When I had my HA, as well as chest pain, dizziness, shortness of breath & nausea, I got lots of pins and needles all down both arms and into my hands/fingers.
Ever since then I've become very prone to getting pins and needles in my arms & hands, way more often than normal.
I've also lost some sensitivity to touch/pressure, so sometimes I drop things. I can't feel extremes of heat/cold as well as I used to either and have burnt my fingers as a result. I've been told it seems to be a sort of peripheral neuropathy, but no one can really explain it to me or tell me if it's temporary or permanent.
I'm 4 mths post HA now. Has anything like this happened to anyone else?
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Callie456
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Only coming off the medication... which I can't do just now. Normal painkillers don't touch it. My GP advised that I bear with it last time I was on this.
If yours isn't medication related, hopefully there's something your doctor could look into for you?
Thanks, Dr doesn't really have any suggestions, except to wait and see and try physio exercises, which I'm doing, but it's frustrating to have no proper answers.
Thanks for the thoughts, I'm not diabetic, I do have a neck problem but it's been checked and it's not that. I think peripheral nerve damage sounds right, I just don't know why.
Hi since my transplant I have suffered badly from this especially at night, my GP said it was peripheral neuralgia and prescribed a low dose of amitriptyline to take at night it really works for me and the symptoms have practically disappeared. Char
Hi they never said and to be honest I probably never asked, I am quite bad for that. I was just so glad when the meds worked and I could sleep without getting woke up with the pains, char
Hi Callie456 yes I've had this down both arms at night only my hands feel like my mouth feels after being numbed at dentist no feeling at all. I do have spine and nerve problems down my right leg for years but this has only started happening down both arms and hands since my HA last May. I wa taken off Amitriptyline at hospital after my HA after about 8 years on it, waiting on my cardiologist follow up appointment in few weeks to ask more questions about it I haven't been seen by anyone since it happened last year unfortunately so still pretty much in the dark about it all. This forum has helped me so much as I see now I'm not alone or going mad with all these new strange things happening to my body. I would push and push to be seen especially as it has caused you to burn yourself.
Thank you for your response, it's a comfort to find others with a similar experience. Yes there's so many new feelings, emotions and sensations with these cardiac problems.I was also glad to find this forum and no longer feel like I'm crazy with it all too. I'll see if I can ask drs again. You've had a very long wait, I hope the cardiology appointment goes well. Maybe they'll start amitriptyline again.
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