Hi @Gabby G , welcome to the forum.My doctor and I are a bit confused about all the symptoms as they said this usually happens with very uncontrolled diabetes.
Hi Gabby G and welcome. My experience was similar to yours, up to a point.Hey there,
Grateful to have found this forum! I just need some advice:
I’m in my early 30’s and had neuropathy symptoms start in 2017. I first thought it was carpal tunnel. It was stable for a number of years but started to spread in my feet with tingling and it’s now continued to get worse.
I have polyneuropathy so it affects a lot of my nerves now including my feet and hands. My left food started to go a bit numb aswell as my right hand with on and off pins and needles. I’ve had trigeminal nerve pain in my temples and pain in my tongue. The nerve pain seems to change every few weeks. I also believe my digestive system has been affected as I have acid reflux ( which I never used to have) and troubles with indigestion now.
I was diagnosed as prediabetic last year on a Hb1ac of 42 ( which surprised me for my symptoms I thought it would be higher). I changed my diet and started exercising and now it’s down to 37 so I’m no longer in the range. However my symptoms still seem to be there and I really was hoping this would change.
My doctor was suggesting it may not be linked but a previous appointment with the neurologist said it’s most likely linked. I’ve had an MRI done which came back fine.
I’m feeling a bit stuck on what to do as I was hoping some of my symptoms would decrease. It’s taking a while to get a referral on the nhs for a neurologist, is it worth looking into anything else. Has anyone had the same experience? My doctor and I are a bit confused about all the symptoms as they said this usually happens with very uncontrolled diabetes.
Hi thanks for your welcome and reply! Yes, it’s all a bit confusing. I’m looking into a few causes with my GP. Unfortunately the previous neurologist rejected my second referral and it will take a while to get another oneThose sound like very unpleasant symptoms, and not at all how you'd expect diabetic neuropathy to manifest if you're only at the absolute lowest threshold for prediabetes.
However, while diabetes is the most common cause for neuropathy, it's by no means the only one.
I hope your doctor has done all the blood tests to rule out various causes?
Hi Kenny,Hi Gabby G and welcome. My experience was similar to yours, up to a point.
Like you I had a range of diabetic symptoms while my BGs were quite low. As well as a dozen other symptoms I developed neuropathy - burning feet, stabbing pains, pins and needles - around 2014. My BG was around 43 at the time, although I only found this out years later. I was firmly assured that I didn't have T2 diabetes as my blood sugar wasn't high enough. I thought - if the medics say it's not diabetes then there's no point me doing anything diabetes related.
So I had about six years of that before my BG eventually rose to the point in December 2019/January 2020 where they told me I did have diabetes. I'd found this place by then and went (very) low carb. By April 2020 my A1c was 36 and the neuropathy had gone. Almost entirely - I still have a slight tingle which is probably permanent but it's not painful.
So I'm with you right up to the point where your symptoms don't decrease. In my view it's the high blood sugar that causes the damage, so reducing that should reduce the damage. The other possibility is that it's something else entirely, and your diabetes is just a coincidence.
In your shoes I'd push hard for the neurologist referral.
No problem - just to complete the story, the "diagnosis at 48" is comparatively recent. There was international agreement in around 2008 that countries would all accept a BG level of 48 as being diagnostic for T2. This agreement however did not exclude anyone diagnosing diabetes at lower BG levels - the 48 was designed as a backstop so comparisons could be made across different healthcare systems - it wasn't done for patients.Hi Kenny,
Thanks for your reply and that’s encouraging to hear you were able to reduce your symptoms!
Finding this forum I’ve also seen a few people mention they did have symptoms even on the pre-diabetic borderline so it’s making me wonder with what you just mentioned! I’m trying my best to stick to a low carb diet, although maybe in the past week or two I haven’t been so strict. I think I may need to take your advice and be a bit stricter.
It seems to be working in the past few months with the reduction in my hb1ac result, just sadly hasn’t had any effect on my symptoms just yet. I’ve bought R-ala and some other supplements in the hopes it will be more helpful and now have got a CGM so will monitor so let’s see if that helps.
Will keep an eye! Appreciate the welcome too
Before I began eating low carb to try to lower my bg levels, I used to have mega problems with acid reflux and other digestive problems, including dreadful bouts of constipation. My worst known A1c was only 41, but I had packets of Rennies stashed in every room of my house, and every handbag too. To manage the constipation I was getting through x3 suppositories daily. (Good thing I could get them free on the NHS!) Eating lower and lower carb, gradually the reflux and constipation went away. It must be years since I needed a Rennie, and I'm wondering what to do with all those un-needed suppositories. It seems a terrible waste to throw them away.. I also believe my digestive system has been affected as I have acid reflux ( which I never used to have) and troubles with indigestion now.
You might like to have a look at the Youtube videos called "Beat Diabetes" by Dennis Pollock. He has often mentioned his own diabetes history, when as a young man he suffered from Reactive Hypo and Hyper-glycaemia. Lots of the thousands of people who have contacted him and shared their stories had all sorts of symptoms long before their A1cs were even at pre-diabetic levels. This happened to me too.Finding this forum I’ve also seen a few people mention they did have symptoms even on the pre-diabetic borderline so it’s making me wonder
Brilliant !I changed my diet and started exercising and now it’s down to 37
I agree, reducing bg levels should stop the damage from getting worse, but not all damage can actually be reversed, or reversing it may take a long time (weeks, months, even years). I am basing this on Dr Richard K Bernstein's classic book "Diabetes Solution". Dr B has generously made a lot of his book available free online.I'm with you right up to the point where your symptoms don't decrease. In my view it's the high blood sugar that causes the damage, so reducing that should reduce the damage.
Thank you for enclosing this link. I kept using my copy as a reference book for years and years. Then I lent it to my nephew, whose house was flooded six months months ago (first time in more than a hundred years). All books were submerged in a meter of water.. . . . . . . . . Dr Richard K Bernstein's classic book "Diabetes Solution". Dr B has generously made a lot of his book available free online.
http://www.diabetes-book.com/read-online-diabetes-solution/
Hi there,Hey there,
Grateful to have found this forum! I just need some advice:
I’m in my early 30’s and had neuropathy symptoms start in 2017. I first thought it was carpal tunnel. It was stable for a number of years but started to spread in my feet with tingling and it’s now continued to get worse.
I have polyneuropathy so it affects a lot of my nerves now including my feet and hands. My left food started to go a bit numb aswell as my right hand with on and off pins and needles. I’ve had trigeminal nerve pain in my temples and pain in my tongue. The nerve pain seems to change every few weeks. I also believe my digestive system has been affected as I have acid reflux ( which I never used to have) and troubles with indigestion now.
I was diagnosed as prediabetic last year on a Hb1ac of 42 ( which surprised me for my symptoms I thought it would be higher). I changed my diet and started exercising and now it’s down to 37 so I’m no longer in the range. However my symptoms still seem to be there and I really was hoping this would change.
My doctor was suggesting it may not be linked but a previous appointment with the neurologist said it’s most likely linked. I’ve had an MRI done which came back fine.
I’m feeling a bit stuck on what to do as I was hoping some of my symptoms would decrease. It’s taking a while to get a referral on the nhs for a neurologist, is it worth looking into anything else. Has anyone had the same experience? My doctor and I are a bit confused about all the symptoms as they said this usually happens with very uncontrolled diabetes.
If you have this it will never go away now all of your nerve endings have been destroyed unfortunately only thing to be done is control your diabetes to avoid anymore damage sorry for your suffering , I have neuropathy in my hands and feet and it’s awful but I take seratonin it’s an antidepressant to help with the pain contact your doctor for options as there are loads of meds to help with the painHey there,
Grateful to have found this forum! I just need some advice:
I’m in my early 30’s and had neuropathy symptoms start in 2017. I first thought it was carpal tunnel. It was stable for a number of years but started to spread in my feet with tingling and it’s now continued to get worse.
I have polyneuropathy so it affects a lot of my nerves now including my feet and hands. My left food started to go a bit numb aswell as my right hand with on and off pins and needles. I’ve had trigeminal nerve pain in my temples and pain in my tongue. The nerve pain seems to change every few weeks. I also believe my digestive system has been affected as I have acid reflux ( which I never used to have) and troubles with indigestion now.
I was diagnosed as prediabetic last year on a Hb1ac of 42 ( which surprised me for my symptoms I thought it would be higher). I changed my diet and started exercising and now it’s down to 37 so I’m no longer in the range. However my symptoms still seem to be there and I really was hoping this would change.
My doctor was suggesting it may not be linked but a previous appointment with the neurologist said it’s most likely linked. I’ve had an MRI done which came back fine.
I’m feeling a bit stuck on what to do as I was hoping some of my symptoms would decrease. It’s taking a while to get a referral on the nhs for a neurologist, is it worth looking into anything else. Has anyone had the same experience? My doctor and I are a bit confused about all the symptoms as they said this usually happens with very uncontrolled diabetes.
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?