same thing when I read Cherie's post. Not fair Cherie - you must share everything you learned.
                        Virginia

                        Comment


                          #13
                          I am just reporting in as Gary ordered.

                          I will be offline from the computer for quite a while. Moving this room around for new carpet, and taking care of some medical issues. I have more specialists than I can count on two hands. I'll return when I can.

                          All of you my good friends, please be well and don't overdo things. I won't be reading here, or anywhere. I'll catch up when I return. I'm not leaving here forever, don't think that. I just have so many things on my calendar, and so many doctors to see, labs to catch up with, and many body parts that need fixing.

                          Sally, please pass on the info to any other peeps. Thank you.
                          Take care..later then
                          carry on..
                          Lady


                          May happiness be at your door. May it knock early, stay late, and leave the gift of good health behind.

                          Comment


                            #14
                            He's skeptical. After being closeted solely with Embryonic stem cell lines for more than 20 years, he does not understand the technology. I told him about Peg before her procedure and he emailed his friend Arnie who does Mesenchymal stem cells (adult rather than embryonic). Arnie said that he had heard of success stories in cosmetic areas such as moving fat cells from one part of the body to another to fill in areas of atrophy. Arnie also said that what Peg had done "made sense" in that the body does not reject its own cells but was not sure how the cells were treated to heal the CNS. So...Mike, on my suggestion, contected stemGenex and Adistem and they told him about this conference which fit nicely into his travel schedule.

                            He also did not know about the CCSVI theories and was intrigued by them. He said he had a whole line of myelin cells growing but no one interested in doing research on an animal model which was needed if this technique was to go to the FDA. He is willing to overnight some of these cells to any researcher that is willing to try them out on an animal model and see if they work so if you know of any clinics or docs who would be interested in this, send me a PM with contact info and I will put the two of them together.

                            He just seems almost melancholy about not having had a breakthrough yet that can help (in more than theory) those of us with diabetes or heart disease or MS. He is open and hopeful going to the adipose cell conference. As I get his impressions I promise to pass them on. Heck! I offered to go to CA and be his guinea pig with David's blessing. He is just not there for human trial with all the years put into this area of research. Said he has gotten it to work in animal models but not found researchers with the cash to take it to human testing level. He is now working with a large group in Israel that is ready to begin human trials on his cell lines.

                            Comment


                              #15
                              Lady, take care, you know where I am, if you need me.:o
                              Love, Sally


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






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