Jump to content
RemedySpot.com

Re: Off-topic: UTIs

Rate this topic


Guest guest

Recommended Posts

>

> I have one now and it is a DRAG--actually, the cure is worse than

> anything. I hate antiobiotics, but the doctor insisted. And what

I

> hate most is that EVERY LITTLE THING affects my legs.

>

> Tom, if you're out there: you talked about d-Mannose a while ago,

> but I only remembered it today. I went out and got some and took

my

> first " dose " today. It says three times a day. I seem to remember

> you taking it once a day...

>

> This is my first UTI in many years, but still, I'm wondering if

it's

> something people with MS are prone to. Anyone know?

>

> And one more thing. I recently read some good advice about MS that

> might be helpful to the new people:

>

> Don't let yourself get too hungry, too hot, too cold, or too far

> from a bathroom!

>

> I needed to vent. Thanks.

>

>

>

--

,

Some people with multiple sclerosis have difficulty emptying their

bladder. Some become incontinent. One of the incorrect self-help

solutions is to restrict fluid intake, but this increases the risk of

bladder infections.

http://www.nationalmssociety.org/Brochures-Controlling%20Bl.asp

Hope you feel better soon.

Artie

Link to comment
Share on other sites

,

I have had MS since 1993. I have never had a UTI. It seems like some people get them and some people don't. I am sorry you have one. I have tried the spasm stuff you recommended from Dr. Lawrence-it has done me no good. Today I think I'm going to take the neurologist up on his suggesdtion of the Bacolfen pump. I'm calling him tomorrow!

-- [low dose naltrexone] Off-topic: UTIs

I have one now and it is a DRAG--actually, the cure is worse than anything. I hate antiobiotics, but the doctor insisted. And what I hate most is that EVERY LITTLE THING affects my legs.Tom, if you're out there: you talked about d-Mannose a while ago, but I only remembered it today. I went out and got some and took my first "dose" today. It says three times a day. I seem to remember you taking it once a day...This is my first UTI in many years, but still, I'm wondering if it's something people with MS are prone to. Anyone know?And one more thing. I recently read some good advice about MS that might be helpful to the new people:Don't let yourself get too hungry, too hot, too cold, or too far from a bathroom!I needed to vent. Thanks.

Link to comment
Share on other sites

yea, thats probably one of the biggest problems, at least for me. I love to eat, and all the wrong things. Maybe she meant to not starve yourself, but eat things that are good for you, like what I dont do. :0)))

Re: [low dose naltrexone] Off-topic: UTIs

Why too hungry? I know the other stuff but too hungry?You can try Uva Ursi for UTI's. Also calld bearberry.Go here for more infohttp://www.umm.edu/altmed/ConsHerbs/Uvaursich.htmlI tried antibiotics for like 6 weeks for my first utiand still had it. Took this and felt a difference in aday or two. Hope this helps.

Link to comment
Share on other sites

LOL. That's the weirdest part for me. I was a vegan

then vegetarian and my former neuro pushed until I ate

the dead things again. I was the ultra-healthy type

all through my 20's, watched my diet, drank lots of

water, all that, then dropped to under 100 pounds and

changed my diet after constant prompting FOR THE

WORSE! Now, I live on coffee, Coke and just bad stuff.

I'm slowly working water and fruits and veggies back

in. Even water was making me puke b4 and the healthy

stuff. I just want to be at least a vegetarian again,

not even vegan. I think my hunger censor is broke

though along with so many other things. LOL Has anyone

else noticed a lack of hunger? Like you just forget to

eat unless prompted?

[HI !]

Link to comment
Share on other sites

>

> I have one now and it is a DRAG--actually, the cure is worse than

> anything. I hate antiobiotics, but the doctor insisted. And what I

> hate most is that EVERY LITTLE THING affects my legs.

>

> Tom, if you're out there: you talked about d-Mannose a while ago,

> but I only remembered it today. I went out and got some and took my

> first " dose " today. It says three times a day. I seem to remember

> you taking it once a day...

>

> This is my first UTI in many years, but still, I'm wondering if it's

> something people with MS are prone to. Anyone know?

>

> And one more thing. I recently read some good advice about MS that

> might be helpful to the new people:

>

> Don't let yourself get too hungry, too hot, too cold, or too far

> from a bathroom!

>

> I needed to vent. Thanks.

>

>

>

=======

, never use antibiotics for a UTI. Get D-Mannose(Dr McCandless

recommends), Uva Ursi, Cranberry capsules(not the juice), Astragalus(natural

antibiotic), Garlic is a great fighter of bacteria. Go the all natural way.

Keep D-Mannose on hand at all times and take 2 cranberry capsules in AM and 2 in

PM for life.

Antibiotics will cause candida. Take a good probiotic up to 4 capsules per day.

Link to comment
Share on other sites

Re: "That's the weirdest part for me. I was a vegan then vegetarian and my former neuro pushed until I ate the dead things again."..."Has anyone else noticed a lack of hunger? Like you just forget to eat unless prompted?..."Yes, me too Donna, but I've made major changes to my diet recently - Best Bet Diet, basically, with other things excluded because I show a sensitivity to them, and trying to fix a Candida problem. I'm losing weight steadily, and I rarely feel hungry. I just make food because I know I have to eat. That's fine for now because I was a bit overweight, but I do wonder if it will change once my weight drops to "thin" again.

I was vegetarian too and a complete health nut for years, and very fit. And I still got MS! Now I can't see a way to be vegetarian, because of the "no legumes" rule on the BBD. My vego heading for vegan son is trying to find a way...but my way is to just buy organic, which hopefully helps with the animal cruelty issues as well as my own health. I don't think my diet slipped quite as far as what you described - sounds like you were on a swinging pendulum! - but it did get pretty bad (read "normal" for Australia and the USA).

Gayle

Link to comment
Share on other sites

Hi ,

Take the D-Mannose 1 tsp. in 8 oz. of water 3 X a day until the UTI disappears....should be about 3 days. Then for maintenance once a day.

Regards,

Tom

[low dose naltrexone] Off-topic: UTIs

I have one now and it is a DRAG--actually, the cure is worse than anything. I hate antiobiotics, but the doctor insisted. And what I hate most is that EVERY LITTLE THING affects my legs.Tom, if you're out there: you talked about d-Mannose a while ago, but I only remembered it today. I went out and got some and took my first "dose" today. It says three times a day. I seem to remember you taking it once a day...This is my first UTI in many years, but still, I'm wondering if it's something people with MS are prone to. Anyone know?And one more thing. I recently read some good advice about MS that might be helpful to the new people:Don't let yourself get too hungry, too hot, too cold, or too far from a bathroom!I needed to vent. Thanks.

Link to comment
Share on other sites

The D-Mannose is also available from Solaray combined with Cranberry extract.

[low dose naltrexone] Off-topic: UTIs

I have one now and it is a DRAG--actually, the cure is worse than anything. I hate antiobiotics, but the doctor insisted. And what I hate most is that EVERY LITTLE THING affects my legs.Tom, if you're out there: you talked about d-Mannose a while ago, but I only remembered it today. I went out and got some and took my first "dose" today. It says three times a day. I seem to remember you taking it once a day...This is my first UTI in many years, but still, I'm wondering if it's something people with MS are prone to. Anyone know?And one more thing. I recently read some good advice about MS that might be helpful to the new people:Don't let yourself get too hungry, too hot, too cold, or too far from a bathroom!I needed to vent. Thanks.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...