Hi,
I’m 9 months post WLE and SLNB for stage 2b melanoma and still have significant nerve pain. I’ve been offered neuromodulation to try and alleviate the symptoms. Every 2 weeks for 12 weeks, however I can’t find any information on what it is or what it entails. Has anyone had this? Any advice /information would be greatly appreciated. Thanks
Hi Catnan
I am sorry to hear that you are having significant nerve pain.
This link has a bit of information.
Neuromodulation :: Royal National Orthopaedic Hospital (rnoh.nhs.uk)
You could also give the Support Line a call and speak with one of the nurses who may be able to give you a bit more information on the treatment and what it entails.
Jane
Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
I think a lot of treatments can sound scary when they are first suggested. Do give them a call and they should be able to talk you through it. They may also be able to suggest other treatments. I have nerve pain following chemo and was prescribed medication. I hope you can find something that helps
Jane
Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
Hi, I phoned the surgeon’s secretary and she has emailed me a leaflet, explains everything and it doesn’t seem scary now! I was offered gabapentin but didn’t want to take it because of potential side effects.
Fingers crossed this does the trick, many thanks for your responses.
That's good to hear. I understand about the gabapentin- it's about weighing up the side effects and potential benefits and seeing what is right for you. I hope you find something that helps
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