mike_maple
Member
- Messages
- 9
- Type of diabetes
- Other
- Treatment type
- Other
Hi Mike and welcome to the forums.Hi folks,
I'm 47 and have had tingly feet off and on for about the last 3 weeks, with the problem getting more pronouced this week. Thought I heard years ago that this was one of the first symptoms. Saw a doctor the other day, he's lined up some tests, but not for over a week. Since then I've really been cutting back on sugar/carbs, though I haven't been totally off carbs as some suggest (just learned this tonight). It's been an emotional time for me I admit with the full realisation of what it means, but have been more positive today and especially being on this forum with the advice given.
Now I learn that Peripheral Neuropathy is a later stage complication! I'm scared stiff! What do I do? Any advice greatfully recieved.
Thanks
Mike
Personally I'd hesitate to make any drastic changes in my diet till I knew what my blood sugar levels were and indeed, even if I had diabetes. At this stage you have some symptoms that may or may not be related to (as yet undiagnosed) diabetes. New diabetics are generally recommended to lower their bg levels slowly, as a too fast drop can cause issues with eyes.Thank you KennyA for your in depth post, much appreciated. I have ordered tonight a glucose meter and will be using it as you suggest. I'm going to cut the carbs out totally until I know more as a precaution. I'd say wish me luck, but you already have done! I'll need it too as going on a cruise ship in two weeks....
All of this depends on the "if you do need to reduce your blood glucose levels" question. If you don't need to reduce, because you're not out of normal range, the meter won't be telling you much useful. Non-diabetic people have variable blood glucose, in response to various things.Thank you KennyA for your in depth post, much appreciated. I have ordered tonight a glucose meter and will be using it as you suggest. I'm going to cut the carbs out totally until I know more as a precaution. I'd say wish me luck, but you already have done! I'll need it too as going on a cruise ship in two weeks....
I am a member of the RHS and a life member of the National Trust. I like to take macro shots of flowers. See here for some of my flower close-up shots at Wisley Gardens.Thanks everyone, that's good to know. Will stay put on the reduced but not cut out carbs then for the moment.
The doctor did mention B12 deficiency, but as I'm overweight and eat too much chocolate and ice cream, I dismissed it as false hope. Will try the supplements you mention Art Of Flowers (ace handle by the way - Florist? Gardener? Passionate gardener myself.)
I am a member of the RHS and a life member of the National Trust. I like to take macro shots of flowers. See here for some of my flower close-up shots at Wisley Gardens.
I’m type 1 for over 20 years, but have been told by 2 neurologists that I don’t have diabetic neuropathy. My recent neurologist diagnosed me with B12 deficiency and I am on mega doses for the foreseeable future. For now, that’s all he has diagnosed me with. I’m terrified and my symptoms skyrocketed when I began the treatment. He wants me to be evaluated for Sjogren’s Syndrome as well, just in case. I don‘t have any of those symptoms though, just dry eye. I have an appointment for that in August.Thanks everyone, that's good to know. Will stay put on the reduced but not cut out carbs then for the moment.
The doctor did mention B12 deficiency, but as I'm overweight and eat too much chocolate and ice cream, I dismissed it as false hope. Will try the supplements you mention Art Of Flowers (ace handle by the way - Florist? Gardener? Passionate gardener myself.)
I agree with this. I have just had my latest bloods back and B12 has gone from being at the bottom of normal to below the lowest number they measure. I am going to ask for a test for pernicious anaemia as I have family history of that, luckily I dont have many symptoms apart from lethargy, bit of fatigue, so I'm hoping it got caught early before it does damage because I've also read that damage can be permanent. Apparently half of B12 deficiencies can be caused by pernicious anaemia which is auto immune so if, like you (and me) have autoimmune diabetes its more likely. Definitely worth getting checked out, they've put me on tablets for now but may need injections if it doesn't improve enough.I’m type 1 for over 20 years, but have been told by 2 neurologists that I don’t have diabetic neuropathy. My recent neurologist diagnosed me with B12 deficiency and I am on mega doses for the foreseeable future. For now, that’s all he has diagnosed me with. I’m terrified and my symptoms skyrocketed when I began the treatment. He wants me to be evaluated for Sjogren’s Syndrome as well, just in case. I don‘t have any of those symptoms though, just dry eye. I have an appointment for that in August.
B12 deficiency is very serious and can bring permanent damage. I suspect I have that.
Please get tested for B12 BEFORE you start taking it. The first number before supplements are what they look at. Not everyone can process it and some need injections or sublingual tablets. Please put a rush on your B12 tests if possible. And, research how to replenish it. Many doctors are not well informed of how much people need to treat a deficiency. Find an expert who can ensure you get enough to help. I thought I was treated last year, but it was inadequate.
Thank goodness you caught it! Man…..that’s a relief. Good idea to test for anemia. Are you going to take B12 sublingual tablets? I’m taking that 1000 mg a day indefinitely for now, I have seen substantial improvement in my body since starting the treatment. The tingling in my hands and arms has stopped waking me up at night and I’m no longer sleeping on my back with arms supported on pillows.I agree with this. I have just had my latest bloods back and B12 has gone from being at the bottom of normal to below the lowest number they measure. I am going to ask for a test for pernicious anaemia as I have family history of that, luckily I dont have many symptoms apart from lethargy, bit of fatigue, so I'm hoping it got caught early before it does damage because I've also read that damage can be permanent. Apparently half of B12 deficiencies can be caused by pernicious anaemia which is auto immune so if, like you (and me) have autoimmune diabetes its more likely. Definitely worth getting checked out, they've put me on tablets for now but may need injections if it doesn't improve enough.
Yes, I've been prescribed 1mg a day, 1000mg sounds a lot?Thank goodness you caught it! Man…..that’s a relief. Good idea to test for anemia. Are you going to take B12 sublingual tablets? I’m taking that 1000 mg a day indefinitely for now, I have seen substantial improvement in my body since starting the treatment. The tingling in my hands and arms has stopped waking me up at night and I’m no longer sleeping on my back with arms supported on pillows.
Correction 1000 mcg sublingual per day. I thought it sounded like a lot, but discovered it’s common to prescribe high doses for those with deficiencies. I suspect at some point the doctor will reduce it.Yes, I've been prescribed 1mg a day, 1000mg sounds a lot?
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