I did find this.
How do I get a referral to a specialist?
http://www.nhs.uk/chq/pages/1094.aspx?categoryid=68&subcategoryid=153
Is there another Dr. in your surgery that you could see to explain how you are feeling about decisions made about your health?
Thank you for posting this link. It sounds quite ominous, with permission to seek diagnosis in the power of one person, the GP. "Your health, your choices," the site is headed. How ironic!
Amitriptyline is an anti depressive drug but it does work to enhance painkillers, I would push for a second opinion
Good luck
Jan
Yes she did say that in larger doses it is used as an anti depressant. I think I will go back and ask for a different doctor.
Thank you
I had massive nerve pain when I was first diagnosed, after lowering my BG levels for a prolonged period I no longer have nerve pain. I hated Amitryptline, and Gabapentin was useless (another antidepressant). At the time the only relief I got was using Tramadol hydrochloride. You need to get to the cause though, and a dr who understands the issues.
I had massive nerve pain when I was first diagnosed, after lowering my BG levels for a prolonged period I no longer have nerve pain. I hated Amitryptline, and Gabapentin was useless (another antidepressant). At the time the only relief I got was using Tramadol hydrochloride. You need to get to the cause though, and a dr who understands the issues.
This is one of the things I am confused about though. There was no nerve pain when I was diagnosed, as my hba1c has come down the sensations are getting worse and the area affected has increased in size around 8 times. It seems to be the opposite way round to what should be happening!
Yes she did say that in larger doses it is used as an anti depressant. I think I will go back and ask for a different doctor.
Thank you
This is one of the things I am confused about though. There was no nerve pain when I was diagnosed, as my hba1c has come down the sensations are getting worse and the area affected has increased in size around 8 times. It seems to be the opposite way round to what should be happening!
So I recently posted about what I had been told was nerve damage in my left leg and following the advice of most on here I went to see my gp. She did some tests and my leg leg was a lot more sensitive (in a painful way) than my right. She then told me that it may or may not be related to my diabetes and that she could prescribe me medication to control the pain... Am I missing something here? I told her I did not want medication and that I wanted to figure out what was causing it so I could resolve this to ensure it doesn't keep getting worse as it is doing. She said she didn't know what was causing it and handed me a prescription. Am I being deluded by saying I feel like I have been completely fobbed off?
http://www.diabetes.co.uk/forum/thr...m-i-being-told-all-is-okay.73730/#post-800732
Edited to add link to previous post.
I had severe critical care peripheral nerve damage following kidney failure last year. My gp said it would clear up on its own- but it wasn't improving (even as my bs righted itself) so I demanded referral to a neurologist who was brilliant and gave me lots of exercises to try before going on pain medication. I'm now seeing improvement in the pain without meds so it can be done!So I recently posted about what I had been told was nerve damage in my left leg and following the advice of most on here I went to see my gp. She did some tests and my leg leg was a lot more sensitive (in a painful way) than my right. She then told me that it may or may not be related to my diabetes and that she could prescribe me medication to control the pain... Am I missing something here? I told her I did not want medication and that I wanted to figure out what was causing it so I could resolve this to ensure it doesn't keep getting worse as it is doing. She said she didn't know what was causing it and handed me a prescription. Am I being deluded by saying I feel like I have been completely fobbed off?
http://www.diabetes.co.uk/forum/thr...m-i-being-told-all-is-okay.73730/#post-800732
Edited to add link to previous post.
My BG was >40 MMOL when I was diagnosed, and apparently had been high for a very long time, a couple of years. The explanation my consultant gave as I had no nerve pain prior to diagniosis, was that the pain was down to a massive adjustment in BG in bringing it into control, which affected my nerves. I found it hard to understand as I didn't have the nerve pain when I had diabetes and it was untreated and undiagnosed. The reality is that I had massive nerve pain when I was diagnosed, and made the transition to managing it with insulin.
2.3 years after being diagnosed I don't have any nerve pain. Hope you can get to a similar position.
Hi Lunar,Every time I try and start pushing for a referral I get made to feel stupid. I asked what had to be done to find out what the problem was and she just gave me a prescription for Amitriptyline and said it might help. I am so angry I'm shaking
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