Tingling sensation in both lower legs is it liver related ????
Liver related : Tingling sensation in... - British Liver Trust
British Liver Trust
No one can know on the forum if your symptoms are liver related, please check with your GP.
So what have these 15 doctors and all the scans and tests revealed? I wouldn't have thought that 15 doctors were useless or know nothing it's perhaps they are just not finding what you think they should but they can't find things that arn't there.
Tingling legs arn't a liver symptom but could potentially be linked with other issues - you previously mentioned a pre-diabetes issue - was this followed up.
You mentioned having an MRI scan - what were the results of that?
Mrcp came back a normal over 2 months ago in the last 7 weeks liver blood tests keep on raising I’m in constant pain under both side of ribs middle of back and right shoulder always burping for no reason bouts of itching all over pale floating stools always pain after food with really bad stomach pains promises of scans off different doctors nothing happens joke really had to paid for mri and this ct scan Saturday with me bloods keep going up was promise another ultrasound said 3-4 weeks just over 4 weeks now and nothing
I have similar symptoms as you. For me, it started with abdominal pains (upper side left, centre, right), burping even just after drinking water, pain after eating, weakness in the legs (especially in the calves), strange stools, pain in kidney areas along with bright (dark?) urine full of flakes. This started nearly 3 years ago. Now, the abdominal pains, burping, pain after eating, and strange stools are mostly gone (sometimes these symptoms return, but now last only a couple of days, and subside). However, I still have the back pain and dark urine (despite drinking 3 Litres of water daily), weak legs, and more.
This past spring I also developed a persistent vibrating feeling in my legs, along with a feeling of coldness in my calves with hair loss (at least 1/2 lost) in the areas of most coldness/worst vibrating sensation.
I also have numbness in the left side of my face, and have lost nearly 2/3 of my hair over my entire scalp, with slightly more loss on the same side as the numb face. First round of hair loss started last summer, and I lost 1/2, ended around Christmas time. The second round started this summer, and is ongoing.
I've had negative scans (abdominal ultrasound, colonoscopy/upper endoscopy with biopsy for H. pylori, MREnterography) negative blood tests (liver function tests, kidney function tests, urine tests)
I've had basic autoimmune blood tests: Basic anti-ENA screen - came back negative, also ANA negative. These were done about 1.5 years ago, so maybe they have changed. The only positive test was low complement (C3 and C4 both low).
I think this is autoimmune/vascular. Could be wrong, though.
I'm thinking about trying to find a doctor who will order tests for antiphospholipid syndrome and vasculitis. It is just so hard, since every time I go to seek help I just get beaten up with "you have anxiety anxiety anxiety!" even though I do not and have never suffered from anxiety. And if I manage to get these tests and they are negative, then I feel that will be the final nail in my coffin, at least when it comes to GPs willing to try anything at all.
In which do nothing
They sure are for ibs when I was in a+e months back doctor there gave me colfac laugh at me and said your too young to have owt wrong with you I’ve not been too doctors since I was 10 years old now just turned 36 always thought are doctors where good now I know they are shit and fob you off most of the time they don’t have a clue ok if you got the common cold
You do seem to be very angry about GPs. If they can see you are angry they can refuse to see you. Maybe you need to be a bit calmer when you see the next one and explain your symptoms in the manner you wish to be treated. If you would prefer to see a private GP, as l know it still isn't straightforward to see NHS ones, for £95 you can get a 30minute appointment. Seeing a doctor is the only way you are going to get a diagnosis and treatment.
If you are concerned your pains are liver related you must give up drinking completely and forget the takeaways..
Hope you are successful next time you see a doctor.
For one I anit touch drink since April another to see 15 different doctors in 8 months in which half of doctors have left the gp which are no longer there summits wrong with the liver for the alt and ggt to go up treble in less then 8 weeks each month I’m getting more sytoms some morning I can’t even put my socks on the pain right side is unreal I wouldn’t be as mad if they knew summit first 4 months pain came and when now it’s constant there anit no good days ill just ride it out like the last doctor told me
Just gone private ct scan Saturday morning hopefully get some answers that’s all I want
Regarding the tingling in your legs, Trust 1 and Laura have given good advice. Those kind of symptoms need assessment by a doctor and then the relevant speciality from this.
Tingling bilaterally is a mine field as it can be caused by so many things that all require different management. Metabolic, central nervous system and peripheral nervous system disorders are just a few examples and then each of those can be broken down into a whole array of disorders and causes.
The doctor is the best way to go. I appreciate it can feel overwhelming and all becomes clouded and messy with multiple symptoms, tests, health care professionals.
Maybe simplify things and write down each symptom one by one in a list under columns like…..
1) What symptom you have right now. (regardless of what’s happened in the past).
2) How it affects you day to day, in terms of social activities, work, mood, worry, pain etc.
3) What you would be able to do if you didn’t have that symptom.
Show them to the GP x
Hi. I been getting the same. Was given gabapentin. Drinking too much caused nerve damage. Neuropathy. Good luck. I know how annoying the tingling is.
Thanks had ct Saturday just waiting on results
Hi. I didn't have any scans for the tingling. I was just put on gabapentin. With cirrhosis and all , I never pushed it. Please let me know how you get on. Good luck 👍
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