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Hi Fellow Groupies

I went to the doctor yesterday and he suspects a stomach or esophogus ulcer.

He did a rectal, ick, and found blood in my stools. So now I have to get

that horrible test done with the scope thing. One down the mouth for the

stomach and one up the rectum for the intestines. the only good thing about

them is they say they will knock me out first.

I kept asking him about candida but never got a response. He wants me to do

a blood test for celiac disease. Sorry but I believe candida and parasites

are the real problem. I am going to follow up with another doctor who sends

patients to an acupuncturist and see if she knows anything about candida. I

won't give up.

When he did the rectal he took sample of my stools and put them on this

cardboard thing, that is how he found the blood in the stools. He said it

could be from the ulcer but wants to make sure. Question? Isn't this what

they use to send to the lab to do candida tests? He has a horrible bed side

manner and it was very late so he didn't answer all of my questions. I hate

doctors who think they are gods. Sorry but just tired of them not listening.

I will call the nurse tomorrow and see if I can get an answer out of her.

He didn't even refill my prescription for the reglan but told me to keep

taking it. The other med we talked about is prevacid which he said works

great for ulcers, keeps the acid down and gets rid of the feeling like I am

having a heart attack heart burn.

This is so slow and when they don't talk and explain things it is so

frustrating. I might try some parastie formula now that I can keep food down

but will go very slow. The stomach is one problem but the candida and

parasties are another. I belong to another onelist group for benzo's and

several of us going off xanax, etc. developed not only candida but parasites.

The ones doing the parasite cleanse say they never felt better. They also

follow the candida diet and did the candida cleanse but the parasite cleanse

is where they got the best results.

I have to keep reminding myself to go slow becuase I usually jump in and

tackle these problems with lots of energy but this time my body just can't

handle it. Everytime I take anything for candida I get worse symptoms right

off the bat.

Thanks to all of you who have taken the time to write to me and offer me your

support. Without it I would be much worse off. Let me know how everyone is

doing and I will keep you posted also.

Thanks again

brenda

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In a message dated 11/11/99 9:04:09 PM Central Standard Time,

1005@... writes:

<< I hate

doctors who think they are gods.

~~~~~~~~~~~~

It's called the god syndrome....many have it

~~~~~~~~~

They also

follow the candida diet and did the candida cleanse but the parasite cleanse

is where they got the best results.

~~~~~~~~~~~~~~~~~~~

what is a candida cleanse?

~~~~~~~~~~~~~~~~~~~

Thanks again

brenda

~~~~~~~~~~~~~~~~~

glad to " see " your feeling better!

Edith

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Hi , How about trying water for the ulcer?

When it hurts take a glass every 15 " This is

recommended in the book Your Body's many cries for

WATER. Aloe juice is also of benefit.

=====

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You are right. I feel like you do also. Myra

Re: Re: doctor

> From: Es9525@...

>

> In a message dated 11/11/99 9:04:09 PM Central Standard Time,

> 1005@... writes:

>

> << I hate

> doctors who think they are gods.

> ~~~~~~~~~~~~

> It's called the god syndrome....many have it

>

> ~~~~~~~~~

>

> They also

> follow the candida diet and did the candida cleanse but the parasite

cleanse

> is where they got the best results..

> ~~~~~~~~~~~~~~~~~~~

> what is a candida cleanse?

> ~~~~~~~~~~~~~~~~~~~

>

> Thanks again

> brenda

> ~~~~~~~~~~~~~~~~~

>

> glad to " see " your feeling better!

> Edith

>

>

> > _

>

> Subscription URL: /subscribe.cgi/candidiasis

>

>

> Send blank message to this e-mail address if you want to:

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> TO UNSUBSCRIBE !!!!!!!!! :

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  • 5 months later...
Guest guest

Hi Alison,

We live in Salem, VA (in the Roanoke Valley) and my daughter Kelsey was

recently diagnosed with poly JRA. Her Pediatric Rheumatologist is Dr. Kathy

Amoroso, the only ped. rheum. in our area. She is WONDERFUL! What part of

VA are you in? I have been hoping to find someone else from VA. I don't

know how close you are to Roanoke/Salem, but if I can help in any way please

let me know! Hope to hear from you soon,

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Guest guest

We are in Fairfax County, Va and see Lipnick in Bethesda, Md.

has been his patient for over 5 years, and we absolutely love

him!! If you want more info, let me know.

Liz

alisonearly@... wrote:

>

> Is there anyone in VA that has JRA? I was wondering what doctor that they

> see.

>

> ------------------------------------------------------------------------

> Your high school sweetheart-where is he now? With 4.4 million alumni

> already registered at Classmates.com, there's a good chance you'll

> find her here. Visit your online high school class reunion at:

> 1/3139/1/_/524922/_/956327332/

> ------------------------------------------------------------------------

>

> For links to websites with JRA info visit:

> http://www.geocities.com/Heartland/Village/8414/Links.html

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Guest guest

We live in Greene Co..That near Charlottesville Va. My son goes to the UVA

hospital. He see Dr. Keasler, he has been seeing he for 13 years since he

has been diagnose with JRA he is a great DR also. I was just wondering what

other good dr. that are out there.

Thank for your reply

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Guest guest

Hi Alison:

I am also in McLean Virginia and we have seen dr Goldmuntz, Dr Patience

White (both at Children's Hospital in DC but they have sattelite offices on

Rt 50 VA) and Dr Lipnick in Bethesda. They are all very good drs. My

daughter has Polyjra (she will be 4 in june and she has had it since she was

18 months). Take care....

________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com

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  • 3 months later...
Guest guest

I am looking for a LLD in the San Diego and Orange

County area. Any suggestions would be greatly

appreciated.

__________________________________________________

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  • 7 months later...
Guest guest

here's a little list of 'candida types'...

There is over 150 species, common one include :

Candida albicans

Candida dubliniensis

Candida famata

Candida glabrata

Candida guilliermondii

Candida humicola

Candida krusei

Candida lambica

Candida lipolytica

Candida lusitaniae

Candida parapsilosis

Candida pseudotropicalis

Candida rugosa

Candida stellatoidea

Candida tropicalis

Candida zeylanoides

wendy

doctor

Hi everyone

Well I had an exciting day today, but have to keep this brief as I feel

exhausted.

I went to see a guy who was recommended to me today about my candida. I

felt between going yellow and not really knowing what I was doing with all

my pills etc, I would go see him.

He had this machine that tested you via frequencies for heaps of stuff,

including candida. I tested positive for candida, but NOT candida albicans.

It was another form of fungus. I was amazed at this, after reading one of

the letters today on the list that said about another woman that found this

as well.

He wants me to stick to the diet of course, but I am not allowed to take

other vitamins for awhile as they might interfere with the treatment. I

don't think Molybdenum would be a worry, he mainly meant big doses of them.

I cannot remember which one he said I had (candida) but he said he doesn't

usually come across this one. I thought " , maybe that's why I have

never been able to get rid of it! " . So I am feeling really positive, as he

said he has a good success rate with candida. He wants to get the candida

under control first, then work on the hormonal/allergies side of things. It

will be interesting to see what happens. I am still cautious, but feeling

like I am o.k. with what he is suggesting. Is anyone familiar with these

frequency machines that send out a frequency to a homeopathic modulation?

Hope I hear from someone who has tried this method, but as he explained,

treatments work better on some people than others, and it may take a bit of

time finding the right one. Hey, he doesn't cost a fortune so I am o.k.

with that. I liked him because he was sensible and make sense. Some I have

been to........we won't go there.

Love to everyone

p.s. Did you know there are 2 New Zelanders on the list now....

Send blank message to candidiasis-unsubscribeonelist if you want to

UNSUBSCRIBE !

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Guest guest

I think it was Candida Astragillis? or something like that - know anything

about that one?

doctor

>

>

> Hi everyone

>

> Well I had an exciting day today, but have to keep this brief as I feel

> exhausted.

>

> I went to see a guy who was recommended to me today about my candida. I

> felt between going yellow and not really knowing what I was doing with all

> my pills etc, I would go see him.

>

> He had this machine that tested you via frequencies for heaps of stuff,

> including candida. I tested positive for candida, but NOT candida

albicans.

> It was another form of fungus. I was amazed at this, after reading one of

> the letters today on the list that said about another woman that found

this

> as well.

>

> He wants me to stick to the diet of course, but I am not allowed to take

> other vitamins for awhile as they might interfere with the treatment. I

> don't think Molybdenum would be a worry, he mainly meant big doses of

them.

>

> I cannot remember which one he said I had (candida) but he said he doesn't

> usually come across this one. I thought " , maybe that's why I have

> never been able to get rid of it! " . So I am feeling really positive, as

he

> said he has a good success rate with candida. He wants to get the candida

> under control first, then work on the hormonal/allergies side of things.

It

> will be interesting to see what happens. I am still cautious, but feeling

> like I am o.k. with what he is suggesting. Is anyone familiar with these

> frequency machines that send out a frequency to a homeopathic modulation?

>

> Hope I hear from someone who has tried this method, but as he explained,

> treatments work better on some people than others, and it may take a bit

of

> time finding the right one. Hey, he doesn't cost a fortune so I am o.k.

> with that. I liked him because he was sensible and make sense. Some I

have

> been to........we won't go there.

>

> Love to everyone

>

>

>

> p.s. Did you know there are 2 New Zelanders on the list now....

>

>

>

> Send blank message to candidiasis-unsubscribeonelist if you want to

> UNSUBSCRIBE !

>

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  • 9 months later...

Hi and welcome

The thought is daunting but it's not too bad taking one pill a day.

You get used to it. Good to hear your doctor is carefully monitoring

your dosage and it's effects.

Kate

cbdevilangel1516 wrote:

Hi i went the 2 to get blood work and my tsh was

35 its gone down but

still not normal hes upping my med. to 100 mg . and i go back the 19

of next mon. for blood work again hope things get better he said i

might have to take this for the rest of my life . HOPE NOT!

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yeah i know but i have to take 2 other pills too

Kate Fraser <Fraserk@...> wrote: Hi and welcome The thought is daunting but it's not too bad taking one pill a day. You get used to it. Good to hear your doctor is carefully monitoring your dosage and it's effects. Kate cbdevilangel1516 wrote: Hi i went the 2 to get blood work and my tsh was 35 its gone down but still not normal hes upping my med. to 100 mg . and i go back the 19 of next mon. for blood work again hope things get better he said i might have to take this for the rest of my life . HOPE NOT!

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LOL! Three pills? That's nothing compared to what I used to

take trying to balance those blasted individual supplements! I know

what you mean, though. I wouldn't want to take a drug every day for

the rest of my life either, if there was another choice. Look into

your other choices........you'll be very glad that you did.

Donna

http://trak.to/life

www.reliv.com

Take control of your health!

wrote:

yeah i know but i have to take 2 other pills too

Kate Fraser <Fraserk@...> wrote:

Hi

and welcome

The thought is daunting but it's not too bad taking one pill a day.

You get used to it. Good to hear your doctor is carefully monitoring

your dosage and it's effects.

Kate

cbdevilangel1516 wrote:

Hi i went the 2 to get blood work and my tsh was

35 its gone down but

still not normal hes upping my med. to 100 mg . and i go back the 19

of next mon. for blood work again hope things get better he said i

might have to take this for the rest of my life . HOPE NOT!

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You got it Donna

My daily intake is 6 pills minimum. That includes no supplements

or vitamins. With those added in I range up to 12 pills daily.

Then if I am experiencing muscle spasms, or joint inflamination, the count

goes up again. And for migraines...And so on.

I know the concept can be overwhelming, but it really isn't to bad

even if it's 3 pills daily. Hang in there and it will get better.

We all adapt. :-)

Kate

Donna wrote:

LOL! Three pills? That's nothing compared

to what I used to take

trying to balance those blasted individual supplements! I know

what you

mean, though. I wouldn't want to take a drug every day for the

rest of

my life either, if there was another choice. Look into your other

choices........you'll be very glad that you did.

Donna

http://trak.to/life

www.reliv.com

Take control of your health!

wrote:

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  • 5 months later...
Guest guest

> Hello group,

> I haven't written in awhile but I was wondering if anyone has a

> way to either e-mail/ write/ call Dr. Cunningham- Rundles?

Yup...

Charlotte Cunningham-Rundles, MD., PhD.

The Mount Sinai Medical Center

1425 Madison Avenue

New York, NY 10029-6574

PH: 212-659-9268

Fax: 212-987-5593

Also if you look up the Mount Sinai Hospital on the web, you will find

her information there too, that is how I found her.

Diane, Mom to Kody

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  • 4 weeks later...
Guest guest

Jeannette,

I do not know how your health care system works but find a new doctor if you

can. I can't believe a doctor would be so rude. Hang in there and keep

looking.

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  • 10 months later...
Guest guest

Donna--

See if you can track down Deb Grossett through TDMHMR. She's a psychologist

and a BCBA and may be able to help with your situation. She's got many

years of experience working with conditions that may be co-morbid with ASD.

I thought I had her contact number. Let me check around and see what I can

find.

CS

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Guest guest

Donna--

See if you can track down Deb Grossett through TDMHMR. She's a psychologist

and a BCBA and may be able to help with your situation. She's got many

years of experience working with conditions that may be co-morbid with ASD.

I thought I had her contact number. Let me check around and see what I can

find.

CS

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  • 10 months later...
Guest guest

DJ -- I don't know about the TX docs (besides that they're at Baylor), but

the doc that I would recommend if you decide to go to Cleveland is Dr.

Vaezi -- here's his info:

http://www.clevelandclinic.org/staff/getstaff.asp?StaffId=3186

The hospital in Cleveland is " The Cleveland Clinic " -- it's kinda like the

Mayo Clinic, only just not as well-known. They are the #2 rated hospital

in the country for GI disorders, and they treat more achalasia per year

than any other hospital in the USA, and probably more than any hospital in

the entire world.

It's actually an entire 'campus' of medical buildings... doctors' offices,

specialty clinics, regular " hospital " buildings, diagnostics, etc. Many

of the newest buildings have " skyways " connecting them, so you don't have

to go outside and across streets to get from one building to another.

They actually even have free shuttle buses that run a route all around the

campus, so that if you need to see a doctor in his office in one building,

then go have some tests done in another building, and then go see another

doctor in yet another building, you only have to park your car once and

they will tell you how to get from point A to point B. Everyone is very

helpful, and they even have an " internal " shuttle bus for those who can't

walk (like the " golf cart " trolleys they use in airports, etc.)

They do tons of research at The Cleveland Clinic (TCC) and are very highly

regarded in the medical community. I have no clue why they're not a

household name like Mayo Clinic... they're less than 4 hours from me, and

I had never heard of them until I joined this group a couple years ago!

Debbi in Michigan

> Thank you for all of the responses for finding help. Someone

> mentioned a doctor at Waco that was not far from me in Okla. Does

> anyone have his/her name and what hospital he/she is at. Also what

> is the name of the doctor in Cleveland and what hospital is it. Any

> help is appreciated, and just knowing that there is hope of getting

> better is nice to know.

>

> Dj

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