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XMRV positive by serology from WPI

Discussion in 'XMRV Testing, Treatment and Transmission' started by gracenote, Feb 23, 2010.

  1. usedtobeperkytina

    usedtobeperkytina Senior Member

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    Sing, well, I don't than the mice. Retrovirologists say they gave us this tricky virus.

    Tina
     
  2. gracenote

    gracenote All shall be well . . .

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    Thanks George.

    I notice that Candace Pert is one of the collaborators.

    There is a thread on Peptide T. Peptide T for XMRV

    All this research is really happening! This is exciting!! I'm excited!!!
     
  3. gracenote

    gracenote All shall be well . . .

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    Sing Nothing you say is off topic. Please say more about this if you'd like. As the starter of this thread, I invite your thoughts.
     
  4. _Kim_

    _Kim_ Guest

    This reminds me of the thread that joyscobby started Zero tolerance to mouse hate.

    I'll echo you Sing and give thanks for every animal that has been or will be sacrificed in the research efforts to diagnose and treat us.
     
  5. Sing

    Sing Senior Member

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    Thanks for replying, Tina and Gracenote!

    I know what you mean, Tina, for not wanting to appreciate mice's role in all this. I get it! But what it means to me is that we are all part of the same biosphere, sharing and affecting each other. I feel interconnected with animals and like the feeling. And now the mice are playing a helping role, as our forerunners also made ill by this retrovirus, so I am wanting to express my feeling of gratitude.

    And, mice have learned to fend off the actual XMRV that we get sick from, so I expect the researchers will learn from that too!

    Just my "animal take" on things,

    Sing
     
  6. oerganix

    oerganix Senior Member

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    Congratulations Gracenote! And many, many hugs!! I hope you can get into WPIs trials soon and that you are in one that works for you!!

    :D:D:D:hug::hug::hug::hug::hug::hug::D:D:D
     
  7. shrewsbury

    shrewsbury member

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    xmrv positive by serology

    dearest gracenote :hug:

    I've been speechless since getting your news. Again, have started to write numerous times and not been able to, or able to get it to 'send' readiness. I know you've been diligent and doing your best to prepare for the results, but you must feel a bit like Alice in Wonderland. It's a new world, with new rules, some whacky characters both friend and foe, all mostly unknown, and all to be explored. You're a pioneer now - one of the first serology xmrv-positives.

    I thank you so much for sharing your news with us. A true opportunity for practicing 'don't know' mind. The ME/CFS world is changing so quickly. While there is still no proof that I know of to show that XMRV causes ME/CFS, there are hints everywhere that it's close, not only for prostate cancer, but for ME/CFS, Autism, maybe MS..............The CROI shows virologists madly racing for their firsts. George's post shows the NCI already starting to try to develop anti-XMRV drugs!

    Across the airwaves, from here, you seem to be living with the news with great aplomb, and grace of course.

    Please continue to take great care of yourself. And know we're here should you need us!

    if:Retro smile::Retro smile::hug:

    [​IMG]
     
  8. shrewsbury

    shrewsbury member

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    Look at the info that's come out in this thread:

    Funkster reports that Belgium is going to do a replication study. That's fantastic. It's the first replication study I've heard of. Is this already a thread in the XMRV testing thread? If not, FUnkster, would you mind starting a thread there so others will know? If you're not sure how - you can PM me.

    And George - what amazing news from the NCI. This has got me so excited - I've been wiggling and wagging my tail and going 'chu' for hours! Same request - I don't think people know about this. Would you mind starting a thread?

    thank you all

    and the times, they are a changin'

    ps - he's so young here!
     
  9. Dr. Yes

    Dr. Yes Shame on You

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  10. shrewsbury

    shrewsbury member

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  11. ukxmrv

    ukxmrv Senior Member

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    IslandFin,

    About the Belgium "replication study". I've also spoken to Redlabs. They are not intending to do a study. They are going to offer the XMRV test as a private test to paying patients only. That's why they went to the USA to learn the right methods.
     
  12. shrewsbury

    shrewsbury member

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    thanks ukxmrv. Even if it's not a replication study, I guess it's still a positive shift in the landscape; a European lab that wants to invest now in providing accurate xmrv-testing.Their business sense must say that this will be a renumerative venture in the long-run. I hope they'll charge reasonable prices.
     
  13. ukxmrv

    ukxmrv Senior Member

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    It's great news Islandfin. One more resource for patients in Europe. Redlabs already offer things like a RNASE-l test and some immune tests. Hard to get here otherwise.
     
  14. gracenote

    gracenote All shall be well . . .

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    Here are some thoughts that Dr. Mikovitz communicated to a source which I have paraphrased. This is third hand information. (Obviously, this does not carry the weight of Dr. Mikovitz said, but I believe it to be an accurate reflection of her current thinking.) I have permission to post.


    It is becoming more apparent that the virus in not being found in large numbers in the blood.

    There have been over 300 verified positives so far.

    The virus has been isolated from over 90% of the (antibody) serology positives.

    When one person who was serology positive, but without detectable virus, was retested when symptoms were acute, the virus was then isolated.

    It may be possible for some to develop antibodies after only being exposed to viral fragments, yet remain uninfected. (This is basically how a vaccine would work.) This could explain how some of the healthy population is positive.

    Some who were expected to be positive have tested negative. Perhaps those who are the least sick and the most sick may not have free antibodies because it is bound in immune complexes.

    It may be possible for some to have an immune defect that prevents them from expressing antibodies at all. They would then require culture testing, or possibly tissue biopsy to find the infection.


     
  15. Adam

    Adam *****

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    Thanks for posting George. I love the fact the NCI refer to CFS as a neuroimmune disease.
     
  16. IntuneJune

    IntuneJune Senior Member

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    This is the group I fall into, I have had vaccine challenges, and I do not produce antibodies..... This certain would change the picture...

    June
     
  17. Cort

    Cort Phoenix Rising Founder

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    Nice catch Adam - neuroimmune disease - has a nice ring to it. :)

    Gracenote had you been tested before (and been found negative?)
     
  18. gracenote

    gracenote All shall be well . . .

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    This is the only test that has come back. I'm still waiting for the 3 other test results from WPI and the results from Panorama.
     
  19. Countrygirl

    Countrygirl Senior Member

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  20. ukxmrv

    ukxmrv Senior Member

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    When I was tested I was the best that I had been for a long while. I had a little more energy than normal and less viral (sore throat, glands etc). I was XMRV+
     

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