This I believe is a misstatement as nerve damage is permanent. Any views on this appreciated.
Oh yes remember this well, so many initial complications. I had the tingling in both feet and fingers. I also had some athletes feet and boils / blisters. I did a lot of reading (when I could see, as my sight was also affected). I didn't lose sensation, but could feel sharp shooting pains at the extremities of fingers and toes and sometimes legs.I’ll tag @Mbaker here for his experience. Not sure it’s with feet, but some relevant experience from memory.
BG is averaging 6.2 mmol down from 12+ in January immediately post diagnosis, so a start. Thanks...Oh yes remember this well, so many initial complications. I had the tingling in both feet and fingers. I also had some athletes feet and boils / blisters. I did a lot of reading (when I could see, as my sight was also affected). I didn't lose sensation, but could feel sharp shooting pains at the extremities of fingers and toes and sometimes legs.
Walking was not recommended, I recall; but I saw the situation as a catch-22 (also I am a rebel). Long story short I walked, and walked as well as dietary changes. Over time, less than a year for me, all of the tingling went - 100% resolved. I have read how long it takes to potentially resolve nerve issues, but it can happen. I have another non-diabetes experience. In my 20's I tripped over a shoe, fell and put my arm through a glass pane, this severed my median nerve in my wrist. It took months for me to be able to grip and use my hand normally, for years I had pain whilst the nerves did their thing. So I have 2 examples of reparation.
Try to get glucose control as soon as you can.
BG is averaging 6.2 mmol down from 12+ in January immediately post diagnosis, so a start. Thanks...
I hope all is well.
That's an awesome improvement. Patience is a virtue, which will hopefully see your complications reduce.
Please send your DSN my way - you don't need her while you are away , and I do.!New My DSN has marked me as "high risk" for foot issues, as I have very cold feet, some tingles and my left big toe failed the tickle test, everything else was fine.
Her rationale was that by marking me as high risk, access to resources with NHS funded podiatry is enhanced.
I'm the same as my feet are often cold, I have lost 3 stone so thought it might be related to thatPlease send your DSN my way - you don't need her while you are away , and I do.!
Mine refused to do a foot check saying I didn't need it, so today I've bitten the bullet and booked a private podiatrist as not sure what it is I have that causes tingling in big toe.
I also now have to wear slippers all the time due to cold, but had put that down to weight loss
I'm 3 stone down too, and finding chairs, and particularly car seats, very hard indeed. My built in cushion has gone!I'm the same as my feet are often cold, I have lost 3 stone so thought it might be related to that
I was contemplating doing the same as you and going private, but she's got me an appointment for when I get back to the UK.Please send your DSN my way - you don't need her while you are away , and I do.!
Mine refused to do a foot check saying I didn't need it, so today I've bitten the bullet and booked a private podiatrist as not sure what it is I have that causes tingling in big toe.
I also now have to wear slippers all the time due to cold, but had put that down to weight loss
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