Diagnosis

[Guest guest]

My dil's Father has just been diagnosed with squamous cell carcinoma (sp?).

It is a fist size tumor in his lung and apparently elsewhere. Does anyone

have info on this kind of cancer?

thanks - Annette

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[Guest guest]

In a message dated 3/16/01 6:58:23 PM Eastern Standard Time, mmgg@... writes:

my older, beloved sister would somehow drag me on top of the house and drop me off.

Hi Gail,

I had to laugh at that one.....sounds like my older sisters and me with my younger sisters.....what fun it was.

Dotsie

[Guest guest]

In a message dated 3/16/01 11:19:13 AM Eastern Standard Time, jcald@... writes:

The pulser is due to arrive next week along with the Colodial Silver--hopefully this will make a difference.

Hi Joan,

I hope this makes the difference for you because it must be discouraging that the headaches returned after all your hard work. I was calculating the amount of hours you've been using the blood electrifier and I figure that you're up to 70 hours at most - did I figure this right? I know that the literature says at least 90 hours and that's with the colloidal silver and the magnetic pulser.

Did the Pounds Hill Clinic have any healing suggestions for your diagnosis?

I'd like to hear more.

<<Does anyone use BE for 2 hours in the a.m. and 1 hour in the afternoon? I have when I feel the headache return.>>

You can use it as much as you feel that you can tolerate.

<<As of one week (at the suggestion of this group) I received colostrum taking 2,000 mg 3 x a day.  Unfortunately this dosage makes me tired, has that affect happened to anyone else? >>

I'm taking the colostrum now and I haven't noticed being tired. I just started taking a product called Prime One Adaptogens and you might want to read about it:

http://www.microenergetics.com/PRIME%20ONE%20MORE%20INFORMATION.htm

I'll let you know how it works.

Dotsie

What are adaptogens?

Adaptogens are biologically active substances found in certain herbs and plants that help the body and mind adapt to the changes and stress of life.

The adaptogens in Prime One cause a change in the stress reaction. The response is sharper, but the production of adrenaline slows down and there is more left in reserve. You are not as quickly exhausted - and fewer hormones are needed to achieve the same effect.

[Guest guest]

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

Joan Caldwell Wrote:

"Questions re: BE What I don't understand is why the BE seems to be loosing its ability? Does anyone use BE for 2 hours in the a.m. and 1 hour in the afternoon? I have when I feel the headache return. "

Hi Joan,

What a story. I'm so glad to hear you are improving! I have split up the time I BE simple because I get busy and need to go someplace. For me, often I'll do anywhere from 1/2 hour to 3 hours at a time. If I only did a small amount of time before I had to go somewhere, I'd continue in the pm. I found the more I did it, the better I felt. However, even 1/2 hour was nice. I have no idea why it wouldn't be working as well for you as before. Maybe try using it 2 or 3 or 4 times a day for a short time and see what happens. I seem to have the best results whenever I use it about 3 times a day, like 1 hour, then 1 and 1/2 hours, then another 1/2 hour to an hour later on in the day. I don't know why it works well for me like that. Then there are days when I don't use it at all. They suggest you use it 2 hours a day for the blood to circulate throughout the body. Don't forget it increases the ATP by 500% so you get the added energy.

"Questions re: Colostrum As of one week (at the suggestion of this group) I received colostrum taking 2,000 mg 3 x a day. Unfortunately this dosage makes me tired, has that affect happened to anyone else?" I had a very hard time, when I first started on the colostrum. I wanted to sleep all day long, and it was a very pleasant sleep. But lets face it, one can't sleep their life away. I had to cut way down and only take it at night. I still only take it at night and only take 500mg. I was able to up the dosage and take it during the day, but this seems to work the best for me. It took me around a couple of months before I adjusted to the colostrum. It was a long time.

"I fear, reducing the colostrum milligram intake because I need to get rid of the Fibromyalgia pain. I seems to be subsiding, but not completely. I believe more time is needed to reverse years of inefficiency."

always says it was the homozon and H202 that has helped his fibromyalgia more than anything else. If I take too much of the homozon it makes me tired and depressed. I find I can only take 1 tsp. a day. You might try and take a very small amount. You'd still be getting benefits from it.

"I realize that this message is long and full of questions, but through education I believe healing can begin."

I don't mind the length or the questions. Sometimes I myself have a lot of questions, but won't ask cause I feel they're so stupid. But there are a lot of really educated people on these lists, and they've always been nothing but kind to me. It seems like there is a real desire to help one another, and I really appreciate the kindheartedness here. I like that.

"If anyone should want to inquire re: Carol Everett, let me know and I'll be glad to share my experience."

I just might do that. Why don't you email me privately? It's so interesting about the fall. I've heard where CFIDS and fibromyalgia might be a neurological problem of compressed vertebra at the base of the brain caused by a fall or illness. They are actually doing brain surgery for it!

To much for me, tho. I'm a big time chicken! So interesting tho. The talk in my family is when I was not much more than a toddler, my older, beloved sister would somehow drag me on top of the house and drop me off. Sisterly love and all, she meant me no harm. It was just a game to her. Don't no if it had anything to do with anything or not.

Again, so glad to hear of your improvement.

God-speed,

Gail

[Guest guest]

Just my opinion, but I would say that if it's possible to obtain a

diagnosis, then you should. (Not all cases of dwarfism can be

diagnosed.) Knowing the type is important in terms of what medical

complications may arise as your granddaughter gets older, and what

sorts of things she ought to be screened for now. For instance, if

she has achondroplasia, the most common kind (half of all cases), she

should be screened for obstructive apnea, central apnea, and

hydrocephalus -- none of which is common, but all of which *can*

occur, and which can be pretty serious.

For more information, go to LPA Online and read " Frequently Asked Questions. "

Dan Kennedy

Internet services coordinator

Little People of America, Inc.

http://www.lpaonline.org

==================================================

Date: Wed, 6 Jun 2001 22:07:21 -0400

From: " Myrna " <anana47@...>

Subject: diagnosis

My 2 1/2 year old grandaughter who is a lp lives with me.

I am her primary care taker.

She has yet to be diagnosed, though we have had a

genetics doctor see her. He took xrays, blood and urine samples;

yet he has not came up with anything.

Our grandaughter is the only lp in our family and many people I

associate with doesn't understand my desire to see her diagnosed.

I believe it is very important! Kiberly Calhoun (on this list) gave me

info to get in touch with Dr. i. I am in the process of doing this.

My question to you is-- is it important for us to know about her

diagnoses or should I drop it.

Thanks for imput.

[Guest guest]

Hi Jody

In most cases, you'd be sent along for a CT scan to confirm the diagnosis and to try and determine how far the disease has spread.It isn't always done though - if the ctoma is reasonably large and especially if the eardrum is down, it would be pretty easy for a surgeon to identitfy. Hearing loss and other symptoms are also an indication. Always helps to get a second opinion if you are really not sure.

I always post this link of an actual ctoma. If will give you some idea what you're dealing with. It is a bit gruesome, so if you are at all bothered by such images then I'd recommend that you don't look at it.

http://www.ghorayeb.com/Cholesteatoma.html

Phil

Was recently told by ear specialist that I have a cholesteatoma. Have had problems with chronic middle ear infections for years and had a hole in my ear drum.Went back to the specialist as ringing in ear has become louder (and with two tones!) and the hearing has deminished (practically non-exsistant)He cleaned out ear and said that there was a cholesteatoma and will need surgery....is it really that simple? Can doctors tell just by looking in the ear? Would certainly hate to have an unneeded op!!! Feeling a little anxious...Jody

---Outgoing mail is certified Virus Free.Checked by AVG anti-virus system (http://www.grisoft.com).Version: 6.0.745 / Virus Database: 497 - Release Date: 27/08/04

[Guest guest]

Yes...well Phil...that is a wee bit gruesome! Thanks, it is

interesting to see what the thing looks like.

Will go and get that second opinion, as specialist just said there is

an indent in eardrum where hole once was...and was too easy to get

appointment with him. I think a good specialist should be booked up

tight!!lol

Thanks for your help...and after watching the posts over the last few

days, I am brought back to earth with thankfulness that it is me with

the problem and not one of my children.

Jody

Down under.

<I always post this link of an actual ctoma. If will give you some

idea what you're dealing with. It is a bit gruesome, so if you are at

all bothered by such images then I'd recommend that you don't look at

it.

[Guest guest]

You will find some -Silver resources online at:

<http://www.lpaonline.org/resources_dwarftypes.html>

=====

Dan Kennedy

Editor, LPA Online

Little People of America, Inc.

<http://www.lpaonline.org>

On 2/21/05 4:26 PM, " kemerlings " <kemerlings@...> wrote:

> 31 years ago when i was bron in rural Wisconsin; a doctor diagnosed

> me with " Russel Silver Dwarfing Syndrome " - why can't i find any info

> regarding this diagnosis? also, is there a newer/better name given to

> Russel Silver syndrome? somebody help me get connected please!

> MK

[Guest guest]

Hi MK,

I also have Silver Syndrome (RSS), and I just wanted to let you know

that there are two RSS specific groups that are available through . One

is the RSS Support group, which is a list of parents of children with RSS and a

few adults who have RSS. The other is called RSS People and is restricted to

adults with RSS only. I'm not sure of the exact addresses to subscribe to each

list, but if you go to the homepage and search for both of them,

they'll come up. I hope to see you on one or both lists soon! Please feel

free to email me privately if I can be of any further assistance.

~Hillary

[Guest guest]

Yes, I do recall this WAS used in the past...why do you ask?

In a message dated 4/18/2007 9:54:49 P.M. Central Daylight Time, cathynesbit@... writes:

Has anyone ever heard of a diagnosis "Static Encephalopathy" being used as a "catch-all" term, maybe not recently but perhaps about 10 years ago?

Thanks

Ahhh...imagining that irresistible "new car" smell?Check out new cars at Autos.

See what's free at AOL.com.

[Guest guest]

My daughter Kim, now 22 years old was given that diagnosis several years back. I am an RN, and never really understood what they meant by it. Somewhere long the line that diagnosis was removed from her long list of diagnosis. Richter

diagnosis

Has anyone ever heard of a diagnosis "Static Encephalopathy" being used as a "catch-all" term, maybe not recently but perhaps about 10 years ago?

Thanks

Ahhh...imagining that irresistible "new car" smell?Check out new cars at Autos.

[Guest guest]

My first thought is that you can get another psychiatrist, who will fill out a

form.

What in the MD's report is inaccurate? Is there a possibility that the MD's

staff pulled out the wrong file, and that someone else's info got entered on

your grardson's form?

I'd approach the MD (by phone if possible) and ask about this, approaching the

situation as if there were some error, compared to what the MD had said in

interactions with you all at your grandson's visits.

-Gail

Bergman <sbergman@...> wrote:

Has anyone ever had a doctor give incorrect and damaging information

regarding a disability? What can be done about it?

My grandson was seeing a psychiatrist last year who filled out a

physicians form for SSI. He was denied. The information the doctor

gave is all incorrect. I have made an appointment to see this doctor to

correct the information, but am afraid the damage cannot be repaired.

[Guest guest]

>

> I haven't ever been formerly diagnosed with Candida but do have

issues

> with overproduction of yeast (chronic yeast infections), and suffer

> also from chronic headaches and acid reflux disease, both of which

I

> have recently heard can be caused by Candida. Any suggestions on

where

> I would start to decide if this could be a cause, and how I would

begin

> to effectively treat it?

==>Hi. Welcome to our group. What is your name please? The place

to start is by reading and learning so you know what you need to do

in order to turn your health around. Start with the article emailed

to you when you joined " Candida Basic by Bee " or read my more

extensive article " How to Successfully Overcome Candida " ;

http://www.healingnaturallybybee.com/articles/menu2_8.php

Also print out the 2nd article on that menu: " Curing Candida, How to

Get Started. "

Once you've read please get back to us with any questions and

concerns. We are here to help you.

The best in health, Bee

[Guest guest]

>

> hi bee,

>

> i was wondering what are the first symtoms of candida?

==>Hi. Welcome to our group. What is your name please? The first

symptoms vary from person to person, and there are tons of them! Most

people don't realize it until they've had it for years. With some

people the first symptom is intolerance to alcohol or sugars, or

toenail fungus, or problems with the genitals in both sexes, or

migraines, or ear infections, or white tongue or upset stomach, etc.,

etc. and the list goes on forever.

Bee

[Guest guest]

get a second opinion.. Then based on your age I think you have to consider

it..

: )

Tom

In a message dated 10/28/2009 2:36:59 P.M. Mountain Standard Time,

ljorichardson0912@... writes:

I was just diagnosed with herniated nucleus pulposus c4-5 and they want to

do surgery. I just had surgery in Feb for c 6-7 and I have also had c 5-6

fused also.

anyone have any suggestions on what to do?

Thank you

__________________________________________________________

Windows 7: Simplify your PC. Learn more.

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[Non-text portions of this message have been removed]

[Guest guest]

I'm sorry you've been through so much already. Were you having symptoms other

than pain? I have tons of herniations but go to surgeons who aren't so quick to

cut on every person they see with disc problems. They do surgery to relieve

compressed nerves or spinal cord compression that is causing symptoms other than

pain.

None of the spine surgeons I've seen, who wanted to do these invasive surgeries,

would guarantee that my pain would be relieved but some said I needed to have

the area stabilized. I tend to go with the ones who know surgery is the only

answer which means a real need in order to preserve nerve function.

I've heard a lot of negative stories and " failed surgeries " when it comes to the

spine.

I'm the type that gets second and third opinions from surgeons who have a good

reputation and affiliated with a good hospital before deciding that surgery is

the best way to treat the problem. Unless, of course, it's an emergency.

Jennette

________________________________

From: <ljorichardson0912@...>

spinal problems ;

neck pain

Sent: Wed, October 28, 2009 5:36:16 PM

Subject: Diagnosis

I was just diagnosed with herniated nucleus pulposus c4-5 and they want to do

surgery. I just had surgery in Feb for c 6-7 and I have also had c 5-6 fused

also.

anyone have any suggestions on what to do?

Thank you

____________ _________ _________ _________ _________ _________ _

Windows 7: Simplify your PC. Learn more.

http://www.microsof t.com/Windows/ windows-7/ default.aspx? ocid=PID24727:

:T:WLMTAGL: ON:WL:en- US:WWL_WIN_ evergreen1: 102009

[Guest guest]

I had back x-rays yesterday on my mid and upper back because on Friday I began

having really bad pain. The x-rays say I have a compression fracture at T-7.

Does anyone know any one know more about this and if there is anything that be

done done to help me. I cannot handle this pain it's just to much.

Janice

[Guest guest]

it is direct immuno florescence(Odell, Clinical Problem Solving dentistry, page 193, edition 3)Regards From: Shipra Bapna <bapnashipra@...> " " < > Sent: Tuesday, March 27, 2012 11:21 PM Subject: DIAGNOSIS

hi..plz help me with this question A 60 year old female attends your surgery complaining of soreness affecting her gingivae. No other area of her oral mucosa is affected, she has no skin lesions and other mucosal surfacesdo not appear to be affected. She is fit and well and is not taking any medication. On examination intra-orally a desquamative gingivitis is present. Your differential diagnosis

lies between

lichen planus and mucous membrane pemphigoid. You carry out an incision biopsy and send the fresh tissue to the laboratory without putting it into formalin. What procedure, performed on sections of fresh frozen tissue, do you expect the histopathology department to perform in addition to conventional staining with haemotoxylin and eosin? A. Indirect immunofluorescence B. Direct immunofluorescence C. Papanicolaou (PAP) staining D. Periodic acid Schiff (PAS) staining E. Immunoperoxidase staining