Treatment for chronic Epstein-Barr virus (EBV)
My son has been suffering with Epstein-Barr virus (EBV) for over a year. I have taken him to an immunologist and infectious disease doctor with no answers. He is always tired and never feels well. He has relapsed with Mono twice in the last 10 months.
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I passed out and hit my head about a year ago. I spent two days in the hospital. They ran bloodwork and did a CT Scan. I was told everything was normal. When I went home and continued to get worse that’s when I saw a Function Medicine specialist. They ran the tests for EBV which came back positive with very high numbers.
I haven’t been able to get this virus into remission and I just continue down this road of exhaustion. I also still had a couple of markers for Lyme in my blood which I was told don’t really mean anything since there were only two. I’ve pretty much given up and just try to understand my new normal and do the best I can.
I was told early on I was depressed and offered antidepressants. I felt my depression was stemming from my life falling apart from being sick. I also had severe anxiety, and again it felt related to the illness. Now that I’ve accepted my new normal, I still feel sadness, but it’s not the same as depression and anxiety. It’s one day at a time and acceptance has been a slow process, but it helps deal with the pain of what my life has become. Some days are better than others.
It is so depressing to not get the answers or a doctor that does not pursue further for a diagnosis. I spent over a year going to so many different doctors. One thing I can assure you of is to seek out the Lord and trust He will take care of you. It will help lessen your worries and insomnia. I will pray for you to find answers and support to get healthy again.
Thank you. I’ve actually been praying and seeking the Lord but sense nothing. I’ve been blessed to have many praying for me to no avail. I don’t understand why this is happening. I’ve been doing my best to try and accept this because it doesn’t appear to be any medical help or answers available. I’m trying to get strong enough to have some sort of life, but it’s exhausting and discouraging. Insomnia and night sweats are one of the the worst parts. That’s when the depression tries to set in, but by accepting this and trying to learn from it, I'm able to at least get a little emotional relief.
I wish more funding and research was available to research this. It’s real and I know many suffer with CEBV.
They ended up denying my referral which I’m shocked. I’ve never been denied a specialist referral. He seemed smug and said it’s most likely a reinfection and not chronic based off my symptoms. I’d still like to have answers as to why I got it again and why numbers are higher. I have a neck ultrasound soon to check my lymph nodes. I prefer not to do a Ct since I’ve done four in the last four years for other issues. Any suggestions on what else I should try?
So sorry to hear he’s going through this. Are there docs you can recommend or articles? This illness is new to me- recently diagnosed. I feel crippled- all joints ache. Had stressful previous job- now retired. I’m at a loss. Is this disease contagious to others? Thank you!!
I don’t know if this will be of any help, and it may not be what one wants to hear, but I, too was a childhood cancer survivor have been struggling with a host of mysterious and progressive health issues including neuropathy. I thought that the EBV+pneumonia that dramatically altered my health suddenly many years ago may have lead to chronic EBV, among other theories.
It turns out what I actually may have is the well-studied and documented RICAD (Radiation induced Coronary Artery Disease) with Chemotherapy induced neuropathy. Despite the names, damage is widespread and not limited to heart and nerves. Treatments are available if diagnosed early but not if delayed. Please look into it if you received radiation, especially if to the chest and neck area, or if you received both radiation and chemotherapy.
I have gone undiagnosed despite early warning signs of first neuropathy, then fibromyalgia, chronic fatigue, and liver and lung damage and now extensive heart damage.
I would not want anyone to go through the *heck* both myself and my spouse have experienced, desperately seeking answers for over 25 years.
I too have had to deal with this for many years and are encouraged to hear what treatments others have found helpful. Thank You
I hope your healing journey is going well. I was wondering if you could share the homeopathic protocol for EBV when hyou have time, thakn you
I hope this message finds everyone in here well and their loved ones as well as can be. Please consider this protocol: cbd tincture for headaches and nerve pain, gromwell root tincture for ebv replication suppressant (add pure shikonin to tincture if symptoms are severe), L- lysine daily and acetaminophen for fever and pain mgmt. You should notice lymph node swelling reduction pretty quickly with the gromwell which has really low toxicity and also helps prevent damage to other vital organs.
90% of the world's population has this virus and I honestly believe it's the root cause of most fatal diseases. But because the greater majority seem fine we ignore the few who suffer tremendously, that is until the majority gets sick later in life at which point the medical professionals don't understand that ebv is the root cause of your ms or lymphoma or heart failure.
Read the studies, you know what's best for you, and keep on fighting.
To Igervasio: Which CBD tincture are you using, and which gromwell root tincture? What is shikonin? And where does one get these things?