Frozen Shoulder after Biceps Tenodesis

Posted , 4 users are following.

My story - I had a successful biceps tenodesis on my dominant arm in Oct.  I developed frozen shoulder and had a cortisone injection at 4 weeks followed by a capsular release at 9 weeks.  I was pain free for 3 weeks and regained flexion, extension and abduction.  I am slightly limited on adduction and extremely limited on internal rotation with extension (hand behind back) and external rotation. I am in a considerable amount of pain that interferes with sleep and work and some daily activities such as dressing and bathing.  I continue p.t. 3x/week since Oct. I also used the passive motion chair for 3 weeks after the capsular release. Any words of wisdom out there?  Will I ever be pain free again and return to my regular activities?

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8 Replies

  • Posted

    Hello,

    I too have Bicep Tendodesis in both of my arms, one having frozen shoulder.

    I've been in PT for 4 months and its gotten better, but still there.

    Dressing and bathing is good, but when I lay on my side sleeping, my shoulders still hurt.

    I was told this take a long time to correct and i've started resistant bands and small weights under the supervision of my PT.  She said we need to build those muscles back up.

    I too had shots in my shoulders, which helped- but the pain is still there- my orthopedic Dr. said this should subside within a year.

    Hang in there- you are on the right track

     

  • Posted

    I had frozen shoulder for 18 months then had an MRI which showed a torn tendon , as physio wasn't helping my specialist recommended surgery for the tendon , which I had in April. While 'in there' the surgeon removed the scar tissue from the frozen shoulder . Unfortunately after surgery the frozen shoulder returned with a vengeance!! I have since had 2 cortisone injections and a hydrodilatation injection which has given me some movement but I am still in a lot of pain , from my shoulder down through my elbow, and there is no way I could sleep on my right side (if I roll onto it at night I wake up in pain instantly). I'm still doing physio once a week but there doesn't seem to be much they can do and the specialist doesn't want to clear it surgically as he believes I am 'genetically prone' to getting it again. Everyone I've spoken too, who has had frozen shoulder , has said that it takes at least 12 months before it even feels a bit better. I'm holding out for April 2017 , but not feeling too optimistic sad. (By the way, with all the anti-inflamatories and pain killers I've been on I have blood tests twice a year to ensure my kidneys have not been affected! - just another thing to be aware of.

    Good luck with your recovery....

  • Posted

    Hi Runnergirl44:

    It's quite the pain we get with FS! I learned from this forum that there are two schools of thot on treatment. One is that you have all the aggressive sorts of treatments & recovery options to make the pain go away in the months ahead, and the other is that you treat it gently, letting it heal & keeping the inflammation cycle down to make the pain go away in the months ahead.

    FS is 'self-limiting' meaning that it will go away! Some have better success with one way than the other. Personally, I quit some very aggessive physiotherapy, opted out of surgery & learned as much as I could about its healing on its own. I've included occasional visits of gentle PT & cortisone every 3-4 months since starting to thaw. I am very functional again, and I doubt surgery or intensive PT would have made much difference to my time line.

    I'd be happiest if the medical community could pin down a cause for FS & treat accordingly. But in the meantime, be encouraged that it does have an end! Lack of sleep makes everything harder. It's good to read back on this forum & learn lots on the nights you're up wandering; it's a good distraction, and there are many tips for managing with this. Here's an example: https://patient.info/forums/discuss/helpful-tips-28439

    In the end, all of us need to choose the treatment plan that we can live with while on the way to recovery - and regular activities again! All the best smile

    Liane 

    • Posted

      Thanks for the tips!  It's interesting to read them and shake my head yes, I understand why you would want to do that.  FS really affects us the same way in our daily activities.  I can now get my arm up on the shower wall to wash and shave.  For me, sleeping and driving seem to be the greatest challenges.  

    • Posted

      Yes, driving for sure! There's a soft latex pad you can buy for cheap ($5) that velcros over the shoulder strap where it lays against your shoulder. It seems too small a thing to work, but it actually makes a huge difference (whether driver or passenger). 

       

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