DOM'S FMS/CFIDS NEWSLETTER
www.fms-help.com
 
October 10, 2008
 
Topics are in PURPLE.  Readers comments are in BLACK.  My comments are in TEAL.
Don't miss the RED TOPICS!
 
Do you like the background color (gray) for this newsletter or the other color (tan) that I used in the last newsletter at www.fms-help.com/092708.htm?  Write dombush@bellsouth.net.  I'm trying to find a color that is easy on the eye - and brain.
 

 
1.  READERS WRITE
 
 
"I spent a couple of hours on your website www.fms-help.com and was delighted at what I read."
 
"I absolutely loved your [site]. It was inspiring, informative and so warm and personal!"
 
"I read your story www.fms-help.com/fibro.htm and it sounds like me. It actually made me cry!"  
 
"As far as I am concerned your site is one of the best that I have found on the internet. I use it regularly when talking to the members of the two support groups that I run."
 
"I am very impressed by your compassion and dedication."
 
"Your website has been a big help this past week."
 
"I just found your website. What a blessing.  I've read as much as I could for today. There's so much you are sharing with us. Thank you."
 
"Fibromyalgia is zapping my life away."
 
"Your website is very well put together and full of so much great information."
 
 
2.  "BEYOND THE DARK CLOUD"
 
Thea Schlosser, author of the CFIDS book, "Beyond the Dark Cloud"  told me she lowered the price of the book on Amazon.com to $4.95. Thea has had a terrible battle with CFIDS and suffered much because of the misdiagnosis and mismanagement by doctors. Her book is written very personally and straight from the heart.  It has gotten mixed reviews on amazon.  I have read the book and think much of it has merit. Thea concludes that CFIDS is a herpes strain virus infection. She also gives other important information about CFIDS, as well as her personal story.
 
 
 
3.  LYRICA
 
From a reader--
 
"I READ YOUR ARTICLE ON LYRICA AND FOR ME IT'S NOT GOOD EITHER.   I WAS IN A COMA FOR THREE WEEKS  WHEN I WAS TAKING LYRICA.   ALL I DID WAS SLEEP.   I MEAN IT WAS GOOD TO FINALLY SLEEP, BUT NOT LIKE THAT.   I WOKE UP FOR AN HOUR AND SLEPT AND SLEPT.  IT WAS HORRIBLE AND DIDNT EVEN HELP WITH PAIN OR ANYTHING ELSE FOR THAT MATTER."
 
 
4.  YERBA MATE
From a reader--
 
"In South America, yerba mate has been revered for centuries as the “drink of the gods” and is drunk daily for optimum health, sustained energy and mental clarity.  Of the six commonly used stimulants in the world: yerba mate, coffee, tea, kola nut, cocoa, and guarana, yerba mate triumphs as natures most balanced stimulant, delivering both energy and nutrition.  The leaves of the rainforest mate tree naturally contain 24 vitamins and minerals, 15 amino acids, abundant antioxidants. In fact, The Pasteur Institute and the Paris Scientific society in 1964 concluded "it is difficult to find a plant in any area of the world equal to mate in nutritional value" and that yerba mate contains "practically all of the vitamins necessary to sustain life.  See http://en.wikipedia.org/wiki/Yerba_mate and
http://www.guayaki.com/index.php?p=mate&id=136."
 
 
 
5.  IT WASN'T FIBRO
 
From a long-time reader--
 
"I ended up having Parkinson’s and severe allergies.  The pain stiffness malaise exhaustion etc were caused by these, not fibro.  It took almost 20 years to figure it out and find solutions.  I now take levo/carbidopa ,IV vitamin therapy and homeopathics and have a life again."

 

6.  CHOLESTEROL-LOWERING STATIN DRUGS LEAD TO MUSCLE PAIN
 
From a reader--
 
http://articlesofhealth.blogspot.com/2008/09/cholesterol-lowering-statin-drug-leads.html
 
 
 
7.  WHAT COUNTRY ARE YOU FROM?
 
 
My newsletter readers are from many countries: U.S., Canada, Australia, United Kingdom, New Zealand, South Africa, Belgium, Israel, Argentina, Cayman Islands, Uruguay, Bermuda, France and Singapore - to name most, but not all, of them.  If you don't see your country on my list, please write dombush@bellsouth.net.
 
 
 
8.  IF A DOG WAS THE TEACHER
 
This has nothing to do with fibro - except maybe give us some pointers on "stress management!"  I loved this email!
 
"If a dog was the teacher you would learn things like: 
 
When loved ones come home, always run to greet them. 
Never pass up the opportunity to go for a joy ride.
Allow the experience of fresh air and the wind in your face to be pure Ecstasy. 
Take naps. 
Stretch before rising.
Run, romp, and play daily. 
Thrive on attention and let people touch you. 
Avoid biting when a simple growl will do. 
On warm days, stop to lie on your back on the grass. 
On hot days, drink lots of water and lie under a shady tree. 
When you're happy, dance around and wag your entire body. 
Delight in the simple joy of a long walk. 
Be loyal. 
Never pretend to be something you're not. 
If what you want lies buried, dig until you find it. 
When someone is having a bad day, be silent, sit close by, and nuzzle them gently."
 
 
 
9.  FIBROMYALGIA & OCCUPATION
For a list of occupations my newsletter readers had when they were diagnosed with fibromyalgia, please visit http://www.fms-help.com/occupations.htm - most interesting!
 
 
 
 10.  ACCUPRESSURE POINTS FOR INSOMNIA & CFS
 
From a reader--
 
Try these points to help you sleep better:  http://www.herbalshop.com/Acupressure/Acupressure_07.htmlSome of them are easier to reach with a Theracane, but the ones in the front & chest should be easy.  Wishing you better sleep & fewer hot flashes!
 
Wow!  These diagrams are intriguing.  I'm going to try this.  We need as many non-drug ways to help ourselves as possible!
 



11.  HOW LONG UNTIL THERE IS A CURE FOR FIBROMYALGIA?
 
From http://www.stopfibromyalgianow.com/fibromyalgia-cure/how-long-will-it-take-to-find-a-cure-for-fibromyalgia#comments--

"Unfortunately, I don't think there will be a "cure," because it's a neurological disorder like MS. It's very difficult to repair damage to the nervous system.

BUT - the fact that researchers have identified it as a neurological disorder, and that we have proof of organic differences in fibromyalgia patients shows significant progress over the last decade.

Other studies have identified a genetic anomaly that seems to make some people more likely to fibromyalgia or TMJ/TMD or other painful disorders.

Knowing that FMS is neurological instead of rheumatological (or psychological, as some claimed) means that there's a much higher likelihood of good treatments coming along. And yes, it also makes it much more likely that somebody will develop a cure."



12.  TANNING BED CAUSED VIRAL REACTIVATION
 
 
From a reader--
 
"I had no idea fms could be caused by mercury.  i had a very unpleasant experience with it myself.  i tried to get mercury chelation rectal suppositories, but could only take two weeks of the proposed 90 day regimen.  (i was told hospital iv chelation could run over $25,000).  it initially seemed to help me feel better but i just had the EBV virus come out of dormancy and i'm back to square one again. i also believe that both fms and cfs are viral related.  researchers still have a long way to go in the field of viruses.  for me i think excessive heat reactivated the virus and they are supposed to start putting warnings on tanning beds concerning viral reactivations, but probably won't in the end."

I believe our condition is viral too, and it affects the brain and nervous system.  See www.fms-help.com for some interesting articles about this subject!
 
 
13.  THE TOP 10 MYCO-TOXIC FOODS
 
http://articles.mercola.com/sites/articles/archive/2003/11/05/toxic-foods.aspx
 
 
 
14.  FIBROMYALGIA & FATIGUE CENTER - FREE WEBINAR
 
http://now.eloqua.com/e/es.aspx?s=949&e=9efd9d0d5da24f148ebc1f542971c738&elq=C6B2D7CFB27149E3A184104C85B4E457
 
 
15.  ALPHA-STIM MACHINE
 
From a reader--
 
"Look up  www.alpha-stim.com  to see what it is, and what it does. It does require having a prescription to purchase one.  My psychologist let me use a "loaner" for a month to see if it would help me, or not before I purchased a product that cost so much.
 
It has helped me have lots more energy, much better mood, I can think more clearly and have hardly any brain-fog anymore.  And, the very best part is that I SLEEP FROM 6-8 HOURS PER NIGHT - along with my regular night time meds,, wwhich include 5 mg Elavil, and one Xanax.  Unheard of for me before the Alpha-Stim.
 
She would be the first to tell you that it doesn't work for everybody - the same way medications don't work the same for everyone.  But this product started working for me after one session of using it.  I am now to the point where I only have to use it once every TWO days.  It has worked miracles for me!!!  This, too has helped with the travel -- I feel so blessed that I can travel in a limited way again.  yaaaaaa!"
 
One day if my ship comes in (and doesn't sink at the dock, haha), I'd like to try one of these for insomnia, but $495 is a lot of moola.
 
 
 
16.  DOM'S UPDATE
 
 
I'm feeling better today than I have in a long while!  Just kicked a virus, and that helped.  I've also slowed down my schedule to a saner pace.  I'm preparing 25 piano students for a recital on Oct. 25 (7 adults and 18 children & teens).  It's soooo rewarding to share my love of the piano with others, and I'm glad I can still work, even if it is limited.  I also serve in music at my church www.fms-help.com/MBC.jpg filling in for keyboard musicians when they have surgery, vacation time, etc.
 
I will be 57 soon, and must admit I'm slowing down.  Strange though....my mother (age 87) runs circles around me!  At my current age she was digging up the yard with my father and planting grass.  She also went on several trips to China with my dad www.fms-help.com/eulogy.htm to see his family (after 40 years of separation due to China being closed for so long).  My brother quipped the other day, "You're older than MOM!!"  Fibro can sure make us feel that way!  I hear from 20-somethings who say they feel like 90.  I rely on various meds and supplements to keep me going - my list is at www.fms-help.com/what.htm. We are all different, but you might get some ideas if you are at wit's end with FMS/CFIDS.  I know how discouraged I felt when I was first diagnosed in 1982 - you can read my interview with Bella Online at www.fms-help.com/interview.htm.
 
Well, that's all for now.  Sorry I can't answer all of my email, but I try to read everything you send.  Visit me on my message board at http://health.groups.yahoo.com/group/dominie.  Nearly 400 newsletter readers are using the board now to offer information, lend support or just vent about fibro.  
 
Yours truly,
 
Dominie
 
 "Bear ye one another's burdens, and so fulfill the law of Christ."  Galatians 6:2
 
 
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DOMINIE'S FIBROMYALGIA & CHRONIC FATIGUE SYNDROME HOMEPAGE

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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.