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Dan Moricoli
  • Male
  • Wellington, FL
  • United States
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REPLY TO TO SONIA MONTUFAR NOV..27 AT 3PM I WOULD LIKE TO HEAR MORE ABOUT YOUR CASE,PARTICULARLY YOUR PRESENT MEDICAL COMPLAINTS AND THEN IWILL TRY TO BE HELPFUL. HERB HYMAN
on Friday
We have a complex neuro endocrine immune dis-ease and each of one of us is affected very differently. Our "abilities" can wax and wane throughout the day. One day we're limping, the next day we are helping someone walk. We're survivor's and we...
on Friday
Hi Geoffrey, I'm so sorry about what you're going through, and that your wife doesn't seem to understand at all. What if you were to print up some information from the internet concerning the illness and the problems that come with it like cognit...
on Friday
Great idea Dan. And what Paula said is great as well, about asking the sufferer what we can do to make things easier for them. And also, sufferers should ask themselves that question (if they haven't already, that is). For example, setting up your...
on Wednesday
 

Welcome!

About me . . .and this website.

I have had ME/CFS since May, 2006 when I had a sudden onset of the disease following a bout of stomach flu. My symptoms have changed considerably during the course of my illness. I consider myself lucky in that my "crashes", while they now occur almost daily, most often only last just a few hours. During these periods I completely loose my physical and cognitive abilities and can only lie down and wait for the episode to pass.

What little energy I possess is very easily exhausted. Virtually any physical exertion or mental stress will trigger a reaction which, if it does not trigger a total crash, will cause my speech to become slurred and I will have difficulty finding and vocalizing words. I will also become very "wobbly" on my feet and then need a cane to get around.

One can get some idea of the impact of my affliction with ME/CFS in one of my "wobbly" periods HERE.

Like almost everyone else with ME/CFS, I struggled with physicians and numerous other medical providers who insisted that "it was all in my head" for over two years before I was fortunate enough to be able to see Dr. Benjamin Natelson, M.D.

Dr. Natelson has guided me towards a significant reduction in my symptoms and greater optimism about my future prospects. If you have not yet done so, please read his book Your Symptoms are Real. You can buy it HERE for as little as $1.31.

A fortuitous meeting with Dr. Herbert Hyman, M.D. in the summer of 2008 got me thinking about the possibility of developing a website. Subsequent meetings with him as well as Marly Silverman of P.A.N.D.O.R.A. and Dr. Kenneth Friedman of the University of New Jersey School of Medicine led me to the development of cfsKnowledgeCenter.com and the ME-CFSCommunity. Each of these three continue to serve on the Board of Advisors of cfsKnowledgeCenter, Inc., a Florida Not for Profit 501 c3 corporation.

My investment in this work has reached well into five figures and I have no more to give. Little can be done now without your assistance. There is no benefactor or foundation supporting us. Our ability to survive now rests with you and the other members of the community.

I invite you to think about the importance of this site to you and ask that you please consider supporting it with a donation commensurate to its value to you. A click on the icon below and a willingness to part with a few dollars, euros or pounds sterling to help yourself and others is all it takes.


Lastly, please let us know what you like, or dislike, about the site as well as any ideas you might have for its development. You can do so by emailing your comments and suggestions to: editorial@cfsKnowledgeCenter.com

I keep thinking about when I will be well enough to go back to fly fishing . . .

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At 6:48am on November 29, 2009, raffi sebouhian said…
Thanks, Dan. My usual thoughts on B-days are of the mothers.--Best, George S.
At 6:46pm on November 28, 2009, Pris Campbell said…
oh, btw, I've had the illness 19 years and week after next have plans for my husband to drive me down to Miami to take part in one of Dr Klimas' studies on genotyping and how the immune system functions on good and bad days. It involves 4 visits over a 2 year period, the first visit being the longest, then wearing a wrist band for two weeks after each to measure activity and filling in an online questionnaire for a short period after each. Her center is about an hour and fifteen minutes south of where I live in the greater West Palm Beach, Fl.
At 6:41pm on November 28, 2009, Pris Campbell said…
Thanks, Dan.
I have a lot of information about myself on the about me page of my website. It's easier to post that link than to type it up again.

http://www.poeticinspire.com/aboutme.html
At 6:03pm on November 26, 2009, Annette Gagnon said…
Thank you Dan,
I appreciate the welcome and look forward to getting to know the community.
Annette
At 9:34am on November 26, 2009, Ramona said…
Wow, thanks for that great on line salute. I love being in control of my own fireworks. Makes me think everyone should have just such a button in real life. I would make for a noisy world though.

I have this disease 40 years. XMRV is key. Of that I am sure. I predicted they would discover a retrovirus 20 years ago.
At 11:47am on November 25, 2009, abot bensussen said…
just wondering if you're the guy using xyrem like i am. let me know please. curious.
At 3:14am on November 25, 2009, Sandy Cooley said…
Hi Dan,
Ever since I read about you and how you "crash" almost every day, I've been concerned about you, and thinking that I should share a bit with you about my husband and what happened to him. He's had this illness for over 25 years, and when he first became ill, he (like most of us) just continued pushing himself and pushing himself until there was absolutely nothing left and he began involuntarily collapsing onto the floor, and even passed out at times. Pretty soon he was completely and totally bedridden. This is after pushing himself so hard for many years (every single day). He thought that if he just continued pushing himself, he'd get better (because we knew nothing about CFS at the time). Well, we realized later on that because he pushed himself so hard for so long, that is why he is so sick today and has remained 97-100% bedridden now for over twenty years! So I'm really feeling that since you are crashing every day, perhaps you should not do as much as you're doing. Maybe you should cut back a little, and try to rest more. Don't get me wrong. It's good to do things and be persistent, but it sounds like your body is trying to tell you something, and that by cutting back and not pushing yourself too hard, you may be able to recover from CFS much sooner than if you keep pushing like my husband did. He suffers every single day with a severe case of CFS, and we know that a lot of it (if not all of it) has to do with him pushing himself too hard for too long. So I just wanted to share this with you, since you've only had it for a few years now. Best wishes to you and please be careful. Thanks for all you've done.

Sandy
At 3:55pm on November 24, 2009, abot bensussen said…
i'm 69 next month and live in san diego. i see a sleep specialist who has me on xyrem. lately i've been confused about this illness. been sick a long time. it's stress related, people seem to think. my dr. says it's a sleep disorder. oversensitive nerves? psychosomatic? and now a retrovirus.....so i don't know what i've got but i do try to exercise 5 days a week and keep my spirits up. i'm married and have 4 kids and 4 grandkids.
At 3:51pm on November 24, 2009, abot bensussen said…
hi, this is abot. dan, are you using xyrem? i think i read this somewhere. am new here and easily confused. i have been using xyrem for more than three years and am much improved. still having problems with energy and vitality. also, neuropathy in my feet. i don't know too much about this illness but have lived with it for more than 25 years. i do my best to be well. somedays it's just so frustrating to try and have a life.
At 11:54am on November 24, 2009, Darlene Blair said…
Thank you dan that was beautiful and very special great day already take care and be safe.
 
 

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