Epstein-Barr and Cytomegalo Virus (CMV) Simultaneously. Complications?

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doublehit008
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Date Joined Oct 2010
Total Posts : 3
   Posted 10/19/2010 10:35 AM (GMT -7)   
sad I have the combination too of CMV and EBV yet I have not experience the sever symptoms of these just the sever fatigue and weakness. Plus concentration is not good either. If anybody has cronic constipation with this I like to know if the Gasro doc will look into to make sure it is not from virus.

I have to take shots ( Gamglobulyn??? spelling shots) soon weekly to put in something to help me fight this my own is not doing a good job. Also with a new medication called Valcyte twice a day instead of Valtrex. I see a hemo doc. My number for cmv is 7.9 last month. And my EBV is now active.

I like to share with other people who have the same treatment.

God bless you all smurf

CMV confused
New Member


Date Joined Nov 2010
Total Posts : 1
   Posted 11/20/2010 8:02 AM (GMT -7)   
Hey there,
Any help would be appreciated as not getting alot of information from my doctor.  My CMV level is 16 but have no idea where that sits!?!  I am now being treated for  GERD as a result but seem to be getting worse. (nearly three months from initial diagnosis).  My Epstein barr was positive but now negative and have chronic fatigue syndrome as a result.

Lifeagain
New Member


Date Joined Nov 2011
Total Posts : 1
   Posted 11/1/2011 4:24 PM (GMT -7)   
For those with EBV:

9 years ago I was diagnosed with epstein barr virus. After another year of debilitating fatigue and being tested again to see that the EBV factors were even higher and being told there was nothing to do, I discussed with my GYN doctor. I was rock bottom. My life had stopped as I had always known. She, being an advocate for women and really seeking to understand all the issues women encounter, said she wanted to start me on Valtrex. She said to stay on it at least 3 months before quitting and see if there was any change. about the 4th month I felt a bit stronger and was willing to try doing things that required a bit more energy (which would usually put me in bed for a week or so) and found that I was fine. My life became completely normal again.

She had learned about Valtrex, which is an antiviral for herpes related virus, at an infectous diseases conference and had found it to be effective for people with EBV or Chronic Fatigue from other illness like FibroMyalgia and others. She had one patient that after being completely bed ridden resumed her life as a professor after being treated. She had now been on it for 11 years.

Valtrex gave me my life back. I decided to go off after about 4 years and my symptoms returned and and it took me 9 months to regain the progress I had found. It has been 9 years now and I have no fatigue as only those who have truly experienced can understand. My doctor says I can try and take 1/2 a dose and see how it works and try going off, but I don't want to risk it until I have a year to spend in bed. I take 1 gram a day. She said some of her patients even required a stronger dose. When I started it it cost about $400 a month and it was worth ever penny because I had no real life without it. Now it is closer to $100 because there is a generic. I don't know if you will find the same results, but if you felt like I did, you will consider anything.

One draw back is that because it was not initially put on the market to treat EBV or fatigue, some doctors are so weird about using it for EBV or other things. It is a safe antiviral, but like anything can have side effects on some people. I have had NO bad side effects at all. If you doctor is not educated about this drug, consider finding one who will consider it. Maybe even an infectious disease doctor. I wish for all those suffering to find a solution to your fatigue. I understand.

Rrose Selavy
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Date Joined Nov 2011
Total Posts : 1
   Posted 11/30/2011 7:18 PM (GMT -7)   
This is a really old forum, so I'm not sure if anyone will even read this but I, too, had CMV & Mono simultaneously in high school. I have no idea how I caught it because I was such a nerd in high school and certainly wasn't kissing anybody, haha. But anyway, I can remember waking up one day and just very suddenly feel AWFUL. My throat hurt worse than it ever had before everrrr. Which says something because I had chronic tonsillitis in middle school and had my tonsils and adenoids taken out. The only way I could describe it to my doctor was comparing the feeling to those performers who swallow fire or can swallow swords etc. I literally felt like my throat was on fire. Eating hurt so bad I cried at every meal for upwards of 2 or 3 weeks. I ended up losing a looott of weight because all I could stand to eat was soup. I was unbearably fatigued. I could sleep in until noon, having gone to bed at 10, and wake up feeling like i needed to sleep more. My glands were extremely swollen. My whole body hurt, so achey.

But anywayyss, you weren't asking about having them currently you were asking about long-term. I was diagnosed with CMV/mono, the combination from hell, when I was 16. I am 21 years old currently and I don't feel like I have ever fully gotten back on my feet. I am always tired. I have been treated with anti-depressants, because as you can imagine being tired and sick all the time interfered with my schooling and my relationships, as well as NuVigil/Provigil that is intended to boost energy. All my blood tests would come back clear and okay, with the exception of cmv and mono antibodies being present. I got so tired of the "you're faking it, lazy college kid" look from doctors. Finally when I was referred to an infectious disease specialist, Dr. Duncan, I was diagnosed with fibromyalgia (at 18!!?) and CFIDS (chronic fatigue immuno-deficiency syndrome) and was put on Lyrica for the body aches. I took Lyrica for a while but I ended up gaining about 25 pounds over the course of a couple of years without changing my life style at all. It also make me even more tired which interfered with normal life...again.

After a wholeee bunch of trial and error...I finally feel okay. Not as energetic as I was pre-mono/cmv, but that could just be growing up. I'm now on Savella (marketed for fibromyalgia but technically an antidepressant), Wellbutrin XL (anti-depressant), and trazodone (anti-anxiety) all those are for other issues but I've never felt bettter.

StillTired
New Member


Date Joined Dec 2011
Total Posts : 8
   Posted 12/14/2011 8:36 AM (GMT -7)   
Reviving this a bit, with maybe a helpful suggestion.

When I initially became sick, I was told I had been recently infected with CMV and HSV. Oddly, no EBV test was done at the time, but much later on I do have positive labs for a prior infection.

Fortunately my doctors were a bit persistent and kept repeating the CMV and HSV tests until they could see development of the longer-term IGG antibodies (as IGM was what was testing positive). Over about a 6 month period, no IGG antibodies ever developed and the IGM tests for both of these viruses went to negative. So, after being told I had a few viruses, persistance revealed that even though I had many positive tests, they were on the acute IGM side and were false positives.

ANA antibodies can cause false positives on these tests - and I've got that as well as ongoing autoimmune issues, and of course EBV. Conclusion in my case was that no CMV or HSV infection ever existed or I was just the miracle person that rid myself of it and all antibodies (Not).

Soooo.. In a nutshell, if you were just told once that you had CMV, I'd recommend asking your doctor for a CMV IGG test just to make sure. You may or may not really have it.

CoachForGrowth
New Member


Date Joined Apr 2012
Total Posts : 3
   Posted 4/20/2012 8:42 PM (GMT -7)   
I'm very curious about what "alwayspray" said in the post dated 1/29/2012. She mentioned a Dr. by the name of Linn and a sugar free diet. I don't see how to contact alwayspray but am very interested in what she said.

I have a history of Lupus, earlier diagnosed as CFS, but now (18 yrs. later) I'm in the process of a workups to identify it as Sjogren's with complications of Dysautonomia and Small Fiber Neuropathy. Additionally, I've was told I had CMV last year and I also see my lab work from showing I was positive for EBV. Now, I'M HAVING SAME but WORSE symptoms so my doctor is doing blood work.

I feel like my neck and underarm lymph nodes are tender and enlarged, but the doctor doesn't feel swollen nodes. I've had this horrible exhaustion (worse than the usual terrible) and sore throat, lump-in-the-throat, and extreme weakness for about 5 weeks. I AM ALWAYS fatigued, but the recent 5 weeks have been much worse. I suspect she will call and say the CMV and EBV has flared again.

Jayci168
New Member


Date Joined Nov 2012
Total Posts : 2
   Posted Yesterday 11:49 PM (GMT -7)   
Hi Everyone
I know this is an old thread and have only stumbled across this now as I too have been diagnosed recently (August 2012) with CMV and EBV simultaneously.

My Dr recently diagnosed me in September 2012 with Post-Viral Fatigue syndrome. I am feeling as this is going on three months now, I have tried to go back to work twice and failed due to having relapses.

I just want to know if those who from the start of the thread made a huge improvement and what did you do? I am reading so many negative comments from doing google about this illness and it would help to hear positive ones.

thanks

Hopefully I will beat this.

ASTEROIDZ
New Member


Date Joined Feb 2013
Total Posts : 1
   Posted 2/26/2013 9:24 AM (GMT -7)   
I am new to this forum.
My blood tests just came back positive for EBV and CMV!!!
Been man-down for close to 4 weeks now, this is terrible!!!
To answer your question NANNEN, yes the headaches do occur and they can be so severe that they cause nausea. I have three kids and need to work, this is such a set back.

Jen13
New Member


Date Joined Mar 2013
Total Posts : 3
   Posted 3/7/2013 9:39 PM (GMT -7)   
I was diagnosed with EBV in September. I saw a specialist in December who did more testing. He diagnosed me with extremely high levels of both CMV and EBV. In the fall I was very sick with extreme fatigue, terrible headaches, sore throat, coughing, shortness of breath, dizziness, anxiety, and concentration problems.
Since then I have been in and out of sickness. My doctor has suggested valcyte but I am hesitant due to the warning labels. I have been eating a very clean diet and have tried to boost my immune system with very high doses of vitamin D, and B 12 complex shots once a week. I am a 51 year old women. I am on disability because my fatigue was too severe to handle work. I am hopeful that someday I will be well again.

Vanessa Sullivan
New Member


Date Joined Jun 2013
Total Posts : 2
   Posted 6/10/2013 11:33 PM (GMT -7)   
Hello all i am 19 and was diagnosed with the EBV virus about 7 months ago
i was taken to hospital before diagnosis and they assumed i had meningitis so they did a lumbar puncture, it came back clear and they sent me home with NO diagnosis, then i was bed ridden for 3 days and taken back to hospital where an MRI was performed and they saw the lumbar puncture had caused a cerebrospinal fluid leak( CSF leak), CSF was coating my back fat so that night they did a blood patch to patch the leak in my spine, every since then i was having ongoing issues and they picked up i had EBV in my blood after they did the blood patch and that the EBV was the cause of why i was so sick that week i went in, they did more MRI's to reassure me that it was just the glandular fever and not another leak that was making me so dizzy, sick, panic attacks, pressure headaches etc...

here i am 7 months later and id love to say i have healed but i still suffer constantly from sever fatigue, muscular aches ( they feel like inflammation all over my body) i was tested for lyme which i do not have, lately i have visited a naturopath and they are going to start treating me soon however i also saw an ayurvedic doctor (almost a spiritual indian herb doctor) and he told me that glandular is almost like a threat is on the body, and i realised the only way i can cure myself is if i remove this threat, now im not going to sit here and say its the MIND because it is a PHYSICAL virus and is horrible and i do believe in medicine , i want to become a doctor and am actually studying pr-med, however im started to think once you can shift that mind frame you can almost boost your health alittle more, and this is by trying to reduce stress, i am an extremely stressed person and the less stress i have the better i have been feeling overall ( less cortisol in the body) i like everybody else WANT a cure but i just dont see a quick easy cure, i also should add my dad has had chronic fatigue for 7 years and i am so scared that will be me but lately i have done a couple things NOT all but some of the things the aryuvedic dr has told me which i think i should pass on to all of you, it had improved my energy and this is eating the biggets meals at breakfast and lunch im talking heaps of food in the day and then he told me to not have or barely have dinner ( i still do but) some days i have implemented this WOW its actually helping but its not just quantity its the food your consuming he said lots of vegetables extrmely nutritious food and i have slightly done that i buy bags of spinach now cook it with lemon and have that with an egg and salad and protein and its actually helping me BUT I SERIOUSLY think i found something that is helping ... ( i know im ranting but im just trying to briefly explain a few things that have helped a little) another thing is!!! DECAF GREEN TEA! i cant have caffeine because of the virus and its apparently not even good to have caffeine when you have it but i saw CAFFEINE free green tea the other day and have had 2-3 cups a day with a squeeze of fresh lemon juice ( soon i will put manuka honey in it too) and wow its actually helping .. before this it was just warm honey and lemon water i was having but now i actually do think this green tea is helping.. try it out it may be in my head but ive felt alot less anxious and stressed lately and also more energy and a calmer feeling! youve got nothing to lose i guess :)

Vanessa Sullivan
New Member


Date Joined Jun 2013
Total Posts : 2
   Posted 6/10/2013 11:38 PM (GMT -7)   
if anyone has decaf green tea and tries it out for a couple weeks let me know how you feel :) its not a cure but it really might help.. it does take a few days tho! and i have only been doing it for a week but something feels like its helping for some reason!!

Jen13
New Member


Date Joined Mar 2013
Total Posts : 3
   Posted 6/11/2013 12:24 PM (GMT -7)   
I had about 6 weeks of almost feeling normal, but tired at night. I do the best when I try to eat all organic, and avoid processed sugar and white flour. Actually all processed foods are bad if you have EBV and cmv. During that time I also took 3 weeks of valtrex prior to feeling better. I tried to walk when I was feeling up to it but I was also very busy. I missed 3 weeks of vitamin b12 complex shots and I completely crashed last week and I am still feeling very exhausted! My dizziness is so bad sometimes that I don't feel safe driving, yet I try to push myself to get out of my house and try to be normal. Sometimes it makes be feel better and sometimes it makes me feel worse. My neice who is 16 is very sick with CFS and has been for around 2years. My other neice who is 19 has it as well.
My younger neice tried valcyte and it helped at first, then she became very depressed and suicidal. It is all so sad! There might be a new medication coming out soon! If I find out anymore information I will let let the forum know!

Jen13
New Member


Date Joined Mar 2013
Total Posts : 3
   Posted 6/11/2013 12:40 PM (GMT -7)   
I am feeling like if you feel positive about it even if you are down and do everything you can to feel better, that there will be healing for this disease. I hope you get better soon Vanessa!

meryil
New Member


Date Joined Jun 2013
Total Posts : 1
   Posted 6/19/2013 2:26 AM (GMT -7)   
Hello everybody! I saw this forum couple of months before but all posts were very old ad i was very bad so i didn't write anything. I was diagnosed with CMV infection last September after 3 months felling very bad. I had seroconversion with very low fever but felt bad for one day. Couple of days before i felt bad lying in bad and couple of days after the seroconversion i felt extremely bad. At that time my baby was 11months and i was breastfeeding. I stopped breastfeeding immediately when i felt bad. The baby is ok. I experienced general malesia, bowel change for 3-4defecations/day, headaches, sore throat for 2months, pain in the lymph nodes, skin strips on the forearms near the palm from the inner side, tickling on my feet. The infection was in June. I started feeling better in September. Never had any intervention for the rectum nor anal sex. In July went in a private lab to test for all known viruses. Only CMV came positive with IgG 938iu/ml ECLIA and can you believe that all doctors said - Oh it is old infection. You have no problem at all. In September I ended up on Pathology. I was lucky the doctor was fantastic and saw my salivary glands and my symptoms and said to test for CMV. In September on ELISA technique the result was 100 with a limit 16-22. This showed that definitely it is a CMV infection. In December i started feeling rectal sensations that last till now. In February i started felling sensations in my breasts and pain in the axylary lymph nodes.The milk path is painful. In March on ultrasound nothing and on mamography nothing. In April o ultrasound cysts in one breast. Still pain in the breasts, sensations in the rectum. Reactivation in the throat many times. In the abdomen also. Painful abdomen with nothing on ultrasound. CONSTANTLY TIRED!!! Starting from April very bad head pain at one point. Twice i felt like something is leaking in my head. Quit my job since my colleagues thought that i don't want to work. My manager called me for a meeting to ask what is going on. He is a doctor and when i told him about the infection he said - oh everybody has this it can not be that infection to cause this problems....
And before this happened i never went to a doctor. Had a perfect pregnancy and perfect delivery with a healthy and beautiful child.
All of you know how it feels.
I am a medical person so i read a lot and this virus is found in 99% of brain tumors, in breast cancers and colon cancers. It is the worst thing ever. I read the post of BABYGIRL1022 she explained all my symptoms.
I ask her if she reads this to post how she feels and what happened with the breast lump. I kindly ask all of you that have any info for a doctor that understands this infection to write me. I plan to buy the drug and take it on my own. I can not deal with this pain and this virus anymore.
From immune busters only gele royal helped me. But only for couple of weeks to feel ok.
This virus is linked for breast cancer in parous women ( i have the articles and i can send you them if you want). With this constant pain in my breasts, this evidence of malignancies and a IgG levels that do not drop i think of mastectomy.
Any of you that have any info please post because not a lot of doctors know about this infections and we can help each other the most.
I ask you with cmv to post about the IgG levels? How fast did they drop? Mine were in March with ECLIA 835iu/ml which is nothing since a 10% +/- if you check in two laboratories is nothing.
I have a lot of info and from what i know is that you can never rid of the virus the only thing is to control it. Keep your immune system up with vitamins, good mood, prayers, love, holidays, nature and check check check your health. Do not miss pap smears, blood checks, mamographs, ultrasounds do all you can to protect yourself. I give my support to all to increase the knowledge for this virus and please feel free to write me if i can do anything.
Let's pray for all of us!
M.

PTW
New Member


Date Joined Sep 2013
Total Posts : 3
   Posted 9/14/2013 2:04 AM (GMT -7)   
I was diagnosed with both EBV and CMV in August 2013 I also have herpes type 2 for over 4 years, I have been ill for the last 5 months, I have been to the DR a few times & then finally got them to do some blood tests 1st one said viral infection then 2nd reported EBV & CMV just over a month ago. I have also been to the sexual health clinic for other test & so far all negative.

I have had skin flushing/rash all over my body for the last 4/5 months & was so unwell for the first month, sitting in front of the fire shivering, but since then i have felt a bit better but still get shivers & shakes expectationally when i go outdoors & some wind hits my skin.

I went to the Dr last night for some more blood tests, he did not like the skin flushing/rash & also detected a heart murmur, so making an appointment with the NHS Hospital.

Does anyone else have skin flushing/rash, did it get any better?

Monolaurin an extract from coconut oil has been shown to remove the skin of the herpes & CMV virus & that kill the virus, I have been on them for 2 weeks, not sure if they are working, has anyone else tried Monolaurin??

jennyO77
New Member


Date Joined Aug 2014
Total Posts : 1
   Posted 8/18/2014 11:29 AM (GMT -7)   
Hi. I had EB 20 yrs ago. Then 5 yrs later I contracted CMV. The Mono that time was so severe that my liver swelled to 3x its normal size and I had to be put on OxyContin for 5 months. I never completely recovered. In fact, I haven't been able to work outside the home since. 6 yrs ago I was diagnosed with Fibromyalgia. My question is, can EB and CMV cause Fibromyalgia? Or is Fibromyalgia, in some cases a form of chronic Mono?

BBBloom
New Member


Date Joined Aug 2014
Total Posts : 3
   Posted 8/19/2014 8:28 AM (GMT -7)   
Hi
Before you go to Mayo it is good to "google" enough to get most out of visit. They get comfussed by too many symptoms.Two viruses sounds like a defect in your immune system. Look up http://primaryimmune.org/
Get copy of all blood test. Google EBV and CMV antibodies you have/had and compare to what they say on-line.
Do same with ANA and SED rate. ANA can be a sign of Lupus or other autoimmune diseases.

BBBloom
New Member


Date Joined Aug 2014
Total Posts : 3
   Posted 8/19/2014 8:32 AM (GMT -7)   
Two viruses sounds like a defect in your immune system. Look up http://primaryimmune.org/
Both EBV and CMV are related to herpes and are successfully treated
with Valcyte, valtrex etc. Google research on treatments to get dose and duration.Shots of IG(immunoglobulin) are ok but IV of IG are better. See if you qualify.

Love NY
New Member


Date Joined Aug 2014
Total Posts : 1
   Posted 8/27/2014 6:29 PM (GMT -7)   
HELP! My mother is extremely sick! She's been in the hospital almost a week with EBV and CMV. She has elevated liver enzymes, critically low blood pressure (was 50/30) and having trouble elevating without tons of fluids, low H&H levels, she was in atrial fibrillation but is now experiencing ventricular tachycardia. The doctors are stumped because they can not find root cause. She is getting worse and worse! We are having her transferred to another facility we hope will know what is causing this. Did this happen to anyone or do you know someone else? We're desperate!

Boyko
New Member


Date Joined Oct 2015
Total Posts : 2
   Posted 10/22/2015 7:06 AM (GMT -7)   
My daughter 14 years old been sick since end of August.2015 with EBV infection. She was in hospital for a week because she had an high fever and swollen lymph nodes and severe tonsillitis.

Happy that no prescription corticosteroids from our doctor.

When we home her energy level was 0, Only goes to bathroom, sleeps 16 hours. And her legs body was so week so EBV virus cause EncephaloMyelitis. EC

We got home started using homeopatic remedies, vitamins, minerals, virgin coconut oil, echinecia, dandelion roots fresh shake and juices, eleminating sugar and healthy food. What is really helped her high dose of Vit C drip 25000ccIV injection. beam-ray.

Planted wheat grace for juicing but makes my daughter vomiting, also offered beetroot juice doesnt like taste. Says togue bean sprouts juice is good after several trail she said it makes her more sick.

Her energy level index point is 2.5. Cant walk fast slow movement climping 10 stairs makes her tachycardia, feeling sick nauseting.

Checking today website www.treatmentcfs.com is very promising.By doctor MA.Lerner.
Will discuss about possible this info with our doctor for possible antiviral valacyclovir treatment for my daughter. Reading posts of people suffering from CFS due to EBV for long years is really depressing.

Today it seems her infection is coming back her eyes swollen and tonsillar crypt in her back wall of oral cavity.

Few days ago ordered GENE -EDEN online and waiting for delivery in few days. Says has no therapeutic effect but helps to boost immune system.

Mom

ro19
New Member


Date Joined Aug 2016
Total Posts : 1
   Posted 8/2/2016 6:28 PM (GMT -7)   
well im seeing this years after the 2008 posting dates but im glad I saw it...I also have suffered with CMV EBV MONO and other issues as well ...all at once.. started in 2013 ....about 2 weeks after a visit to my dentist spent almost the whole year in bed (other than the initial 4 doc visits and recurring specialist visits .. suffered greatly unfort. symptoms were rash extreme fatigue no appetite head neck and eye aches swollen spleen and liver fevers on and off +++ I didnt want the antibiotics I didnt want the anti virals I didnt want my spleen out I didnt want vaccines they were pushing sooooooo I went the natural route .. YES IT HELPED ALOT AND I MEAN ALOT
I still take natural supplements to keep it in remission/dormant
this is what worked for me during the initial 3 months - oil of oregano capsules . immuno g prp. lymph tone 2. vit d spray. b12 spray. liposomal vit c. and a few other supportive tinctures and minerals depending what my symptoms were
so now its 2016 and ive had my first "awakening" of the cmv ebv and mono wow its hard to be going through it again HOWEVER its much less severe than last time ..I had let my healthy eating go stopped working out and had gotten way to stressed with things and WHAMMMMO immune system crash so I totally suggest whatever u do ..EAT HEALTHY STAY ACTIVE AS POSSIBLE (WITHOUT PUSHING YRSELF STAY AWAY FROM DRAMA AND STRESS AND LISTEN TO YR BODY!!!!!!!!!!!!!!!
Hope this helps someone

NewGuy102
New Member


Date Joined Jul 2016
Total Posts : 1
   Posted 8/22/2016 7:03 PM (GMT -7)   
i have all of the above lyme, epstein , cmv and more it is just devastating. Did the tic give me all of this?

Outtamymind
New Member


Date Joined Sep 2016
Total Posts : 1
   Posted 9/17/2016 10:11 AM (GMT -7)   
Wow......I can't believe I've found this! I've been suffering for 8 weeks now with random and varying symptoms!! At first I thought I'd got some sort of diseases like HIV but all my tests have come back negative.
I will be sure to discuss this with my doctor when I next see him because this is unbearable if indeed it's what I've got!
Below are my symptoms.

Night sweats (early on don't get them now)
Sweaty palms and feet (again early on and very minor if at all nOw)
Swollen tonsils (very bad early on but mild when recurring, they do come up a lot)
Mild sore throat (only had this twice and it's very mild)
White tongue (changes daily)
Leg weakness (intermittent)
Jaw weakness (happened once but couldn't eat)
Dizziness (happened once same time as the jaw weakness)
Stomach grumbling (happened after week 4 Upto week 10, happens early now)
Mild cough (1 day only)
Muscle aches (intermittent and recurring)
Diarrhoea (1 night! Stools are much harder to pass now)
Headache (once only)
Balance loss (Infrequent but happens)

So tests I've had done

HIV tests
16 days
18 days
28 days
51 days
61 days
All negative

FBC
At around 3 weeks after symptoms started came back normal?!?!?!?
Sed rate
Thyroid
Liver function

I'm having more bloods done Monday and will see the doctor a week after.

If this is what I've got it's one messed up illness!!

Hope you're all well

nikki69
New Member


Date Joined Sep 2017
Total Posts : 1
   Posted 9/27/2017 10:49 AM (GMT -7)   
Cmv, ebv, herpes, shingles... are all complications of a suppressed immune system. Latent viruses like herpes and shingles that 85% if the population has are reactivated. Try having them all at once and bring bedridden for 18 months and counting. Osp-A poisoning (aka Lyme disease) is the culprit. Osp-A from a Borrelia infected tick acts as a fungal antigen on your B cells shutting them down. When your B cells are shut down you're not going to produce antibodies so any of your lab tests for certain conditions are not going to be accurate. They'll tell you its false positive if you do test positive at all. It's not autoimmune (allergy), it's the opposite, sub immune. Have your cd57 (for NK cells, not T cells) checked by Igenex labs. You'll see your immune system in the toilet. Without NK cells you have no first line of defense against viruses or tumorous cancers. No one cares. This country's NIH has no department of immunosuppression, only the opposite - allergy (autoimmune). This is an acquired immune deficiency. The AIDS (not from HIV) of our time. Ever hope to gain wellness and have someone figure out how to solve the problem of B cells shut down without reactivation of them creating a cytokine storm we likely wouldn't survive? Prosecute the LymeCryme first. TruthCures.org

emotions
Regular Member


Date Joined Mar 2005
Total Posts : 162
   Posted 10/25/2017 6:07 PM (GMT -7)   
I also have IgM positive for EBV and CMV. These viruses have not cleared in a long while.

Last winter I had low grade fever 99.6-100 for about two months. I go through periods where I am ok then get extreme exhaustion then anxiety, then depression. I have night sweats, headachy, sore throats, feel like I can't focus, concentrate, memory and memory issues. Achey legs. Joints no longer hurt but did many many years ago when I had positive Lyme. I have also had Lyme and confections throughout the 15 or so years.

Mostly concerned with depression and anxiety now and brain fog so much that I need a lighthouse or a fog horn!

These viruses are difficult and cause a lot of brain issues.
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