Exercise and Everyday Living | Arthritis Information

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Hello, folks. From time to time I read allusions to the role of exercise in coping with PMR. This is a concern of mine because while disinclined to engage in it, on the one hand, I find that not doing so leads to muscle atrophy, on the other hand. I used to work out for onehour three times a week at the gym, but have not been able to return since May, 2007 when this hit me. I would be most interested in knowing more about other poeple's experiences in exercising. Do you find it helpful? Does it require a simple (or courageous) act of will to get started and maintain it? What is the aftermath when finished each exercise session. I read that "light exercise" is recommended. For those who do this, could you share how you define "light" when putting into practice?

Also, my apologies for the add-on of this important question, but do any of you find that there is a connection between allergies and PMR?

Lastly, Libeth, I suspect you're really on to something essential when you speak of just managing everyday living, as you did in a response to an earlier post. I think that this may, understandably, sometimes be a neglected area because of the pain, malaise, and even depression that so many of us endure. Yet attending to it in an appropriate way may be a useful area along the spectrum of treatment and one that we can take control over. I imagine what "appropriate" way amounts to for each of us may differ, but perhaps we can all share what that is for us with one another from time to time. 

Still deriving so much help and support from this essential forum. Thanks all. 

Hugh

 

 

 

 

 

 

 

My ap

Hugh, since my rheumy told me I did not have PMR, but offered no
explanation for what is wrong with me, I find that I have been reversing
my position on what to do with the situation. Instead of focusing on the
name of my "affliction" and the details of the the pain, discomfort, and
limitations, I am working on shaping my life around them. I have been
examining what is important to me, what I can eliminate, how I can
continue to do what is meaningful to me, even if it is for 15 minutes
instead of 2 hours. Instead of thinking how I used to feel when I went
into the studio, I am trying to focus on what I am able to do now, and
proceed from there. Is it simple or courageous? I don't know, but it
seems to be necessary. Exercise is important, I tell myself, just keep
moving. I walk to the post office every day with my dog, she needs the
exercise and so do I, even if I have to sit down for a few minutes several
times during the 1 mile walk. I go up and down the stairs in my house
often, (it is cheaper than a stairmaster at the gym), I care for my house
and garden in small bites of time and effort. Is all this working? I"ll let
you know!

Libeth

Libeth, thanks so much for taking the time to provide us all with such a thoughtful summary. It makes lots of sense to me. I think you have developed a great attitude -- concentrating on what you can do and not the label of what you may have. I guess it is frustrating though to be "dismissed" with no diagnosis and no alternative offerred by your rheumy. I haven't been formally diagnosed yet, but am on prednisone. In any event, I've come to the conclusion that I just can't wait for doctors to give me direction and feed me with pills. Whatever help they can offer is fine, but I must carve out a life for myself within the acknowledged limits I (as we all do) face. Otherwise, giving in to this "thing" leads to a downward spiral. Yes, please do let me know how things ago. I'd appreciate it. I'll do the same. Wishing you all the best,

Hugh

Libeth and Sean,

You two seem to have a handle on things quicker than I did. It took me a LONG time to come to grips with rearranging my life and to stop worrying and grieving about what I couldn't do any more. I'm like you, Libeth. I have certain things that I refused to give up, though I couldn't do them with as much time  or intensity as I did before. I am happy to say that has all changed over time. I am now done with the PMR, and I am getting back to a more "normal" life. For me, it did work.

Hugh, the exercise thing IS very important. You just have to find what and how much you can do. With me, it was an ever-changing process. I never quite figured out how much was too much or too little. I just knew that if I didn't do some sort of exercise, that I would end up feeling worse. If I did the exercise (walking, very light weights, swimming or pool exercises...), I would still hurt, but the hurt was a constant thing anyway, so as long as it didn't get worse, I was good. I still got deconditioned, because I couldn't do what I did before, but at least I was doing something. It is important to do some stretching, too. I wish our insurance covered massage therapy, or that I could afford to go frequently. I can't afford to go even infrequently, and I know that regular massage would help so much. So I have to concentrate on stretching at home. Things are gradually getting back to pre-PMR status (of course, now I have to take older age into consideration

It seems each of us is affected differently by this disease, and gets different levels of relief from our medication.  For me, before the prednisone, I still had to be physically active every day because I have a small horse farm, so had to clean stalls & water buckets, handle the horses, etc.  It became very difficult until I started on prednisone.  I found that as I worked and the muscles warmed up (I guess) it became easier and I felt better.

Since being on prednisone, again, I've had no choice but to remain physically active.  Over the past year and a half, there have been times when my arms & shoulders were stiff & ached, so I had to fill my wheelbarrow only half full, etc., but as before, it feels better once I get "warmed up".   I can imagine if I went for even a few weeks without such activity, I would probably suffer for it later if I tried to resume, as it requires a certain level of fitness.

I am lucky enough that, even if I have some aches & stiffness, I am still physically able to saddle & ride my horse, so my "quality of life" has not altered significantly from my pre-PMR days.

Ruth, I am so glad for you that you are able to continue working with your
horses - even on a reduced schedule. It must help you to keep going.
My daughter used to ride combined training, and when she was preparing
her horse for an event, she used interval training to bring him to a level
of fitness. Perhaps you know about it. We talked about using that
program to deal with PMR. I have been doing a version of that and I think
that it is helping. Instead of focusing on how much I need to do, I
focus on the length of time I spend and the periods of rest in between. I
think it is important to monitor those periods carefully, and not to spend
too much time on either one. Incidentally, I am not living with horses
anymore, and I miss those beautiful creatures, their soft noses, the
nickers of welcome, their grace of moment. Enjoy yours!

My dogs MADE me go out and keep walking......

 My friend MADE me go swimming with her and I endured the pain of doing the breaststroke .My arms would be killing me but I kept going.

I think it is important to do gentle exercises as not to atrophy the muscles .

I find that walking is good for me.  I hate to repeat myself, because I don't know who has read what or who is new.   I initially stressed my knees on an exercise bicycle.  My knees hurt the next day and continued to hurt.  I had a low grade lower back pain for about a year.  I had gone to a physical therapist and that helped at the time.   I was doing Pilates for 20 minutes every other day.  This did not help and I had groin pain.  I was doing leg lifts and stressing my groin area.

When I stressed my knees, I couldn't turn over in bed or get out of a chair.  I went to a chiropractor and that did not help too much, other than he had  a physical therapist working with him.  One time he suggested a massage.  For me that was not good.  The next day I felt like I had been whipped with bicycle chain.  Every muscle in my body hurt.  To much pressure was applied.

I stressed my arms because I used them to lift myself in bed and out of chairs.

Now I realize....whatever muscles I stress, they take a while to heal.  I think PMR has given me moderately high blood pressure.  I didn't have high blood pressure until a couple years ago.

The picture is coming clear.   My left arm hurt more than the rest of me.  In fact, I would say it hurt about the same before I took Prednisone.  I'm no longer on Prednisone.  The doctor said to take my blood pressure every day and report back to her in a couple months.  The other night I took my blood pressure and shooting pains ran up my shoulder.  It was then I realized my arm hurt because of taking my blood pressure and putting pressure on them every day.   I was stressing those muscles/veins.

I was working on antique furniture this summer and I could work on it for a couple hours each day and my arms didn't hurt too much.   Spend more time than that and I had pain.

I know now that is why we hurt, we are stressing muscles/veins.  Some say their buttocks hurt...mine used to before I started getting better.  That is because we sit on our bottoms and put pressure on that area. 

PMR in my opinion is adrenal fatigue.  It is just not putting out enough stuff to fix up the muscles/veins that we use and when we over work them to much they hurt.

We do need to keep moving, but have to be careful to not stress our bodies.    Mary

 

[QUOTE=marianne1952]

Did not do it on my own....did not want to ....but......

My dogs MADE me go out and keep walking......

 My friend MADE me go swimming with her and I endured the pain of doing the breaststroke .My arms would be killing me but I kept going.

I think it is important to do gentle exercises as not to atrophy the muscles .

[/QUOTE] [QUOTE=marianne1952]

Did not do it on my own....did not want to ....but......

My dogs MADE me go out and keep walking......

 My friend MADE me go swimming with her and I endured the pain of doing the breaststroke .My arms would be killing me but I kept going.

I think it is important to do gentle exercises as not to atrophy the muscles .

[/QUOTE] Thank Goodness for dogs. I had to go out twice a day there was no-one else to take her. Otherwse I would have stayed indoors feeling sorry for myself. I am sure the regular exercise is responsible for my no longer "seizing up" JuliaDogs are life savers..not only for excersise but also ...they are great listeners .....and great  company!Plus....you ahve someone to focus on other than  yourself in this horrible time . They are good for mind body and spirit. I do not understand anyone can live without them!

Hi Marianne!

At the moment we have the golden retriever that we often take care of.  I have a problem with my right foot, so I cannot help to walk with him (I seem to have gout after a week´s visit to Portugal some weeks ago - gout used to be called port wine toe in Sweden when I grew up, so the name could fit in this time). Especially my wife likes the dog but I get more and more fond of him. When I was OK he helped me to get up early in the morning those days that my wife went to work and also in the middle of the day. As we live in a hilly area, he helps me to walk uphill - he is so strong that he pulls me when he is determined to go faster.

We have had great weather although it is getting colder and one night last week we had night frost.

Ragnar

Dogs are indeed life savers! I have a corgi, she insists we go for a walk, I let
her off the leash for a little run, and watch her with amusement while she
chases squirrels, smells every bush, looks for crumbs that might be edible.
She is at least a laugh a day, and her devotion warms my heart. Her
welcome when I come home is always exuberant and affectionate every time.   
Priceless!


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