Does anyone else suffer from chronic back pain across the middle of their back? I know it's all to do with poor posture and weakened muscles. I do try to stand straight, but the pain is so great, especially after cooking a meal. Also affects the back of my neck and makes my head feel too heavy for my body!!
BB, your Eagle Brand Medicated Oil helps, but makes me smell a bit like a eucalyptus tree! Anybody got some good exercises for strengthening back muscles?
I get back pain after walking about 6 miles. It's clearly linked to my stoop (which predates my diagnosis 11 years ago), lean to the side (which I first noticed 5 years ago) and twist (1 year). I assume that they are caused by dystonia. I find that I get straighter after taking levodopa, and this causes much of the pain to go away.
Posture is the key, but that's easier said than done.
Impressed that you can still walk 6 miles. That's great. Three is my limit, on a good day and I'm only 4 yrs. diagnosed. Interested to hear that Levodopa helps, as I'm due to go on Madopar next week. Really hoping the back pain might ease, it makes me so tired. Many thanks for your reply and keep mobile!
I see a McTimoney Chiropractor every so often. McTimoney is much more gentle than the bone-cracking type usual chiropractic treatments. Doesn't feel as if he's doing much at the time, but it helps to straighten me out. I get a lot of lower back pain, mainly due to osteo arthritis. Costs a bit, £ 45 a session, but worth it. Recently he has been treating my stiff and painful neck, pain probably due to whiplash effect of several backward falls over last few months. It is sooooo much better now. He recommends the "cat camel" exercise to Improve back and neck mobility - lots of videos on you tube.
I've had back pain on and off for years following a fall down some stairs, but for the last year or so it's been pretty much constant, lower left back with spasms across the whole lower back which make me freeze until they ease off.
Have you tried physiotherapy? You should be able to get a few sessions on the NHS through your GP. Short term, some stretching exercises might help. If you visit the website for Flint House in Goring on Thames (it's a Police rehab centre) and click on the 'Physio' tab, there is a video of lower back / spine stretches. They may help, just try them and see.
I've also bought a foam lumbar support cushion online which seems to ease the pain when watching tv etc. I still get up very slowly to avoid my back going into spasm!!
Thank you for your helpful replies. Yes, I have had neurophysiotherapy sessions (6) and some of the exercises shown on the Flint House video, are the ones I already do. Just watched it, so thanks Richard for drawing it to my attention......will definitely be trying those out. I sympathise with you over your spasms too, they really are very painful. I get less of them now, since taking Chia seeds on a daily basis.
I do see a chiropractor, every 3 months, who specialises in people with Parkinson's and I feel great afterwards. She also does acupuncture on my shoulders and lower back. Charges £30 for half an hour, so not too bad. If I could afford it I'd go for a massage every week too!
Also wear a back brace from time to time, but don't want to get too reliant on that. I'm hoping the Madopar will help........reluctantly going down the conventional meds. route now. I suppose we all deal with our condition in whichever way works best for us. I just wish more people knew about Parkinson's and could get some insight into the psychological and physical torture it can cause.
All the best to you both. I hope you can manage your pain and thanks again for sharing your thoughts.
Hi Twinks...I also get awful painful neck, shoulders and upper back and my GP who is a qualified accupuncturist gives me regular treatment also i do exercises every day given to me originally by a physio. I was very interested to read about the Chia seeds....how long have you been taking them? do you cook them or add them to your food? hope you don't mind me asking but i would like to try them, would it be best to get them from a health shop do you think?
Sorry to hear you're a fellow sufferer! It's no joke, is it? Good that your GP can help by doing acupuncture though.
I've been eating Chia seeds for nearly a year now. You can get them from health food shops, but I buy them online. (much cheaper). I just sprinkle a teaspoonful on my cereal every morning, or add them to a salad, or you can put them in anything really. If you put them in a drink, they will swell up and become quite thick, so it's always a good idea to drink plenty of fluid when eating them, or they could clog in your oesophagus. Why not google it and find out more. They really have helped relieved my constipation, cramps and muscle spasms.
I get shoulder and elbow pain every night.I have walking difficulties and have tried stroke rehabilitation for 22weeks but improvements in my mobility are very small I have vascular parkinsonism .waiting for a physiotherapy appointment.I am 71 years of age.
I have recently suffered agony beyond belief with a trapped nerve but that is not your problem methinks, yes the stooping posture PD inflicts on us is more than likely a big contributor , I chose Acupuncture for the ache,,2yrs ago, and just had to wait for the nerve to reset. can recomend AP though it works well Regards Fedexlike FED
Hi Fed, yes I read your post about how your trapped nerve got better. Hope it stays untrapped! Since starting on Madopar in June, my back pain is a lot less. I still get some shoulder pain (right shoulder...affected side), but if I press my fingers into the top of my arm, it goes away. In fact putting pressure anywhere on my affected arm and squeezing hard makes it feel like the muscles are working properly again, instead of feeling like a heavy lead weight. Does that make any sense? My PD is not the tremor type, but slowness of movement and dexterity, all down my right side. May try acupuncture.......can you get it on the NHS?
Sorry to hear you are suffering with back pain as you know I get quite painful joints myself hence the heat rub as you said the massage helps but is not affordable weekly have you possibly looked into having this treatment at your local university or college as the students training in this need people to volunteer to have massages so they can qualify its been suggested to me we could get this at a good reduced rate.
Yes its available in vhs sorry NHS and it does work when I t was suggested to me I thought cobblers ,, but I agreed to a 4 week treatment in my right shoulder ,, this was 5yrs ago and it never came back until I am made to sleep on my right side by necessity due to the Ddopa pump being on that side, I am due any day to go in for the tubes of this device changed this will only be a day job so im told but knowing my luck they will probably take a leg and a ear ? the latter only on loan ????lend me yr ears?? so it is pain in my right shoulder coz im always leaning on it.
Hi Twinks....i have just read your post and like you i have had awful pain in my shoulder particularly the right side, again the affected side. this has been going on for at least 7 years. I was sent to an Orthopeadic surgeon, plenty of physio, Hydrotherapy and finally found it was one of the symptoms of PD, though i was not diagnosed until 2013. The shoulder pain went across my back between the shoulder blades, into the neck and my head always feels heavy and woozy, down the arm and now into the hand which is quite stiff and goes rigid at times. The shoulder eventually froze up completely and was excrutiatingly painful and so i had an op called an MUA (Manipulation under anaesthetic) that gave me back much more movement but as the years have gone on the pain and stiffness is my worst symptom. My wonderful GP is a qualified Accupuncturist and every 4 weeks or so he treats me. He and i can feel straight away the release of the muscles as he inserts the needles, it is almost like a popping feeling. Occassionally he has had to cancel and i reallly notice the difference. I find that has been the only treatment to help me and afterwards i can actually turm my head to the right quite easily. Sadly none of it lasts long but i would recommend trying it for yourself....we all react differently but i would say to make sure that you find a reputable qualified person to treat you. I am very lucky that my GP does not charge his patients but to be honest i would pay for it....as it helps me.
I hope this info helps you.....and that you soon get some relief Twinks
You know I said the pain in my lower back and left thigh had eased, then ceased altogether , well its back and yesterday my Consultant consulted me or one of the Nurse Specialists did and asked me to attend the PD clinic today at 2.45 which we did , and as my walking any further than 2 or 3 yds is impossible beloved piloted me in our wheel chair into his office causing much damage to the furniture en route,and I was informed I have a serious possibly dangerous prolapsed disc which as a result of my condition (parky) may exclude surgery, hmm, bugger, its most unlike Mr Lucky Luck to visit old fed these days but I am or have been seriously battered of recent, however injections into the area are a possibility has anyone had this done and how long does it last re killing the pain either way It seems this is going to be a rush job maily to ease the aaaaaaaaaaaaaaaaaaaaahhgonising pain obviously but also to prevent losing the use of my legs which is occurring now and again,,also PD is worsening making the pain worser ?? Prostate symptoms are playing catchup ,old Dee Pression is also chucking his £2 coin into the pot ( yes £2 , brexit you know it was 20p) and to round off I am becoming very deaf, as is my lady, we have some peculiar conversations so if you reply can you type a little louder please,,THANK YOU
Thank you Dolly, for the info and advice about acupuncture.......very helpful. Sorry to hear you suffer too with pain. Since being on Madopar (July), my pain has thankfully got a lot better. If I stand cooking or baking, for any length of time, then I do get it across my shoulder blades.
Oh Fed, I bet you're FedUp. So sad to hear that your pain has come back and the possible reason is a prolapsed disc. You sound in AGONY........so how do you manage to keep your sense of humour and make all your problems sound lighthearted? This friggin' disease has a lot to answer for.
I can sympathise with the deafness, as my right ear is totally blocked with wax and putting drops in has only made it worse. I get a certain pleasure out of the snap, crackle & pop going on in there though. And no, I didn't put a Rice Crispie in my ear! My deafness has come at completely the wrong time, as I am the Prompt in our village pantomime and opening night is tonight!! Cinderella had better make sure she hears the clock strike midnight, 'cos I might not!