Neck pain: Hi everyone, my wife has had... - Multiple System A...

Multiple System Atrophy Trust

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Neck pain

Oliverwindsor profile image
6 Replies

Hi everyone, my wife has had MSA for a while now, she also uses a CPAP machine at assist her at night. She is experiencing extreme neck pain and her head has somewhat dropped forward. So my question, has anyone experienced this nasty neck pain, could it be the CPAP machine or more likely, is it part or the MSA problems?

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Oliverwindsor profile image
Oliverwindsor
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6 Replies
Yanno profile image
Yanno

Hello Oliver, neck and shoulder pain, sometimes called coathanger pain, is a symptom of low blood pressure may be caused through postural hypertension. Another post this afternoon also talks about low blood pressure perhaps have a look at my reply there and also the MSA Trust Factsheet is well worth reading. It can be found here. msatrust.org.uk/wp-content/...

Take care, Ian

Oliverwindsor profile image
Oliverwindsor in reply toYanno

Hi, thanks for that, it’s silly really, to be honest I should have realized, however, to get a second opinion doesn’t hurt. Thank you again, perhaps I should be monitoring her blood pressure more often. Regards.

Orla789 profile image
Orla789

Hello Oliver I ave msa and suffer with a very stiff sore neck which I don’t think is related to low blood pressure as my body has been ok so far. I think it’s probably due to muscle weakness and rigidity. I also have lumbar back pain which restricts how long can stand up eg I find I need to sit to brush my teeth. The pain intervention consultant cannot help and thinks it’s due to a dreid out vertebral disc. However I know that this is a frequent symptom for other MSA sufferers so I think it is part of the disease. I don’t (yet) use a CPAP machine.

Wishing your wife some relief.

TK-67 profile image
TK-67

my mum has an antecollis, as her muscles contract, it pulls her head forwards, it was the first real indicator that her initial PD diagnosis was wrong. Mum tried botox injections but sadly it didn't help. Occupational therapy and physio may be able to help with coping with it. There is an outside chance if she is still taking parkinsons type drugs that this can make dystonia worse with MSA so worth checking with your consultant.

binnyrox profile image
binnyrox

Hi Oliverwindsor

I used a cpap and now a bipap. In the 5 years using it, I have not experienced neck pain from it other than from sleeping in an awkward position

However as my MSA progresses, I have developed a forward head posture which has caused me great discomfort. The therapists explained that the muscles are no longer in balance, some being shortened and other being lengthened unnaturally

I spent quite a while in therapy and with diligent home exercises - it did help with the pain

When the doctor started me on Madopar (levodopa) just a few weeks back, the posture improved remarkly during the "on" periods.

And I took the window when I felt good to do more physical activity. Movement really helps ward off and delay the progression including the forward head posture

I was advised to do a few minutes every hour rather than a heavy session once a day

Hope this helps

Lou117 profile image
Lou117

My Mum was experienced very bad ‘coat hanger’ pain particularly in her shoulders. She now has a Buprenorphine patch which has helped her greatly. She also uses paracetamol and ibuprofen when needed.

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