Have you had the foot Neuropathy tests.......i.e the clinician asks you to close your eyes and you say when you can feel a pin type thing touching each toe? Technically I suppose you could ask a friend to do it although I seem to remember some sort of doppler/ultrasoundy thing used to measure circulation also?Hi, looking for some advice, I've been type 2 Diabetic for 2 years. My last HBA1c results were 59 which i know is not great but have been feeling fine. Over the last month I have had constant tingling in hands and feet more so the feet. I have seen my local Dr who simply says reduce blood sugar levels. I exercise every day. Any advice appreciated to get rid of this tingling. i have read about peripheral neuropathy which is quite alarming. I'm not sure if I have the 1st stages. Anyone else experience this sort of thing? Any advice appreciated.
Yes me - in my feet. A mild form of it. Since radically reducing carbs this has stopped and stayed stopped.Hi, looking for some advice, I've been type 2 Diabetic for 2 years. My last HBA1c results were 59 which i know is not great but have been feeling fine. Over the last month I have had constant tingling in hands and feet more so the feet. I have seen my local Dr who simply says reduce blood sugar levels. I exercise every day. Any advice appreciated to get rid of this tingling. i have read about peripheral neuropathy which is quite alarming. I'm not sure if I have the 1st stages. Anyone else experience this sort of thing? Any advice appreciated.
Hi, looking for some advice, I've been type 2 Diabetic for 2 years. My last HBA1c results were 59 which i know is not great but have been feeling fine. Over the last month I have had constant tingling in hands and feet more so the feet. I have seen my local Dr who simply says reduce blood sugar levels. I exercise every day. Any advice appreciated to get rid of this tingling. i have read about peripheral neuropathy which is quite alarming. I'm not sure if I have the 1st stages. Anyone else experience this sort of thing? Any advice appreciated.
A GP I saw a few years back suggested using a treadle from an old sewing machine or similar to work the feet if doing a desk bound job.I have Vit B 12 injections, one a month. Not sure if mine is related to diabetes (I’ve had poly neuropathy for ages) or the same as my brother and father who both have it (two long thin streaks- no diabetes). Anyway whatever the cause, I find it helps. Sub lingual tablets work if no injection possible.
The owner of my gym, who has trained extensively in Germany and US, says to roll my feet on a hedgehog ball. If nothing else it helps the circulation.
Fibromyalgia, polymalgia, and asthma in my list too along with a host of others! I couldn't do without this forum, have lost five stone now since diagnosis three years ago but still got a little way to go with BG levels. I too stagger my carbs I don't think I could do intermittent fasting unless being asleep counts!I was diagnosed with Non-diabetic peripheral neuropathy a few years ago - via a neurologist, with nerve conduction tests.
Blood tests done then (not earlier by my previous, useless, GP in spite of reporting the problems several times, and having falls because of it) showed I had folate anaemia.
So when I was diagnosed with diabetes last year this was my main concern.
I joined the lowcarbprogram, went on their low carb programme and my blood sugar went down within a couple of weeks. Since then I've had two HbA1c results in the normal range. I am usually very careful about staggering my carbs rather than eating them in a single meal, and staying within my target. (I've had a few difficult days due to extra stress, but managed to keep it down below 110g even then. Fear of diabetes affecting my legs and eyes is a huge incentive to stay low carb.)
Both here in the low carb forum and on the programme there are tips on substitutes for rice/potatoes/bread/cereal, plus great recipes and support.
Thank you. Just ordered some ALA and will give it a go. This forum is so good for ideas and advice.My peripheral neuropathy developed gradually over many years. It began with with itchy feet particularly at night and in the winter. This was followed by tingling in the hands and feet then pins and needles. 18 months ago following a cut in my diabetic medication I got the sharp pains and a regularly occurring stinging that sometimes feels like the skin is being ripped off.
I have received the following good advice form this forum and my diabetic clinic.
Vitamin B12, preferably sub-lingual
Cut the carbs. Since last July I have followed the Low Carb Program and my A1Cs are much improved 9.7 Feb 2018 to 6.9 Feb 2019
Alpha Lipoic Acid. This helps to repair damaged cells the immediate cause of the pain reaction of the nervous system. The clinic suggested up 1800 mg per day. I take 4 x 400 mg per day and if I miss a tablet the condition rapidly gets worse.
Keep your feet warm as the contraction of blood vessels in the feet and hands when they are cold worsens the condition.
Keep going to the gym especially anything that pushes blood out to the feet and hands. I do very rapid walking on a treadmill when warming up for weight lifting.
I also have healing prayer at Church but this may not be for everybody.
All of these have coincided with an end to the deterioration in my condition and there is now a gradual improvement.
Find out what works for you and do it now before things start to get worse.
I did use the R-ALA but is is very expensive in Canada. I find using a much higher dose of the ALA works just as well and a lot cheaper. Choose what works best for you.Get R-ALA, not just ALA. Many say it's far more effective
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?