Infectious Mononucleosis :: Recurring Glandular Fever
Jan 30, 2006
Living with Recurring Glandular Fever
Many people who catch glandular fever (Epstein-Barr virus) recover completely, but for a significant minority, like me, the virus hides from the immune system. I believe that this ability was discovered in the late 1960s. I heard of it in a BBC science programme in the early 70s, and immediately recognised my situation.
I caught glandular fever (without complications) in spring 1967 when I was a youth. Those who are affected by recurring symptoms, will recognise my case, where the symptoms receded imperceptibly slowly. It took about 9 months from being infected before I felt more or less normal again - for a while.
I pass on my experience of coping with this condition. There is bad news and good news.
The bad news is that the symptoms recur throughout life - that is for those who have difficulty clearing the original infection. A cure might emerge, but I am assuming that this will not happen. The good news is that, in time, the symptoms become gradually less of a problem.
The bad news is that one needs to adapt one's lifestyle in order to deal with this. The good news is that one can live a normal life. There are many with other lifelong conditions, who are far worse off.
Any virus illness (cold, 'flu) will trigger the symptoms. Something as common as catching a cold runs as follows. One feels unwell (exhausted), with no symptoms. About 2 days later, the cold symptoms start, accompanied with swelling of the glands in the throat and/or cheeks. The swelling is not very noticeable to others. One has a slightly raised temperature, and feels quite ill. After 4 to 10 days, the cold symptoms and swelling subside, but the feeling of exhaustion remains. This can last 4 to 6 weeks, or 6 months after a bout of 'flu.
How can you cope? There are a number of measures.
1) Smoking exacerbates the symptoms. If you are a smoker, you will be one of those who find stopping smoking relatively easy. You will soon learn to avoid smoke-filled places.
2) Should the symptoms start, treat as for a cold, or 'flu. You will feel exhausted, and a good thing to do is to get a lot of sleep.
3) It is worth getting a 'flu vaccination, if you can.
4) Exercise - you won't feel like exercise, and it is wise to rest while the cold symptoms are there. Once they are gone, and the feeling of exhaustion remains, that is the time to resume vigorous exercise. I think it might be the raised body temperature which helps to fight off the symptoms. In the case where you go to the gym, you will have to force yourself against the feeling of exhaustion for the first time, and even the second time, but by the third time, you realise that you are much fitter. The exhaustion will go. Regular exercise helps ward off the problems, and the fitter you are, the better you will manage.
5) Avoid catching colds. You will find that you have become especially susceptible to colds. There are many things involved here, from a good, varied diet, a daily multivitamin/mineral tablet (don't overdose), cough sweets in the bus/train etc.
The best advice, and perhaps the most difficult and lifestyle threatening, is to follow what (great) grandmother told you, "Wrap up warm!" Think how she would say, "Put on your sweater/scarf/hat/woolly socks before you go out!" You think. "It is not cold outside". You know it isn't "Cool", and you don't want your friends to laugh at you.
If the summer weather is really hot, you can get away with fashionable wear. Otherwise, the bad news is that keeping warm maybe "uncool" but if you ignore this, you will suffer. Ideally, you should keep on the verge of perspiring, and if the surrounding air is fresh and cool, that is the ideal. Avoid stuffy environments. Avoid becoming too hot, sweaty and wet, and then getting chilled. However, if you can arrange to change into dry clothes and not become chilled (as when you go to the gym), all well and good!
I found these lifestyle adaptations very unwelcome. You will have to find your own way to cope. Thinking of these matters will help, and you can lead a normal life, with bouts of extreme exhaustion from time to time. Take comfort in that these will become less severe, and maybe less frequent as the years pass. Otherwise, you are quite normal. You can achieve what you are capable of intellectually, and physically. Face up to the occasional difficulties, and be determined to succeed with your life. Epstein-Barr will not prevent you.
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Spontaneous splenic rupture in infectious mononucleosis. How will his body fight the infection without his spleen.
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Back in January 2012 I contracted Glandular Fever and was sick for a couple of weeks. Ever since then I have had a sore throat on and off and nothing it doesn't seem to be getting any better. I get frequent mouth ulcers, the back off my throat is almost always red and patchy with ulcers and sometimes I even get the on my uvula.
I have seen my GP about this a year or so ago and was referred to a throat specialist who pretty much told me to wait it out, but it is very frustrating considering it's been over three years. I have also noticed that alcohol seems to make the problem worse, but being at uni I didn't have much chance to avoid it. My general health is relatively good, if I pick up an infection intend to fight it off quickly and don't get that sick. It's just this which is more frustrating than anything. The only other thing I would say is that I do have mild hay fever and always seem to wake up with phlegm in my throat so I'm not sure if this attributes to it.
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I was diagnosed with Glandular fever back in September after a blood test but first had swollen glands in June, I still have swollen glands now and am really worried. Is it normal to have swollen glands for 4-5 months?
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I previously posted about my night sweats but now I have a new symptom. Mostly in the morning, my forehead and sometimes my face feels hot but I don't have a fever. In fact my temp. will be a degree below normal. My body will feel a little warm but not as much as my face and forehead. Does this sound like mild hot flashes?
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I am 52 years old. I just discovered that a recent blood test came back positive for mono markers. My doctor told me that I am RECOVERING from mono but I can't remember EVER having mono! I've been suffering from fatigue and body aches (along with shortness of breath) for 3 months now. So, how long is this going to last and how is it possible to be recovering from something I don't ever remember having?
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I have recently been diagnosed with EBV. I didn't present with the "normal" symptoms. I first experienced joint pain, then muscle pain, followed by extreme fatigue and muscle weakness. That lasted for about a month, then I developed sharp electric pains in my nerves and associated muscle weakness and numbness that comes and goes in my arms and legs. The nerve sensations have lasted for about 2 months. I seem to be healing
As I haven't experienced as many sharp electric pains, just numbness and tingling. I have been to a neurologist and have had an MRI of the head and neck which came back normal. Has anyone ever experienced anything of this sort of nature? I've been experiencing symptoms from EBV for 3 months now.
It's also important to note I was tested for Lyme and other blood work was done. Everything was normal except the ebv (which showed I had either contracted ebv in the last 6 months or it was.
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I just started getting really bad pain exactly where my spleen is. Whenever I stand up or am sitting there comes a really sharp stabbing pain. I can't breathe on deep or eat alot, all I can feel is this pain. Someone said it's because they mono, I've had mono but I'm not sure what that has to do with your spleen.
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I am a 30 year old female who was diagnosed with mono April 19, 2014. It has been quite the challenge caring for my 7 month old and having to take time from work. I never had the fever, although I have the other fun mono symptoms such as discomfort in shoulder blades and under ribs from liver and spleen. I have visited both my physician and GI doctor and they can not feel any swelling which is good. I am 6 weeks into the disease and feel pretty good. I am happy to report my bloodwork came back normal yesterday. Last night, my 7 month old kicked me in the back (upper left side of my shoulder) while sleeping next to me. My anxiety alarm went off. I am not in pain, however I am feeling a light discomfort in the side and back of ribs. Of course I'm freaking out and thinking something is wrong with my spleen....anxiety can do terrible things to the brain...so maybe its all in my head? Someone told me you would need a blow to the abdomen in order to rupture the spleen and not to worry. How would I know if my spleen ruptured?
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I don't have mono but this was the best place I could think of to ask this question since an enlarged spleen is a common problem of mono. I've had pain in my upper left abdomen since March and finally had a CT done of the area. Lady I saw at the clinic originally thought I had mono from where my pain was and my fatigue, but test was negative. CT report I got from the hospital shows 12.9 cm spleen and I'm a 21 y/o female if that makes a difference. I'm in the process of trying to find a PCP instead of just random people at the clinic, so once I get that settled I'll make sure to ask them. Just wondering if this might possibly be the cause of the pain or if I should look elsewhere?
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I've had abdominal pains for about 9 months now. At first, they were sharp, so I went to the doctors. They were all over my abdomen (upper left, lower right, lower left back, etc. [sometimes in my upper left chest]) Literally, anywhere over the core of my body. After an ultrasound, it turned out I had an enlarged spleen. From blood tests, they discovered that had mono.
6 months passed, I got another blood test. No mono, but I still had the pains. I got another Ultrasound, and still had an enlarged spleen.
Just a month ago, I got another huge panel of blood tests and they all came back normal. But I still had the pains. I then got a CT scan, and it again showed that everything was normal, except for the fact that I only had an enlarged spleen.
Could my spleen still be recovering from mono? My doctor told me not to be too worried, but it still worries me because I get them everyday. And how could my enlarged spleen (on the left side) account for pains all over my body?
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Is it possible to have pain in spleen, liver and Kidneys with Mono. I have these issues on and off for 2 years now. I can't find any doctor that can help me resolving these issues. It's very frustrating and I am not sure how long i can handle these?
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Hi I just had a friend pass away from what they believe was Sepsis. But they aren't sure just yet. His organs and fluids came back great. There doing blood tests and we won't know exactly what it was until mid March. I was just wondering if his family and friends should be concerned about getting it?
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So last friday night, my cat bit me on my lower leg. I washed it coz my mom got mad at me with water and soap. Yesterday I feel fatigued (probably due to my brother's birthday and I cooked half the day ugh) and just this morning when I woke up my throat feels itchy and I have had chills. I don't have fever but feels like about to have a flu. I had myself vaccinated after waking up but still feels chilly. Is it rabies? My cat looks well anyway so I don't think she has rabies but I want to be sure. Everyone in my family has had flu last week so I'm not really sure.
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This should be a title to a horror movie, not the title of a post,in another attempt to gain some insight to what is inhabiting the largest organ of my body.
Am I really delusional? the dermatologist diagnosed me as being a cracked egg,I'm a victim of domestic violence and therefore,my brain has made up an imaginary situation, to take me away from the emotional trauma...he says I may also be psychotic, I've mutilated my skin,picked and scraped away at myself,simply because I'm convinced that I am unworthy of my vulnerable protection,my defenseless,pink skin...NO.
I HAVE SOMETHING IN MY DAMN PORES.
That man....he scared me more than any violence, domestic or random! I'm looking to find a slight insight,other than Demodex,scabies,botfly,or the largest bodied Demodex...the one that causes mange in dogs. They're very small but damn it...they're very visible! I thought I had pinpointed where they hail from predominantly... I was wrong. I researched myself...tried different creams...permethrin, high dose cortisone,tea tree...still popping out of the open pores,sometimes sebum sometimes alone. Thread like but also grain of rice like,can't see them move,think they may be in my mouth as well. When I haven't slept for 24 hours( I work a lot) they bite(?) And it feels like I walked through fiberglass,then they come out! Yep,uninvited terrorists and I'm the host. What is this?
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I got back from a 2 month trip across Eastern, Central and Southern Africa about 6 weeks ago. A few days after I got home I felt quite unwell, fever, headache etc and I was concerned I may have contracted malaria as I wasn't brilliant at remembering to take my pills. So I got referred to infectious disease department who tested me for lots of travel related illnesses. I was negative for malaria but came back positive for tick borne encephalitis and also Rickettsia (related to African tick fever) I think.
I am actually feeling fine now but they called me in for the results ... I'm just a little confused as from what I've seen on travel health websites is that you can't get tick borne encephalitis in africa! I didn't know this at the time so I didn't say anything to the doctor. You get it in Asia and Europe..I did go to Asia about a year and a half ago but would it be possible for this to still show up in my blood?
I'm just a bit worried as I know this disease can be potentially deadly or cause lasting neurological problems and there's no treatment. I'd feel a bit better knowing I definitely caught it from the earlier trip to Asia as then I know it would have made me much sicker by now if it was going to.
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This weekend I discovered some worms in my stool which is a first as with my current problems I have been quite observant of my body over the months. I'm planning to go doctors this week when I can call up Monday.
I've been to the doctors a couple of times over the past few months with problems, which I can obviously point to my new discovery, however I was diagnosed with the usual stress etc. after my blood deficiency tests a month back came back normal. I still knew something was wrong because of the patterns. Before this discovery I was pin-pointing it food allergies / sensitivities as my symptoms seemed to peak after meals.
It started with a fever back at the start of February. The next week I was getting chronic nausea and headaches (seemed to be shortly after eating). I went to the doctors and reassured I was fine. I was getting a lot of small muscle twitching, nerve pain, general fatigue, especially after meals and anxiety. I cut gluten from my diet and noticed my symptoms seemed to drop by 90%, although my whole diet changed so it could of included over things. After that point I've been sensitive to some foods e.g. after having a banana or orange juice I will itch and have felt a lump in the back of my throat which I assume could of been contributing to my symptoms. The banana gave me noticeable chest pains, maybe cause bananas are a known laxative and I was annoying the worms!
I will also mention I have a few cats and sometimes interact with dogs. I can eat rare steak quite occasionally. I'm in the UK as well and haven't traveled for a while, last was Sri Lanka December 2014.
What worms do the <attached photo> look like? Sorry for the grossness. I figured pin worms or hook worms from what I read but I guess the symptoms are a big clue. I will have to get a stool sample I assume, but obviously want to be on the biotics as soon as possible so I can return to normal as the last couple of months have really impacted me.
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I have a worm infestation in my face. They travel around under the skin leaving tracks and bursting holes into my skin. they create glass like balls that split the skin open and move around my skin with ease.
I first reported it 3 months ago and the doctors totally ignored me treating me for a secondary infection that was caused by open wounds in my face. They have given me 4 courses of antibiotics treating the wrong infect but totally ignored what I was telling them about the worms.
The worms whatever they are are very sharp and wherever they travel through in my face the skin collapses, leaving it like plasticine and it causes tiny splinters that are as sharp as anything that embed themselves in the inside and outside of my skin right down to the lowest skin level. My skin is also producing a clear sticky substance which feels like little shards of glass if I touch it. All in all, it really couldn't be much worse except for the fact they have made a hole around my mouth which they can look out of. I am totally sane!
I am in pieces. I've been telling the doctors what it is and they have totally ignored me. Even refusing to refer after an A & E i visited confirmed I needed to be referred as the lesions had been on my face for so long.
I discovered I had private medical care through my company which now thank god means I've seen my first dermatologist. He's referred me to another dermatologist that apparently knows more about things in the skin who I'm yet to see. Even though he's now put me in the right direction, I'm not convinced he was sure it is worms. I can pull 1/2 inch worms out of my skin bit by bit. They look like thread worms and never come out intact, you pull little bits off of them. It leaves worm shape dents in my face and they feel like little match sticks under the skin. Nobody is taking me seriously as people don't really get worms in the face.
They have totally destroyed me skin and I have bad scarring. I have never had acne and had no scarring. This has all been caused in the last 3 months. I dread to think how many are alive in there now they've been left so long.
Has anyone ever heard of anything like this?
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CDC states in Literature Physicians do not have enough education in regards to Hemochromatosis
Toxoplasmosis is an emerging infectious disease that may not be as rare as they think it can come from cats other mammals fleas cockroaches rare meat more...it affects the muscles liver heart brain throat can cause birth defects jaundice premature birth stillbirth miscarriage cerebral palsy or defects later in life blindness deafness is linked to Schizo/bi-polarism more.
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Are there diseases that can sort of "mask" as mono, yet be something else? Can something else other than EBV test you positive?
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I am a 29 year old female. Around 19 years ago, I had slipped capital femoral. Around 6 months ago, the same pain started to occur. I went for a dye injected MRI and the results were inconclusive due to the pins interfering with the magnets. The pain has gone away for the most part with a few outbreaks but about two weeks after the injection, I found a pea-sized hard movable lump in my groin, painless unless manipulated a lot . I spoke to my general practitioner about it going on 6 months ago, and he said keep an eye on it but confirmed it was a swollen lymph node. I am scared to go back but the lump has stayed consistent, possibly enlarged. Should I be worried? I have had insomnia and I have narcolepsy, so it's very rare for me. I am always tired, but again have narcolepsy and hypothyroidism .
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