*** DOMINIE NEWSLETTER ***
JULY 2005
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Web FMS-HELP.com

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

To read Topics 26-50, click on www.fms-help.com/July2005Page2.htm:
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."
 
"Your newsletter is a high point in my month!"  [NOTE FROM DOMINIE:  You can find current and back issues of the newsletter at www.fms-help.com/newsletters.htm.  Use the SEARCH feature to find specific topics discussed in the newsletters.]
 
 

 
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--
 
http://www.supernutrient.com/fibromyalgia.cfm?pageInfo_ID=5
 

 
4. ASPARTAME DETOX
 
From a reader--
 
http://www.sweetpoison.com
 

 
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
 
http://www.geocities.com/capitolhill/4277
 
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. THEY WERE NOT HAPPY BECAUSE THEY WERE OVERLOADED WITH MAIL. I WAS HAPPY BECAUSE WE SUCCEEDED
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. 
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.
 
[NOTE FROM DOMINIE:  This subject has been addressed many times in my newsletter.  Here's a link to Dr. Lowe's site for those who want to pursue the subject of thyroid and FMS: http://www.drlowe.com/QandA/askdrlowe/mostrecent.htm#November%208,%202004]
 

 
17. VIDEO ON FIBRO
 
From a reader--
 
www.healthscout.com/video/1/10050/main.html
 

 
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 
 
I got this link from a reader about milk substitutes: www.panix.com/~nomilk/milkalt.txt
 

 
19. CHILDHOOD TRAUMA & FMS
 
From http://tropicaltraditions.com/chronicfatiguesyndrome.htm--

"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

CONTINUE READING THE JULY 2005 NEWSLETTER (TOPICS 26-50): www.fms-help.com/July2005Page2.htm
 

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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