Hi there. Very new here. Just second post can anyone tell me what does it means that i have faint pulse at the front part of both feet. My feet are very cold all the time even with two socks it doesnt help.
Kindly anyone can help me with this and also as i been visiting the gp quite a bit past few months he told me to change the surgery as all of sudden i am not in the catchment area..... Help mee
Thanks. I will give it a try hopefully it helps. Its getting really bad every passing day.There are something called raynauld's socks, gloves and other far infrared stuff that can be bought and some podiatrists use tens therapies for the neuropathy on top of that. There are special kinds of neuropoligists who deal with both Raynauds (the cold extremities) and the neuropathies.
Thanks a lot i really appreciate your help. I am very upset since been told about it.I would give your old doctor's surgery a ring and ask them for clarification.
You may be outside the catchment area, but until you find another surgery, get registered, and see a doctor there, you are still under the care of your old surgery. The transfer, including finding a new surgery and getting registered can take months, and during that time your feet will need medical care.
If you ring the surgery and ask the receptionist, she will probably confirm that you can continue to see your old doc, or can suggest another alternative.
Well worth a phone call to find out!
Hi, I suffered from Raynaud's disease in the hands when I was first diagnosed with T2. It's very strange to see your hands turn white and go numb, shouldn't happen too much in the warmer weather though. My main neuropathy problem has been numbness, tingling and pain in the feet, particularly when trying to sleep. That's mainly gone now I have got into the non-diabetic range with LCHF.There are something called raynauld's socks, gloves and other far infrared stuff that can be bought and some podiatrists use tens therapies for the neuropathy on top of that. There are special kinds of neurologists who deal with both Raynauds (the cold extremities) and the neuropathies.
did you try a tens machine to zap the nerves back in consciousness?
Thank you @Contralto I hadn't heard of a TENS machine until your post, so I looked it up. I can see how it might work, but thank goodness I don't have a neuropathy problem now. I believe they used to do this sort of thing with dead frog's legs back in General Science days.did you try a tens machine to zap the nerves back in consciousness?
Would you consider using a supplement called lipioc acid for nerve damage in your feet?thanks everyone for sharing. There has been one more issue all of sudden i started to get hypos whereas I was going fine. I am on 2000 mg of metformin and the dr keeps on saying that metformin doesnt let you get hypos. If that is not getting me hypos in other words it means that metformin keep the blood sugar levels high.. Its been 4 times in last 8 days all of sudden my sugar level drops to 4 or less. Thew numbness has increased in feet has increased. I am trying to get an appointment of dermatologist but they just gave me photographic appointment which i didnt understand.
I visited couple of gp but they barely let you talk to the actual gp u have to take a shot in the dark. I have requested to let me meet the gp as you cant simply just get registered anywhere. I have seen reviews on the nhs website. The patinets number is 6000 plus which is so much. there is waiting time of 10 days for appointment which is unreal. I dont know what is happening. Its becoming really difficult. The stress levels get too high at times which makes me depressed. I am feeling really lost.Would you consider using a supplement called lipioc acid for nerve damage in your feet?
Have a search here and ask users any questions?
Hope GP still supporting you? Any signs of a new gp?
Obviously a large practice can offer you more services, lesshospital visits maybe? Mine is a small practice but very friendly. No practice can do everything hun. You could give a smaller practice a try and if not for you change to a bigger one/health centre?I visited couple of gp but they barely let you talk to the actual gp u have to take a shot in the dark. I have requested to let me meet the gp as you cant simply just get registered anywhere. I have seen reviews on the nhs website. The patinets number is 6000 plus which is so much. there is waiting time of 10 days for appointment which is unreal. I dont know what is happening. Its becoming really difficult. The stress levels get too high at times which makes me depressed. I am feeling really lost.
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