Subject: Never Lose Your Keys, Wallet, or Purse Again

From: Never Lose Anything Again <[email-masked]>
Date: Mon, 19 Jan 2015 12:29:00 -0800

Why didn't I think of this Atompub-archive!

I can't tell you how many times I've spent hours searching
for my keys or wallet. It's always at the worst times too-
right before work, an important meeting, or trying to catch a flight.....
Soooo Frustrating!

I know that you have told me that this happened to you too, thats why I wanted to tell 
you about this http://www.waslost-nowfound.com/misemployment/decontaminates/erupting.php 

It will hep you find your keys, and much more. You'll never loose one of your valuables
again.... Thank me later :) 

Happy New Year

158abe06976e4ffe1ce736f92c83562c-158abe06976e4ffe1ce736f92c83562c158abe06976e4ffe1ce736f92c83562c

Settings: http://www.waslost-nowfound.com/washrags/edited/extending.html  - TAP Advances
49 KALKO DR
WOLCOTT, CT 06716
My slow decline started with a unknown chest infection and manifested from there. Fast forward 6 months and was tested for EBV, CMV, HHV6 (Labcorp). I was told that my elevated IGG HHV6 was causing my CFS. My titers were only at a 2 with anything being over a 1 as positive (although 2 doesn't seem high for a reactivated virus IMO). I started Valcyte and only made it three days with extremely bad flu type symptoms. I stopped Valcyte due to the reaction and now have taken three IV infusions of Cidofovoir (vistide). 

After the three days of Valcyte my titers jumped to 3. After the second infusion, they jumped to 9. So far other than herx type reactions/worsening of symptoms for the last month on antivirals, I cant say its helped yet. My titers have skyrocketed during treatment so I don't know what that means other than upsetting the virus I guess. I will try to report back down the road as this treatment is scheduled to go on for months before the Dr. says I could notice a change. Its only been about 1.5 months so far and supposedly could be for up to one year if needed.
IGM Igenex/CDC Positive 
23-25 IND, 31 +, 34 IND, 39 +, 41 +, 83-93 +
IGG: 
41 IND
MTHFR C677T homozygous
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jeanneac
Veteran Member

Date Joined Feb 2009
Total Posts : 1661
    Posted 1/7/2015 3:56 PM (GMT -7)   	
Sorry to hear you've been sick Joey. So, the CFS hasn't been going on that long, it was more like an acute illness after which you had igue? It can sometimes take a long time to get over some viruses. 

For me, it's been a long, chronic thing. I have no recollection of ever getting sick with these viruses unless it was mistaken for the flu when I was younger. I do remember getting a few really bad cases of the flu in my 20's. 

I hope you see some progress soon.
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jkn913
Regular Member

Date Joined Nov 2013
Total Posts : 114
    Posted 1/8/2015 6:53 AM (GMT -7)   	
I have FM and most likely CFS also. I had mono in my early teens, but saw a huge shift in my health and all these debilitating symptoms after I had the West Nile about 7 years ago.

Yes, I do believe that these illnesses are related to viruses, flues and other body stressors we may have had. It is not contagious like other viruses, so how and why we get it is a mystery.
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jewelrylady
Veteran Member

Date Joined Jun 2008
Total Posts : 678
    Posted 1/8/2015 11:35 PM (GMT -7)   	
For me the CFS just seemed to come on out of the blue. I don't remember a beginning, I was under a long term stressor & when it was over the igue continued to get worse & worse. I don't think I was ever sick with something but I can't say that I wasn't. My grandson was really ill for about 2 1/2 years & it is all a blur now. When it was over & he was okay, I had CFS. When people ask me if I had a virus or some other illness, I have to say I don't know. I do know that I had CFS more then a year before his last surgery because I was trying to make speghetti for a benefit dinner & I was crashing & just thought I was stressed & tired, now I know it was a crash, all to familiar. 

Has your Dr found out the reason for your igue? Have you been dx'd with CFS? I hope you don't have it & the igue is treatable.