Chronic Fatigue Syndrome Community
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Welcome to the community and thank you very much for your story and comprehensive advice.
It is so nice of you to share your time and energy with us and I am sure your advice will help many women and men in this group.
Take care and keep in touch with any further updates on your situation and any other advice you might have for us.
Many thanks once again.
Kind regards,
Sergio
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Welcome to the community.
1Butterfly82, I too have had low energy and exhaustion symptoms from an early age (15). I will be 41 next month. I was diagnosed with CFS last year.
I do not live in the US as I think you might do, so I cannot unfortunately advise you on health insurance.
However I am here if you need to chat about our illness.
Take care and I hope you feel better very soon.
Kindest regards,
Sergio
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I hope that when you read this you are feeling much better.
Not much information is out there regarding the link between the Epstein-Barr Virus and Chronic Fatigue Syndrome, however I have read on many occasions posts by sufferers of Mononucleosis who contacted the EBV, that they have experienced symptoms associated with CFS.
I too at fifteen contracted a viral infection and have since been suffering with CFS. I will be forty one in May.
I suggest that you try and contact a doctor who specializes in CFS. Please refer to the following post kindly provided by knyb007.
"knyb007 responded:
I've been there. I was sick about 6 years ago and had all the troubles you explained and more. Doctors couldn't find anything wrong with me. They weren't doing the right tests. I'll spare the details and just get to the solution. If you are on the east coast, contact Dr. Ritchie Shoemaker in Pocomoke City, MD. If you are in the Southwest, contact Dr. Michael Gray in Benson, AZ (outside Tucson, AZ) These are two of the most highly qualified doctors who know what to look for, how to diagnose and treat people with chronic fatigue. I have seen both of these doctors and am happy to say that I am on my way to full recovery.
I could be wrong, but I suspect that perhaps you have long thin limbs, are or were pretty flexible and either you or people in your family have a history of soft tissue damage such as cartilage. These are genetic characteristics of a group of the population that are susceptible to environmental toxins that the immune system is not able to properly deal with and clear from the body. About 25% of the population is like this.
If you are unable to see either of these doctors, ask your own doctors about levels of VEGF, TGF beta 1, MSH, C4A.
Good luck."
I hope this information was useful to you.
Good luck and I hope you recover very very soon.
Take care and keep in touch.
Kind regards,
Sergio
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Welcome to the community!
The symptoms are definitely there, however I suggest that you try and get it diagnosed by a doctor.
No pains for me at the moment (touch wood) although I too get palpitations and sometimes my heart even skips a beat. What I have learned to do is probably one of the few or the only thing I can do and that is to try and stay calm. It usually goes away after a few seconds.
Please find below some information that knyb007 posted that might be of use to you.
knyb007 responded:
I've been there. I was sick about 6 years ago and had all the troubles you explained and more. Doctors couldn't find anything wrong with me. They weren't doing the right tests. I'll spare the details and just get to the solution. If you are on the east coast, contact Dr. Ritchie Shoemaker in Pocomoke City, MD. If you are in the Southwest, contact Dr. Michael Gray in Benson, AZ (outside Tucson, AZ) These are two of the most highly qualified doctors who know what to look for, how to diagnose and treat people with chronic fatigue. I have seen both of these doctors and am happy to say that I am on my way to full recovery.
If you are unable to see either of these doctors, ask your own doctors about levels of VEGF, TGF beta 1, MSH, C4A.
I hope that I have been helpful and that you feel better very soon.
Take care and keep in touch.
Warm regards,
Sergio
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I hope that when you read this reply you are doing well.
I personally do not have any experience on this particular matter, so I suggest that you ask an obstetrician specific questions regarding CFS and pregnancy. Also maybe get in touch with doctors specialized in CFS such as: If you are on the east coast, contact Dr. Ritchie Shoemaker in Pocomoke City, MD. If you are in the Southwest, contact Dr. Michael Gray in Benson, AZ (outside Tucson, AZ)
These are two of the most highly qualified doctors who know what to look for andhow to diagnose and treat people with chronic fatigue syndrome.
Even if it is just giving them a call or dropping them an email, they might be able to offer some advice.
If you are unable to see either of these doctors, ask your own doctors about levels of VEGF, TGF beta 1, MSH, C4A.
[br> I hope this information is of use to you.
Take care and keep in touch.
Warm regards,
Sergio

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I hope your day is going well.
Please find below a post that might be of use to you.
knyb007 responded:
I've been there. I was sick about 6 years ago and had all the troubles you explained and more. Doctors couldn't find anything wrong with me. They weren't doing the right tests. I'll spare the details and just get to the solution. If you are on the east coast, contact Dr. Ritchie Shoemaker in Pocomoke City, MD. If you are in the Southwest, contact Dr. Michael Gray in Benson, AZ (outside Tucson, AZ) These are two of the most highly qualified doctors who know what to look for, how to diagnose and treat people with chronic fatigue. I have seen both of these doctors and am happy to say that I am on my way to full recovery.
If you are unable to see either of these doctors, ask your own doctors about levels of VEGF, TGF beta 1, MSH, C4A.
[br> I hope it is of use to you and that you too get on the road to full recovery.
Take care and keep in touch.
Warm regards,
Sergio
View Thread

I hope you are doing well.
Thank you very much for taking the time in trying to help Sadiejoe.
As you can see she needs all the support she can get.
See Sadiejoe, you are not alone.

Thank you very much once again.
Take care and keep in touch.
Kindest regards,
Sergio
View Thread

I am a 40 year old British citizen born in London England of Spanish (Spain) decent and have been suffering from CFS for over 25 years. I used to live in the US in Grand Prairie Texas near Dallas where I was married. I now live in Cádiz in the south of Spain.
Sadiejoe with my story I do not want to depress you, on the contrary I would like for it to be able help you see things a little clearer. I totally sympathize with your situation as I first had to put up with the incredulity of my family and then from my wife which eventually cost me my marriage.
The important aspect of the situation is YOU, as YOU are the one who is ill and although it is understandable that your husband has difficulties understanding YOU and your condition and that of course it would be great for YOU and for all of us that our loved ones were to be supportive and understanding, as I say it is YOU who is the most important part of this situation.
Your husband needs to come on board with you situation 100%, if that is possible and understand that your condition is genuine as who would want to be in this situation if they had a choice? I say nobody.
YOU need to do your research (as I think you are doing) on doctors and treatments and try to increase your quality of life.
Energy permitting, I am here in this community quite often, so you do have someone to talk (type) to and if you wish to contact me via email, my email is: sergiokay@yahoo.es.
Take care Sadiejoe and keep in touch.
Warm regards,
Sergio
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You did it,

They appear once you click Submit.
Computer literate I'd say.

Take care.
Bye for now.
Sergio
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) I Just would like to bring this more to attention.HELLO FELLOW COMMUNITY READERS AND MEMBERS, MAY I PLEASE KINDLY ASK YOU ALL TO HELP KEEP THIS COMMUNITY ALIVE AS THIS WILL HELP FIND SOLUTIONS FOR OUR HEALTH.
JUST BY REPLYING OR POSTING. EVEN IF IT IS JUST BY PRESSING THE KEY ON YOUR KEYBOARD THAT HAS THE COLON ( : ) CHARACTER AND SUBMITING THE COLON CHARACTER ( : ) AS A REPLY OR AS A POST, THIS WILL TELL US THAT AT LEAST PEOPLE ARE READING THE REPLIES AND THE POSTS AND WILL ENCOURAGE THE CONTINUITY FOR FUTURE POSTS AND REPLIES, AS TWO LITTLE EYES ( : ) WILL CONFIRM THAT THEY ARE BEING READ
. MANY THANKS IN ADVANCE AND APOLOGIES FOR ANY INCONVENIENCE.
Kindest ragrds,
Sergio

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