Menopausal Frozen Shoulder
Posted , 99 users are following.
Any ladies with frozen shoulder who are peri menopausal/menopausal and not on HRT should have a serious chat with a (preferably female) GP.
I suffered for ages (two male GP's dismissed the idea of it being hormonal) before being diagnosed with menopausal adhesive capsulitis by a Nurse Practitioner who researched the subject for her thesis. This is also sometimes known as menopausal tendonitis/arthritis. After a month of being on conjugated estrogen (Prempak C) it is like someone has 'oiled' my shoulder. I felt like I had completely seized up and my bicep and shoulder muscle were like concrete. I am now able to do gentle exercises to free the adhesion, and can now lift my arm (impossible for months) to wash and dry my hair/shave under arms etc. Estrogen is the WD40 of the body, and without it, in some women the soft connective tissue goes hard and brittle. Not all women suffer from joint/connective tissue problems in menopause,. but interesting it is usually the ladies who were a bit smug, because they got got to 50/55 ish with no real symptoms or hot flushes - then bam, being hit like a ton of bricks with frozen shoulder. I also had stiffness and pain in the other shoulder, other large joints, elbows and fingers. Mornings were terrible, it could take up to ten minutes to actually get OUT of bed, and sleep? Forget it, being woken with shoulder pain every half an hour.
HRT is not for everyone, but AC was ruining my life. Given that the prognosis for recovery can be up to seven years ...I decided the risk was worth it.
i would never EVER have thought that simple 'hormones' could cause so much pain and change me from being a fairly fit 50 year old into a crippled 90 year old.
Google menopausal frozen shoulder/menopausal tendonitis/arthritis and go and see your GP ladies!!
14 likes, 270 replies
sandra196521 Lesley998
Posted
I'm 50 and have a frozen shoulder left for almost 3 years en for aprox 6 months now on the right side. Hope by the way my English is good enough...
Lesly I do recognise 80% of what you are writing.... It's such a bad "disease" ... pain pain and a lot of stifness also in other joints. I will call my GP comming Monday. I think in Holland there also is a special ladies clinique. Will try to find that. I think and hope they must know more about the hormone treatment when you have a frozen shoulder. Since jan 12 I do not work anymore (I am a secretary and can't work with my computer, mouse etc.)
Now I have Zaldiar as a painkiller. 3 x time a day at the most. I take 1 of 2 a day. It's tramadol with paracetamol. I does help but it makes you sleepy and I feel it is not a cure...
I hope the hormone treatment will help. As you wrote before, I also don't want to get it in other partas of my joint. I also feel my left hip a bit and after sitting whilst watching tv for example I feel 80 years when I get up... Muscles or joints... ?
Anyway, I felt I had to reply, thanks a million for letting know your experience! I can't type as much... you know the frozen shoulder
How are you doing now?
Bye Sandra
jacqueline23588 Lesley998
Posted
In march I had a full hysterectomy after a
large fibroid caused a dvt in my leg. In June I woke up with a really painful shoulder that
just appeared over night no reason for it I
have never heard of this being s symptom of the menopause so I am wondering I I should see the doctor about it its still painful and tender I have what seems like every symptom hot flushes terrible night sweats aches and pains all since the op my doctor wouldn't give me hrt because I am 53
caroline_b-m Lesley998
Posted
Thanks Lesley, I will get myself some oestrogen 'wd40'!
Caroline
bobbysgirl Lesley998
Posted
I've read through a lot (not all) of this thread.
I thought my problem was due to a combination of a riding accident 20 years ago (I landed on my right shoulder) and dislocating the same shoulder in a fall 6 years ago. I just thought old war wounds were catching up with me.
Recently the pain has got much worse and like many ladies here I can't dry my hair properly any more! I automatically reach for something with my right hand, then have to send my left hand in to rescue it. I can lift my arm, but can't bring it down without agonising pain
About a year ago I askedmy GP for HRT. We had discussed this before and come to the conclusion that I would try other things (Sage tablets etc) first. Well I tried them and nothing helped with the flushes etc. He gave me Kliofem and I have been MUCH better with it.
Unfortunately I have fibroids and cysts and have suffered with Endometriosis and recently have had some breakthrough bleeding and stopped the HRT.
I'm on the list to see a NHS Physio, but in the meantime have gone private. My Physio is a lovely young girl who has worked miracles with the stiffness in my shoulder but I can't afford to keep seeing her and the pain is getting worse.
After reading your thread I am convinced that the frozen shoulder is hormone related so what to do??? Should I start the HRT again and have reduced pain, no hot flushes and a good nights sleep - with a slightly raised risk of cancer. Or give in to the bogieman and NOT take HRT?
Anyone have any ideas?
april35137 Lesley998
Posted
I also have frozen shoulder. I have had it since December 2014.
In March I started taking Black Cohosh in a few forms (meaning a Whole Foods brands Daytime/Nighttime tablet, a Pure Black Cohosh tablet during lunch and a Menopause One multi vitamin that include Black Cohosh at lunch as well). They have helped considerablly with my hot flashes, night sweats and mood. I feel MUCH better. And about 3 months later my Frozen Shoulder seemed to become less painful.
Literally, the day after the pain was lessened I saw a specialist that said MUA was perfect for me, but we decided to try the Cortisone shot first. It has been 10 weeks and I am still pain free. Because of this I have been able to start exercising and using that arm somewhat. I am definitely still frozen as I do not have 100% mobility but it is better and I am pain free.
So not sure if the Black Cohosh helped - it definitely worked for me on with the Menopause symptoms. I wanted to avoid HRT for a while so was happy to get decent results from this option.
The fact that my Frozen Shoulder is potentially linked to my menopause was a revelation. I see so many specialists that no one doctor has all the information - meaning my GYN and Endocronlogist knew about my Menopause. My GP and Ortho knew about my Frozen Shoulder.
I have an appointment later this month to bring my GP up to speed on EVERYTHING.
All I can say is the 7 months of pain wore me down so much. Nothing could touch it and while Black Cohosh probably will not work for everyone - and it is not a fast remedy - I do know it helped get rid of 90% of my menopause symptoms (within 2-3 weeks) and seemed to maybe help with my shoulder somewhat after an extended period of time (3 months).
I went off one of the tablets and had hot flashes come back wtihin the week so just decided to get back on all the tablets and they went away again. Black Cohosh mimics hormones in our bodies (without actually being a hormone). Will not work for everyone.
All this being said - I KNOW how terrible this affliction is. It wore me down and I was so miserable, tired and unhappy. I tried physcial therapy, airrosti - just about everything. Found when I did exercise (with a LOT of efford) my shoulder would warm up and feel better - but that took a lot for me. I could not wash my hair, shave or do anything with my right arm being frozen.
I constantly feel like my left arm is tightening and I just do exercises to try and keep it moving every other day (weights and push ups etc... ). One of my hips is clicking and painful when I do certain exercises (not walking, running or anything simple thank goodness) - so I am fearful of getting Frozen Hip too. But I find exercise and positive thinking helps. If my body freezes up in multiple places - and I am in that kind of pain I will definitely have a problem.
So I am open to HRT if needed, but will continue on Black Cohosh for now and will get another cortisone shot this fall if it is needed - but am hoping I can get to the other side in 2016 without it.
If you can get to a less painful place - I do recommend exercise to help. If nothing else, it also helps take are minds off the aches of aging too :-) I have not felt better in the past year and am thankful I got to this place through some devine luck honestly - taking one herb to help with menopause somehow helped with my shoulder (not realizing they were linked in the first place which makes so much sense now).
So if you are female, over 45, having some menopause symptoms and Frozen Shoulder/Hip - I would recommend giving Black Cohosh a try. If it does help somewhat and you are open to a cortisone shot... do that. The shot HURTS but within 24-48 hours I was pain free.
I am doing some light exercises and am now probably at 60-70% mobility. I can sleep - which all helps my mood. I feel the downward spiral has been broken and while I am not over this yet - I can try to do things that will make it all better. Before I was in such pain, I could not do anything to help myself.
So thank you all for this post. It was a revelation to learn about the connection. I am hoping to avoid MUA and just work through this with exercise, Black Cohosh and positive energy/thought. Oh - and getting all my doctors on the same page. When I have my bone density scan next January I will be sure to tell her and my Endocronologist about my Frozen Shoulder and Hip concerns. They scan my hip every year to ensure I am not losing bone density.
An important lesson for certain. With the fractured healthcare system here in the US - you have to really work hard to ensure you get the care you need, deserve and want. And with a painful issue like Frozen Shoulder that is not always easy.
My heart goes out to all those who suffer from this - so please do not give up. Have a strong heart and faith you will come out on the other side. I am not out of the woods yet, but I have hope now which is something.
Cheers~
April
bobbysgirl april35137
Posted
I was up and down a ladder today, painting. I did have help, but I'm sure I'm going to suffer for it tonight and tomorrow. Still the job is done now and is looking good, so it was worth the pain!
april35137 bobbysgirl
Posted
I am sorry it did not work for you, but yes, once it starts to lighten up, I recommend doing exercises as they seem to be helping me.
Good luck...
April
maria58274 Lesley998
Posted
OK this could all just be a coincidence but seeing this discussion has got me wondering. Trouble is, I have little confidence in my GP buying into this. The GP practice has had many staff changes and I rarely see the same doctor twice. They just check back my notes and repeat what the last doctor said. Hope I'm not just clutching at straws here but this has given me something to think about!
april35137 maria58274
Posted
The specialist believes it is Frozen Shoulder and that is what matters most.
I am taking Black Cohosh for my symptoms and had a cortisone shot which helped me. I am at 85% mobility and no pain. Still not 100% but can live and hope to get it back in the next 6 months.
It has been 3.5 month since my shot so I assume it has worn off and I am still okay for pain.
Good luck and just keep looking for what works best for you. Ultimately that is what matters most with this little understood affliction.
April
Vaughny64 Lesley998
Posted
Going to make appointment with nurse practicioner
Thank you
Th0mkat Lesley998
Posted
I'm now so frustrated to be dealing with this again and would love to discuss and gain support from those of you who have been through this before.
Best regards
Kathy
Th0mkat
Posted
tara75402 Th0mkat
Posted
d59025 Lesley998
Posted
double FS sufferer here. About 7 yrs at age 45 I first got it in my non-dominant shoulder, then one year later, just as I was starting to thaw on that side, I got it in my dominant shoulder. I had a very bad case of it, particularly in that first non-dominant shoulder. 2.5 yrs after the whole ordeal started, at age 48, I was pretty much back to normal. Now I'm 52, and my dominant shoulder has started to exhibit terrifyingly familiar serious pain. I startled Googling for info on FS recurrence and ended up here.
What I wanted to add re: hormonal factors is that as I've gone through a very rough perimeno patch over the last 2 years, I've done a lot of research about what actually happens to women's hormones during the perimenopausal transition, and contrary to popular belief, estrogen levels typically do *not* decline until you are almost completely all the way to full menopause. Rather, estrogen levels typically *increase* during the perimenopausal transition as your body tries harder and harder to compensate for a failing reproductive system. So while I absolutely do believe that the prevalence of FS in women betwen 40-60 is related to hormonal changes, I am certainly not convinced that the problem is falling estrogen. Rather, I suspect the problem is too *much* estrogen, probably in combination with other hormonal changes as well. So starting estrogen/HRT before you are fully into meno may be adding fuel to the fire and may be making the FS worse, not better. Hope this is grounds for careful consideration and further research for you all.
Peace and best wishes to all,
D
d59025
Posted
maria58274 d59025
Posted
Having googled this, it doesn't seem entirely straight froward - nor do the varous web articles I read say exactly the same thing. It would seem that Estrogen levels can rise above normal and then drop rapidly about 6-12 months before full menopause - other sites say it fluctuates erratically during perimenopause before dropping off. This may well vary between people - after all, some women sail through menopause without any issues - others (like me) do not! It's generally only those who do have problems that the doctors see and investigate. I suspect that if estrogen is a contributary factor, it is this dramatic drop or fluctuation that is at fault. Estrogen has an important role in maintaining collagen, so any disruption to our supply - either too little or maybe even too much - could have some role in this. Lack of estrogen does contribute to skin thinning and general joint pain is an accepted menopausal symptom for some women.
It would be good if some proper research was done to find out for certain. Finding the true cause and contributing factors that may help in finding an effective cure for this awful condition.
d59025 maria58274
Posted
In my case perimeno was accompanied briefly by a very severe case of adult onset asthma, which to the best of my ability to research (again not well understood by modern medicine), is likely also associated with spiking estrogen levels accompanied by diminished progesterone levels. So that's part of why I've been suspecting estrogen as a culprit in my FS as well.
Couldn't agree with you more that more research is needed!!
Best,
D
Oliveria d59025
Posted
So she was under some kind of just progesterone treatment.
I may look in to it, myself.
d59025 Oliveria
Posted
Estrogen is such a complicated hormone in its effects. I read a huge amount about it when my asthma came on. One can't simply say "it's good" or "it's bad" or "it increases inflammation" or "it decreases inflammation", because it has so many different effects on so many different systems in the body through so many different receptors and mechanisms and co-factors. It's very, very complex, which I guess is why modern medicine still doesn't understand problems like FS and hormone-related asthma.
Thanks for your inputs!