I had hydrodilation in my left shoulder twice. The injections weren't uncomfortable - unfortunately they made no difference. My left shoulder has been painful for two years now (agony earlier on).
I can just about shave my underarm on the left side now.
My right shoulder has been affected since last Christmas. I had hydrodilation after my second covid jab (they wouldn't do the procedure until I'd had the second vaccine). The first part of the procedure which dilates the area was utter agony I asked the practitioner to stop. He assured me the steroid part of the procedure wouldn't hurt. It did. I swore then that I wouldn't have that procedure again. It worked though. The pain eased and I was able to sleep better. It has worn off now and I dare not have another hydrodilation - it was truly horrendous.
I cannot reach far with my dominant hand/arm. I have to be really careful showering, getting dressed and undressed as I have really restricted movement. I cannot reach shelves. I cannot lift/hold grandchildren for any period of time. I cannot sleep on my right side. I cannot lift this arm high enough to get a razor in there - which is how I gauge how well I'm progressing. I have to force a ball deodorant in there somehow. Cannot have my usual hair do because I cannot get both hands to the back of my head - when I see either of my daughters they do my hair for me otherwise I can just about manage to brush it then leave it. I usually have a bun/clip it up. I hate my hair down - it's too hot and I feel messy. I can't blow dry my hair or use straighteners.
The worst part is the lack of sleep. It's the worst torture. My sleep has been affected for two years.
I've no idea how people have managed to get strong pain killers for this condition. I've just managed to get some 500/30 cocodamol prescribed. Perhaps I don't complain loud enough. Can't really take them as prescribed as they make me incredibly woozy and cause terrible constipation.
I don't talk about the pain and inconvenience to people now as they are probably fed up of hearing about it and think that I should've recovered by now.
I was thinking that at least I'd got it out of the way/been there done that - only to be told that you're more likely to get it again if you've already had it.
Can't bear to think about it.
I do think that health care professionals underestimate the effects of lack of sleep. This is by far the worst part of having a frozen shoulder/shoulders.
It's bloody torture.
The fact that I also have a broken big toe at the moment makes me want to give up. Did this almost 4 wks ago - went to the fracture clinic yesterday to find out that the break hasn't started to 'fill in' yet and I could be in pain at least another 8 weeks. So I have to persevere with my Forest Gump shoe for the foreseeable future.
Staying asleep is something that is impossible for me to achieve. I constantly wake myself up because of varying degrees of bone pain and finding it difficult to get comfortable because lying in the only comfortable position becomes uncomfortable after 20 min.
I apologise for length of post.
Frozen shoulder - awful condition.
Was also told that physio was a waste of time as it doesn't shorten the overall recovery time.