Re: Professor of Molecular Biology/Microbiology on XMRV in CFS
Uploader Comments (DysautonomiaMD)
Top Comments
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Hi Margaret,
This is great news, Lord willing, soon the research will be complete and there will actually be a treatment available for sufferers of Dysautonomia and all other associated diseases.
Get well soon, Margaret, I think it's just one of those days as I too, am feeling under the weather. My prayers are with you.
With Love from your Brother In Christ,
Jeff
All Comments (12)
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Thanks, I tend to be optimistic because if I see a big wave coming, I'm gonna put my surfboard out and try to ride along with the wave!
Time will tell all, and more research includes 1 NIH grant to cover 5 or 6 researchers across America. Then compare results with ? over 1000 people. That would be a better step, to replicate the research; this will take years.
But I am still happy and agree that in the right hands, this information will contribute to science not just for CFS, as you state.
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Yes, thank you. I don't know what the impact will ultimately be (no one does yet), but am sure God has a plan.
God Bless You Too,
Margaret
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My prayers are with them and you, my dear Sister In Christ!
God Bless,
Jeff
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There is every reason to be optimistic and may God Bless these people and protect them from any harm.
Lots of Love,
Margaret
thanks for keeping in touch its appreciated, over here in the uk i amsure our med folk still are trying to deny love and best wishes good luck with your garden look forward to seeing it soon ours over here in uk are covered in snow!!!bbrrrrrr its soo cold :)
kimpurdy1 2 years ago
No prob. I just happened to see it on TV, and I never watch TV....so it was pretty cool and as I watched, I thought of all the YT people that would be happy to hear the WP Institute is getting it from all sides..
...may we continue to pray that their work is blessed, and stays focused on the patients.
...sometimes, money and fame change people so much...but they started research because of their own child.
I choose to believe the best: good intentions lead to discovery lead to cure. Optimist.
DysautonomiaMD 2 years ago
I love when people share good things happening. Thank you for sharing. unfortunately, I do not live where this kind of caring is happening. Being rare, I've found, means wasting and just treating the symptoms. :( I can handle it, but I know a few who need more than that. I have paraneoplastic cerebellar degeneration. And all I see are men in white coats play with their new toy and then pt it on the shelf. It's good to see people caring!~ YAY! Hugs- SHAY!
bennasdwarf 2 years ago 4
Hiya, thanks for the Comment. Nice.
..too bad there are not more women in white coats looking at you; perhaps sympathy and compassion need more of a place in the art of science.
I hope you know God, and His Son, Jesus. He is with you and loves you just the way you are. You will influence many lives, many medical professionals will be in awe to examine you.
Am sure it gets old, to be of such scientific interest. I hope some one is looking out for your mind and soul, too. Dr M
DysautonomiaMD 2 years ago
I was all over this 6 wks. ago when it was first announced. I have since had a change of heart, and will further explain in an upcoming video. Happy New Year!
Suzanne42 2 years ago 2
I know that many doubters exist re: the WP Institute and the XMRV, but.....many doctors do not 'believe' in CFS. Perhaps deep down, they still think people are pretending. Am sure some are, so that makes it harder for us.
You are right; there is much controversy and people are envious that the Institute charges so much ($450), reportedly, for the blood test.
Of course, there needs to be time, more research, mulit-center trials all combining data, etc. It is too soon to draw conclusions...
DysautonomiaMD 2 years ago