Is anyone else with MS always thirsty?
Is anyone else with MS always thirsty?
seem like I can't get enoutgh liquid, luckily I like water, seems like I ALWAYS havef to have some liquid, it that just me or normal?
- flautenmusik
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I think it is diabetics related.
see http://www.thisisms.com/ftopict-15188.html
yet another pice of the puzzle that fits in neatly into the low-glucose hypothesis.
see http://www.thisisms.com/ftopict-15188.html
yet another pice of the puzzle that fits in neatly into the low-glucose hypothesis.
I've always been very thirsty and as a result my doctors have tested me for diabetes a number of times. I don't think it's due to the MS, but I also have never had an explanation for it other than that I like water.
on 2nd thought i do sweat a lot when I'm hot (and as many on here I get hot easily) so maybe it's something to do with that, but I have no real idea.
on 2nd thought i do sweat a lot when I'm hot (and as many on here I get hot easily) so maybe it's something to do with that, but I have no real idea.
- lyndacarol
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- flipflopper
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I had my first relapse in 1999 (later officially diagnosed as ms) and I have been extremely thirsty all the time since about 1998. After my first relapse (optic neuritis), I asked to be tested for diabetes. I have been tested for diabetes every year for the past 12 years and I definitely do not have diabetes. I have also been tested for numerous things but my tests results have always been normal. So I am always thirsty and I have not found an explanation for this yet...
From recent papers, I understood that insulin resistance starts developing long before you are diagnosed with diabetes. That may perhaps be as much 10 years or more. Also the process of demyelination and nerve damage has started earlier, but the signs, in our case MS, will only show up much later.
We are breaking new grounds here. The key metrics to qualify and quantify will need to be determined. I think the posting by Lyndacarol is extremely important here as we may need to look for early indicators.
insulin resistance is also thought to be the cause of other neurodegenerative diseases as ALS http://www.als.net/forum/default.aspx?g=posts&m=326324
http://care.diabetesjournals.org/conten ... 984.1.full
We are breaking new grounds here. The key metrics to qualify and quantify will need to be determined. I think the posting by Lyndacarol is extremely important here as we may need to look for early indicators.
the link between nerve damage and diabetics has been known for a long time: http://diabetes.niddk.nih.gov/dm/pubs/neuropathies/lyndacarol wrote: ... If your GP or endocrinologist has tested your glucose level and it is "normal," ask that your fasting serum insulin level be tested. (I suspect the insulin level will be above 7 UU/ML.)
insulin resistance is also thought to be the cause of other neurodegenerative diseases as ALS http://www.als.net/forum/default.aspx?g=posts&m=326324
http://care.diabetesjournals.org/conten ... 984.1.full
Re: Is anyone else with MS always thirsty?
Can somemeone explain why the MS patients feel constantly thirsty?
thanks, Hector
thanks, Hector

Re: Is anyone else with MS always thirsty?
Hi,
I'm the opposite. I rarely feel thirsty but when I do drink water I seem to need a lot. It's like I forgot I was thirsty and drinking something reminds me.
Regards,
I'm the opposite. I rarely feel thirsty but when I do drink water I seem to need a lot. It's like I forgot I was thirsty and drinking something reminds me.
Regards,
Re: Is anyone else with MS always thirsty?
hector wrote:Can somemeone explain why the MS patients feel constantly thirsty?
thanks, Hector
The thirst can is caused by the of SETRUSITOL (overactive bladder) which causes dry mouth.

Re: Is anyone else with MS always thirsty?
I have also been very thirsty with MS and have been tested for diabetes and my doctor said that it is probably any of the interferon's which are causing my mouth to not produce saliva and thus making my brain think that I am thirsty
Re: Is anyone else with MS always thirsty?
I have overactive bladder and I'm always thirsty. This is from like 3-4 years before being diagnosed with MS and might have been the initial symptoms. Doctor's don't have explanation for either one of them besides MS, they blame everything on it.hector wrote:hector wrote:Can somemeone explain why the MS patients feel constantly thirsty?
thanks, Hector
The thirst can is caused by the of SETRUSITOL (overactive bladder) which causes dry mouth.
Re: Is anyone else with MS always thirsty?
Just for the record I don't have extreme thirst. I have PPMS.