theeicebear
Active Member
- Relationship to Diabetes
- Type 2
Hi all,
I was diagnosed with diabetes 7 years ago. I had been going to the doctor's with medical issues for a long time. One of which being my feet. As they were/are very painful and I have pins and needles in them all the time. Obviously now with hindsight it's peripheral neuropathy. He said it was anxiety!
He basically said at some stage that he never thought it to be type 2 diabetes as I was too young! I'm 44 now, and obviously was 37 when diagnosed and have probably had it since I was 27.
I contacted one solicitor about a medical negligence claim but they basically said no in a long and polite way.
I'm not after quick "compo" or anything like that, but I know in old age that'll no doubt need some care and it's obviously not cheap. I think I have a case because you cant say you are too young for diabetes and not diagnose it.
I have peripheral neuropathy, diabetic retinopathy, and I'm 99.9% sure I have gastroparesis (which was being diagnosed until the pandemic ruined that).
Have you had any experience or have an information that could help?
Thanks in advance!
I was diagnosed with diabetes 7 years ago. I had been going to the doctor's with medical issues for a long time. One of which being my feet. As they were/are very painful and I have pins and needles in them all the time. Obviously now with hindsight it's peripheral neuropathy. He said it was anxiety!
He basically said at some stage that he never thought it to be type 2 diabetes as I was too young! I'm 44 now, and obviously was 37 when diagnosed and have probably had it since I was 27.
I contacted one solicitor about a medical negligence claim but they basically said no in a long and polite way.
I'm not after quick "compo" or anything like that, but I know in old age that'll no doubt need some care and it's obviously not cheap. I think I have a case because you cant say you are too young for diabetes and not diagnose it.
I have peripheral neuropathy, diabetic retinopathy, and I'm 99.9% sure I have gastroparesis (which was being diagnosed until the pandemic ruined that).
Have you had any experience or have an information that could help?
Thanks in advance!