Hi Nicole. My BG's are good at night (and most days - being on a pump has really helped that). I take thyroid medication and low dose Amitriptyline which was prescribed to relax muscles as part of treatment for CFS. I'm not bad with veggies - could always eat more. And I take B12 tablets and last time it was measured it was just below mid of ref range which was why I started supplementing it so I would expect it to be better. I do take co-codamol when the pain gets bad. It helps but I'm very aware of dependancy issues so wary of taking it too often. What is frustrating is that the diagnosis of CFS is kind of a catch all for many medically unexplained symptoms and I would prefer to get a more accurate diagnosis. Thanks for your suggestions! K
Hi DCUKMod,
I have tried NDT, T4 only, T3 only, T3 & T4 combo. I've been under medicated, over medicated, properly medicated (in terms of results - which include FT3, antibodies etc). I've tried different diets, loads of supplementation, different exercise regimes and none of it has made any significant improvement in terms of pain and fatigue. I have been T1 since 1986 and for many years I didn't manage the condition well. Luckily during that time I only passed out once and had a few infections but nothing serious. I've been really on top of things from a diabetes management perspective for almost 20 years now, although I've no doubt the early years did some underlying damage.
Sorry to go back to my initial query but do you know if its possible to have neuropathic pain in legs with none in feet? Cheers, appreciate your help, K
Hi Kev. I have peripheral neuropathy and I have no pain in my feet. They are on the numb side though. With me the PN manifests as a really weird water trickling down my legs sensation along with an ache and almost a restless legs feeling. If you speak to your DN they can run a test on you which measures the electrical activity in your feet to see of there is any nerve damage. Hope that helps.
I've been fortunate enough not to have neuropathy to date, but I should think it possible to have neuropathy anywhere there are nerves, although the extremities, with their more ad more delicate nerve endings, will probably be more susceptible.
Do you eat gluten-free? I was strongly advised, based on a few factors by the Endo I see that many with auto-immune conditions do well GF. For me, my gluten intolerance means when I find myself accidentally "glutened", I have extreme fatigue, joint pains, brain fog, and erm,...... "digestive disturbances".
Some of the symptoms you describe occur across a real variety conditions, so they can, as you are finding, be tricky to pin down.
Yes I'm with you 100% on this. I am GF but when I either lapse or eat it accidentally it definitely disturbs my system and is a contributor to fatigue, sluggishness and digestive problems. I read that Gliadin, the protein in gluten, is similar in structure to the thyroid and if you have hashimotos (I do) then the immune system will see gluten as a target to be destroyed!
Kev - I am atypical everything. It's a wonder my brain allows my fingers to type typical.
I don't have Hashi's. In fact when I first saw my current Endo, he ordered up a raft of about 40 blood tests (in addition to the usual stuff), based on my family history of AI conditions. He was aghast I didn't (at that time anyway) have any AI conditions. His parting shot was along the lines of "keep an eye on that diabetes. LADA is a sneaky condition."
Charming.
Have you gone dairy free, as well as GF? His words on that have so far only met my deaf ear!
Yes I am DF as well. Like being GF its a struggle at times both in terms of willpower and "hidden" ingredients. Eating out is like playing russian roulette with my digestive system. I'm hoping that I don't get any more AI conditions - especially lupus. My mum has that and it's nasty. I would love to have a body which could properly differentiate between friend and foe. Instead it's a question of trying to keep the friendly fire to a minimum.
How's your circulation Kev?
I would describe it as reasonable Jo. I do get cold feet sometimes. Spoke to a diabetic nurse yesterday and she is going to enquire about the test kazwbb mentioned earlier in the thread and hopefully organise one for me.
I have Neuropathy in my feet and legs. For me, the pain feels like its stabbing and stinging along with a sensation of boiling water being poured on me (usually all at the same time). Its very painful and I have been prescribed a low dose of Pregabalin which helps take the edge off the pain. As I am on quite a few other meds, they have to keep the dose low. Drugs such as Co-Codamol or Ibuprofen don't help with Neuropathy pain. I'd discuss options with your GP. Good luckThanks Kazwbb. I will ask my DN for that test. Do you mind if I ask you what, if any, pain relief you use for your neuropathy? Cheers K
I have Neuropathy in my feet and legs. For me, the pain feels like its stabbing and stinging along with a sensation of boiling water being poured on me (usually all at the same time). Its very painful and I have been prescribed a low dose of Pregabalin which helps take the edge off the pain. As I am on quite a few other meds, they have to keep the dose low. Drugs such as Co-Codamol or Ibuprofen don't help with Neuropathy pain. I'd discuss options with your GP. Good luck
Hi all,
I have a dull pain mostly on the front of my thighs but sometimes on the calves. Occasionally on the thighs it feels like numbness and a bit tingly. My knee and ankles are sometimes a bit stiff but not really problematic. I have no issues with my feet however.
I never feel refreshed after a nights sleep and often have the pain in my thighs upon waking. Consultants have said its a symptom of M.E./CFS as I also have severe fatigue especially in the mornings.
So my question is - could it be diabetic neuropathy and does anyone else have experiences of something similar? I thought neuropathy started with hands and feet?
Many thanks, Kev[/Q
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