EBV - Reactivation / Chronic EBV
Hi, My son (17) just got diagnosed with reactive / chronic EBV he is an athlete with dreams of playing in college. He is really struggling, and we cannot find a doctor to help him. This is his test results.
EBV VCA IgG (U/ML)
>750.0
Comments: Above high normal
EBV VCA IgM (U/ML)
< 0.0
EPSTEIN-BARR EARLY AG IgG (U/ML)
20.1
Comments: Above high normal
EPSTEIN-BARR NUCLEAR AG IgG (U/ML)
>600.0
Comments: Above high normal
His DNA PCR was negative.
He is resting and eating healthy with some supplements - a little worried to just start giving him a ton of stuff though. He is 3 months ( or longer) into this reactivation and just getting worse. He had mono in early 2022 and covid / Vaccine.
Worried this is progressing. We are willing to travel just need to find help!
Thanks!
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Hi @denistenis, I'm tagging @worriedmom123 to make sure she sees your question to her about her son.
How is your daughter doing? What symptoms does she get and how does she manage them?
I just turned 15 in 1973 when I was diagnosed with mononucleosis and strep throat. I was quarantined for 4 months. With paralyzed vocal cords creating an inability to verbally comminate or even swallow. I lived on split twin pops which I would shove down my throat to melt and help with the pain, and give me the only nutrients I got.
In the next 5 decades or so, I was diagnosed with mononucleosis at least once per year. And a few times more than once in the same calendar year. Then in January in 2018 I was listening to a talk regarding Hashimoto’s Thyroiditis (which I also have) They mention the percentage of Hashimoto’s patients that also test positive to EBV. Then it was like in passing they mention Monolaurin.
So, I started my own research. From there I began taking it daily. After I got over the first die-off phase, I began noticing that while even one else was catching a cold or a flu bug, I was not. This alone was very weird.
Since I started taking Monolaurin, I have only gotten sick twice. And that was only because I screwed-up in the ordering of the supplement, and was without it for 3 weeks or so. So, in case I screw up the ordering again, I already have some on hand.
Personally, I would recommend anyone struggling with lingering issues with EBV to do your own research on monolaurin. Then just go for it..
Oh, and the reason why it is suggested to start with lower dosage is because of what is called die-off. It is true. Die-off sucks. It is not like you are really sick or anything, but at about two weeks or so in of taking monolaurin daily you will just feel icky for a few days. This is just the toxins given off by the dying virus cells. And it may happen more than once.
Oh, as a side note I was able to speak again eventually (took about a year), but I could no longer sing. Not that I was ever good at it or anything. I but I have always missed being in choirs.
I was also fortunate that when I met my new primary care physician a few years ago, she was very familiar with monolaurin, and was pleased with my imitative and progress.
I also have chronic reactivated EPV. I perpetually feel like i am either getting or recovery from mono/EPV. I take 2000mg L-Lysine tablets a day when in a flare and 1000mg a day as preventative. These help me keep alot of symptoms at bay. I will look into Astra-isitis as it sounds like it can help with my inflammation issues.
I j e been dealing with Lyme disease and other auto- immune illness- different doctors choose different labels- but my recent EBV lab result is 750 on EBV Viral Capsid IGG and I do not think my doc knows what to think! I am so short of breath and tired all the time- supposedly my Lyme is in remission but I feel sick- and so sick of feeling sick! Trying to help my husband finish up our house and am almost useless! Do not know what to do next!
Lisa, my dear, so very sorry to hear your woes. Health affects our whole life, every facet. I recently had a similar experience with UTI chronic, and got sepsis in October. Nearly died in hospital, had no symptoms but the exhaustion and fatigue and foggy mind for two weeks till a friend took me to ER where they kept me for two weeks. I was seeing ninjas before l got better the day before l was released. First, please take many deep breaths, as you are able, and give yourself a break. Let someone else help your hubby and do all the stuff except take care of you. That’s your only responsibility right now. I’m 78 now, still youngish for my age, and used to be Superwoman at all times. I know better now— your emotional state, sleep, and self care are all important with autoimmune disorders and you have more than one. I don’t know if you have kids that need your time etc, but try to hire out what you can or ask family and friends. The doctor issue is another issue, considered Mayo? 20 yrs ago they diagnosed me and prescribed a Rx (l still take) in two days’ visit. They are fabulous. Or you might get references from them for the best specialists in your area. It’s almost a given that someone can ID your issues and take care of it to give you relief! It will happen. For now, you just breath a few deep ones when you feel overwhelmed, and love yourself as you deserve. The world will go on, and you must get better to enjoy the ones you love. Nothing is more important than that. I send you blessings and wish you resolution soon. We on this blog know your pain and care. Keep in touch with updates on here, you will get some more educated responses than mine. Vicki