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Post by moreattention333 on Aug 10, 2018 7:46:20 GMT
isolote virus means :
Nucleic acid sequence, virus characteristics。 better Drug resistance,
and Nucleic acid sequence, virus characteristics conld be enough
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Post by lior30 on Aug 11, 2018 1:21:51 GMT
My wife just told me right now that she didn't understand why her tounge is white, then she showed me her tounge, just like mine, her tounge is very white and it's looking like oral thrush. I'm so frustrated, we both have the same symptoms, very dry palms- our skin is just peeling, joints pain, abdominal pain, grumbling stomach, weird headces feel like a stabs in the brain, etc. We are both very ill, what should we do? She want a baby but I'm not ready to have a baby, she is pushing me very hard, but I'm so so afraid that this disease will transfer to the baby, so i told her that I am not ready yet. It's now 11 months from the exposure, the symptoms arr chronic and not going anywhere, I have a changes in my toe nails, inflammation of the gums, sensitivity of the scalp, change in the bones of my fingers that looks like Ramutid artrtis. I am so devastated, so scard, what will be in the future, when the doctors will do something?? Just wanted to share it with you guys, thanks for listening, you are the only who can understand the feelings.
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Post by Calm on Aug 11, 2018 2:21:34 GMT
My wife just told me right now that she didn't understand why her tounge is white, then she showed me her tounge, just like mine, her tounge is very white and it's looking like oral thrush. I'm so frustrated, we both have the same symptoms, very dry palms- our skin is just peeling, joints pain, abdominal pain, grumbling stomach, weird headces feel like a stabs in the brain, etc. We are both very ill, what should we do? She want a baby but I'm not ready to have a baby, she is pushing me very hard, but I'm so so afraid that this disease will transfer to the baby, so i told her that I am not ready yet. It's now 11 months from the exposure, the symptoms arr chronic and not going anywhere, I have a changes in my toe nails, inflammation of the gums, sensitivity of the scalp, change in the bones of my fingers that looks like Ramutid artrtis. I am so devastated, so scard, what will be in the future, when the doctors will do something?? Just wanted to share it with you guys, thanks for listening, you are the only who can understand the feelings. I would say if you can mentally and financially handle it then have the baby! Honestly the best thing for your wife would be to get pregnant. Her immune system will reboot and many women are able to overcome this because of that. The first year and a half to two years are the worst. Then some get remission. But your baby will be ok just keep the breastfeeding to 6-8 weeks.
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Post by moreattention333 on Aug 12, 2018 2:44:01 GMT
Some one said he contact your cdc and nih.what is the way he contact.what he said .what did cdc and nih reply?actually Only one isn't enough.we can't keep the disease only we know.numbers patient suffer the disease .we can do anything to survive and make us better.unless we make the disease know by media and gov.everything will be easy.
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Post by PZ on Aug 13, 2018 3:33:08 GMT
Omar, how are you doing on the anti-malarials? Are you taking hydroxychloroquine?
Has it stopped the fat loss in the face at all?
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Post by moreattention333 on Aug 14, 2018 2:28:50 GMT
moreattention33, keeponrolling, others - what you are saying makes sense. I e-mailed old admin a few times asking him to not close the forum completely, we'll see what happens next. If he ignores we'll have to think what to do about google search results, nonetheless - please do not post member e-mail addresses here without their permission in the future, I edited the post with his e-mail address. I'm not sure if it was the best thing to do given the situation, maybe if more people e-mailed him he'd at least consider creating a permanent link to this forum on the old forum since it still shows up in search results, but user privacy is important and I doubt he'd want his e-mail being posted online, so that's that for now. If you have his address - do e-mail him if you think shutting down old forum was not a good idea etc. we should change new forum name same as the old 。the early the better。what else we can do
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Post by Sux on Aug 14, 2018 4:29:28 GMT
Lol just forget this forum. Name change won’t happen all data is lost. See that other users are more active on Phoenix rising forum. So this forum will bleed to death.
Good luck to all the other who didn’t found alternative forum with people who give support.
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Post by moreattention333 on Aug 14, 2018 4:47:35 GMT
Lol just forget this forum. Name change won’t happen all data is lost. See that other users are more active on Phoenix rising forum. So this forum will bleed to death. Good luck to all the other who didn’t found alternative forum with people who give support. Phoenix?i don't know Hey .what's the url. Change name can be friendly to Google
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Post by omar2011 on Aug 14, 2018 12:44:27 GMT
Omar, how are you doing on the anti-malarials? Are you taking hydroxychloroquine? Has it stopped the fat loss in the face at all? In a week maybe , am just dealing with some issues
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Post by omar2011 on Aug 14, 2018 12:45:33 GMT
Lol just forget this forum. Name change won’t happen all data is lost. See that other users are more active on Phoenix rising forum. So this forum will bleed to death. Good luck to all the other who didn’t found alternative forum with people who give support. Do you have cfs ? Try to post some crazy ideas of unknown infection like you guys do here and you will be blocked + it’s a hall different case
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Post by scaredmatt on Aug 14, 2018 16:37:57 GMT
Do you have cfs ? Try to post some crazy ideas of unknown infection like you guys do here and you will be blocked + it’s a hall different case That's exactly what happened to me. I tried to tell my story and ask some questions. They blocked all my messages and "kindly" requested me to go find help somewhere else. In other words, they basically told me "You don't have CFS, and therefore you are not welcome here". Those bastards...
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Post by omar2011 on Aug 14, 2018 18:58:29 GMT
Do you have cfs ? Try to post some crazy ideas of unknown infection like you guys do here and you will be blocked + it’s a hall different case That's exactly what happened to me. I tried to tell my story and ask some questions. They blocked all my messages and "kindly" requested me to go find help somewhere else. In other words, they basically told me "You don't have CFS, and therefore you are not welcome here". Those bastards... This language is not appropriate! They have there scale and range of symptoms which is some how different, yes there are sick people like us there but they don’t bring hiv like virus and conspiracy stuff Patients there are smart and long term sick , they manage to keep there fourm by staying away of what new patients keep thrown here so they don’t look crazy and get medical attention and they barley have some so don’t blame them A lot there are the same but being a cfs patients is better than being crazy with hiv phobia as they referred to Chinese patients
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Post by moreattention333 on Aug 15, 2018 1:04:04 GMT
<title>UID (continued from old forum) | UID</title>
please change it <title> unknownstd unknown mystery virus infectious disease </title>
i used to make web. the second tittle is friendly to google. to patient
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Post by moreattention333 on Aug 15, 2018 2:51:41 GMT
all patient in sent me message to me ,there can be used when we went nih.
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Post by scaredmatt on Aug 15, 2018 14:09:07 GMT
Patients there are smart and long term sick , they manage to keep there fourm by staying away of what new patients keep thrown here so they don’t look crazy and get medical attention and they barley have some so don’t blame them. I beg to differ, my friend. My first post there was a reply in a thread about an Undiagnosed Immunosuppresion. I never brought up the HIV-like virus subject. I only asked help because I was going through the same issue (and there were many members discussing the subject). My reply was blocked and then I was asked to introduce myself in the proper forum section. I did exactly what I was told, but they sent me a PM saying that I didn't have CFS (just because I didn't match ALL symptoms in their list, but I surely have MOST of them) and I wouldn't be allowed to post there. I know there are many people in that forum who could help me, but the admin/moderators won't allow me to join them. I think the best option is to create another profile using a fake email and make up a feasible story to make them believe I have CFS.
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