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Hello Everyone, just a question for those of you who are also afflicted

with Lupus. My rheumy couldn't decide what was wrong with me because I

presented positive for lupus, Hepatitis and RA. He consulted with a

hemotologist who said I have lupus. Now I will have to go back to rheumy and

see what kind of treatment there is available. This seems a very difficult

disease to diagnosis but the symptoms are muscular and skeletal pain

chronically. Does anyone have any good treatments going on?? Does anyone

know if there is a specialist I should see or just the regular rheumy?

Thanks for any help!

Suzanne

-- [ ] Hello I am new and would like to know somethings

Hi my name is ,

I have had Fibromyalgia and sjogrens syndrome for 10 years now and

have just started Antibiotic therapy from my Rhuematologist. I was

wondering if anyone is on the therapy and the success of the therapy.

I am a self employed caterer and find it hard to do my work most of

the time especially since I have to do most of the work out in the

weather and I live in Upstate New york.

Would like to talk to someone and share

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Guest guest

Suzanne,

I don¹t have lupus so I can¹t tell you anything from experience. I¹ve

collected some links and

put them on my site:

http://rheumatoid.arthritis.freehosting.net/Lupus.html

I hope this helps

a

> Hello Everyone, just a question for those of you who are also afflicted

> with Lupus. My rheumy couldn't decide what was wrong with me because I

> presented positive for lupus, Hepatitis and RA. He consulted with a

> hemotologist who said I have lupus. Now I will have to go back to rheumy and

> see what kind of treatment there is available. This seems a very difficult

> disease to diagnosis but the symptoms are muscular and skeletal pain

> chronically. Does anyone have any good treatments going on?? Does anyone

> know if there is a specialist I should see or just the regular rheumy?

> Thanks for any help!

>

> Suzanne

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Guest guest

Suzy, I highly recommend Dr. Wallace's " The Lupus Book (2nd

edition). " Of all the books I've read for patients with rheumatic

diseases, it is the best. Wallace is thorough and writes in a very clear

manner. Despite the complexity and wide spectrum of lupus, he has

written a very concise and understandable guide for patients and their

families.

http://www.amazon.com/exec/obidos/tg/detail/-/0195132815/102-4592148-2532168?v=g\

lance

This article, 'Management of lupus erythematosus: recent insights, " also

by Dr. Wallace, is quite important reading:

http://www.rheumatology.org/annual/sessions/Dr%20Wallace.pdf

There is much current, reliable information at the Hospital for Special

Surgery on lupus:

http://rheumatology.hss.edu/phys/diseaseIndex/lupus.asp

A rheumatologist is the specialist you need if you have lupus, although

you may have others you may consult depending on just what sort of lupus

you have and how it has affected you (or might). It would be wise to see

a rheumatologist who has a lot of experience treating lupus patients.

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

Re: [ ] Diagnosis

> Hello Everyone, just a question for those of you who are also

afflicted

> with Lupus. My rheumy couldn't decide what was wrong with me because

I

> presented positive for lupus, Hepatitis and RA. He consulted with a

> hemotologist who said I have lupus. Now I will have to go back to

rheumy and

> see what kind of treatment there is available. This seems a very

difficult

> disease to diagnosis but the symptoms are muscular and skeletal pain

> chronically. Does anyone have any good treatments going on?? Does

anyone

> know if there is a specialist I should see or just the regular rheumy?

> Thanks for any help!

>

> Suzanne

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  • 1 year later...

Dear ,

When you have dates let me know, I'd love to come up to Denver and visit with you. Things will be a blur for the next month, but you'll be so glad when it's over. Anything I can do let me know!

Colorado Springs

[ ] Diagnosis

Well...hello again. Got my diagnosis. I have failed fusion with flatback. I wasn't surprised about the flatback, but I was about the failed fusion. Anyway...surgery is scheduled for October. They will remove my Harrington rod which is no longer connected at the bottom. It seems L3 & L4 are severely degenerated (causing the numbness in my left leg). L3 and L4 will be fused with a cage replacing the disc, and 2 rods, 4 screws to hold it all together (and some bone from the front of my hip & some BMP). Good news is that since I did not fuse at L3/L4, the doc can create some more natural curve to my spine to minimize flatback. Bad news is he goes in from the front this time and from the back...long recovery. I will find out more details this month...as I have many questions to get answered to get mentally ready for this. I do have a supportive family and husband to get through this which is good. I wanted to also thank you all for your input as I went through this waiting period. God bless.

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,

I am trying to remember and didn't locate it on a quick search...Did

you see Dr. Kumar? I suspect I am not the only one that cannot

remember.It seems there are a few advantages to getting things done so

quickly, but as said, the next month will no doubt be a blur. If

you haven't already, do check out all of the wonderful tips on

preparing for surgery and ask whatever questions you think of...I will

be taking notes as well!

Best wishes to you.

kamala

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,

Wow, that is amazing to think you are going from diagnosis to

surgery in just a couple months. You are very brave.

I went back to see who your surgeon is...I am confused...did you go

to Colorado and is that where you are having the surgery? Is that

your second opinion? It sounds like you are getting pretty much the

same " treatment " we all get...although I was lucky that only the

very botton of my HR had to be removed. I think after all these

years having it out would have been a challenge....And of course

this all meant the muscles in my upper back didn't get traumatized

so it might have been a tad easier recovering. None the less, I

still felt like a huge MAC truck had run me over.

Will you surgeries be one or two days?

Please count on us for anything you need.

Take Care, Cam

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In a message dated 9/7/2005 9:40:16 PM Eastern Standard Time,

morningsunranch@... writes:

I gave up on doctors a long time ago

and have never been healtier.

,

I am with you. Western medicine has only caused more problems for me.

I did have a stool test done which told me which bacteria and yeast i have

and what to use to kill it. That was very beneficial and i have made great

progress. I have been fighting low grade fevers for the last 2 years. Since i

started killing my bad bacteria, i haven't had a fever in over a month.

I was told that my fevers were from lyme disease and i would have to stay on

antibiotics until i was symptom free. Well, if i had followed that advise,

i would have destroyed my gut and made my candida even worse than it was. My

doctor didn't even mention the fact that yeast could be part of my problem.

I strongly feel that because i developed a candida problem, it made my

dormant lyme become active. Also, i had surgery for endometriosis which what

finally broke " this " camels back. It all adds up. Its not just one thing.

So,

there is not one thing that will fix the candida. There is not a magic

bullet. It is a combination of diet, exercise, supplements, positive thinking

amongst other things.

Blessings,

Jordan

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The doctor that performed my original HR surgery is performing this

one. I fly down and meet with him on the 23rd. I have talked to other

patients of his and they all were extremely happy with him (I didn't

get their names from him either) and the team he uses. He has a team

he has worked with for many years and has performs many of these

types of surgeries. He mentioned he could leave the rod in and take

the end off as you said...but he said the only disadvantage to that

is that in the future it could slip again/more. I would rather have

it out than go through this again...even if the chance is remote.

They said I had a good fusion on the rest of my back which will make

the HR easier to remove. It is one long surgery. They will go through

the front first to insert the cage and get bone from my hip, then go

through the back to finish the fusion with 2 rods, and 4 screws...and

take the HR rod out. I have done research and have a list of

questions for when I go down to see him. My mother is a nurse and has

helped with a lot of what I need to know and ask which has been a

blessing.

I know this seems fast...but I am noticing more issues with my

comfort level each day and I worry I am going to have more nerve

damage, pain, etc. if I wait. And...I am getting to where I can't

pick up or do a whole lot with my babies. It's bugging me bad.

Thank you for your support...

> ,

>

> Wow, that is amazing to think you are going from diagnosis to

> surgery in just a couple months. You are very brave.

>

> I went back to see who your surgeon is...I am confused...did you go

> to Colorado and is that where you are having the surgery? Is that

> your second opinion? It sounds like you are getting pretty much

the

> same " treatment " we all get...although I was lucky that only the

> very botton of my HR had to be removed. I think after all these

> years having it out would have been a challenge....And of course

> this all meant the muscles in my upper back didn't get traumatized

> so it might have been a tad easier recovering. None the less, I

> still felt like a huge MAC truck had run me over.

>

> Will you surgeries be one or two days?

> Please count on us for anything you need.

>

> Take Care, Cam

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If you have to convince your doctor that you are sick, you need another

doctor. ALso if friends or family can't understand you are not feeling well,

that is their problem. Just start getting well and then you wont have to

convince a doctor or have ammo to counter questions with family. I would not

waste my money getting tests the treatment will be building your immune

system and you can do that on your own. I gave up on doctors a long time ago

and have never been healtier.

-- Diagnosis

Hi everyone,

New here and still struggling a bit with accepting (and having others

accept) what seems to be wrong with me.

I'm just wondering how many of you have been diagnosed by a " proper "

brush cytology test and how many, like myself, have suspected

candidiasis through consultation with a naturopath or similar. Perhaps

there are also those who have self-diagnosed?

What does it take to convince your GP to request this test for you? It

would be nice to have some orthodox ammo to counter all the questions

I get.

Thanks to all,

Mucusarus

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Hi Jordan,

BOth husband and I believe we had lyme also. Never a confirmed Dx. My

husband had the chronic fevers also and major joint pain. For me my symptoms

were the chronic infections and nuerological stuff. The candida then takes

over and has a whole list of symptoms all its own!

You are so right that inorder to get well we must have a combination of

things. I think so many get stuck on a diagnosis and then try to just treat

that particular disease symptom. That just will never work and for some

reason the doctors have not quite noticed that year after years their

patients just keep coming back sicker and sicker. Glad you are on the right

track. I can tell with my experience with lyme, you must keep your immune

system strong. I have a good amount of supplements I take everyday, I rest,

eat good organic healthy foods and drink only filtered water. Good luck to

you.

From: jbgoth@...

,

I am with you. Western medicine has only caused more problems for me.

I did have a stool test done which told me which bacteria and yeast i have

and what to use to kill it. That was very beneficial and i have made great

progress. I have been fighting low grade fevers for the last 2 years.

Since i

started killing my bad bacteria, i haven't had a fever in over a month.

I was told that my fevers were from lyme disease and i would have to stay

on

antibiotics until i was symptom free. Well, if i had followed that advise,

i would have destroyed my gut and made my candida even worse than it was.

My

doctor didn't even mention the fact that yeast could be part of my problem.

I strongly feel that because i developed a candida problem, it made my

dormant lyme become active. Also, i had surgery for endometriosis which

what

finally broke " this " camels back. It all adds up. Its not just one thing.

So,

there is not one thing that will fix the candida. There is not a magic

bullet. It is a combination of diet, exercise, supplements, positive

thinking

amongst other things.

Blessings,

Jordan

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Dr. Lowe in Wheatridge Colorado. He performs surgeries at Lutheran

Hospital and Denver Childrens Hospital.

> ,

>

> Would you mind giving the name and location (hospital) of your

doctor?

> It could prove helpful to others in the area at some point.

>

> Thanks!

>

> kam

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...Thank you. I am scheduled for October 17th at Lutheran

Hospital in Wheatridge, provided I don't change my mind after my

visit with the doctor in person. One thing I have read that I have

questions on is inflamation of the pancreas after back surgery. Do

you know anything about this? I didn't have it when I got my HR at

14. I have had a 1/3 of my pancreas removed when I was 11. I gave my

doc the op reports so he is aware. I still may get a second opinion

from Kumar...I just might have to do it long distance (after my

sister in Littleton picks up my xrays and does the transporting for

me).

> Dear ,

>

> When you have dates let me know, I'd love to come up to Denver and

visit with you. Things will be a blur for the next month, but you'll

be so glad when it's over. Anything I can do let me know!

>

>

> Colorado Springs

> [ ] Diagnosis

>

>

> Well...hello again. Got my diagnosis. I have failed fusion with

> flatback. I wasn't surprised about the flatback, but I was about

the

> failed fusion. Anyway...surgery is scheduled for October. They

will

> remove my Harrington rod which is no longer connected at the

bottom. It

> seems L3 & L4 are severely degenerated (causing the numbness in

my left

> leg). L3 and L4 will be fused with a cage replacing the disc,

and 2

> rods, 4 screws to hold it all together (and some bone from the

front of

> my hip & some BMP). Good news is that since I did not fuse at

L3/L4,

> the doc can create some more natural curve to my spine to

minimize

> flatback. Bad news is he goes in from the front this time and

from the

> back...long recovery. I will find out more details this

month...as I

> have many questions to get answered to get mentally ready for

this. I

> do have a supportive family and husband to get through this which

is

> good. I wanted to also thank you all for your input as I went

through

> this waiting period. God bless.

>

>

>

>

>

>

> scoliosis veterans * flatback sufferers * revision candidates

>

>

>

>

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Dear ,

Anything I can do to help if you want a second opinion just let me know. I'm up in Denver fairly often since my daughter lives up there and I take the Granddaughter everyother weekend. I could run the X-Rays to Kumar if you'd like, just let me know when they are available, no pressure, just trying to help. I know you have prior experience with your doc and feeling comfortable is most important. Just would be good to see if Kumar concurs with your doc on treatment, always good to have options.

On the pancreas, I know zero about that complication. Put it out to the other members, maybe they know this one.

When is your doc appointment in Wheatridge? My second surgeon Dr. O'Brien was located right next to Lutheran Hospital, been out there tons of times, so if you have surgery there I could come by and visit. You'll do great, and life with your young ones will be much improved when you are in a lot less pain. I'm pulling for you!

[ ] Diagnosis> > > Well...hello again. Got my diagnosis. I have failed fusion with > flatback. I wasn't surprised about the flatback, but I was about the > failed fusion. Anyway...surgery is scheduled for October. They will > remove my Harrington rod which is no longer connected at the bottom. It > seems L3 & L4 are severely degenerated (causing the numbness in my left > leg). L3 and L4 will be fused with a cage replacing the disc, and 2 > rods, 4 screws to hold it all together (and some bone from the front of > my hip & some BMP). Good news is that since I did not fuse at L3/L4, > the doc can create some more natural curve to my spine to minimize > flatback. Bad news is he goes in from the front this time and from the > back...long recovery. I will find out more details this month...as I > have many questions to get answered to get mentally ready for this. I > do have a supportive family and husband to get through this which is > good. I wanted to also thank you all for your input as I went through > this waiting period. God bless.> > > > > > > scoliosis veterans * flatback sufferers * revision candidates > > > >

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Thank you, , for the info about your doc.

It seems mid-October is going to be quite busy around here! I hope

all goes well for you, too!

kam

> ...Thank you. I am scheduled for October 17th at Lutheran

> Hospital in Wheatridge, provided I don't change my mind after my

> visit with the doctor in person. One thing I have read that I have

> questions on is inflamation of the pancreas after back surgery. Do

> you know anything about this? I didn't have it when I got my HR

at

> 14. I have had a 1/3 of my pancreas removed when I was 11. I gave

my

> doc the op reports so he is aware. I still may get a second

opinion

> from Kumar...I just might have to do it long distance (after my

> sister in Littleton picks up my xrays and does the transporting

for

> me).

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  • 1 month later...

,

What are your symptoms??? Also if you and boyfriend have the same thing you

would not need to worry about being intimate at this point unless one got

well and the other was still sick. GIna

-- Diagnosis

How does everyone know that they have yeast? I'm experiencing some of

the symptoms of cadidiasis, but every culture the doctors take comes

back normal and everyone keep stelling me I appear healthy but I don't

FEEL well and I would think that it's something autoimmune or

something tot hat effect, but my boyfriend has the same symptoms, so I

don't know what else to do. We've seen 9 doctors and a dentist between

the two of us, including an ENT, various dermatologists and ID. We're

afraid to touch each other.

How does everyone know how to treat themselves? Thanks

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I don't have any of the GI symptoms that everyone is mentioning, but we're both

having problems with our mouths.

We're worried about touching each other because sometimes I feel good, sometimes

he feels good, it varies. It started last winter and then we were ok all

summer, we had never been sexually intimate for the 9 months we've been

together, but recently I started um... doing things for him and now our problems

are resurfacing. I have a vaginal infection, my lips are dry and chapped, I have

a disgusting taste in my mouth that I can't describe, I wake up with white cakey

mucous in the corners of my mouth and sometimes my tongue burns. He has the

same problems and also he feels flushed a lot, like he ahs a fever but he

doesnt, pimples near the lips and other various little things that I can't

currently remember but that you wouldn't even consider worrying about if it

wasn't alll happening at the same time. All the doctors I've seen say my mouth

looks normal, I've had the full battery of STD testing and everyting is normal.

He's a virgin.

I'm at a loss, really. If this ISN'T yeast, which is entirely possible, I have

no idea what it could be and I don't know who else to turn to for an answer when

everyone keeps telling us we're fine. It's so frustrating.

" Kindscher (Charter) " <morningsunranch@...> wrote:

,

What are your symptoms??? Also if you and boyfriend have the same thing you

would not need to worry about being intimate at this point unless one got

well and the other was still sick. GIna

-- Diagnosis

How does everyone know that they have yeast? I'm experiencing some of

the symptoms of cadidiasis, but every culture the doctors take comes

back normal and everyone keep stelling me I appear healthy but I don't

FEEL well and I would think that it's something autoimmune or

something tot hat effect, but my boyfriend has the same symptoms, so I

don't know what else to do. We've seen 9 doctors and a dentist between

the two of us, including an ENT, various dermatologists and ID. We're

afraid to touch each other.

How does everyone know how to treat themselves? Thanks

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Hi ,

First of all I want to commend you on waiting on the sex with your boyfriend

that is a good idea. What you are describing does sound like oral thrush.

I don't know why the doctors cannot detect it. Have you done the simple spit

test first thing in the morning??? You can look up exactly how to do it

online, its very simple and it gives you pictures and everything to compare

to . You need to get your immune systems up and running better, balance the

bowels even though you have no bowel symptoms The bowels is where

everything starts. You need to change your diet to akaline foods, eliminate

all sugars, processed foods, high glycemic carbs. Just eat meat, vegies,

drink lime juice, coconut oil, and other coconut products, garlic, onions.

Its not that hard to get rid of when you change the diet and get the immune

system optimal.

-- Re: Diagnosis

I don't have any of the GI symptoms that everyone is mentioning, but we're

both having problems with our mouths.

We're worried about touching each other because sometimes I feel good,

sometimes he feels good, it varies. It started last winter and then we were

ok all summer, we had never been sexually intimate for the 9 months we've

been together, but recently I started um... doing things for him and now our

problems are resurfacing. I have a vaginal infection, my lips are dry and

chapped, I have a disgusting taste in my mouth that I can't describe, I wake

up with white cakey mucous in the corners of my mouth and sometimes my

tongue burns. He has the same problems and also he feels flushed a lot,

like he ahs a fever but he doesnt, pimples near the lips and other various

little things that I can't currently remember but that you wouldn't even

consider worrying about if it wasn't alll happening at the same time. All

the doctors I've seen say my mouth looks normal, I've had the full battery

of STD testing and everyting is normal. He's a virgin.

I'm at a loss, really. If this ISN'T yeast, which is entirely possible, I

have no idea what it could be and I don't know who else to turn to for an

answer when everyone keeps telling us we're fine. It's so frustrating.

" Kindscher (Charter) " <morningsunranch@...> wrote:

,

What are your symptoms??? Also if you and boyfriend have the same thing you

would not need to worry about being intimate at this point unless one got

well and the other was still sick. GIna

-------Original Message-------

" on the web.

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Thanks ,

I'm definitely going to do the spit test first thing in the morning.

The images of thrush that I've seen online don't really appear to

match what's going on in my mouth though, I don't have any white

patches, neither does he.

I just wish there was another way to get a concrete conclusion. It's

so weird that between the two of us, no one can come up with a

diagnosis. Is that common?

> ,

>

> What are your symptoms??? Also if you and boyfriend have the same

thing you

> would not need to worry about being intimate at this point unless

one got

> well and the other was still sick. GIna

>

> -------Original Message-------

>

> " on the web.

>

>

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yeast infection

back to: health guide | all healthnotes indexes | health concerns index

shop related departments

. yeast infections

. probiotics

search for more

. see results for 'yeast infection'

continue shopping

. all drugstore.com departments

Also indexed as: Candida vaginitis, Candidiasis (Vaginal), Vaginitis

(Candida)

See also: Chronic Candidiasis

a.. Introduction

b.. Checklist

c.. Symptoms

d.. Treatments

e.. Dietary changes

f.. Lifestyle changes

g.. Supplements

h.. Herbs

i.. References

Vaginal yeast infections are one of the most common reasons that women

consult healthcare professionals. Yeast infections result from an overgrowth of

a species of fungus called Candida albicans.

Checklist for Yeast Infection

Rating Nutritional Supplements Herbs

Lactobacillus acidophilus

Boric acid

Cinnamon

Echinacea

Oregano

Tea tree oil

See also: Homeopathic Remedies for Yeast Infection

Reliable and relatively consistent scientific data showing a

substantial health benefit.

Contradictory, insufficient, or preliminary studies suggesting a

health benefit or minimal health benefit.

An herb is primarily supported by traditional use, or the herb or

supplement has little scientific support and/or minimal health benefit.

What are the symptoms of yeast infection? Yeast infections are a type of

vaginitis. The hallmark symptom of a yeast infection is itching of the external

and internal genitalia, which is often associated with a white discharge that

can be thick and/or curdy (like cottage cheese). Severe infections lead to

inflammation of the tissue and subsequent redness, swelling, and even pinpoint

bleeding.

How is it treated? Yeast infections (vaginal candidiasis) can be treated

either with oral antifungal medications (e.g. fluconazole [Diflucan®]) or

topical antifungal medications (e.g., miconazole [Monistat®], clotrimazole

[Gyne-Lotrimin®]). Doctors often prescribe antifungal medications for insertion

into the vagina, either as a cream using a special applicator or as a

suppository, for three to seven nights. Antifungal cream may be applied

topically to the vulva (external genitalia) to help relieve itching.

Dietary changes that may be helpful: Some doctors believe that a

well-balanced diet low in fats, sugars, and refined foods is important for

preventing vaginal infections caused by Candida. In one preliminary trial,

avoidance of sugar, dairy products, and artificial sweeteners resulted in a

sharp reduction in the incidence and severity of Candida vaginitis.1 Many

doctors advise women who have a yeast infection (or are predisposed to such

infections), to limit their intake of sugar, fruit juices, and refined

carbohydrates. For persistent or recurrent infections, some doctors recommend

that fruit also be avoided.

Another trial found that dramatic increases in intake of several sugars in

healthy people partially increased stool sample levels of Candida, but only in

12 out of 28 people.2

Lifestyle changes that may be helpful: According to one study, yeast

infections are three times more common in women who wear nylon underwear or

tights, than in those who wear cotton underwear.3 Additional predisposing

factors for Candida infection include the use of antibiotics, oral

contraceptives, or adrenal corticosteroids (such as prednisone).

Underlying health conditions that may predispose someone to Candida

overgrowth include pregnancy, diabetes, and HIV infection. Allergies have also

been reported to promote the development of recurrent yeast vaginitis. In a

preliminary trial, when the allergens were avoided and the allergies treated,

the chronic recurrent yeast infections frequently resolved.4 In most cases,

sexual transmission does not play a role in yeast infection. However, in

persistent cases, sexual transmission should be considered, and the sexual

partner should be examined and treated.

Nutritional supplements that may be helpful: Lactobacillus acidophilus is

a species of friendly bacteria that is an integral part of normal vaginal flora.

Lactobacilli help to maintain the vaginal ecosystem by preventing the overgrowth

of unfriendly bacteria and Candida. Lactobacilli produce lactic acid, which acts

like a natural antibiotic.

Lactobacillus acidophilus can be taken orally in the form of acidophilus

yogurt, or in capsules or powder. It can also be administered vaginally. In a

controlled trial, women who consumed 8 ounces of Lactobacillus

acidophilus-containing yogurt per day had a threefold decrease in the incidence

of vaginal yeast infections and a reduction in the frequency of Candida

colonization in the vagina.5 In another trial, women who were predisposed to

vaginal Candida infection because they were HIV-positive received either

Lactobacillus acidophilus vaginal suppositories, the antifungal drug,

clotrimazole (e.g., Gyne-Lotrimin®), or placebo weekly for 21 months.6 Compared

to those receiving placebo, women receiving Lactobacillus acidophilus

suppositories had only half the risk of experiencing an episode of Candida

vaginitis-a result almost as good as that achieved with clotrimazole.

Many women find relief using an acidophilus-containing yogurt douche daily

for a few days or weeks, depending on the severity of the infection.7 Three

capsules of acidophilus or one-quarter teaspoon of powder can be taken orally

one to three times daily. Acidophilus can also be taken preventively during

antibiotic use to reduce the risk of Candida vaginitis.8 9

Boric acid capsules inserted in the vagina have been used successfully as

a treatment for vaginal yeast infections. One study demonstrated that 85% of

women who used boric acid vaginal suppositories were cured of chronic recurring

yeast vaginitis.10 These women had all previously failed to respond to treatment

with conventional antifungal medicines. The suppositories, which contained 600

mg of boric acid, were inserted vaginally twice a day for two weeks, then

continued for an additional two weeks if necessary. Boric acid should never be

swallowed.

Are there any side effects or interactions? Refer to the individual

supplement for information about any side effects or interactions.

Herbs that may be helpful: A small, preliminary trial found that a

mouthwash with diluted tea tree oil was effective in decreasing the growth of

Candida albicans and in improving symptoms in AIDS patients with oral Candida

infections (thrush) that had not responded to drug therapy.11 People in the

study took 15 ml of the oral solution (dilution of tea tree oil was not given)

four times per day and were instructed to swish it in their mouth for 30 to 60

seconds and then spit it out. For use of tea tree oil as a mouthwash, one should

not exceed a 5% dilution and should be extremely careful not to swallow the

solution.

Many doctors recommend that people with recurrent yeast infections take

measures to support their immune system. Echinacea, which has the capacity to

enhance immune function, is often used by people who suffer from recurrent

infections. In one study, women who took echinacea experienced a 43% decline in

the recurrence rate of yeast infections.12

The essential oil of cinnamon contains various chemicals that are believed

to be responsible for cinnamon's medicinal effects. Important among these

compounds are eugenol and cinnamaldehyde. Cinnamaldehyde and cinnamon oil vapors

exhibit extremely potent antifungal properties in test tubes.13 In a preliminary

study in people with AIDS, topical application of cinnamon oil was effective

against oral thrush.14

A test tube study demonstrated that oil of oregano, and an extract in the

oil called carvacrol in particular, inhibited the growth of Candida albicans far

more effectively than a commonly employed antifungal agent called calcium

magnesium caprylate.15 However, clinical studies are needed to confirm these

actions in humans.

Love and Light

Blessings too!

-Blakeslee

Http://www.loveandlight.com

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Re: Diagnosis

> ,

>

> What are your symptoms??? Also if you and boyfriend have the same thing you

> would not need to worry about being intimate at this point unless one got

> well and the other was still sick. GIna

>

On the other hand there are many strains of fungus and bacteria. It's possible

one has more potent strains that could be spread to the other making the

other worse.

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Both husband and I went for years without diagnosis of our illnesses. It

turns out we had late stage lyme disease. Having Candida was just one of the

many symptoms that went with that. There are just too many illnesses and not

very good diagnostics. That is why I believe that supporting the bodies

immune system and getting the bowels healthy will make a huge difference no

matter what you have.

-- Re: Diagnosis

Thanks ,

I'm definitely going to do the spit test first thing in the morning.

The images of thrush that I've seen online don't really appear to

match what's going on in my mouth though, I don't have any white

patches, neither does he.

I just wish there was another way to get a concrete conclusion. It's

so weird that between the two of us, no one can come up with a

diagnosis. Is that common?

--- In candidiasis , " Kindscher (Charter) "

<

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Sorry to hear you have to make these decisions alone and that your

hubby is in Iraq! Hopefully we can make you feel not so alone in this

since we've all been there!

I'm not sure why your doc would write that as the diagnosis instead of

just plagio, but that is the characteristics of plagio.

Where do you live? Is there a helmet provider in your area? Check

out our Database section, there is a helmet/band locator in there, you

just type in your state at the top and it will bring up all the

providers near you.

Lacy

Waydon 1 year

DOCgrad

www.waydonsnoodle.com

>

> My 5.5 month old son saw the pediatric plastic surgeon today about the

> flat spot on the side of his head. The doctor said it was cause from

> laying too much on that one side. His diagnosis was moderate and

> about a 6 on a scale of 1-10. The doctor said that he needs a

> helmet. On the paperwork that the doctor gave me to send to the

> insurance he had checked that the condition was " anomilies of the face

> and skull bones " instead of " plagiocephaly " . What is the difference?

>

> Also, the insurace we have is Tricare. Does anyone have any

> experience with getting them to pay?

>

> All of this is new to me and my husband is in Iraq. It is difficult

> not having him here to help me make decisions. I would appreciate any

> advice you can give me.

>

> Thanks in advance!

> Missy

>

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Sorry to hear you have to make these decisions alone and that your

hubby is in Iraq! Hopefully we can make you feel not so alone in this

since we've all been there!

I'm not sure why your doc would write that as the diagnosis instead of

just plagio, but that is the characteristics of plagio.

Where do you live? Is there a helmet provider in your area? Check

out our Database section, there is a helmet/band locator in there, you

just type in your state at the top and it will bring up all the

providers near you.

Lacy

Waydon 1 year

DOCgrad

www.waydonsnoodle.com

>

> My 5.5 month old son saw the pediatric plastic surgeon today about the

> flat spot on the side of his head. The doctor said it was cause from

> laying too much on that one side. His diagnosis was moderate and

> about a 6 on a scale of 1-10. The doctor said that he needs a

> helmet. On the paperwork that the doctor gave me to send to the

> insurance he had checked that the condition was " anomilies of the face

> and skull bones " instead of " plagiocephaly " . What is the difference?

>

> Also, the insurace we have is Tricare. Does anyone have any

> experience with getting them to pay?

>

> All of this is new to me and my husband is in Iraq. It is difficult

> not having him here to help me make decisions. I would appreciate any

> advice you can give me.

>

> Thanks in advance!

> Missy

>

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Missy,Welcome. I know this hard and I feel for you not having hubby with you to help. God Bless him, and tell him I said Thank You. The diagnosis is the same as plagiocephaly, just worded different. Maybe that will help with insurance,LOL. Have you found a provider for the helemt or band yet? I cannot help much on the Tricare issue, but we have a couple people right now working on the same issue, so maybe you can all work together. There is an insurance database here where you can look up who got Tricare to pay and how.Please know that you are doing the right thing by seeking treatment for your son. I am not sure who you will be using, my son wore the Doc Bnad by Cranial Technologies and I made him a website to help others. You can take a look at it, to get an idea of how the treatment process works and what kind of results you can expect. I have lots of pictures and talk about the associated risks, and the ups and downs of the journey you are about to embark on. It's called My Banded Baby and I hope it helps. You stay with us here and we will try our best to provide the support you want and need during this time. CAROLG >> My 5.5 month old son saw the pediatric plastic surgeon today about the > flat spot on the side of his head. The doctor said it was cause from > laying too much on that one side. His diagnosis was moderate and > about a 6 on a scale of 1-10. The doctor said that he needs a > helmet. On the paperwork that the doctor gave me to send to the > insurance he had checked that the condition was "anomilies of the face > and skull bones" instead of "plagiocephaly". What is the difference?> > Also, the insurace we have is Tricare. Does anyone have any > experience with getting them to pay? > > All of this is new to me and my husband is in Iraq. It is difficult > not having him here to help me make decisions. I would appreciate any > advice you can give me.> > Thanks in advance!> Missy>

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