DOM'S NEWSLETTER
www.fms-help.com
 
  Tulips 
March 1, 2008
 
A compassionate informative newsletter for people with FMS (Fibromyalgia Syndrome), CFIDS (Chronic Fatigue & Immune Dysfunction Syndrome) and M.E. (Myalgic Encephalomyelitis)
 
SCROLL DOWN TO CHECK OUT 25 INTERESTING TOPICS IN PURPLE
 

 
1.  READERS WRITE
 White Water Rafting 
 
"Thank you for all the articles you find and share.  It’s so good to be in the same boat, even if my life jacket is a bit more damaged."
 
"I just got done reading you 100 tips to coping with fibromyalgia at www.fms-help.com/tips.htm.   It's a frustrating, draining, and painful thing to deal with.  Thank you for taking the time to spread the knowledge you've learned."
 
"You know how it is when people who are otherwise healthy DO NOT have a CLUE as to what's going on in your body.  Please continue to send me your E newsletter.  It just helps to know someone else is out there who cares."
"Thank you so much for being there continually in this storm of so many peoples lives."
 
"I am really learning a lot from your website www.fms-help.com. I am a registered nurse and have worked in nursing leadership for years."
 
"Thanks for your devotion. It is very appreciated! The topics are always what we need."
 
"Your story www.fms-help.com/fibro.htm is just like mine.  As I was reading what you have to say, I felt as if it were me who had written it myself."
 
"Just read through most of your website. Very informative."
 
"Your newsletter is such blessing! I know I say it almost every time I receive a newsletter, but it really is!!"
 
"You have sent me some awesome info.  I love it. You inspire me to keep looking, studying, and hang on for hope. At the little local FMS monthly meet, I spread you around like honey and all were impressed even the hardheaded ones."
 
"I came across your brilliant website today and have bookmarked it for later reading."
 
"You are definitely a light in the world of fibro people and I am truly grateful I found you out there."
 
"I am just really happy to have found your information regarding fibro!  I have been suffering now for two years.  Most every thing I search for on the internet is not free.  I am grateful that you have shared your experiences www.fms-help.com/fibro.htm and helpful tips www.fms-help.com/tips.htm."
 
"This is a wonderful site www.fms-help.com for people with fibro."
 
"I stumbled across your site this morning.  Thank you for sharing your story and experiences with those of us who cope daily and hourly with fibro.  I especially LOVE the sleep discussion and info on it."
 
"I was very impressed with your website."

 
2.  MERCURY REMOVAL DID NOT HELP FIBRO OR TINNITUS
 
Reader 1--
"I bought into the mercury and pain/tinnitus theory.  After having all my amalgams removed and cavitations cleaned out and many chelation treatments to remove metals, guess what?  My savings were gone; I still had the symptoms and the tinnitus was still there.  I was one of several persons who went through these steps to get better and none of us would do it again if we were advised to. It didn’t help. We still have fibro and tinnitus.

Mercury can aggravate the ringing and the primary offensive source is seafood. There may be a correlation between the increase of symptoms when eating foods high in mercury. I have found it true in my case. I find it best to stay away from seafood that is not wild caught in deep waters well away from shore;  also fatty seafood of any kind. I tried experimenting to see the effects of high fatty fish and sure enough the ringing in my ears got worse, especially in the right ear. I do take EPA/DHA capsules and they are pharmaceutical grade. These have been purified to remove metals and other contaminants in fish. So that way I get the omega 3’s so important to our health.

The American Academy of Physicians put out a good report on Tinnitus about 4 years ago that listed among its causes  neurological and metabolic disorders (thyroid, high lipids, and vitamin B12 deficiency). Many of us with fibro have been diagnosed with some or all of these.

This is just my two cents worth from my own expensive efforts to alleviate my many fibro, loud ear symptoms. I found other things worked to help me improve very much but it has not helped the wretched ringing, hissing, and siren sounds especially in my right ear. Keep us posted please on tinnitus. Perhaps someone has or will learn of some things that REALLY work. For me, avoiding foods that contain mercury are the best I can find for the ringing."

Reader 2--
"I, too, suffer from tinnitis....it can be as gentle as a ringing in the back of my head to the sound of a car horn so deafening I cannot describe it.  Being a product of the 50's and free dental care at a local dental school, I  had a mouthful of mercury fillings, and due to a sudden dental flare in 2003, I spent  over an entire month  in a dentist's chair;  she had to remove all my fillings and after having  completed the work  to correct my problems,  she gave me nice, new 'white' fillings.  Having the mercury removed was something I was very excited about, but I am sorry to say that I have yet to have any positive results from it.  As a matter of fact (and coincidentally as well, for I know it Is NOT the cause), I have become worse due to a complete body covering of myofascial pain - it is a LAYER of pain, especially in both legs entirely."
 
Reader 3--
"I spent about $1500 6 years ago to have all my silver fillings
removed. Then had to take special supplements for a year because it
is impossible to remove them without toxic release. Did not have many
but was told to get them out because they were linked to Fibro and
auto immune problems.  Here I am today with the symptoms I had back then plus many more.
Waste of money and was not a pleasant experience."
 
     
3.  MORE ON TINNITUS (RINGING IN THE EARS)
From a reader about the article in the last newsletter at www.fms-help.com/021708.htm--
"Tinnitus just started this year and is driving the musician part of me crazy.  Loud noise seem 10X loud some days.  The specialist had me on Cipro to help my ears, but they’re still about the same, just with less pain.  I have to go back for a hearing check and I’m going to cross both my fingers and toes on this.  I need my hearing, especially as a mother.  I hate the fact that Fibro has stolen so much of my life and time already."

 
4.  CELL PHONES & INSOMNIA
From a reader--
"The cell phone article www.fms-help.com/021708.htm was particularly interesting.. we had on our NY news a report that you should ot let your cell phone charge up at night in the room  in which you sleep. There is a low frequency sound that disrupts the sleep cycles..I moved mine to the dining room and I think it does make a difference."
 
 
5.  RIBOSE
From a reader--
"I have been taking Ribose powder  twice daily, and cant believe the difference it has made. I feel mentally alert most of the time, even though I still forget to do things!!!!!!  I might not always have the energy to do what I want to do, but at least I have reached the stage of wanting to do something.  I think only a fibromite would really appreciate that statement. But one thing I have noticed on it - I laugh more than I use to.  It makes me feel like me."

 
6.  ANTIBIOTICS & YEAST
From a reader--
"I saw in your newsletter www.fms-help.com/021708.htm that you avoid antibiotics until you are too sick to do without them because they destroy the good bacteria in the gut.  My GI doc has me take Culturelle (found in the digestive health section of Wal-Mart and drugstores) if I need an antibiotic. It puts back the good bacteria.  You can do the same with yogurt that has live cultures.  Much better than suffering."
This is a great tip!  I take acidophilus when I am forced to use antibiotics, but sometimes still get a problem with yeast....ugh.....maybe I should take more.
 
 
7.  GLUTEN-FREE HELPS
Reader 1--
"In the few months that I've been gluten free (or maybe not so long as it takes awhile to find out all of the stuff that gluten is in - had to buy a new toaster for example),  my IBD and stomach bloating have completely disappeared.  My pain level has really diminished (except for a week long flare following a dental extraction)  and my smell/chemical sensitivity is much, much better.  Before, I had to hold my nose whenever I walked down the detergent or bug spray aisle in the grocery.
 
The best book to read is "Dangerous Grains" - but I'd spent 8 hours a day for several months investigating all of the reasons for even having fibro. Bought every fibro book and bookmarked dozens of articles regarding food intolerances and their symptoms.   Found a great new doctor and was tested for a variety of things.  Neurotransmitters, insulin, thyroid, growth hormone, vitamin d, etc - all normal.  My ANA was elevated and my iGg antibody test was sky high.  My doctor (who believes that 40% of the population has a gluten sensitivity) suspected that I have it.
 
I just had new blood work done and will get the results back next week. I will let you know if there are any changes with my new blood work.  I am currently taking Soma only but take about 20 various supplements, as well as eating lots of fresh fruits and veggies. I try and walk at least a mile or so every other day."
 
Reader 2--
"I am an RD and have celiac. The best website I have found for gluten free diet is www.celiac.com - it is excellent and has been very helpful for my patients.  The basic thing is no wheat, barley, rye.  This does not mean you cannot have corn or rice gluten. Oats are controversial but you need to choose a plant that doesn't produce anything else.  The simplest way to do it is to eat only plain meat and veggies and fruit (I can't eat fruit because fructose is a  problem with me and my IBS as well as others - this has been published as well).  I also recommend the specific carbohydrate diet and the body ecology diet.  I truly believe you have to have the probiotics and fermented foods to get better.  They also host at www.glutenfreeforum.com but you can access it from the celiac site."
 
 
8.  POST TRAUMATIC STRESS DISORDER (PTSD)
From a reader--
"I finally found out my fatigue is due to PTSD and have found some relief through Glenn Schiraldi's book, "The Post Traumatic Stress Disorder Sourcebook."   Basically the trauma keeps the stress locked in my body; so I have been using the beginning of "Saving Private Ryan" and/or "Shawshank Redemption" to assist me in changing my perspective so that I can grieve. It works!  It is life or death.  The grief has to come out, so I induce it to change my feelings and so far it works."
I do believe many of us with FMS/CFIDS have PTSD as a precipitating factor.  You can do a Google search of Ashok Gupta's theory that CFS begins in the amygdala as a result of stress - also see my previous newsletters with this topic at www.fms-help.com/newsletters.htm.

 
 
9.  SPELT IS NOT GLUTEN FREE & GREAT PLAINS LAB
From a reader--
"I just wanted to make a correction on
one of your user's submittal at
www.fms-help.com/021708.htm.
Reader number 3 under the gluten free topic
refers to spelt as gluten free.  She is correct that spelt is recommended
on the Type O blood type diet, but spelt DOES contain gluten.  So readers
who want to try a gluten free diet should
be wary of spelt, barley, and
rye.  I've read conflicting information on oats.  To be gluten free you
must avoid all grains except for rice, millet, quinoa, amaranth.
  Those are
the only gluten free grains I'm aware of so far.  It is easy to go gluten
free.. you can still have potatoes, squash, and the grains I mention. I was
on  the blood type diet for many years and found it very helpful , but then
my condition worsened ( I was still wheat free, but using spelt flour
liberally).  I recently was tested by Great Plains Labs and tested positive
for yeast/fungus.  I'm now on a diet to not feed the yeast ( no grains, no
sugar of any kind including honey, maple syrup, etc, no alcohol, no aged
cheese, no vinegar, no dairy, no fruit, no fruit juice, nothing
processed) and Nystatin a drug to kill the yeast.  I've been on the diet
for 2 weeks and the drug and I am thinking much more clearly.  I urge your
readers to go to the Great Plains Lab website and take a look.  Their full
acid test (urine) that tests for fungus/yeast and other things, is now
covered by Blue Cross Blue Shield.  As are many of the other detailed
tests. They also do food allergy testing (this was not covered by blue
cross blue shield).  It will be interesting to see where the candida/yeast
treatment leads.  I am on the fence regarding Lyme Disease versus
Autoimmune versus Candida versus FMS.  After 10 years of an FMS diagnosis,
I suffered a bout of optic neuritis with some loss of vision in one eye and
increasing neurological symptoms. I did not test positive for autoimmune.
I did test positive for Lyme on IGENX lab's western blot , but no according
to CDC critieria.   Lyme Disease, FMS, and Candida (which some Dr.'s
believe to be the root cause of autoimmune) all overlap in symptoms.  I
wish I had gone down the Candida testing path 10 years ago, before my
condition worsened.  I encourage your readers to get food allergy and
candida testing by Great Plains Labs.  They specialize in Autism and
killing the yeast is a key treatement today for Autism.  It is interesting
how much overlap there is between FMS, CFS, and Autism when you look at
some of the testing that is done by Great Plains Labs.  There is a Dr. out
of Maine - Dr. Amy Yasko, who believes this is not coincidence, but there
is a similar root cause with the body's inability to detoxify.
I emailed Yvonne regarding the lab she used for
yeast/candida testing.  It was Great Plains Lab.  That is what started me
down the yeast route. 
http://www.immunesupport.com/library/showarticle.cfm?id=8334&T=CFIDS_FM&B1=EM092607F."

 
 
10.  CELIAC DISEASE - ROOT OF FIBRO SYMPTOMS?
From a reader--
"I am reader #4 in the newsletter at www.fms-help.com/021708.htm.  Like reader #3, I am a type O blood type who had read the book "Eat Right For Your Type", and had switched from whole wheat bread to spelt, ultimately settling on Berlin Bakery's bread.  In 2003, my peristalsis stopped and I got very ill.  I sought professional help from an RN who is a colon hypdrotherapist and nutritionist.  I was advised to eliminate grains, fruit, and certain other foods to combat a candida overgrowth.  Last year, I started eating the spelt bread again, along with rye bread in restaurants.  For the last few years, my pain and stiffness was much worse.  I could tell though, that the pain and stiffness were a lot worse the day after eating spelt bread.  From my new holistic doctor, I know that glands in our bodies, like our adrenals, excrete hormones that help us deal with poisons (that is a very general idea).  So, by eliminating the poisons, it just makes the messages our bodies are trying to tell us so much clearer when we are exposed to the poisons. 
 
Celiac disease is a very insidious disease, and a very serious and deadly disease.  One needs a very good doctor who is experienced with the disease, and its hundreds of other diseases and symptoms it can cause.  A good place to start learning about the disease and the gluten-free diet is www.celiaccentral.org.  A good support group, like the yahoo group SillyYaks, is also necessary for diagnosed celiacs.
 
Regarding the diet, wheat, rye, barley and all of wheat's derivatives and relatives, including spelt, must be eliminated.  One has to read about the history of the cultivation of wheat to understand that today's wheat is a grass that has been reengineered by man, and has 55 times the gluten of the wheat of biblical times.  My doctor told me that the Bible instructs us to sprout grains before eating them, which eliminates most of the gluten.  However, that won't work for me now.  Dr. Kenneth Fine, a leading researcher, has identified some gluten-intolerance genes besides the two celiac genes.  His research found that 81% of Americans have some sort of gluten-intolerant gene(s).  I have both the most common celiac gene and another gluten intolerant (non-celiac) gene.  That makes me more sensitive to gluten and makes my symptoms worse.  People can have 2 celiac genes, and their sensitivity is the worst
 
You do not become ultra-sensitized to gluten by avoiding it.  You become ultra-sensitized to it by having a celiac gene, consuming gluten, and having the gene be turned on by some sort of physical or mental stress or trauma.  And, you are more likely to become sensitized to it if your mother does not nurse you long enough when you are a baby, or, as in my case, not at all."
 
 
11.  GLUTEN FREE DIET NOT ALL IT'S CRACKED UP TO BE
From a reader--
"I am a Gulf War veteran from the first Gulf War (1990-91), and I have tried every diet on the books plus a few diets I made up on my own with my doctors' approvals. I cannot work at my profession any longer, too young to be retired. But my "sense of purpose" is to do what I do best -- investigate and report on Gulf War Illness and all of its ugly stepsisters like Fibro and Fatigue. I have 17 years of experience in investigating both law and medicine as it pertains to Gulf War Illness, et al (my legal term for those ugly step-sisters).
 

    I have found abundant peer-reviewed medical literature and numerous specialized physicians backing up my educated theory on drug and food sensitivities that accompany these chronic, debilitating illnesses. EVERYBODY's food and drug sensitivities (they are NOT allergies) change as the disease waxes and wanes. Food avoidance for a time can be a healthy thing -- cutting out FOREVER entire segments of the food pyramid and/or whatever bothers you is a terrible thing and can actually change your pH balance, causing even more damage to the fibro and fatigue system overall.

 

    The very best way to address food sensitivities is to detox either orally or though IV infusion therapy. Avoiding gluten means avoiding many of the grains that are essential for producing energy at the cellular level. And usually, it is not the gluten at all that is bothering the fibro or fatigue "victim". It is either fungal overgrowth in the intestine or sensitivity to molds that begin to grow the instant breads and grains leave the oven, dropping toward room temperature. Both fungus and mold cause depression. Mold causes incredible, debilitating pain.

    I have found that I am extremely sensitive to raw nuts and raw whole oats if I have not "de-toxed" in a while. Neither of those foods contains gluten. However, nuts always have mold on them. I cannot explain sensitivity to raw oats, other than they are a "sleep enhancer". (Can't sleep? Just try one or two oatmeal raisin cookies at bedtime. Works for me every time.) I bake my own bread, so preservatives and gluten are not the issue. I have tried gluten-free recipes. I have switched from rye to organic whole wheat to potato based to multi-grain to whole oats flours. I even bake my own white bread. And I have found that I can tolerate all of them as long as the bread is toasted or still hot. I cannot eat sandwiches or hamburgers or hotdogs because the bread is cold and chock full of mold. I never use a microwave oven -- for health reasons related to Gulf War Illness and radiation poisoning. And I do not believe that microwaved breads are mold free, even while still hot if you use a microwave "roll warmer".

 

    Detoxing requires a multi-faceted approach. I use prescription-strength Diflucan, an antifungal agent that targets both the gut and the adjacent female organs. I have never suffered from female fungal infections, but I do fully understand what they are. Fungal infections start in the intestine because most people do not eat enough dairy cultures to keep the gut flora in balance. I was raised on farm and ranch foods and products, so I have never had a short supply of buttermilk, cheese, yogurt, sour cream, cream cheese, or kefir, which I make myself with organic whole milk and kefir granules. Even organic whole milk has been processed so that it is deficient in dairy cultures. I cannot tolerate regular milk, yet I am not lactose intolerant, never have been. I personally believe that fibro and fatigue victims should consume dairy cultures with every meal. I take probiotics and digestive enzymes prescribed by my doctor every day. They are available at www.immunesupport.com and www.OrthoMolecularProducts.com.

 

    Secondary to oral fungal detox, I use prescription-strength antifungal shampoo on the days that I do not take the Diflucan (oral tablet). My doctor prescribes 2% Ketaconazole shampoo. I leave the shampoo on my hair at least 5 minutes during my warm shower so that it soaks into the scalp to the subdermal "fatty" layer. Fat underneath the skin stores nasty stuff, such as toxins, fungus, parasites, bacteria that can cause acne, probably herpes viruses such as cold sores and genital herpes or genital warts, heavy metals, and the "stuff" that Type II diabetes is made of. Depleted Uranium, a heavy metal nuclear waste used in all munitions and military ammunitions since at least 1985, causes my scalp problems. I suffer radiation poisoning apparent mostly underneath my scalp in the fatty tissues.

 

    I also suffer systemic candidiasis, which means Candida Albicans is thriving in my blood stream. For most fibro and fatigue victims, systemic candidiasis is a result of not getting rid of fungal overgrowth in the gut while the nasty stuff was still contained therein. For women, it is also an indication that they did not take antifungals or use antifungal vaginal creams while they were taking antibiotics or other medications that feed fungus.

 

    Third, I take oral blood-and-liver detox capsules just one day per week. They are available at most whole foods stores. Major ingredients are Hawthorn extract, Red Clover, Garlic, Burdock Root, Goldenseal Root, Ginger Root, olive leaf extract, grape seed extract, oregano oil, capsicum (high-grade cayenne pepper), CoQ10. Not all blood and liver detox capsules contain all of the aforementioned. These detox capsules make me very, very sick the day of and the next day. And stool has a strong, metallic, rather sickly smell the next day. But I feel like a million bucks the very next day. As an alternative that is milder than capsules, I take Healthy Heart, extract distributed by Tahitian Nonie, available to distributors and members only. Anyone endeavoring blood-and-liver detox should have plenty of prescription pain meds available, and plan on sleeping through most of the 24-hour process. Drinking filtered water, more than a gallon per 24 hours, is critical. You won't be hungry at all, believe me. The two types of capsules that I take most frequently are Heart Support by "NOW FOODS" www.nowfoods.com, and Detox Blood Purifier with Goldenseal by Crystal Star, by Linda Page, PhD and Traditional Naturopath. She is author of the book "Healthy Healing - A Guide to Self-Healing for Everyone". Before taking ANY of these over-the-counter detox capsules or extracts, all fibro and fatigue victims should talk to their treating physicians. Detox CAN make you feel as though you are suffering a heart-attack because of the flood of fungus, parasites, heavy metals and toxins leaving the body through the stomach and gut in such a short period of time. I experience incredible abdominal swelling with intestinal pain. 

 

    Fourth, and not readily available to most fibro and fatigue victims, is IV infusion therapy. I have been on weekly IV therapy since I could finally tolerate it so frequently, November 2006. The detox includes extremely diluted pharmaceutical grade hydrogen peroxide (7% H2O2 extremely diluted in dextrose solution), dimethyl sulfoxide (DMSO or sulfur compound), glutathione (another sulfur compound), and pharmaceutical-grade garlic extract. You can find M.D.s who administer such IV infusions by visiting Oxidative Medicine Division at American College for Advancement of Medicine (www.acam.org) website. In the Oxidative Medicine menu option, type in your zip code instead of a doctor's name or an area of practice of medicine, and then SCROLL down manually to see the results of your search. These doctors do NOT accept insurance, but you can file your own claims for reimbursement. Most states have "health freedom" laws that force the health insurance companies to pay for at least a portion of the cost of IV infusion therapy. Also, Medicare supplemental insurance will cover at least part of IV infusion therapy.

 

    For everyone reading my comments, I wish you happy eating anything that you want, after you successfully start your detox program with your physician's nod of approval. And just for me - if for no other reason - stay away from colonics, colon cleansing, and doctors who insist that you need radiation scans of your gut. Those three habits will kill you quicker than a single glass of hemlock."

 
 
12.  LYRICA
Reader 1--
"I thought Lyrica was going to be my wonder cure till I wanted to kill myself !! I have struggled with this horrible illness CFS/Fibro for 8 yrs now . I have beed anxious and depressed off and on. I decided to try the Lyrica bc I have tried "all things under the sun " that is legal anyway ....( there has been extreme pain moments ....if I wasnt the person I am...you never know ) anyway , I started on 75 mg ...1 a day . I felt great !  Or so I thought . My dose was increased gradually over weeks and as the pain decreased my moodiness, anxiety, depression and suicidal thoughts increased. I told my husband on 2 different nights to "just drop me off at the mental hospital!"  Well, needless to say I am now off Lyrica and slowly as the doses decresed , I started to get my self back , pain & all 25 -30 lbs of weight gain too. So to those it helps - GREAT.  But it's not for me. I just wish the government would take notice and put a warning label bc more woman are coming forward to tell their story regarding the severity of complications from Lyrica."
 
Reader 2--
"I was put on Lyrica last month.  It did take away almost all of the symptoms but unfortunately it upset my stomach something fierce.  To the point that I have stopped taking it for the moment anyway?  I may try again later?  I had the same kinda problem with Celebrex, it did help with the symptoms but after I took it for a couple of months I ended up in the emergency room with bleeding from my stomach.  Maybe best just to stick to the pain meds?"
 
 
13.  CANDIDA (YEAST OVERGROWTH)
From a reader--
"I am not alergic to gluten but I do feel Sooo much better when I limit my intake of yeast products (yeast overgrowth causes inflammation), non organic meat ( bc of chemicals ), processed foods, high acidity foods, fried and or very fatty foods, refined sugers, sodas( No sodas at all )  etc . I dont drink alcohol, smoke, I try to exercise when I can.  I have talked to 100's of woman who say they overall feel better when they eat foods in the God made natural state as much as they can."
 
 
14.  TYPE A PERSONALITY
From a reader--
"I could really relate to your section on Type A personality www.fms-help.com/tips.htmI am going through the withdrawal from who I have always been right now. It is difficult."
I sooo understand this!  I have to say NO to a lot of things I would very much like to participate in and things I would love to accomplish with my life.  Stress is my worst enemy.  I have to avoid it like the plague!
 
 
15.   SOCIAL SECURITY DISABILITY
From a reader--
"I was told yesterday by yet another lawyer that because I haven't worked in over 10 years, I will never be able to collect ss disability.  You might want to spread the word.  My neck and back are so bad that I can't even get a job much less hold one down."
See www.fms-help.com/disability.htm for Dom's newsletter readers' advice on getting SSD for FMS/CFIDS.
 
 
16.  HOW DOES YOUR BODY KNOW WHEN TO SLEEP?
http://www.womentowomen.com/fatigueandstress/insomnia.aspx - "So how does the body know when to sleep? Deep in your brain lies a tiny but powerful cluster of nerve cells called the suprachiasmatic nucleus (SCN) that works 24/7 as your internal clock. It is not just a sleep clock, but governs many biological activities such as cell regeneration, detoxification, patterns of brain activity, and production of important hormones that regulate the sleep/wake cycle." 
Too bad their sleep suggestions don't work for most fibromites - only normal folks.  My "sleep clock" broke when I was a teenager.  I am now 56.  My insomnia story is at www.fms-help.com/sleep.htm.
 
 
17.  SED RATE
People with FMS generally don't have an elevated SED RATE (blood test).  Here's info on what a "SED RATE" is (article is from a reader)--
Sedimentation rate (sed rate) measures the speed at which red blood
cells settle to the bottom of a test tube. The presence of certain
abnormal proteins in the blood can cause red blood cells to stick
together and sink to the bottom more quickly.

Sed rate is a screening test for many different diseases. A high sed
rate is not specific to any one disease. Possible causes include:

    * Infection
    * Inflammatory diseases, such as rheumatoid arthritis and lupus
    * Blood cancers, such as leukemia and lymphoma
    * Cancers that have spread (metastasized)

An elevated sed rate may indicate an underlying problem. But further
testing is needed to identify the cause of the problem.
 
 
18.   TEN COMMANDMENTS FOR INTERACTING WITH THE CHRONICALLY ILL
(Boy are these good!)
http://www.anapsid.org/cnd/coping/looksick.html
 
 
19.  THE LOSS OF SADNESS
From a reader--
This book sounds trippy:
The Loss of Sadness: How Psychiatry Transformed Normal Sorrow into Depressive Disorder
By Allan V. Horwitz, Jerome C. Wakefield
Allan V. Horwitz and Jerome C. Wakefield argue that, while depressive disorder certainly exists and can be a devastating condition, the apparent epidemic in fact reflects the way the psychiatric profession has understood and reclassified normal human sadness as largely an abnormal experience. This system is fundamentally flawed, the authors maintain, because it fails to take into account the context in which the symptoms occur.   "Relentless in its logic . . . It has caused me to rethink my own position and how the authors' concerns might best be handled." ~ from the Foreword by Robert L. Spitzer, M.D., Professor of Psychiatry, New York State Psychiatric Institute.
 
 
20.  DOES PAIN WEAR OUT YOUR BRAIN?
From a reader--
http://chronicfatigue.about.com/b/2008/02/21/does-pain-wear-out-your-brain.htm
 
 
21.  MIRAPEX HELPED
From a reader--
"I have had fibro and migraine half my life.  I have been disabled with it since 2000.  This past summer I saw a specialist in Shreveport that put me on new meds and treatments.  I think he saved my life.  He has since moved on to Washington, D.C. and all I have is his email address.  But I will tell you what I am taking because of him.  I think the main thing that has helped is Mirapex 3 mg.  My mother had Parkinson's Disease and was treated with Dopamine.  Dr. Wood has done research and found that the dopamine in Mirapex (used mostly for restless leg syndrome) helped his patients with fibro.  It has done wonders for me.  I tell all my friends who have chronic pain or fibro about it.  One of my best friends recently got on it and it made a distinct improvement in her pain and energy level.
 
That is what it has done for me.  I have a great deal more energy than I have in 10 years.  My pain is more tolerable an not as debilitating.  I even feel "happy", which is a word I haven't felt since I was 16 years old, and I am 57.  I contribute most of this to the Mirapex.  I began at 1 mg. and titrated up to 3 mg. daily.  I never had any side effects from it, although I was warned about nausea and possibly falling asleep during the day, none of which happened.
 
I also take a small amount of cortisone daily to "jumpstart my adrenal glands".  This might be one of the reasons I have more energy also.  I take natural thyroid instead of the synthetic and Ambien CR to sleep.  If you are interested, I will give you the entire regime he put me on, but I would like all of your readers to know about Mirapex and that it could possibly be the answer they are looking for."
To read more comments about Mirapex from newsletter readers, go to www.fms-help.com/newsletters.htm (search "mirapex")
 
 
22.  CHERRY JUICE
From a reader--
"I started taking 2 ounces of pure tart cherry juice everyday , after 2 weeks the fibro pain is gone about 85%."
I'm for anything that helps alleviate the miseries of fibro.  I have been pain free for many years now by taking a powerful antioxidant.  Prior to that, I had debilitating fibro pain for 14 years.  A current list of things I use is at www.fms-help.com/what.htm.
 
 

23.  DANGERS OF NEW COMPACT FLUORESCENT LIGHT BULBS

Incandescent bulbs are being banned in the next few years - but look what is replacing them!  These new bulbs leak mercury when broken!  Besides this info online, our local Jacksonville Florida Times Union newspaper had a story on this last week!  Disturbing!

What to do when compact fluorescents crack

February 26, 2008

Compact fluorescent lamps contain small amounts of toxic mercury that can vaporize when the bulbs break, creating a potential health risk for infants, young children, and pregnant women. If a lamp does break, follow these cleanup procedures:

Keep people and pets away. Open windows, and leave the area for 15 minutes before beginning the cleanup.

  • Do not use a vacuum cleaner, even on a carpet. This will spread the mercury vapor and dust and potentially contaminate the vacuum.

  • Wear rubber gloves.

  • Carefully remove the larger pieces and place them in a secure closed container, preferably a glass jar with a metal screw top lid and seal like a canning jar.

  • Next, scoop up the smaller pieces and dust using two stiff pieces of paper such as index cards or playing cards.

  • Pick up fine particles with duct tape, packing tape, or masking tape, and then use a wet wipe or damp paper towel.

  • Put all waste into the glass container, including all material used in the cleanup. Remove the container from your home and call your local solid waste district or municipality for disposal instructions.

  • Continue ventilating the room for several hours.

  • Wash your hands and face.

    As a precaution, consider discarding throw rugs or the area of carpet where the breakage occurred, particularly if the rug is in an area frequented by infants, small children or pregnant women. Otherwise, open windows during the next several times you vacuum the carpet to provide good ventilation.

    SOURCES: Maine Bureau of Remediation and Waste Management; Mercury Policy Project

    Also, a reader sent this in:
    "Are incandescent bulbs being banned?  I can't use many of the fluorescent bulbs because of the way they oscillate in output of light.  It makes me have really bad migraines.  I have some of the fluorescents in my house but only the really expensive kind that don't have light wave issues.  Does anyone else have that problem with fluorescents?" 
    Yes.  I do.  Please send comments to dombush@bellsouth.net.
     
     
     
    24.  SHAKE A VIRUS TO DEATH?
    http://articles.mercola.com/sites/articles/archive/2008/3/1/a-new-way-to-kill-viruses-shake-them-to-death.aspx
     
     
     
    25.  DOM'S UPDATE
     Business Woman 
    I've been feeling well lately.....this week I was almost delirious with happiness at being able to teach without grueling fatigue.  If every day could be like that, life would be a cinch!  A list of things I currently use is at www.fms-help.com/what.htm.  We are all different, but this might be helpful to some of my readers.
     
    I had been waiting for a "good day" to visit my dear friend Curtis (86) in a nursing home.  Curtis is the gentleman I mentioned in my last newsletter who almost had to have his legs amputated a few weeks ago.  He now has congestive heart failure and is bedridden.  In 2004 I helped Curtis make a singing CD of some very old, beautiful hymns - he sang and I played the piano.  (I also sang two songs with him on the CD - we used to sing duets at church.)  Curtis has a wonderful voice - even at age 83 when he made the CD.   I asked Curtis how he would feel if I offered his CD to my readers.  He was all for it!   I know it will be a blessing to many, particularly the elderly!  I wish I could send it for free, but I have to ask a few dollars to cover costs, as I am broke. 
     
    Recently I gave Curtis's CD to my mother's Sunday School class - these are ladies in their 80's and 90's whom my mother refers to as "The Girls!"  (Ha!)  They loved it!!   If you want a copy, please email me at dombush@bellsouth.net and I'll send you a list of the 18 hymns on the CD and how to get one.  If you have elderly parents or grandparents, they will love hearing someone their own age sing the old hymns that you rarely hear anymore, unfortunately.  In his younger days, I think Curtis must have sounded like Caruso!!)  Most importantly, Curtis's life backs up his songs!  He has gone through many trials and tragedies, but has made lemonade out of lemons.  He is an amazingly kind and generous soul who has lived his life to help and serve others.  Some of my readers enjoyed my Christmas CD www.fms-help.com/CD.htm, and I am certain that Curtis's CD will find a niche in your heart as well - particularly with elderly listeners.  Nothing would thrill Curtis more than to know that others are enjoying his music!  I would love to do this for him before he passes away, so please write soon if you want the CD. 
     
    I'll close with a poem sent in by a reader--
     
     
    GOD KNOWS BEST
     
    "Our Father knows what's best for us,
    So why should we complain...
    We always want the sunshine,
    But He knows there must be rain.


    We love the sound of laughter
    And the merriment of cheer;
    But our hearts would lose their tenderness
    If we never shed a tear.


    Our Father tests us often
    With suffering and with sorrow;
    He tests us, not to punish us,
    But to help us meet "tomorrow."


    For growing trees are strengthened
    When they withstand the storm;
    And the sharp cut of the chisel
    Gives the marble grace and form.


    God never hurts us needlessly,
    And He never wastes our pain;
    For every loss He sends to us
    Is followed by rich gain.


    And when we count the blessings
    That God has so freely sent;
    We will find no cause for murmuring
    And no time to lament.


    For Our Father loves His children,
    And to Him all things are plain;
    So He never sends us "pleasure"
    When the "soul's deep need is pain."


    So whenever we are troubled,
    And when everything goes wrong,
    It is just God working in us
    To make "our spirits strong."
     
    Thinking about this poem, for me two good things came out of having FMS/CFIDS since June 1982.  First, I know in my heart that I would most likely have become a hard-hearted soul, lacking sympathy for others' weaknesses and looking down on their struggles.  So if my illness is what God uses to keep me in tune with His loving heart and keeps me humble toward my fellow man, then it has been a good thing.   Secondly, I have met all of you!  The joy of our friendship - even though it is due to mutual suffering - has been a blessing that I can never thank God for enough!  Thank you for being there for me for so many years - ever since www.fms-help.com began in 1996.  And I will be continue to be there for you as long as God gives me strength to continue my newsletters, or until a cure is found (that works for ALL of us!)
     
    Yours truly,
     
    Dominie
    dombush@bellsouth.net
     
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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.