Is there anyone here who identified EBV as their root cause?
I just got my blood results which showed that I had an infection in the past. No unusual given 90% of population carry it but having Hashi I am now considering this could be my root cause as I already ruled out many other common offenders.
I spoke with my mum and she said I had a rather bad āfluā at the age of 7 which antibiotics would not cure. Doctors could not determine what was wrong and it took weeks for me to recover. We now think it was my trigger as I started to exhibit hypo symptomatic soon after.
I want to try and tackle this beast, is there anyone here with tips of what worked for them?
Iāve read Izabella Wentz books, she herself was triggered by EBV, and have her suggestions: NAC, Lysine, Vitamin C and D, antiviral herbs. Is there anything else worth trying?
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AnnaSo
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I am almost certain my Hashi's was triggered by a severe and long lasting ( 10 years) bought of Glanduar Fever. It took 10 years for me to make antibodies. No other person in my family have suffered from any kind of thyroid disorder. I believe it can reactivate and live in the thyroid gland so I had a comprehensive test recently to rule this out. I believe the EBV can severely damage our immune systems and so resulting autoimmune disease is not difficult to imagine.
Hi Baobabs! Isnāt that intriguing. More and more I read about the EBV more Iām starting to see that autoimmune connection.
I never really suffered a bout of bad flu, not that I could remember, until I had a chat with my mum who reminded me of an infection I had as a kid. Doctors thought it was mumps but I already had mumps before so that couldāt be it. No one ever determined what it was. We now believe it must have been EBV showing off. Soon after I started to show hypo symptoms- sleepy, cold, a bit plump. Things got worse as I got older until got diagnosed hypo at 18, Hashi at 21.
Have you ever tried anything to eradicate the virus?
No I haven't as there appeared to be nothing at the time but someone recently claimed to have trialed some anti viral treatment but when I asked the person to elaborate, I heard nothing more. I am not sure the extent of research linking EBV to Hashi's but I do believe a reasonable body exists. Did you have a blood test to see if you have or have had the virus? My dose of the virus was very severe, swollen liver, vomiting and hospitalised. The aftermath of ME was ghastly.
There has been plenty of post regarding EBV in fact. Shaws was kind enough to share a link to them.
I have been reading up today and there are research papers pointing EBV as trigger for autoimmunity, Hashimoto inclusive. Iāve read that EBV was found in the thyroid of 80% of Hashimo patients versus none in control sample. Thatās a staggering fact!
Iāve heard about it being a trigger first time when reading Isabella Wentz book Root Cause few years back. Iām going to revisit what she has to say about it in her books. She has chapters in both. I also heard about a guy called Anthony Williams I believe. Heās a bit of a weirdo, saying all sort of nonsense like spirits guiding him but apparently a lot of people have seen improvements with his protocol for EBV. I havenāt had a look yet, not sure I can take a medical advise by someone like him though.
Virus's are always difficult to deal with. thought I was on my way out of life when I contracted EBV. I have never felt so ill in all my life, far worse than Hashi's. I didn't care if I died. In fact I thought it would be a relief!
Interesting ! I just tested positive for EBV but I canāt recall ever having mono ( Iām assuming thatās the common name ?!)... just a bad flu once for 10 days. I was diagnosed with hashimoto in 2016.
Really interesting yes! Iām gobsmacked. I knew about the EBV-Hashimoto connection but was unaware I had the virus as could not recall going through mono. As mentioned in my post, telling my mum about the blood result she reminded me about a bad infection I had as a 7 year old. We think that was it as hypo symptoms developed after.
How are you getting on with your Hashi treatment? Have you ever tried doing something to fight the virus?
TBH Iām am a bit new to this hashimoto world. I was diagnosed but never treated until 6 months ago , started NDT by my naturopath. A GP ran the EBV tests and I tested positive for EBV Antibody IgG and my results for EBV Antibody IgM were equivocal ( not sure what it means. Negative is <o.8 and equivocal is 0.8-1.2, mine was 1.10 ) . My naturopath says this mean I had a virus in the past and says no treatment is necessary (hm )...but from what you are saying , the virus is still in oneās system ? Perhaps I should get tested again. So in your case does it mean the virus is still active even though you got sick in the past ?
The virus never leaves. It can remain dormant for lifetime or it can reactivate and trigger issues such as Hashi or other autoimmune conditions. My virus is dormant at the moment but itās still hiding (I believe in my thyroid, in one study 80% of Hashis had EBV in thyroid) and causing antibodies. Iāve started a protocol to eradicate it with supplements.
Oh Iāve learned so much just from this post! Just when I thought it was nothing .... Iāll definitely be looking into supps to help with the virus. Thanks Anna
It seems people's reaction to the virus can be very varied and it is possible to not know you have had it. If anyone has Hashi's it is worth being tested for EBV to see if it is still active. I did just to ensure my symptoms were not related to the virus. I felt terribly cold and fatigued when I had it. Actually I've just realised what I've said! I was freezing in the height of summer. Perhaps this was the beginning of my thyroid destruction?
I had glandular fever when I was a teenager and have had the virus reactivayed twice since (Iām almost 40) with the last instance seeming to have triggered CFS/ME.
Iām very interested in Isabella Wentzās protocol - Iāve seen sheās had a few books out, which one have you read?
Isnāt it terrible how much damage one little virus can make. Really sorry to hear about your triggered CFS apparently that very common. I myself also suffer from it. I caught a cold from a colleague recently and it took me 4 weeks to get back on my feet and I got a range of other new symptoms like painful body. I was freaking out it was an Fibromyalgia making an appearance but it now went away.
I have both of Isabellaās books. They are quite similar but also different. 1st Root Cause, is more theoretical. 2nd Hashimoto Protocol is more hands on and solutions orientated.
Iāve just started on high dose Vitamin C and Lysine. I continue with Zync. They are all antiviral. I make sure I have some for of coconut everyday. Will see how I go with that. I have VitD deficiency so also working on this one.
Sorry to hear youāve got the same issues. Letās hope we can both be healthier and more energetic soon!
Thanks for your reply, I think I might get the protocol book, sounds most helpful.
Iām taking quite a few supplements including the ones youāve mentioned. I do feel like my constant sore throats and neck pains practically went away after Iād started taking Lysine 3 times a day, so hopefully these things are helping even if itās not always obvious how!!
Lets hope we get there! Would be nice to catch up and track progress from
time to time if you fancy? š cheer each other on! š¤
I have found a weird thing that since starting supps Iām having a strange glands pain. Not sure if thatās related but canāt see where that would come from otherwise, would be quite a coincidence.
It would be lovely to keep in touch š and perhaps share any success/tips we come across!
Itās difficult to know what triggers what when youāve got a couple of health conditions and youāre trying multiple things to help isnāt it? I know I can be guilty of starting more than one thing at a time so often canāt really tell exactly what benefit or otherwise come from them!
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