*** DOMINIE
NEWSLETTER ***
JULY 2005
Scroll down this page to read Topics
1-25:
1. LETTERS FROM
READERS
2. SEX AND FIBRO
3. FIBROMYALGIA - A STUDY OF
DEMONS
4. ASPARTAME DETOX
5. DR. WHITCOMB
6. A "JELL-O" DAY
7. R.E.S.C.I.N.D.
8. LETTER TO OPRAH & MILLION LETTER
CAMPAIGN UPDATE
9. STRESS
MANAGEMENT
10. DRAMAMINE FOR
SLEEP
11. CYMBALTA
(revisited)
12. CANDY'S
FIBRO T-SHIRTS
13. DOWNLOADABLE PRESENTATION ABOUT
M.E./CFIDS
14. AOL USERS
15. TRAUMA TO THE BODY CAUSES FIBRO
ONSET
16. LOW THYROID &
FMS
17. VIDEO ON FIBRO
18. MILK
SUBSTITUTES
19. CHILDHOOD TRAUMA &
FMS
20. CANDLES &
TOXICITY
21. COCONUT OIL
(revisited)
22. ARTICLE IN WOMAN'S DAY
MAGAZINE
23. MEMORY FOAM PILLOW
24. VAGUS NERVE & DEPRESSION
(revisted)
25. COUGH REMEDY MAY HELP
FIBRO
26. HELP CHILDREN WITH
CFIDS
27.
"THE THIEF OF MANY LIVES"
28. ADRENAL SUPPLEMENTS OR
NOT?
29. KEEP THE PSYCHOLOGISTS AT
BAY
30. LUNESTA (revisited)
31. ZOPLICLONE FOR SLEEP
32. LOOKING ON THE BRIGHT
SIDE
33. CANDIDIASIS (YEAST
OVERGROWTH)
34. HOW TO SEARCH MY SITE &
NEWSLETTERS
35. PROVIGIL (revisited)
36. DIZZINESS & HEAD
RUSHES
37. IVMT = INTRAVENOUS MICRONUTRIENT
THERAPY
38. XYREM (GHB) FOR SLEEP
(revisited)
39. FIBROMYALGIA & FATIGUE CENTERS
(revisited)
40. COLLAGEN FOR PAIN & SLEEP
(revisited)
41. WALL STREET JOURNAL ARTICLE
(revisited)
42. TENSION INDUCED PAIN
DISORDERS
43. SUGAR & WEIGHT
LOSS
44. CREON
FORTE
45. ROSIE HAMLIN
CAMPAIGNS FOR FMS AWARENESS
46. CFIDS LOBBY
DAY
47. IS FIBROMYALGIA
INHERITED?
48. WORKING FROM HOME
(revisited)
49. SPIRITUAL UPLIFT
CORNER
50. DOMINIE'S PERSONAL
UPDATE
1. LETTERS FROM
READERS
"I have been
reading through your 100 tips www.fms-help.com/tips.htm and trying
some of your ideas because doctors have failed to
help me!"
"I'm a 26 year
old, married, mother of 2. I have
fibro/CFIDS and it has taken over my life, I am so weak and in pain all the
time. I used to work 2 jobs and go to school, now I can no longer work and I'm
forcing myself to not drop out of school. I am like you, I used to
work so hard and go a million miles a minute, and now I am trapped in this body
that makes me feel like I'm 100 years old dying of cancer, but I look
healthy. I am getting so depressed, I can't even take care of my
baby anymore! I really need help! I have a million things I want to say but my
arms hurt so bad already that I can't type anymore! I want my life
back!"
"Your site www.fms-help.com has helped me more than any
other one I have been on."
"I came across your website by accident and found it to be
very helpful and inspirational. I have suffered with
CFIDS for many years beginning when I was 18 (after a severe bout with mono and
a throat staph infection that had me bedridden for 4 months). I went off
to college, and got a masters degree in teaching (although I was exhausted and
chronically sick.) I tried to teach, but like you, had to give it up
due to my chronic infections. I picked up everything the kids had, and
eventually became bedridden. I ended up doing office work for a long time,
and had cycles where I was fairly well, only to be followed by an infection that
would leave me weak and often bedridden for months at a time. With the onset of menopause my system crashed again, leaving me with
severe, chronic sinus infections, where I was so weak I could not walk without
assistance. I finally applied for disability. I am 50 now, and
the last 4 years have been a real struggle. I already do many of
the things mentioned on your list
www.fms-help.com/tips.htm It
is comforting to know that there are others out there with a similar history and
illness profile. I am in a small support group, however
your
history [
www.fms-help.com/fibro.htm &
www.fms-help.com/fatigue.htm]
is the closest to mine that I have come across."
[NOTE FROM DOMINIE: I think this lady and I must be
clones!]
"I am reading everything you sent me today. I am just amazed! Now I am sure
I had this lovely illness as far back as high school."
"I would like to thank you from the bottom of my heart, when I was first
diagnosed with fibro I had no clue and never associated it with the
constant agonizing pain I was in, finally after many months of
denial and at the point of ending my own life I found your website
www.fms-help.com.
I was lost and needed information. I wanted to learn more about my
condition as the pain had over taken my life and
I felt like a prisoner in my own body and
home. I joined a fibro group on line and feel like I am starting
to take what is left of my life back. I have come a long way since I first
stumbled onto your site. I was a healthy energetic woman with a wonderful job I
loved and always active with my kids, till someone made a poor choice and pulled
out of a parking lot and t-boned me, he never saw me. Then tried to blame me. I
am still in litigation for this as it has been so hard to try
and prove my case. I pray we settle it as I could not go to court. I
want to thank you for also taking the time to send out the news letters as
I am sure this must be very hard on you at times. Just know your love and
compassion saved my life and has given me a new outlook
and slowly I am re-inventing the woman I once was.
May God bless you greatly for everything you have done for women like me."
"Thank you or your website www.fms-help.com.
I send it to all my
fibro-friends."
"We live in a time of medical advancement but no one can tell me what is
wrong. The more I thought about it the more I realized that if was going
to me up to me to find my answers. My doctor is great but I think he is as
frustrated as I am that my body doesn't respond to treatments that most
people respond to. Your web site has some very useful
information. It is nice to know there are people in the same boat I am in
because for the most part I am
looked at like I am crazy and need to just get over it."
"Thank you for struggling to help our disease a kind of recognition over
the world
www.fms-help.com/letter.htm
Unfortunately during the 80's and 90's, there was no evidence of physiological
signs, and consequently this disease has been easily classified in the
depressive disorders and treated accordingly without clear improvement.
Even if you were not depressive at the beginning,
your doctors hastened your depression! I have been
suffering first of CFS after a
mononucleosis and a
car
accident since 1991, that took 5 years to improve. Unfortunately, in
1997, after a
back surgery, FM developed shortly after....My
biggest frustration was coming from the doctors still embedded in their
depressive syndrome stuff. Thank God that some of them started to go further
into research and find some body deficiencies and dysfunctions.
Considering the high expenses that this disability cost to the
government, it would be worthwhile that it involves some funds to hasten the
research in this area. I hope this letter will help a little; if we
were in shape, we could organize a walk, but I think Internet is our best bet
for the moment.
If we are lucky, a very rich person suffering or having
a close relative suffering from it, could help us to inform and educate the
media, essentially through TV which remains the best route of
information."
"Thanks for sending me all your
information. It was very timely. You even sent something that I didn’t ask you
to send and I know it was a God thing. As you
know, FM makes us feel so bad and even though I have a wonderful husband, I was
feeling yucky towards him this morning about little stupid things. Then, I
opened my e-mail and there was your article on marriage www.fms-help.com/marriage.htm. Thanks so much. I’m
a mature Christian and know better than to be feeling like I was and just needed
a quick kick in the pants. God is really teaching me to not go by my emotions
about how I’m feeling towards my husband, but to trust God to meet all those
needs."
2. SEX AND
FIBRO
From a
newsletter reader--
"Do you have
problems with sex--pain and desire? I wonder how much of this supports my
pain because of the stress on marriage and the lack of desire for
intimacy. Has this ever been addressed in your
newsletter?" [NOTE FROM DOMINIE: Comments,
anyone? Anything sent to me will quoted anonymously, as
always...]
3. FIBROMYALGIA - A STUDY OF
DEMONS
From a
reader--
4. ASPARTAME
DETOX
From a
reader--
5. DR. WHITCOMB
[This article has been removed.]
6. A "JELL-O"
DAY
From a reader--
"I am having what I call a "jell-o"
day: although I felt I slept fairly well and enough last night, I
am having a day of fatigue and slowness, like trying to walk
through jell-o all day!!!! Luckily, this kind of day usually occurs for
only one day, not a whole string of them!!" [NOTE FROM
DOMINIE: What a great description!]
7.
R.E.S.C.I.N.D.
Repeal Existing Stereotypes about
Chronic, Immunological
and Neurological Diseases
Lots of fascinating articles related to FMS/CFIDS/ME!
8.
LETTER TO OPRAH & MILLION LETTER CAMPAIGN UPDATE
As everyone knows, the Million Letter
Campaign was a great effort to get the attention of the media and
government regarding FMS/CFIDS. Pattie
Caprio, MLC Founder, made this comment: "WE WERE TOLD THAT SHOPPING
CARTS FULL OF MAIL WERE RECEIVED.
/smaller>/color>/fontfamily>THEY WERE NOT HAPPY BECAUSE THEY WERE
OVERLOADED WITH MAIL. I WAS HAPPY BECAUSE WE
SUCCEEDED/bigger>
WITH A LOT OF MAILINGS FROM ALL OVER THE
WORLD." See www.fms-help.com/letter.htm for
updates on the results of our campaign thus
far. /bigger>
After our letters went out on May 1, 2005,
Pattie found out from the Oprah show that we need to contact her by email, which
many of us did on May 12, 2005, International Fibromyalgia Awareness Day.
Hundreds, if not thousands, of emails were sent to Oprah! Below is one
from a newsletter reader--
"Dear Oprah, Today, May 12th is Fibromyalgia
Awareness Day. Fibromyalgia is a devastating invisible disease that attacks
millions. I have had Fibromyalgia for many years and just recently officially
diagnosed. Until the official diagnosis I have suffered several misdiagnoses,
costly not only in money, but job opportunities, relationships, self esteem.
etc. My family paid the price right along with me. My story is much like
several million suffers, yet to be heard from, mostly women, and we need your
help to get recognition from; and to educate the Health-care, Insurance,
Medicare Pharmaceutical Companies and States Assistance just to name a few, to
fight the ignorant labels such as Hyprocondratic, Psychosomatic, made up
illness, depressant (or just plain crazy) and on and on resulting in
years of constant pain, and financial losses. This disease is
not terminal unless you count those that could only escape the pain or
losses by suicide. There is a wealth of heroic stories of
Fibro-Fighters trying to help eachother at your fingertips by
contacting the "Million Letter Campaign" originators Pattie Caprio (570)839-1399
Email ivorycgd@noln.com or
Dominie Bush at dominiebush@bellsouth.net or at www.fms-help.com or
my-self, Cathy Buchner under this profile heading. Thank you for
requesting ideas - you are a great support to so many; I so hope you and
your staff finds this cause of interest for one of your shows. Always a
fan...Cathy"
Below is a quote from Hubert Humphrey that is
fitting in relation to the Million Letter Campaign for Fibromyalgia and Chronic
Fatigue Syndrome Awareness--
"The moral test of
government is how it treats those who are in the dawn of life, the children;
those who are in the twilight of life, the aged; and those who are in the
shadows of life, the sick, the needy, and the
handicapped."
9. STRESS
MANAGEMENT
From my brother--great advice!--
A lecturer, when explaining
stress management to an audience, raised a glass of water and asked, "How heavy
is this glass of water?" Answers called out ranged from 20g to 500g. The
lecturer replied, "The absolute weight doesn't matter. It depends on how long
you try to hold it."
"If I hold it for a minute, that's not a
problem. If I hold it for an hour, I'll have an ache in my right arm. If I hold
it for a day, you'll have to call an ambulance. "In each case, it's the same
weight, but the longer I hold it, the heavier it becomes."
He continued,
"And that's the way it is with stress management. If we carry our burdens all
the time, sooner or later, as the burden becomes increasingly heavy, we won't be
able to carry on." "As with the glass of water, you have to put it down for a
while and rest before holding it again. When we're refreshed, we can carry on
with the burden."
"So, before you return home tonight, put the burden of
work down. Don't carry it home. You can pick it up tomorrow. Whatever burdens
you're carrying now, let them down for a moment if you can. Relax; pick
them up later after you've rested. Life is short. Enjoy it!"
And then he
shared some ways of dealing with the burdens of life:
* Accept that some
days you're the pigeon, and some days you're the statue.
* Always keep
your words soft and sweet, just in case you have to eat them.
* Always
read stuff that will make you look good if you die in the middle of it.
* Drive carefully. It's not only cars that can be recalled by their
maker.
* If you can't be kind, at least have the decency to be vague.
* If you lend someone money and never see that person again, it was
probably worth it.
* It may be that your sole purpose in life is simply
to serve as a warning to others.
* Never buy a car you can't push.
* Never put both feet in your mouth at the same time, because then you
won't have a leg to stand on.
* Nobody cares if you can't dance well.
Just get up and dance.
* Since it's the early worm that gets eaten by
the bird, sleep late.
* The second mouse gets the cheese.
* When
everything's coming your way, you're in the wrong lane.
* Birthdays are
good for you. The more you have, the longer you live.
* You may be only
one person in the world, but you may also be the world to one person.
*
Some mistakes are too much fun to only make once.
* We could learn a lot
from crayons. Some are sharp, some are pretty and some are dull. Some have
weird names, and all are different colors, but they all have to live in the same
box.
* A truly happy person is one who can enjoy the scenery on a
detour.
10.
DRAMAMINE FOR SLEEP
From a reader--
"I also want to thank you for your site, and suggest an alternative method
for sleep. Last night I took a Dramamine (car sick pill) and a 0.5
melatonin and I slept for 4 hours straight! This was a first, the best
sleep I've had in a long time. I was able to sleep for two more hours
after that. I thought you might want to put Dramamine now as a possible
help for sleep. If one tablet doesn't work, two might work.
You don't feel drowsy in the morning with it, it's over the counter.
I used it years ago (before fibromyalgia), and thought I would try it
again."
11. CYMBALTA
(revisited)
From a reader--
"I read your message at the
site http://www.fms-help.com/April2005.htm
I've been on Cymbalta for four months. I don't know what
I feel anymore. Loss of memory for one thing, disoriented, light
headed. It isn't helping my Fibro."
12. CANDY'S
FIBRO T-SHIRTS
"FIBROMYALGIA....WHAT'S THAT?"
T-SHIRTS
Are you tired of explaining to everyone what
fibromyalgia is? I know I am!!! Here's a
wonderful T-shirt by Candy Morris that will do the job
for you! You can visit Candy's site at
www.nhws.com/fm/index.html and read what the shirt says on the back.
You will want to order at least one!
13.
DOWNLOADABLE PRESENTATION ABOUT M.E./CFIDS
From a reader--
Presentation by Professor
Malcolm Hooper
http://www.mesupportnorfolk.org.uk/media
Myalgic Encephalomyelitis is
a serious life-changing physical illness, recognised by the
World Health Organisation (WHO); listed at ICD-10-G93.3 as an organic-biomedical
neurological disorder. This classification is supported by a
considerable body of peer-reviewed clinical and research evidence. For
example, SPECT and PET brain scans of M.E. sufferers have revealed
physical tissue damage and severely reduced cerebral blood-flow
– made worse by exertion. Autopsies have confirmed such damage/infection.
In spite of this, in the UK, ME/CFS sufferers are being
systematically persecuted and driven towards an outrageous
situation where they shall be (mis)treated as psychiatric
patients and face reduced access to health services and welfare
benefits.
Professor Hooper's presentation and the associated documents
reveal the compelling truth about the biomedical nature of M.E. and those who,
in the face of this evidence, assert that “M.E. is simply a belief, the belief
that one has an illness called M.E.” (Prof. Simon Wessely, source).
[NOTE FROM DOMINIE: In the U.K. and many
other countries, Myalgic Encephalomyelitis (M.E.) is the name for Chronic
Fatigue Immune Dysfunction Syndrome (CFIDS).]
14. AOL
USERS
If you have AOL and are not receiving my newsletter via
email after requesting it from me at dombush@bellsouth.net, here's some advice
from a reader--
"I have AOL 9.0 and have learned to check my spam
file every morning. People who are having trouble getting your
newsletter should check their spam each day. When an e-mail they want has been
directed to their spam file, they can point their browser to the e-mail they
want to receive and then click on 'This is not spam.' They should then
get e-mail from that source MOST of the time; however, AOL will still
direct it to spam sometimes."
NOTE: If you will put my two email addresses in your
email address book, there's a better chance the newsletter will go
through--Dominie Bush dombush@bellsouth.net and dominiebush@bellsouth.net
15. TRAUMA TO THE BODY
CAUSES FIBRO ONSET
Most of us with FMS/CFIDS can point to a stressful event or
physical injury that triggered our illness. This one was sent in by a
website reader and I thought it was very interesting--
"I've had fibromyalgia and chronic fatigue syndrome for
eight years now. It
is very hard to work and take care of your family with a
illness like this.
I started feeling sick after pulling some muscles lifting
a heavy [grass] catcher
into the trash. I mowed the lawn in the front yard
and the back yard without
empting the catcher until the end. It was getting
dark out and I wanted to
hurry up. I didn't feel bad till the next day. All
the muscles in my neck
and shoulder were hurting. I went to the doctor and he
said I had bursites
from the injury. He gave me some medicine and sent me
home. I started having
fatigue, chills, muscle aches, twitching
muscles, muscle spasms,
constipation, sore spots, acid refux, panic attacks,
impaired concentration and
memory. There is so many symptoms I can't remember
them all. I had to do my
own research to find out what was wrong with
me. I found out the name for my
illness and took it to my
doctor, because after three months I wasn't getting
better. My doctor
said I was right about the type of illness so he started
trying me on
different medications to see what would help. Later I found out
this illness
runs in the family so it is genetic. We don't know what
causes
the illness, because there needs to be more tests to find out what
causes it.
We need your help!!!! There needs to be more research on
fibromyalgia and
chronic fatigue. More and more people are getting it, and if
it is genetic, we
are passing it down to our children."
[NOTE FROM DOMINIE: My personal theory is
that those of us with FMS/CFIDS have somehow "blown a fuse" in our bodies.
The immune system has become overwhelmed and can't seem to right itself after
this. Strange that lifting this heavy grass catcher caused all of the
problems this patient mentioned, but I can believe and relate to what she said,
because I've experienced things like this myself and also heard variations of
this same story from thousands of people all over the world in the past 9 years
with my website. The Million Letter
Campaign www.fms-help.com/letter.htm
was our most recent attempt to gain national recognition of this illness and
hopefully more attention and research will be devoted to finding what is causing
this!....and eventually a CURE!]
16. LOW
THYROID & FMS
From the Fibromyalgia & Fatigue Center
newsletter--
Are All Chronic Fatigue
Syndrome/Fibromyalgia Patients Low Thyroid?
There is mounting
evidence that hypothyroidism is present in the majority of and possibly all
chronic fatigue and fibromyalgia (CFS/FM) patients. The problem is that standard
blood testing that consists of TSH, T4 and T3 does not detect it. Thus, many
CFS/FM patients are erroneously told over and over that their thyroid levels are
fine. TSH is secreted by the pituitary in the brain, telling the thyroid to
secrete T4, which is not the active thyroid hormone. T4 must then be converted
in the body to the active thyroid hormone T3. When T4 and T3 levels drop, the
TSH should increase indicating hypothyroidism. This is the standard way to
diagnose hypothyroidism. There are, however, many things that result in
hypothyroidism but are not diagnosed using the standard TSH and T4 and T3
testing. This method misses thyroid problems with CFS/FM patients 90% of the
time. First of all, there is clearly pituitary dysfunction in these diseases
from a variety of causes, including viruses, bacteria, stress, yeast,
inflammation, toxins, pesticides, plastics and mitochondria dysfunction.
17. VIDEO ON
FIBRO
From a reader--
18. MILK
SUBSTITUTES
Many people (including me) feel better not
drinking milk. For a complete discussion of why you might want to
avoid milk, see www.notmilk.com
19. CHILDHOOD TRAUMA &
FMS
"There is also some other research and
anecdotal evidence that CFS and fibromyalgia seems to happen to people who have
had major trauma such as childhood abuse. It is thought that
this type of thing affects the pituitary/hypothalamus area of the
brain interfering with proper function. Studies have found that these
people have disturbed brain electrical function. Others have
called it the "delayed stress effect" and say that trauma builds up in the brain
as electrical disturbances and imbalances. Practicing meditation, prayer or some
relaxation technique regularly is said to greatly help. Research is being done
with EEG training to help these people. EEG trains the brain to balance itself
electrically and to relax the body. Research with children raised in abusive
situations has found that that they have up to double the output of
adrenal stress hormones and tend to be in a heightened alert
state all the time. When followed to adulthood, researches have found
that in adulthood they often develop low energy problems or
other metabolic disorders. These type of people also do not respond well to
thyroid hormone (thyroid hormone resistance). They have suppressed
metabolisms, basically. Violent prison inmates from abusive childhood situations
were found to have greatly reduced cortisol output. It can be speculated that
some abused children later suffer adrenal burnout. Without sufficient adrenal
hormones thyroid hormone can't work properly. Dr. David Derry found that
traumatized people who develop hypothyroidism often need very high doses
of thyroid medication to function normally."
20.
CANDLES & TOXICITY
From the FCI link e-newsletter--
The following
article is to inform you about the toxicity of many candles. A wick that sticks
up probably has a lead wire in it; one without a wire will fall
over. It is also better to avoid fragranced candles.
Wick-ed Candles: They "Light up Your Life"
and Endanger You and Your
Children
By
Dr. Gloria Gilbčre, ND, PhD
Chemical toxicity comes in many
seemingly innocent disguises. One such toxic substance, not readily known by the
general public, is the candle wick. In 1973 the EPA Administrator urged a
mandatory ban on all candles with lead-containing wicks. As a result, a
voluntary ban was approved and then not complied with or even monitored. An EPA
study in 1974 determined "Burning only
two candles three hours each day on a regular basis in the home could increase
exposure to airborne lead by a factor of 5 or more. This exposure to lead from
candles could equal or exceed the exposure to airborne lead associated with the
busiest freeways in America." [This statement was made at the time when leaded
gasoline was still fairly commonplace.] "Inhabitants of homes in which lead wick
candles are burned could be exposed to substantial incremental quantities of
lead which, if continued on a regular basis would pose a significantly high risk
to health, especially among children." The EPA determined that burning
candles with lead-containing wicks exceeded the current EPA air quality standard
by over 10 times. Yet, today candles containing lead are still being
manufactured and sold! [NOTE
FROM DOMINIE: I was visiting in a home recently where a lot of fragrant
candles were burning. I think it was too much for my immune system to
handle. I felt distinctly unwell when I left, and the
fatigue lasted a number of days. Three years ago, I had a very severe
allergic reaction in my eyes from a candle I received as a gift. Those of
us with FMS/CFIDS/MCS have to be careful about things in our environment--even
something as simple as a candle.]
21. COCONUT
OIL (revisited)
From a reader who recommended coconut oil to
me last year. I wrote to find out if it was still helping him.
Here's what he said--
"It is great! I take 3 spoon 3 times
a day and I'm more relaxed, more alert or less tired. Also in a better
mood. Losing weight, good eh? I highly recommend it. It is getting the
right fat in the system. Dr. Mercola is also another one that recommends
it. Try the small first and you will see the difference."
22. ARTICLE IN
WOMAN'S DAY MAGAZINE
From a reader--
"There's a short but good article in the May
31st issue of Woman's Day magazine about chronic pain. If we could get
'letters to the editor' going out whenever there's a good
article about pain, we could help raise consciousness even more. I'm
sending a letter. Just thought I'd pass this on."
23. MEMORY
FOAM PILLOW
From a reader--
"I have a memory foam pillow and I love it. I
agree with you that it does help keep my neck in proper alignment while
sleeping. Now if I don't sleep on it I can really tell the difference. (My
mattress has a pillow top so it does well also.)"
24. VAGUS
NERVE & DEPRESSION
From a
reader--
High-Tech Depression Fighter
People who
suffer from depression but are resistant to medication may find relief with
Vagus Nerve Stimulation (VNS) therapy. The stimulator
is pacemaker-like device implanted in the chest and attached to the vagus
nerve on the left side of the neck. It sends a regular pulse of
electricity to stimulate mood-regulating regions of the brain. VNS therapy
is currently approved for treating epilepsy and is covered by insurance.
It is expected to be available to depression patients later this month.
Source: Mark
George, MD, professor of psychiatry, radiology and neurology, and director,
brain stimulation laboratory, Medical University of South Carolina,
Charleston. [NOTE FROM DOMINIE: See another article on the
vagus nerve in the November 2004 newsletter at http://www.fms-help.com/November2004.htm -
it's topic #10.]
25. COUGH
REMEDY MAY HELP FIBRO
Source: University of Florida; Date: 2005-05-19
www.sciencedaily.com/releases/2005/05/050519141247.htm
Fibromyalgia
Patients May Benefit From Cough Remedy, UF Study Finds
GAINESVILLE, Fla. -
Dextromethorphan, an over-the-counter medication that silences coughs, may help
fibromyalgia patients quiet over-reacting nerves that amplify ordinary touches
into agony.
A University of Florida study documents, for the first time,
that dextromethorphan temporarily reduces the intensity of fibromyalgia
"wind-up," a snowballing pain response to minor, repetitive physical contact.
The discovery, described in the May issue of The Journal of Pain, also
enables researchers to rule out one suspected cause of the phenomenon.
Fibromyalgia is an incurable illness that causes widespread muscle
aches, stiffness, fatigue and sleep disturbances, according to the National
Fibromyalgia Association. An estimated 10 million Americans suffer from the
condition, most of them women. Current treatment strategies include pain
medication, exercise, stretching, sleep management and psychological support.
Though the UF study did not establish guidelines for using
dextromethorphan clinically, it suggests the drug may eventually be an option
for treating fibromyalgia and other conditions involving heightened pain
sensitivity, said rheumatology expert Roland Staud, M.D., a UF associate
professor of medicine and the study's principal author.
"I think it's
one piece of the mosaic," Staud said. "We currently have no single therapy in
chronic pain that has a big effect. So what this really means for chronic pain
patients is that they need to use a whole host of different interventions to
decrease the pain they have. And in this, dextromethorphan may have a role in
the future."
Dextromethorphan is popular in cold remedies because it
elevates the threshold for the coughing reflex but does not cause physical
addiction, according to the U.S. Drug Enforcement Administration.
But
fibromyalgia patients should not resort to self-medicating by taking cough
syrups for pain, Staud cautioned.
"Like every medication,
dextromethorphan has side effects," he said. "At high doses, patients can have
problems related to memory and confusion."
The underlying cause of
fibromyalgia remains unknown, but in the past 25 years substantial progress has
been made toward understanding the mechanisms behind specific features of
fibromyalgia, Staud said. One is central sensitization, a feature of many
chronic pain conditions in which the central nervous system - the brain and
spinal cord - somehow magnifies pain signals to abnormally high levels, said
Staud, who is affiliated with UF's McKnight Brain Institute.
Central
sensitization is associated with wind-up, a phenomenon in which repeated touches
- even handshakes or pats on the back - geenerate lingering pain that increases
with each new contact, he said. A normal form of achy, lingering pain known as
secondary pain affects anyone who suffers an injury.
The UF researchers
- Staud, neuroscientist Charles Vierck, Phh.D., psychologist Michael Robinson,
Ph.D., and Donald Price, Ph.D. - were surprised to learn that dextromethorphan
eased fibromyalgia patients' wind-up pain to the same degree it soothed
secondary pain induced in healthy volunteers, Staud said. The results indicate a
long-suspected cause of wind-up may not exist.
Previous studies at other
institutions had shown that dextromethorphan blocks the action of a chemical
messenger called N-methyl-D-aspartate, or NMDA, which relays pain impulses in
the spinal cord. Many fibromyalgia researchers have theorized that wind-up is
caused by abnormalities in the spinal-cord structures that process NMDA.
The UF results suggest those structures function normally but that pain
impulses are more amplified in fibromyalgia than in healthy participants, Staud
said.
"This has refocused much of our research now," he said. Future UF
studies will attempt to pinpoint where the pain impulses are originating.
In the current study, researchers worked with 14 women with fibromyalgia
and 10 women who did not have the disease, using mechanical devices that tapped
the participants' hands repeatedly. One part of the study involved contact with
a heated probe, the other used a small rubber-tipped peg. The intensity of the
heat or pressure of the stimulation was individually adjusted so that all
participants reported feeling the same degree of pain.
Researchers then
gave each participant a capsule containing 60 milligrams of dextromethorphan, 90
milligrams of dextromethorphan or a placebo containing none of the drug, and
asked them to rate the amount of pain they experienced when the stimulation was
repeated.
With the heat stimulus, 90 milligrams of dextromethorphan
reduced wind-up pain, but 60 milligrams was no more effective than the placebo.
With the pressure stimulus, 90 milligram and 60 milligram doses were equally
effective, reducing wind-up pain.
The UF study indicates the need for
further research on dextromethorphan, said fibromyalgia expert Laurence Bradley,
Ph.D., a professor of medicine with the University of Alabama at Birmingham's
division of clinical rheumatology and immunology.
"This is a topic
that's actually received very little attention so far in the literature,"
Bradley said. "It would be a disservice to start to recommend that either
patients or physicians begin experimenting right away with dextromethorphan,
because I think there's some important questions about how to minimize the side
effects with this agent."
Another reader sent in this
article--
Cough Remedy for
Fibromyalgia
(Ivanhoe Newswire) -- Fibromyalgia patients may have
a new over-the-counter remedy to relieve pain. A study from the University of
Florida in Gainesville shows a cough medicine called dextromethorphan (also
known as Robitussin Cough Calmers, Sucrets Cough Control or Suppress, among
others) temporarily reduces the intensity of "wind-up," a snowballing pain
response to minor repetitive physical contact.....http://www.ivanhoe.com/channels/p_channelstory.cfm?storyid=11319
DISCLAIMER: I am
not a
medical doctor. I am a fibromyalgia/chronic fatigue syndrome survivor. The
purpose of this website is not to diagnose or cure any disease or malady, but is
presented as food for thought. This information cannot take the place of
professional medical advice. Any attempt to diagnose and treat an illness should
come under the direction of a physician. No guarantees are made regarding any of
the information in this
website.
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