Does PT help at all?

Posted , 15 users are following.

I'm new to this forum and am sure this question has been asked before, but does PT help or is it a waste of time?  I've done 8 sessions (while also diligently performing the exercises at home) and there's been no difference.  Does this just have to run its course?  My FS stemmed from an arm injury.  How long should I expect it to last?  It's so frustrating that I cannot play catch with my kids, among other things.

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  • Posted

    Mine has been going on for a year and a half.  I did 20 PT sessions last year (the most my insurance would cover - I'm in the US) and I did feel some benefit.  Did it cure it No, but I did get a bit more range of motion while I was going.  I would have loved to have gone every week but it would have cost a small fortune.  I'm getting there, the Dr hopes no more than another 6 months - urgh!
  • Posted

    Hi Jill

    I have found that physio usually agrivates my shoulder a gentle massage by a physio is good but they tend to want to do rough massage .

    But ive had acupuncture. Cortisone injections.pyhsio.and hydradialation and they have all seemed to make it worse so i personally say let it run its course but every one seems to be different.

    I now have a frozen left shoulder and bursitis in my right that i had injections in both a week ago and have been in worse pain ever since and now have a lot less movement in my right shoulder .

    I have been working on lighter duties up to about 4 weeks ago and my good shoulder was deteriorating really quickly while stil trying to work then i was to the point of being so stressed and not much sleep ect .

    I got a bad cold and just so run down now you have to really try to take care of yourself during the process as if your employed your employer and work cover will try to keep you doing too much and people say yeh but its only your shoulder but the constant pain and lack off sleep catch up to you after a while .

    I have had my frozen shoulder for 10 months now and work cover a trying to push the specialist to operate but i am hesitant as i have a heart condition.

    So dont let people push you around and if your paying for physio then make sure your getting one that helps not hurts you.

    As if its a work cover physio they just try to hurry you back to work and can cause a lot more damage so be careful.

    And it can take upto 2 years to come good depending on life factors of age ect.

    But try not to let it get you down there are lots of people in the same boat.

    Lauren

    • Posted

      Shame man..I can surely agree tht domestic cleaning really worsen the situation. .I was doing so well till I decided to start cleaning nd tht just set me back..my motion instantly became less the next morning with excruciating pain..After a cortisone shot nd a week of bed rest nd hectic pain killers I am back as I was before the domestic cleaning. .hang in thete
  • Posted

    Your joint is inflamed. Laying down scar tissue to imobilize your joint is how our bodies protect the joint.  If you can keep moving your arm as much as possible and accept some pain with this action, you may not have as much work to do when it finally starts to thaw in regaining your ROM.    There is a belief that timing is everything and too much pt may keep you inflamed.   1-2 years of work may be ahead of you.  Sorry. 
  • Posted

    I'm sorry but I have to strongly disagree with those that advocate the "no pain, no gain" approach.  I may be wrong but it seems to be more prevelant in the US than the UK.   While keeping your shoulder moving as much as possible and gentle stretching excercises may be helpful the advice I've always been told is to stop if it hurts.  Some eminent shoulder consultants tell patients to actively avoid physiotherapy at all, until the thawing stage, as it can do more harm than good.  It may be that the people who advocate this do get better in time - but so do others that don't go through this painful therapy

    Sorry to be contraversial - no offence meant to those who gave the opposite advice but I just had to point out that this view is not universally accepted.  Do some research, read through other posts on here and use your own judgement.  I know we're all different and what works for one, does not necessarily work for someone else but painful physiotherapy is not the only way forward.  What has worked for me is hydrodilatation and gentle (non-painful) excercising.  After about 14 months, I am almost back to normal, have about 80% plus of my movement back and have been without pain for 6 months.

    Good luck Jill - try to remember it will get better in time.

    • Posted

      Yes, I agree with all of this maria and just posted my comments below.  The trouble is we all want instant results and sometimes push the medical profession to cure us asap and we are in such terrible pain with it we would gladly chop our own arm off at times.  If I could wave a magic wand for everyone on here I would and it would allow everyone time off work while in the painful first stage, a proper pain management programme during this stage and a massage of the whole arm and neck at least 3 times a week when able and consistent advice when starting PT movements again in the recovering stages.  A third party to give family members advice on this lengthy debilitating condition to get them to pull their weight around the house more and offer sympathy and tea when needed.  I would avoid all intrusive injection treatments and operations if at all possibe but this depends on the cause or trigger for the FS and any other complications.  I would wish for there to be a clear and quick diagnostic route with a specialist FS advisor and supporter in every healthcare setting and some financial help from the government for those who cannot manage when going through this acknowleding that we are not malingerers! 
    • Posted

      The problem is, there is too little known about this condition, so there is lots of conflicting advice, even from the professionals.  Added to this, we don't look ill and many of us soldier on as best we can, so others think we are OK or putting it on if we complain.  I found this forum invaluable for getting advice and support from fellow sufferes who are the only ones who truly know what we're going through!
  • Posted

    I was told (and have read) that PT helps in about 90% of cases.  In my case, I was among the 10% for whom it didn't work, so they recommended that I discontinue. 
  • Posted

    Hi Jill,

    I have had 7 sessions of it and I don't think it's helping me either.

    I am more sore and painful after it.

    It seems like so much pain to move a millimeter more.

    I am wondering if just doing light exercises to keep it moving is good enough...

    I too am wondering if letting it take its course with painkillers and a little movement is best..

    • Posted

      Hi K

      Wait till after ur painful stage b4 u start PT again. .PT is more fore stretching ur tendons for ROM ..Hopefully then it will benefit u..All the best.

  • Posted

    Hi Jill. I may not be the same case because i had surgery twice for a broken humerus. I have suspected frozen shoulder but it is post operative stiffness as opposed to idiopathic fs. However, i can attest that intense therapy is helping me considerably. But it took a while to start seeing results. I only did 2 sessions of basic physio a week for the first 6 weeks and saw no range of motion improvement. I then started seeing a chiropractor who specializes in ART sports therapy and i began to get bk range of motion immedistely. So i do physio 3 times a week and ART twice. Mon-fri. I then walk 1 hour every day while doing the exercises and stretching on my own 3 times a day. It is very painful while they manipulate my arm but it stops as soon as tyhey stop--- that is whats key. If your pain settles right away after the stretching then it is ok.

    Keep the faith! I had many crying sessions over the last 10 weeks but i believe im turning the corner with this dedicated rehab schedule

  • Posted

    Hi Jill,  not that it is going to help you but I really don't agree with the 'no pain, no gain' attitude - sorry Bobby smile My FS also stemmed from an injury and I eventually listened to my body and common sense and truly believe this awful thing will run its course come what may. PT made it worse and glad I stopped it. By putting yourself through even more pain could also cause issues with an underlying injury if that hasnt been properly diagnosed first as FS then overides everything.  When you have gone through the first painful stage of FS and the pain dissapears but there is limited movement then is the time to gently start the regular exercises in my opinion.  I always ask any doctor or PT if they have had FS because as you know until anyone does they have NO IDEA the level of pain and trauma.  Also some are wrongly diagnosed and it is not a real FS.  Fortunately I finally met one who did have FS and her advice to me was try not to fight it, accept that you are going to be less active for a while and be kind to yourself.  Dont stop doing everything but know your limits, it does get better  biggrin)  I am now pain free and with full movement returned.   Sometimes you just have to slow your life down and benefit from therapeutic therapies to help you through.  It is one of the most frustrating things to happen and I wish you all the best with whtever path you choose biggrin
  • Posted

    Thanks everyone for your responses.  Much appreciated.  I intend to go to 1 or 2 more PT sessions and then re-evaluate.  I'm concerned that it may be doing more harm than good at this point as I don't think my original injury has completely healed yet.

    I had not even heard of the term "frozen shoulder" until I was diagnosed with it.  I certainly feel for everyone else going through this!

  • Posted

    Hi Jill...

    You can tell by the passion on this thread that different things work for different people. I'm in the "gentle physio" camp, only because I tried a different therapist in the "no pain no gain" camp & I'm sure it set me back some weeks because my shoulder wanted to heal, not have yet more rips & tears to cope with. The best thing I did for myself was to quit.

    I started exercises again some months later when I could feel the ROM returning - thawing! And I'm in physio again for my second FS - so far so good. Here is an insightful journal article about this that may be helpful to your physiotherapist - it was to mine. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096148/

    There are lots of good tips on this forum to help you through. Use FS as a teachable moment with your kids in the meantime. You can't play catch now, but you will again one day!

    Liane smile

    • Posted

      Hi FS, This evidence article "AC use the evidence to intigrate your interventions" left me more confused than ever. I can understand a genetic frozen shoulder being left to freeze and stay frozen and then defrost. But if you say an injury or stroke or post surjical restriction or rotator cuff or cardiac condion causes a frozen shoulder are we led to believe that they as frozen shoullders therefore as the orthopaedist says no physiotherapy. This seems to fly in the face of modern physical therapy practice where early intervention is of the essence, so say the researchers. This article it appears  to have no new research of it's;own but a regurgitation of myths of the past.Let us know how early would your PT rehab these so called Frozen Shoulders.
    • Posted

      Hi Frozen Stiff: I would disagree that the cause *is* 'genetic' because a cause has not yet been determined. We'd all be happy if we knew! The article is from 2010, so that's decisively "modern". And the gist of the article is which interventions are most effective e.g. posterior glide is something my PT is doing as early intervention on my second FS, with benefit. The article is by definition a literature review & discussion paper intended to amalgamate best practices; it's doesn't claim to be a research paper. Hope this helps to mitigate your confusion!

      Liane

    • Posted

      Hi meant to reply sooner but here we are now. Google "Frozen Shoulder unraveling the enigma, T D Bunker". Let's know what you think.

    • Posted

      Hi Frozen Stiff - thank you. Bunker says he can nail down 'the cause' as appearing to be a fibrosis, a collagen contracture. It seems true that's the condition; however, it's not the cause - unless I missed it, he doesn't say what initiates this collagen matrix, which, to me, would be the cause. (The closest he comes is a 60% genetic correlation from what he himself describes as a small study.) I'm glad he implies surgery is indicated only for those who did not respond to conservative treatment. In his one FS group though, he went ahead and did arthroscopies at least once on all of them (sounds like whether or not just an MUA would have sufficed. That's sort of like saying all term pregnancies can be successfully treated by C-section.) What's important is that he notes that our generation is one step closer to understanding FS. This paper was written almost two decades ago, and I hope the research like this for true FS sufferers will continue! New products like Xiaflex could well be on the right track that way. Thanks again, Liane

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