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Hypermobility and recovery from trapped nerve | MaeveMadden

Hypermobility and recovery from trapped nerve


  • Hi Ladies,

    I just wonder if anyone else has Joint Hypermobility?

    I've always been flexible and to be honest I had kindof forgotten that a doctor once "diagnosed" me as having Joint Hypermobility because it has never really affected my daily life. Yes I sit weirdly, I'm 37 and can still do the splits and I can partially dislocated my own shoulders my tensing muscles but it has never had a negative impact. Until now.

    Just before Christmas I was having some twingey pain in my back that would shoot down the back of my leg which I self diagnosed as a bit of sciatica. It got to the point where I went to the doc and they prescribed some anti inflammatories and referred me to a physio. Unfortunately, the night after seeing my Doc I shifted in bed and trapped a nerve in my lower back. Agony doesn't even begin to describe the pain.

    It got so bad I was sobbing and begging my husband to call an ambulance (because in my head I was thinking it would be the fastest way to get pain relief). I collapsed twice trying to get downstairs and I ended up stuck on my living room floor for twelve hours while the ambulance service told me to call my GP and my GP then cocked up my prescription and then by the afternoon what he prescribed that morning hadn't touched it so I ended up on a cocktail of naproxen, co codamol, diazapam and tramadol. 

    So now I'm left with nerve damage in my left leg/foot. Most of the feeling has come back in my leg but I can't feel the left hand side of my foot properly and my leg is a little weak. I've seen an Osteopath who realigned my spine and pelvis that had both twisted, causing the sciatica and the trapped nerve but the nerve takes time to recover.

     

    Does anyone else here suffer with JHS? Have you been given any advice on how to strengthen the ligaments (I was told by my osteopath I have likely overstretched my ligaments and they're not holding my skeleton in place tightly, hence the twisted pelvis and spine). I'm terrified of trapping the nerve again but I so miss working out, I tried to follow an upper body workout but I had to stop at walkouts because I just can't bend like that at the moment. I've gone from hypermobile to pensioner and it's really upsetting.



  • Hi Chloe, 

    I just read your post. I don't have any expertise or advice but I wanted to say that I had read it and I'm sorry to hear you're having a rough time. Physical pain can have a really negative impact on emotional wellbeing. You are not alone ❤️ I hope you get the answers you need. Take care xx


  • Hi Chloe,

    I am so sorry to hear this! When I was little I was diagnosed with JHS and did strengthening then. However, I do still struggle with it, especially in my shoulders.

    My advice would be to just maybe watch the workouts and see what feels okay. If you can't do some of the moves perhaps you could think of an easier version or alternative (or just rest and wait for the next set of moves)?

    I would also ask your doctor for advice as they may be able to send you to a physio specialist who can help you strengthen them or knows of exercises you can do at home! There might be some YouTube videos too! I know it must be so frustrating but you will get there! I hope this helps! 

     


  • @Hannah Tomsett @lauren gray thank you both. I think what I'm struggling with is that this is the first time my body has been through a big injury like this and I'm frustrated at how long it's taking to heal but also scared that it could happen again and a bit freaked out that my body isn't just going to keep going and going if that makes sense. This is the first time I've felt "old", in the sense that I have to be careful with how I move and I'm nowhere near as flexible as I normally am.

    I'm currently waiting for a physio referral to try and get some guidance on how to get stronger.

    Thank you both for listening /reading x


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