coccyx pain: hello, I’m having issues with coccyx... - Ataxia UK

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coccyx pain

dansybelle profile image
5 Replies

hello,

I’m having issues with coccyx pain and am wondering whether it’s another exciting (😒) symptom of FA.

I’m still ambulatory so not a wheelchair user but am having the problem when sitting on an upright chair- so I’m avoiding doing that as much as I can but it’s not always possible. I bought a special coccyx relief cushion for my office chair but if anything it has made it worse.

My GP has just given me loads of painkillers, which I am reluctant to take. She also suggested acupuncture.

Has anyone had this problem and what helped?

Thanks 😊

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dansybelle profile image
dansybelle
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wobblybee profile image
wobblybee

🤔 If you’re on Facebook..you could ask this on one of the Friedreich Support Groups

🙂This link might be helpful

nhs.uk/conditions/tailbone-...

MSW_91 profile image
MSW_91

Hi there

I hope you are well.

I experience coccyx pain too. I also have late onset FA.

I’ve found that baclofen has helped to ease the pain (I take 1x 10mg tablet at night). I also do a cobra stretch every morning.

I work in a desk based job and had a lot of discomfort when sitting for prolonged periods. I now use a sit-stand desk which has helped to reduce stiffness and muscle pain.

I hope that’s useful!

Best wishes

Matt

dansybelle profile image
dansybelle in reply to MSW_91

Thanks for replying Matt. Does your dr think it’s related to FA? I am late onset too but not sure how I’d cope with standing a lot! I work from home so am working from bed or sofa atm- not ideal! I have an app booked at the drs in a couple of weeks so will mention bacolfen. I was wondering about requesting and MRI? Have you had one? Have you got a link to the stretch you do?

So many questions! 🤔

Cheers

Danielle

MSW_91 profile image
MSW_91 in reply to dansybelle

Hi Danielle

I haven’t asked if the coccyx pain is linked to FA. I just assumed it is as my discomfort started alongside my other FA symptoms. It isn’t debilitating for me so I’ve just learnt how to alleviate my discomfort and manage it :)

And yes, I’ve had two MRI scans (brain and spine) but these were a few years ago during my journey towards a diagnosis. My first was in 2016, second in 2020. Since FA was confirmed through a genetic test I haven’t been offered any further MRI scans.

And sure. Yoga with Adrienne was recommended to me by a friend who is a personal trainer. There are lots of different videos on YouTube. Here is the cobra one: youtu.be/n6jrC6WeF84?si=oJz...

Just to add this one works for me but you may find something that’s a better fit for you. I attend a weekly stretch/yoga class so have picked up various stretches from the instructor. Some suit me and I’ve incorporated them into my daily stretch routine, others don’t so I don’t do them. Have you seen a physiotherapist? They might have some good suggestions.

If you have any other queries do let me know.

All the best

Matt

medea profile image
medea

I've been in a wheelchair with FA for many years and never had coccyx pan. I don't think it' s directly linked - perhaps indirectly. Anyway there are pleny more exciting symptoms to look forward to! ! Sorry I''ve no practical help.

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