Hydrodilatation - my experience
Posted , 76 users are following.
I've decided to start another thread on here to document my experiences with Hyrodilatation (also spelled Hydrodilation or known as Arthrographic Distension) and how well it works for me over the next few weeks or so.
A brief background, in case anyone didn't read my original thread. I started with odd pains in my shoulder in spring, this year, with no apparant cause and I assumed I'd just pulled a muscle or something like that and hoped it would go away on it's own. It got worse over the summer and I also started to lose movement. I had the usual excrutiating pain on knocks or jerks and aches right down my arm. Pain, lack of sleep and loss of movement finally drove me to the GP in September where I was diagnosed with a frozen shoulder. I managed to seek physiotherapy with Bupa (or I'd still be on the NHS waiting list) and was recommended by a physio to see a consultant with a view to Hydrodilatation.
I had my Hydrodilatation this afternoon - 14th December. A few hours on and I'm feeling fine. I was very nervous but the procedure itself went well and took 15-20 minutes in total. I'd worn a vest top, which meant I didn't need to wear a gown and just dropped my straps off my bad shoulder. I was asked to lie on my front, with a pillow for support. I'd thought the procedure was done via x-ray guidance but it was in fact ultrasound guided. The doctor explained what was about to happen and did an initial scan of my shoulder area before giving me a local anaesthetic. He then put in the needle for the hydrodilatation, which administered first some cortisone and then saline. He said I might feel some pushing and to let him know if it became painful. There was some discomfort but I wouldn't describe it as painful and within a few minutes, he said the saline had started to leak out of the joint and the procedure was over. He did another scan and checked my movement before and after - there was perhaps a couple of degrees improvement but nothing drastic. I left the hospital with a plaster on my shoulder and feeling fine. He said I might experience a bit of aching once the local anaesthetic wears off but the cortisone should kick in within a day or two and should improve things pain-wise.
Physiotherapy is recommended within a few days of the procedure and I have an appointment with the physio on Friday morning and another to see the consultant again in about 6 weeks. So far, so good but it remains to be seen how sucessful it has been in improving pain and getting my movement back. I can currently lift my arm about 90 degrees in front, slightly less at the side and very little behind my back.
I will document my progress over the next few days and weeks, for anyone else considering this treatment. Hope this information is of help to someone and fingers crossed that the procedure works for me!
8 likes, 220 replies
claire50742 maria58274
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I have been suffering for 6 mnths with this. Wow, I thought I was going to go mad. In dsigust at my GP telling me that I was letting it get to me, (no soid sleep for 6 mths nd not missing a day of work might I add) I changed GPs. I went to see a new one on Monday who ordered a CT scan of my neck. I have had an MRI of my shoulder and it showed a spur, bursitis, a small tear in my shoulder and frozen shoulder. He thinks that the intense pain is due to something going on in the neck. He has also recommended the treatment that you are discussing. Likewise, I feel I am desperate enough for nything right now. It will be the first CHristmas that I simply am to tired to bother with although with 2 small grandchildren I shall make an effort.
How can something like this affect so much of your life? How can they look at you with an expression that almost says "another middle aged hormonal woman moaning about a sore shoulder"
Perhaps I am simply over sensitive!
Anyway - this wonderful new GP prescribed me Tramadol - one at night. I took it reluctantly last night and whoo hoo I had 3 hours of continuous sleep! Small steps forward finally!
Wishing you well. Keep us posted!
maria58274 claire50742
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My treatrment hasn't miraculously improved my shoulder movement (it does for some) - though I do think it's a bit better. I suspect for me that slow and steady progress is more likely. It has however left me largely pain-free, which for me is my main priority.
Hope you get treatment that gives you some pain relief soon - we all know how painful it is and how desperate it makes you feel. I'll also be spending my Christmas Day with 2 grandchildren (aged 3 and 10) so know how much that means to you. Hope they help keep your mind off the shoulder, at least for a while. Best wishes for a peaceful Christmas and hope you start to feel much better soon. Take heart in knowing it WILL get better!
Lambchop2 claire50742
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claire50742 Lambchop2
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Yes I had a great Christmas day with both little ones taking my mind off the pain for a while. I intend to get something done. I am a teacher and need to work. I feel I have 6 weeks to make a start on some treatment. The thing is, it is aslow process here and although I am willing to pay to go private, the waiting lists are extraordinary, nothing seems to be a priority either....
Like you Maria, I am certain the drop in hormones is linked to it. In my opinion, there is not enough research being made into this condition, whic, while not urgent or life threatening, is most debilitating.
Claire
jayne48141 claire50742
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Hi,
I had FS for months! Doctors did MRI of my shoulder, found a small tear, but thought my problem was my neck so did MRI of my neck. Sent me to a neurosurgeon who said it wasn't, but didn't know what it was and sent me to a phyziatrist who yanked my arm up above my head and almost passed out from the pain. He didn't know what was wrong. I went to another Dr 4 states away and they diagnosed FS in 5 minutes! Did a cortisone injection which helped the pain within 72 hours. Started physical therapy twice a week. That was in beginning of March and it is now middle of May and it's coming back again like the cortisone is wearing off. I won't make it through this again! The worst pain I've ever been in! Good luck with yours!
CynCash maria58274
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Nattytee maria58274
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maria58274
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I have long hair and in recent years, have taken to wearing it up, twisted round and held in place by one of those hinged claw clips. My freezing shoulder made this increasingly difficult and I remember the exact day in September when, however hard I tried, I could no longer do this. I remember crying with sheer frustration.
Over Christmas I noticed that it was getting a little easier to wash my hair with 2 hands. I decided at first to try to plait my hair at the back - again, something I haven't been able to do for some time. With a little difficulty I managed it. Then I tried the clip - again, not exactly easy but I got it in place and felt elated. OK, to most this seems very trivial - but to me it's a small victory and gives me hope for better things in the New Year. At last, there looks to be some light at the end of this dark frozen tunnel.
Good luck to all of you and lets hope the New Year brings us all some relief from this awful condition!
pollmadoll64 maria58274
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jayne48141 maria58274
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Showering, washing my hair, and drying off with a towell was so incredibly painful I didn't even want to do it! Less than 3 months after the cortisone injection and it's starting to come back! I'd finally started getting through the depression it caused the first time!
CynCash jayne48141
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Hi Jayne, I have FS in both shoulders, the left started 11 months ago so I'm through the worst of the pain but now just diagnosed with FS in the right! It is extremely painful, can hardly use that arm at all and was contemplating a cortisone shot. I've heard mixed reviews. Did it help you with the pain? And how long did that take? Thanks so much!
jayne48141 CynCash
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claire50742 maria58274
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I feel guilty moaning about it, I am sick of listening to myself. My nextdoor neighbour has terminal cancer, how could I even think of moaning about my shoulder, alas I do though..................
As my husband reminds me, with a serious disease, injury, broken limb etc. people recognise it and are prescribed painkillers. With a FS, I have had to fight for an xray, analgesics, ultrasound and 2 MRIs.
Ridiculous really!
maria58274
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Slowly but surely, my movements are improving. Putting up my hair gets easier every day and a couple of weeks ago I realised I could fasten my bra, without sliding it round the front. It's still a little awkward but getting easier all the time - such little things can feel like a major achievement! I've found the best way of excercising for movements behind your back is in the shower - sliding the bad arm up with the help of the other one when soapy makes it much easier. I can't get my arm right up yet but it isn't causing me any major issues, so as long as I'm without pain, I'm happy continue exercising and getting the movement back slowly.
I'm still unsure whether my other shoulder is starting to freeze. Some days I have a slight ache and tight feeling at the top of that arm and into my shoulder - but other days it is OK. I'm hoping it will be OK but if not, will seek help a lot earlier than I did with my right shoulder.
My consultant was happy with my progress and said the movement should continue to improve in time. He said to go directly back to him, should I have any further issues or pain or if my other shoulder does freeze. I'd have no hesitation going for an earlier hydrodilatation, should that happen. I'll report back, if there are any dramatic changes - either good or bad.
Good luck to all of you going through this awful condition and I hope you too can find some releif!
pollmadoll64 maria58274
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maria58274 pollmadoll64
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