*** DOMINIE'S NEWSLETTER (PAGE 1) ***
OCTOBER 2003

www.fms-help.com/October2003.htm

DISCLAIMER: I am not a medical doctor. I am a fibromyalgia/chronic fatigue syndrome survivor. The purpose of this newsletter 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 newsletter.
 
Scroll down further on this page to read the articles for topics 1-14: 
1.  LETTERS FROM READERS
2.  SAUNAS AND FMS
3.  TYPE A PERSONALITY AND FIBRO
4.  MAGNESIUM FOR MUSCLE TENSION
5.  STRESSED OUT
6.  TENDINITIS AND FIBROMYALGIA
7.  NEURONTIN (revisited)
8.  VITAMINS AND MINERALS
9.  FMS OR CFS?
10.  SEROTONIN AND FMS
11.  PROTEIN HELPS BRAIN NEUROTRANSMITTERS
12.  SIT COM STAR WITH FIBROMYALGIA
13.  A.D.D. AND FIBROMYALGIA
14.  SOUND AND THE PARASYMPATHETIC RESPONSE

Click here to read the articles for topics 15-25 below on PAGE 2:
15.  FOODS AND INFLAMMATION
16.  FOLIC ACID AND DEPRESSION
17.  KIDS' ALLERGIES
18.  ZOLOFT AND OXYCONTIN
19.  LOWER MUSCLE COLLAGEN IN FIBRO PATIENTS
20.  CAN A CANCER DRUG HELP CFS?
21.  COSTCO HAS LOWEST PRICES ON DRUGS (AND WHY)
22.  CONSTIPATION A PROBLEM?
23.  SPIRITUAL UPLIFT CORNER
24.  DOMINIE'S PERSONAL UPDATE
 
==========================================
 
1.  LETTERS FROM READERS
 
"I have really enjoyed the August newsletter http://www.fms-help.com/August2003.htm  I have been copying the newsletter each month since I first started reading it...I have put all the newsletters in plastic inserts in a notebook -  and it is a world of information - much better than anything you can get from the doctors who are attempting to treat us."  [NOTE FROM DOMINIE:  You can find the current issue of my FMS/CFIDS newsletter, as well as back issues at http://www.fms-help.com/newsletters.htm]
 
"Thank you so much for taking the time to put your marital harmony manual http://www.fms-help.com/marriage1.htm on the internet.  I am so blessed to have read it tonight.  I have printed out a copy to read as when I am discouraged.  I wish I could have had it this past year.  I suppose the Lord knows the timing better than me.  It has been a very rough year and I have a feeling the Lord is not through yet.  This will come in handy to say the least." 
 
"I share your newsletter and now website http://www.fms-help.com with anybody that I learn has Fibromyalgia or any of the other related illnesses. There is so much information, it's amazing!"
 
"Just want you to know that the immune balancer has helped me tremendously.  I started employment in a new position this past February, and have not missed one day due to sickness.  That is a record for me!  During the Spring and Fall allergy seasons, I have needed to add Allegra D and decongestants at times, but at least I am able to keep going with less symptoms."  [NOTE FROM DOMINIE:  I'm SO glad to hear this!!  I too have enjoyed incredibly better health since I starting taking the immune balancer 2 years ago.]
 
"Thanks for all the great info and wonderful service you provide."
 
"I'm just thankful that when I found out that I was a Fibromyalgia victim, your site http://www.fms-help.com was about the only one that really gave an in-depth hands-on report on the syndrome."
 
"I must agree Terri Beens article [MY NAME IS FIBROMYALGIA] is superb http://www.fms-help.com/mnif.htm and I am sure anyone who has Fibromyalgia would agree with every word.  Hopefully anyone who does not who reads this may understand that a bit more."
 
"I have been reading all your info on CFS http://www.fms-help.com/fatigue.htm and Fibromyalgia http://www.fms-help.com/fibro.htm and can't thank you enough for sharing all that you have been through.  I have suffered with this and constant pain in the whole body for so long I do not remember what it is to feel well!!" 
 
 
2.  SAUNAS AND FMS
 
From correspondence with a doctor--
 
"The sauna idea came because I heard of Mycobacterium as part of the the (FMS) problem, so if you recreate a safe but long state of fever, I suppose you can kill the bug and feel more relaxed after that."
 
 
3.  TYPE A PERSONALITY AND FIBRO
 
From a newsletter reader--
 
"I am 50 years old and was diagnosed with fibromyalgia July of this year.  I quit my job last May of 2002 because of so much physical pain and mental stress I was having. Didn't know what was going on with me.  I was diagnosed with osteoporosis in 2000 and I thought that maybe that was my problem. I thought after I quit my job maybe a few months of rest would cure me.  I was wrong.  Still had lots of pain.  I starting seeing Dr's to see what was going on with me. The first one I went to said I need to get a new bed exercise more. The 2nd one said I also need to exercise more, lose weight and get back to work and that I had chronic pain syndrome. He said that he would put me on narcotic to help with pain. The last Dr. I saw a couple of months ago who is a woman Dr. knew what was wrong with me, it was fibromyalgia.  Up until 2 months ago I knew nothing about this disease.  It was a relief for me to know that I wasn't crazy and that I did indeed have a reason for feeling so bad.  I have worked most of my life and a type A personality.  Never saying no to anything and going the extra mile for family,friends, etc.  Always trying to keep a smile, caring for others and letting myself and my health and welfare be put on the side lines."   [NOTE FROM DOMINIE:  This is so typical of many of us with fibro....we need to take good care of ourselves, not just others!]
 
 
4. MAGNESIUM FOR MUSCLE TENSION
 
From immunesupport.com's Tip of the Day--
 
"Some researchers believe magnesium holds the key to resolving many types of chronic pain. In the body, magnesium converts vitamin D, which the body needs to take advantage of bone-strengthening calcium, into a form that it can use efficiently. By contributing to increased bone density, the mineral may help stall the onset of osteoporosis. Magnesium may also help to ease tension headaches, muscle cramps, muscle strains, and muscle tension. If you have a magnesium deficiency, you may experience excessive muscle tension, which may trigger muscle spasms, restlessness, tics, and twitches."  (Source: The Women's Guide to Ending Pain: An 8-Step Program, by Howard S. Smith, M.D., and Debra Fulghum Bruce, M.S. Published by John Wiley & Sons, Inc.)  [NOTE FROM DOMINIE:  See my tip about magnesium at http://www.fms-help.com/tips1.htm#20 ]
 
 
5. STRESSED OUT
 
From immunesupport.com's Tip of the Day--
 
"If your fibromyalgia leaves you feeling "stressed out" frequently, exercise can help desensitize your body to stress. A study published in February 2002 in Arthritis Care and Research confirms that a combination of cardiovascular exercise and strength training helps women with fibromyalgia increase their strength and endurance, and reduce their fatigue, pain, stiffness, and depression."  (Source: The Women's Guide to Ending Pain: An 8-Step Program, by Howard S. Smith, M.D., and Debra Fulghum Bruce, M.S. Published by John Wiley & Sons, Inc.)  [NOTE FROM DOMINIE:  This is generally good advice, but I can remember when even the slightest physical activity caused days and even weeks of severe fibromyalgia pain.  If this is the case with you, please read my 100 Tips for Coping with Fibromyalgia and Insomnia at http://www.fms-help.com/tips.htm  and also my personal fibro story at http://www.fms-help.com/fibro.htm  The only people who understand what it's like to have this illness are those of us who have it!]
 
 
6.  TENDINITIS AND FIBROMYALGIA
 
From immunesupport.com's weekly bulletin--
 
The aim of this study was to evaluate the role of common tendinitis in fibromyalgia. Twenty female patients with primary fibromyalgia syndrome, 20 with secondary fibromyalgia syndrome and 20 female controls, matched by age and body mass index, participated in the study.
http://go1.warp9ems.com/go.pl?tu=34554153-15826
 
 
7.  NEURONTIN (revisited)
 
In the last couple issues of the newsletter, readers have been writing in about their experiences (positive and negative) with Neurontin. 
 
Here is another comment I received--
 
"I have been taking neurontin for my fibromyalgia and the neuropathy from whatever (radiation, diabetes, fibro)   I do not take as much as the MD wants me to take (which would be l200 - l800 mgs per day).  I h ave found when I have the burning, searing, pain in my back and shoulders just 300 mgs. of it helps me  quickly.  If I take 600 mgs. at one time it makes me too drowsy.  It seems that neurontin is being prescribed for a lot of health problems and not just as a seizure drug.  I have found some good results from taking some neurontin."
 
 
8.  VITAMINS AND MINERALS
 
Some people find help with vitamins and minerals, herbs or immune system balancers.  Anything we can do to naturally supply our bodies with what it needs to stay healthy is better than using drugs when there is a function breakdown.  Fortunately, we have the internet to do research and become informed about the many options available to us.  I sure wish the internet had been available back in 1982 when I was first diagnosed!  I had to rely on the few paragraphs I found in the Merck Manual in the public library for an understanding of my newly diagnosed condition (then called "fibrositis").  For an interesting starting place on the net, check out my 100 Tips for Coping at www.fms-help.com/tips.htm
 
 
9.  FMS OR CFS?
 
From immunesupport.com's newsletter--
 
Chronic Fatigue Syndrome and Fibromyalgia: Important Similarities &
Differences -- Dr. Charles Shepherd writes, "In view of all the recent discussion about areas of overlap between ME, Chronic Fatigue Syndrome, and fibromyalgia syndrome, here are what I believe are some of the key areas of similarity and difference." 
http://go1.warp9ems.com/go.pl?tu=31915365-14960  [NOTE FROM DOMINIE:  I developed FMS in 1982.  My fibromyalgia story is at http://www.fms-help.com/fibro.htm  Five years later in 1987, I developed CFIDS after a lingering viral illness.  My CFIDS story is at http://www.fms-help.com/fatigue.htm  These accounts maybe helpful to read if you're trying to compare symptoms.]

10.  SEROTONIN AND FMS
 
From immunesupport.com's Tip of the Day--
 
Like other rheumatic diseases, fibromyalgia could be the result of a genetic tendency. When a woman with this tendency is exposed to certain emotional or physical stressors (like a traumatic crisis or serious illness), there is a change in her body's response to stress. Scientists theorize that one of these body changes is a low level of the hormone CRH (corticotropin-releasing hormone), resulting in higher sensitivity to pain and more fatigue, including the fatigue one experiences after exercise.  This hypersensitivity to pain may in part be from low levels of serotonin. Lower levels of serotonin cause a lower pain threshold and disordered sleep. The end result may be the chronic widespread pain of fibromyalgia. Some studies show that women have approximately seven times less serotonin in the brain, which may explain why FMS is more prevalent in women. Abnormal transport of serum tryptophan (a precursor for serotonin) has also been described in clinical findings.  (Source: The Women's Guide to Ending Pain: An 8-Step Program, by Howard S. Smith, M.D., and Debra Fulghum Bruce, M.S. Published by John Wiley & Sons, Inc.)  [NOTE FROM DOMINIE:  See my 100 Tips for Coping with Fibromyalgia and Insomnia at http://www.fms-help.com/tips.htm  Remember that I am not a doctor....just an FMS/CFIDS survivor.]
 
 
11.  PROTEIN HELPS BRAIN NEUROTRANSMITTERS
 
From immunesupport.com's Tip of the Day--
 
If pain leaves you feeling fatigued and lifeless, you may want to increase the amount of protein you eat, particularly foods like tuna, chicken, or turkey that are rich in an amino acid called tyrosine. When we eat protein food, this increases tyrosine, which boosts the levels of dopamine and norepinephrine, two brain neurotransmitters that increase a feeling of alertness and boost concentration.  (Source: The Women's Guide to Ending Pain: An 8-Step Program, by Howard S. Smith, M.D., and Debra Fulghum Bruce, M.S. Published by John Wiley & Sons, Inc.)
 
 
12.  SIT COM STAR WITH FIBROMYALGIA
 
Check out this site about A.J. Langer, an actress with FMS who is speaking out! - http://srino.com/aj/aj_langer_fm_aware.html   However, she does not wish to be an advocate for people with fibromyalgia, according to the article.  This information was sent in by Terri Been, author of "My Name is Fibromyalgia," which helps people understand what it's like to have FMS.  With Terri's kind permission, you can read her article on my site at http://www.fms-help.com/mnif.htm
 
 
13.  A.D.D. AND FIBROMYALGIA
 
From newsletter reader, Patsy Stephens.  Stimulants help some people with fibro pain--see http://www.add-fibromyalgia.com
 
 
14.  SOUND AND THE PARASYMPATHETIC RESPONSE
 
From immunesupport.com's Tip of the Day--
 
Perhaps the most popular relaxation modality is music therapy. Whether New Age, rock, jazz, or classical, many people find that music distracts them from the painful moment, helping to reduce mental stress. In fact, in some hospitals, staff members give patients tapes of soothing music and reassuring voice-overs to use during surgical procedures. In clinical studies, both doctors and patients agreed that listening to music produced greater decreases in peaks of tension, and produced greater compliance with relaxation practice. While the studies are limited, it's thought that music therapy can help to improve mood and pain tolerance. This therapy is thought to enhance the parasympathetic response through the effects of sound, encouraging relaxation at a deep level. (Source: The Women's Guide to Ending Pain: An 8-Step Program, by Howard S. Smith, M.D., and Debra Fulghum Bruce, M.S. Published by John Wiley & Sons, Inc.) [NOTE FROM DOMINIE:  On several occasions in the past, despite my lifelong sleep disorder, I found that having my husband read to me in bed helped me fall asleep within just a few minutes, as opposed to a few hours!  There was something about his low resonating voice that calmed and relaxed me at a deep level in my brain.  Now if only I could get him to read to me every night!!.....but he doesn't like it when I fall asleep when he is reading--it seems like an insult....actually, it is a great compliment!!!   I need my bedtime story!!  Maybe I should make a tape of his voice??  Another thing that used to help me was listening to the scriptures on tape read by a low male voice.  I used to wear headphones and would drift off to sleep that way.  Listening to music sometimes does the same thing for me, but not always.  I have to distract myself to go to sleep.  If I think about going to sleep I will stay awake.  Another trick I read about is to think about your toes, then roll your eyes upwards, then think about your toes, then roll your eyes upwards.  Do this slowly, and before you know it, you will be yawning and relaxing.  Think of a cat rolling her eyes up into her head as she becomes sleepy.  Another thing I do to invite sleep is to think back into the past of a happy peaceful memory....the further back into the past I go, the more I start to feel relaxed and sleepy.  I think it is because the past is certain, it is done and cannot be changed.  The future is uncertain and I am prone to worry and anxiety, so it is better for me to think about the past and not the present or future when falling asleep.]
 

 
CLICK HERE to read TOPICS 15-25 on Page 2.