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?
0 likes, 8 replies
sue35966 runnergirl44
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
runnergirl44 sue35966
Posted
tracy12563 runnergirl44
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 . (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....
runnergirl44 tracy12563
Posted
tracy12563 runnergirl44
Posted
FSconversations runnergirl44
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
Liane
runnergirl44 FSconversations
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.
FSconversations runnergirl44
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).