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Yes, I do, almost identically. Unfortunately I almost always bite off more

than I can chew and pay for it. The severity of spasms has increased

considerably just lately.

It seems that my mask is either all smiles or an angrier frown, I am rarely

aware of which of the two I'm wearing. I can see by how others react.

Smiley comes on when I am in the most discomfort (preserving energy, maybe,

since smiling takes less??) Frowny happens when oddly I'm feeling better.

I need a mirror these days to tell which is which.

_______________________________________

about dry mouth, I found this one today

_________________________________-

There are many causes of decreased salivary gland function. the most

common

causes of oral dryness include medical therapies and systemic disorders.

Loss of

water and metabolites results in dehydration which can lead to a decrease in

salivary flow and thus, xerostomia. Dehydration may be due to insufficient

water

intake; loss of water through the skin due to fever, excessive sweating or

burns; loss of blood; diarrhea; renal insufficiency and subsequent water loss

due to diabetes insipidus or diabetes mellitus; or protein malnutrition.

The medical therapies that interfere with salivary function are

dominated by

radiotherapy to the head and neck, drugs, and surgical and traumatic

etiologies.

Damage to the salivary glands with resultant xerostomia can be caused by

radiation therapy to the head and neck region, including the salivary glands.

Radiation-induced xerostomia is usually permanent when bilateral radiation

treatment of the salivary glands cannot be avoided. One study found that the

resting flow rate of parotid saliva was reduced fifty percent, twenty- four

hours after the administration of only two-hundred-twenty-five CGY of

radiation.

After six weeks of treatment using two GY per fraction, for a total dose of

six

thousand CGY, the reduction was more than seventy-five percent. another study

found that there was a progressive decrease in salivary flow following

radiation

therapy, throughout the three-year course of the study. If possible,

clinicians

should make every effort to minimize exposure of the major salivary glands

during radiation therapy. In addition, patients scheduled for therapeutic

irradiation should be referred to a dentist for needed dental treatment

prior to

initiating irradiation.

Xerostomia can also result from systemic diseases, most commonly Sjogren's

Syndrome. Sjogren's Syndrome affects salivary and lacrimal functions as

well as

connective tissue, and following rheumatoid arthritis, is the most common

autoimmune rheumatic disease. It may occur in a primary form in the absence

of

other diseases, or in a secondary form as a complication of other autoimmune

rheumatic disorders such as rheumatoid arthritis, systemic lupus

erythematosus,

or scleroderma. Sjogren's Syndrome most often is diagnosed in women over

forty

years of age. Xerostomia is found in greater than ninety percent of Sjogren's

Syndrome patients. Other systemic disorders such as graft-versus-host-disease

and the diffuse infiltrative Lymphocytosis Syndrome, secondary to HIV

infection,

may also result in xerostomia. Additional systemic disorders that can cause

dry

mouth include sarcoidosis, amyloidosis, type five hyperlipidemia, and the

Eosinophilia-Myalgia Syndrome.

Interference with neural transmission affecting the salivary glands can

result from certain medications; autonomic dysfunction; CNS conditions such

as

Alzheimer's disease; trauma; or a decrease in mastication resulting in

salivary

gland atrophy. Hypoplasia of the parotid glands has been reported in patients

with Melkersson- Rosenthal Syndrome, a rare disease which classically

produces a

fissured tongue, salivary gland hypofunction and facial hemiparesis. Dry

mouth,

a sore and bald tongue, and angular stomatitis are common findings in

Plummer-Vinson

Syndrome.

Many medications, prescription and OTC, can cause xerostomia through their

anticholinergic or antiadrenergic properties, and clinicians must be aware

that

combinations of certain drugs may heighten this effect. In fact, it is

estimated

that there are more than four hundred drugs that have the capacity to cause

oral

dryness. A smaller number of drugs have been shown to actually induce

salivary

gland hypofunction. Commonly used medications with a high potential for

causing

xerostomia include tricyclic antidepressants; antihistamines;

benzodiazepines;

phenothiazine derivatives; and antiparkinson medications. Other drugs that

can

cause dry mouth include narcotic analgesics; appetite suppressants;

anticholinergics and anti-spasmodics; antiemetics and antidiarrheals;

antihypertensives, especially diuretics; and psychotropic agents.

Xerostomia may

also be considered a manifestation of anxiety or depression, even in the

absence

of medication use.

Contrary to popular belief, xerostomia is not a natural consequence of the

aging process. Studies have shown that changes in salivary gland function as

people age are modest changes, and not all salivary glands are affected. The

clinical impact of aging on salivary gland output is not considered to be

significant. If the elderly appear to be more affected by xerostomia, the

cause

is likely related to an increased usage of xerostomia-inducing medications

or a

higher incidence of certain systemic disorders that may cause xerostomia.

There are a number of clinical signs and oral complications associated

with

xerostomia. Oral sequelae may include foamy, viscous or ropy saliva; dry,

cracked lips; burning, fissured or lobulated tongue; dry, pale cheeks;

swollen

and/or painful salivary glands; frequent thirst; difficulty chewing;

difficulty

swallowing, or dysphagia; speech difficulty, or dysphonia; and impaired

taste.

Another manifestation can include an increased incidence of oral infections

such

as candidiasis, which is a common finding in individuals with xerostomia, and

may have an indolent presentation called chronic erythematous candidiasis.

Rampant tooth decay may result from the absence or decrease in the

cleansing and

remineralization benefits of saliva, with attendant increase in the

concentration and activity of acidogenic oral organisms and a reduction in

the

clearance of sugars from the oral cavity.

Generalized exocrine hypofunction may also cause symptoms of dryness in

anatomic locations other than the mouth. These complications include

dryness of

the throat; difficulty speaking; hoarseness; dryness of the nasal mucosa;

impaired olfactory function; dryness of the eyes, or xeropthalmia, with

burning

and/or itching and blurred vision or light sensitivity; dryness of the

skin, or

xeroderma; constipation; and dryness, burning and/or itching of the

vagina.

It is obvious that xerostomia is not an isolated symptom. In fact, one

study

states that patients with xerostomia complain on average of approximately

three

other symptoms. When xerostomia is chronic, the oral and systemic

complications

can be serious and debilitating. These may include not only recurrent oral

candidiasis and accelerated caries, but also sleep disruption; fibromyalgia;

weight loss; malnutrition; sialolithiasis; and bacterial sialadenitis. Not

surprisingly, each of the complications associated with xerostomia requires

attention in terms of diagnosis, treatment and management, which is one

reason

why a multi-disciplinary team approach to treating xerostomia is so

important.

This includes accurate diagnosis of both the etiology and the degree of

salivary

hypofunction.

Certain tests can be performed to assist in determining the etiology of

salivary dysfunction. these include tests for dry eyes; blood tests to help

determine the presence of an autoimmune disorder; imaging tests such as

isotope

scans to study the metabolic status of the major salivary glands; salivary

scintigraphy to assess glandular function; special salivary tests to detect

the

presence of antibodies associated with autoimmune disorders; and evaluation

of

depression and other psychological disorders. The simplest test, and a very

significant one, is sialometry, which measures the flow rate of saliva.

Unstimulated whole saliva can be collected for a specified time and

measured in

terms of milliliters or grams per minute. In contrast, stimulated whole

saliva

can be collected for an equal length of time by chewing paraffin wax or

placement of a two percent citric acid solution on the tongue to stimulate

flow.

In general, patients whose unstimulated flow rate is less than or equal to

zero-point-one milliliter per minute, and whose stimulated flow rate is less

than or equal to zero-point-five milliliter per minute, should be evaluated

for

xerostomia-inducing disorders. However, because of the differences in

individuals and a very large " normal " range, these parameters

must not

be used rigidly.

Many experts have observed that the visual condition of the oral mucosa

often

does not correlate to the subjective feeling of the patient. Many patients

who

appear to have a moist mouth complain of severe dry mouth, while others who

appear dry may not complain at all. Some experts suggest that baseline

unstimulated and stimulated whole saliva flow rates should be obtained for

all

patients, particularly in the dental office setting, so that volume changes

can

be evaluated more objectively. Well established methods are also available to

measure the function of the salivary glands individually.

Treatment of xerostomia consists of therapeutic modalities designed to

eliminate the cause of the condition, or if this is impractical, to provide

preventive palliative treatment designed to provide relief of the symptoms.

It

is important to provide treatment for the various sequelae that may develop

as a

result of dry mouth. Regarding primary treatment for xerostomia itself,

stimulation of salivary flow through pharmacologic, mechanical or other means

will provide the most efficacious relief of symptoms and the best chance to

avoid future complications. The success of stimulating salivary flow

depends on

the degree of remaining salivary gland function.

A masticatory stimulus can be provided by regular chewing action. The

use of

low caloric, sugarless foods such as celery or carrots can help stimulate

salivary flow. The frequent use of sugarless chewing gum has been shown to

increase the output of stimulated parotid saliva and increase the pH and

buffering capacity of whole and parotid saliva, thus helping prevent tooth

decay. Chemical stimulation of salivary flow may be achieved by substances

such

as citric acid, sour and sugarless candies, or lozenges. It should be

mentioned

that prolonged use of acid-containing substances can lead to dissolution of

tooth enamel and irritation of dry, sensitive oral tissues. To alleviate this

potential problem, oral moisturizing substances using a low concentration of

citric acid saturated with calcium phosphate have been developed to stimulate

salivary flow without the demineralizing effects of acids. These products

should

not contain alcohol or phenol, and should contain a sweetener such as

sorbitol

or xylitol that does not promote decay. occasionally, copious use of oral

moisturizers containing artificial sweeteners may be limited by the

development

of diarrhea.

Oral pilocarpine, the systemic sialagogue that has been studied

extensively,

is a plant chemical substance obtained from the leaflets of South American

shrubs from the genus pilocarpus. In tablet form, given in a total daily

dose of

fifteen-to-thirty milligrams per day, pilocarpine has been shown to be

effective

in stimulating salivary glands that have not been totally ablated by

radiation

therapy for head and neck carcinoma. Treatment results depend on residual

gland

function, and the optimal dose level for each patient must be assessed. In

proper dosages, few cardiovascular side effects have been found, although

pilocarpine tablets are contraindicated in patients with uncontrolled

asthma and

acute narrow angle glaucoma. The lowest effective dose should be used to

maintain optimal salivary flow. The continuing effects of this drug depend on

regular use. There is no daily crossover effect. Following radiation

therapy, it

may take up to 90 days of continued use before a noticeable salivary flow

increase is appreciated, although an increased awareness of oral wetness is

noted by many patients soon after pilocarpine therapy is initiated. Research

data suggest that earlier treatment with pilocarpine tablets may be

appropriate

for many head and neck cancer patients who experience dry mouth symptoms

early

during the course of radiation therapy. When xerostomia and related sequela

are

not transient, which is often the case, lifelong therapy with pilocarpine

tablets may be indicated. Use of pilocarpine for treatment of dry mouth and

dry

eyes due to Sjogren's Syndrome is now under study.

For individuals whose salivary glands do not respond to systemic or

stimulatory treatment, or have a minimal response, " saliva

substitutes " have been developed to moisten and " coat " the

oral

tissues. A true substitute for saliva has yet to be developed. Artificial

saliva

substitutes and mouth wetting agents may be used with some success,

although the

majority provide only short-term relief of symptoms, and can cause

irriration of

oral tissues during long-term use. All individuals with xerostomia should

drink

small sips of water or noncarbonated, sugarless liquids in order to moisten

oral

tissues and increase oral comfort. Room humidifiers can also be of benefit in

promoting moisture of the oral tissues and tissues of the upper aerodigestive

tract during the night, particularly during the winter months when rooms

may be

dry and overheated and the relative humidity is low.

Oral complications of xerostomia which require treatment include increased

dental caries; oral infections; dehydration of the oral tissues; compromised

chewing, swallowing and/or speaking; and oral pain. Dental caries associated

with xerostomia typically affects the gingival third and the incisal edges or

cusp tips of teeth, and teeth which generally have a low caries incidence,

such

as the lower anterior teeth, become more susceptible to decay. Because

patients

with xerostomia are more prone to tooth decay, their intake of sugar should

be

eliminated or greatly reduced as much as possible. Substances such as

sorbitol,

xylitol, aspartame, lycasin and saccharin may be substituted for sugars

because

they are not degraded into organic acids by oral bacteria. Dietary

counseling is

important for individuals with xerostomia.

Fluoride should be placed onto the teeth daily at home and during routine

dental visits, to help prevent tooth demineralization and decay. Self-applied

topical dental gels, rinses or foams can be used as a brush-on product or

placed

into fluoride carriers which resemble mouthguards. Such fluoride products

containing neutral one-point-one percent sodium fluoride or zero-point-four

percent stannous fluoride are available for home use. Chlorhexidine gel can

be

placed in a carrier which enhances the ability to control cariogenic flora in

cancer patients with xerostomia. more frequent dental care is important for

these patients. Depending on the caries risk, patients may need to be seen

every

three-to-four months.

Fungal infections frequently occur in patients with xerostomia, and

patients

with removable prostheses may be especially susceptible to such infection.

These

infections can be treated with a variety of antifungal agents. A

chlorhexidine

rinse can serve as a valuable antimicrobial adjunct, including use as a

soaking

agent for toothbrushes and dental appliances in order to prevent recurrence

from

reseeding. Dry mucosal tissues can be treated with frequent sips of water,

moisturizing gels or vitamin e oil, and cracked lips will benefit from

hydrophilic-based non-alcohol lubricating agents such as those containing

aloe

vera or vitamin e. Localized sore areas can be cautiously treated with

topical

anesthetic agents, but the patient should be warned that these may interfere

with taste and temperature sensation. The " masking " effect of

topical

anesthetics on soft tissues can be a problem when tissues awaken following

meals

or toothbrushing, and the natural gag reflex that protects against food

aspiration can be inhibited. Care should also be taken in preventing

frictional

tissue irritation by dental prostheses. Difficulties in swallowing and

speaking

that result from xerostomia may require specialized therapy from

speech-language

pathologists.

Xerostomia is a symptom associated with many causative factors. The

diagnosis, treatment and management of xerostomia and its sequelae involve a

multidisciplinary team of health care professionals. Psychological as well as

physical factors must be evaluated and appropriately addressed; hence, the

knowledge of the associated systemic as well as the oral consequences of

xerostomia is imperative.

Saliva is not simply water. It is a complex bodily fluid that is an

essential

component of oral health and balance. The vital role of saliva, taken often

taken for granted, becomes painfully and dramatically evident when this

remarkable fluid is significantly reduced or missing. No one understands this

better than the individuals who suffer from xerostomia and its myriad related

complications. When all involved health care professionals communicate

effectively and work together to meet the total needs of the xerostomic

patient,

the patient's quality of life and overall health can be greatly enhanced.

__________________________________________________

hope it's helpful

My emails have been received in backwards order all weekend, thought it had

to do with my server, might have been solar flares or something.

aletta mes, vancouver, bc canada

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

Site: http://www.aletta.0catch.com

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