5-21-06
FROM DOMINIE:
 
MOLD UPDATE
 
Dear Fibro Friends - I have received SO many good suggestions from you. THANK YOU FOR CARING ABOUT ME AND TAKING THE TIME TO WRITE!  I have gotten myself out of the moldy environment and am now a "visiting" piano teacher, going to students' homes to give lessons.  So far, so good.  I have been out of the "sick building" for 1 week and hope to improve.  I am investigating many of your excellent suggestions as well.  Several suggested oregano oil for the chest heaviness and breathing problem.  WARNING TO EVERYONE:  Don't work (or live) in a moldy building!  Dire health consequences will result!  Check these out:
http://www.mold-survivor.com/symptoms.html
http://www.doctorfungus.org/
www.moldacrossamerica.org
www.moldwarriors.com
http://palimpsest.stanford.edu/byorg/abbey/an/an18/an18-6/an18-602.html
 
BAD DOCTOR UPDATE
 
Yes, I am planning to report that horrible doctor I saw last week...just haven't had time yet....trying to get an in-home schedule going for my students.  One reader suggested always taking a man with you to a doctor's appointment.  That was certainly the case here.  My husband went with me 2 weeks ago when I first saw this doctor.  He was distant toward us but professional.  The second time I went back alone was when he started his temper tantrums and accusations.  Another reader suggested that he could have Tourette's (since he had facial tics) or even the beginnings of Alzheimers (because he was quite elderly).  Another reader sent this article on cognitive impairment in older physicians: http://www.medscape.com/viewarticle/532007?src=mpFor stories from readers about good and bad doctors, see www.fms-help.com/doctors.htm
 
Well, that's all from me personally.  Below are some interesting emails I received from readers recently....
 

READERS WRITE:
 
 
EXPLAINING YOUR ILLNESS

Me and a few of my online friends have decided to make this an official "Pass a Spoon on Day". A day that we set aside time to ask people in our lives to take a moment and read The Spoon Theory.  You might have seen this before.... but every now and then... even I need to be reminded. Reminded to make good choices, to listen to my body, to take care of myself, and to stop beating myself up for things I can't do, but to appreciate the things I can.  It would mean alot to be if you took the time to read it. It explained in simple words what I was not able to explain for years.  Hopefully by reading this short essay, you will gain more compassion for not just me, but for many people who suffer every day by "hidden sickness, disease and pain. So if you haven't read this at all, or if this a re-visiting.... take a look http://www.butyoudontlooksick.com/the_spoon_theory/

Christine


CYMBALTA HELPS
 
I have been taking CYMBALTA for about 1 month now and LOVE it. It helps depression, pain, and anxiety. It is the best drug I have had since I was diagnosed with FMS over 20 years ago.........Char

FMS-------------WHAT A MESS-----------DON'T TAKE A LICK'N----------JUST KEEP ON KICK'N"


MAGNETICS

I was diagnosed with Fibromyalgia and Chronic Fatigue in 2002 after years of suffering and expensive medical tests. I have tried thousands of dollars worth of medical treatments and alternative therapies. The most effective long lasting relief for me came from a recommendation from my chiropractor. He introduced me to products from Nikken. I was skeptical but willing to try anything after all I had been through. Within two weeks of using some of the products, I had more energy, was less depressed, and had less pain. These products have been written up in numerous medical journals and the sleep system is the only bed to be endorsed by the World Federation of Chiropractors.  I use these products (which include whole food nutritionals, air, water, and sleep systems as well as drug free discomfort relief products) to this day and believe I would not be nearly as well without them. I do not take any medications and have not for over three years. I feel better than I have felt in ten years.  As I have recovered and been able to work a bit more, I wanted to do something that allowed me to help others heal as well as provide me with an abundant reliable income without having to return to to a toxic and confining work environment.This company has provided financial health for me as well.  I would love to share this with as many fibro and chronic pain/fatigue sufferers as I can. Getting a thriving life back is possible for all of us.  My email address is: shesastarus@yahoo.com

Kristine


 
READER HAS BAD EXPERIENCE WITH DOCTOR
 
I have had the same experience with a Rheumatologist to whom I was referred by my regular MD. He didn't "shout" at me, but he basically told me that there was "no such thing as Fibromyalgia", and that I should just get out more with my husband!!!! I told him that if there was "no such thing as Fibromyalgia, why is there a Fibromyalgia Support Group at the hospital that meets every Thursday"? He said that it was just a chance for women to get together and talk, and had nothing to do with any "real" illness!!!! I needed his report in order to keep receiving my SSDI, so I was "patronizing" but civil to him, and he did agree that I was unable to work and was "disabled" but he thought that it was just all in my head. So, please don't feel alone!!!
 
Dianne
 

 
Well, that's all for now.  I still say the best stuff I have found is the immune balancing  powder (been using it since June 2001).  Every time I go off of it, I slide back, so it has become my lifesaver and the foundation of what I do for my health. 
 
Til next time,
 
Dominie
www.fms-help.com
 

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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