Pilates and PMR - and other benefits of exercise

Hi everybody!

I've noticed that a few people have mentioned Pilates in their posts and since I feel that I benefited considerably from the Pilates classes I went to before I was diagnosed I thought I'd stick together a few thoughts of my own and ask what others thought too as there have been a few threads about non-drug coping with PMR.

First a bit of my background: I had the symptoms of PMR for nearly 5 years before I was diagnosed and tried a whole range of physical therapies, both privately and through the NHS, to try and get some relief. I'd been using my local ladies-only gym quite a bit when the PMR started - it manifested itself as agonising pain in my thigh muscles when I tried to use the cross-trainer or bike. Over a period of a few months I realised that I was less and less able to cope with the classes I attended and decided I would have to change to a gym with a swimming pool if I was to get value-for-money. It was a case of \"it's an ill wind that blows no good\" because by my changing to a gym a few miles away a whole new world opened up to me. There was a pool - where they held an aqua aerobics class every day - and they also had a few different Pilates and yoga classes. I was too scared to try the yoga but I had done Pilates before and found the new teacher was even better - and eventually I did try the Iyengar yoga class which was also superb.

Pilates was developed by Joseph Pilates, a German who came to England in 1912 and was interned during the First War. During this time he developed a system of pulley-like machines to allow injured patients to work against resistance whilst still in bed to prevent muscle wasting. Many Pilates studios still use this type of equipment in their training but what is much more often found in fitness studios/gyms is what is called modified Pilates - based on the mat exercises developed by JP. The exercises have been adapted by physiotherapists over the years and former back patients are often surprised to find how many of the exercises are very similar to ones they have been taught by their physios. The emphasis is on strengthening the \"core muscles\" - your internal abdominal muscles - in particular, and on control. There are no points to be scored by doing more and faster or bigger repetitions of the exercises and you are encouraged to work at your level at all times. When your core muscles are strong it improves your posture which, in turn, helps with back pain, joint pain and, perhaps strangely, stamina.

Not all the exercises are done on a mat, there are also a whole range done in a standing position and I found them to be excellent for getting my shoulders and hips mobilised. Very occasionally we worked with a gym ball (the big diameter ones you can sit on) and I really enjoyed that.

I can hear you saying \"But if I got down on a mat I'd never get up again\"! It sometimes used to take me far longer than the others to get into position - especially a comfortable one - but my teacher was doing a college course in sport science and was specialising in rehabilitation. Her placement towards the end was 4 weeks at Catterick at the Army barracks, working with soldiers after injury. This meant she was particularly helpful to any of us who had health problems and she adapted any movement that proved too difficult or showed us something else to do. She consistently encouraged us not to take any notice of what others were doing but to work at our own pace and level.

Over the 4 years I did Pilates I saw a massive improvement in my posture and mobility - and remember, this was before I was diagnosed as having PMR but had the symptoms! I found it easiest when I had had an aqua class beforehand or some other opportunity to get loosened up but even without that, the warm-up series of movements we did at the start of the class were perfect for lindering the shoulder and hip stiffness.

One-to-one classes are the ideal, I suppose, but they tend to be seriously expensive. However, there are teachers out there who are excellent who work in fitness studios and even council gyms! My gym membership was an off-peak one aimed at the retired - Monday to Friday until 5pm and was very reasonably priced at £35-ish, particularly when you consider that I had up to 5 aqua classes, 2 Pilates and 1 yoga class available to me. In most places an aqua class alone costs over £5 by the time you pay for the entrance to the pool and the class and I won't even think about yoga classes! And I also had the use of the gym (I hated it, boring!) and the pool, sauna and steam room - also brilliant for PMR, I found. I had had lots of physio and 2 very good Pilates teachers who were very interested in making sure they were teaching well and correctly so could tell if a teacher was competent or not - and never went back to a dodgy one, especially anyone who sang the \"no pain, no gain\" mantra. A good way to go about it might be a few high standard (expensive) classes, maybe with a physio, to start with and then look for something more reasonable at a studio. And judging by the texts I keep getting from my old gym 18 months after leaving to move here they seem to be desperate for custom in the recession and the prices should be competitive!

In addition to the mobility and strength benefits of going to the gym I found that it also gave me the impetus I needed to go out - even on a day when I felt so down all I really wanted to do was go back to bed! If I had a morning class I didn't go to any great shakes getting dressed (by which time I would have been so exhausted I would have to sit for half an hour before I could do anything else). I put on my swimming costume and used the pool-side shower or gym stuff and showered afterwards - with the easiest top and bottoms I could find, no-one cared at the gym! It was much easier afterwards. I made some new friends - but I knew I would always have some company - and that helped the depressive mood of PMR no end. And I definitely felt better!

Has anyone else got any thoughts in this regard that others might find helpful or encouraging?

cheers from a slightly wintry northern Italy (snow down to 1700m - Midsummer's Day tomorrow, global warming? Yeah right!)

EileenH

:D I have always been a great believer in exercises to keep the body flexible and supple and started off many years ago doing Hatha Yoga. I have done some pilates and found it very good also. What puzzled me a few years ago, was the fact that, despite years of careful and regular exercising, my body was becoming qiuckly more and more painful and stiffer in the shoulder and hips areas. Not only that, but I felt really ill and couldn't figure out what was going on. It was only after moving house and changing my GP practise that Polymyalgia was diagnosed and treated. The prednilosone has made a dramatic difference and I can now do my daily yoga again and I feel so much better. I do feel that one must try to do some kind of gentle exercise every day, but don't overdo it becuase fatigue can soon set in. I don't know whether I'm lucky or unlucky as far as sleep is concerned because I only seem to get a good sleep on every alternate night. The other night, I am wandering about looking for things to do that won't disturb the neighbours.

Just a little postscript to all this, but I found doing pilates and basic stretching and toning, with the correct breathing and pulling in of tummy muscles, has made a dramatic improvement to my pelvic floor muscles.

Look away men, but after childbirth it was never quite right down there, and 2yrs of exercise has made a huge difference!

A positive for pmr!!!

Hello Eileen et al

I have mentioned previously my Tai Chi exercise which I have found of enormous benefit - it combines stretching, breathing, meditation and the Tai Chi Form itself (the latter exercises my little grey cells in particular!). I always feel incredibly energised after each class. It has improved both my balance and co-ordination, both affected by my PMR. A bonus is that it doesn't involve getting up and down off the floor, still a no-no for me. I somehow can't bend my knees enough or weight-bear through my legs to the standing position. Whether this is due to the year of spending so long in bed and total lack of mobility, I don't know, but before steroids, unlike you Eillen, any movement at all let alone exercise was out of the question. There must be different degrees of PMR which renders some people able to keep moving in spite of their pain whilst others are horrendously incapacitated. My ESR at the outset was as high as 92 and my CRP 157(!) so perhaps that had a bearing.

I also attend an exercise class to music called \"Extend\" run at the local Community Day Centre, some of which is standing and some sitting, sometimes using hoops, and sometimes balls to squeeze whilst working the arm muscles. The teacher is such fun as are a few members of the class and we often end up rolling about with laughter - a real tonic! Sadly I'll have to miss my class tomorrow because of an emergency dental visit - yet another load of enamel has broken off another tooth today......another crown looms, the 4th in the last 12 months (the last one only 3 weeks ago!) I haven't read of anyone else on here losing their teeth to the steroids but perhaps that's because, unlike me, everyone is able to take calcium supplements.

Good advice Wallis re the pelvic floor exercises - the bladder is a muscle, and we know what steroids can do to those!

Madge - do hope tonight is one of the of the alternative good kind!

Keep up that exercise everyone but know when to stop!

Wimbledon looms......not much exercise for me then in the next couple of weeks!

MrsO