First of all, keep in mind that I am unable to diagnose you because I am unable to examine you, this forum is for educational purposes.
Tinnitus (ringing in the ears) can have many different causes. A common cause is hearing loss that occurs over time, from noise exposure, wax buildup, viral labrynthitis, Ototoxic drugs, Meniere's disease etc. From the decription that you provided I suspect that you had a viral illness that partially involved your inner ear. This will likely get better overtime, but can also lead to chronic neck and/or balance problems. The pressure sensation sounds like typical low level chronic daily headache syndrome. This can be caused by eye strain (10 hours at a computer per day), poor sleep (I imagine Iraq is stressful) and overuse of over the counter medications. Starting a medication to prevent chronic daily headache will help with the tension, such as Elavil or Zanaflex once daily at night. Neck physical therapy and altering your lifestyle can also be helpful. I suspect your tinnitus will improve with time, but I would suggest audiologic testing. If your symptoms recurr or do not improve then you may consider an MRI of the Brain, some centrally acting pathologies can also cause your symptoms such as an acustic neuroma or multiple sclerosis.
I hope this has been helpful.
Musculoskeletal System
Joint pain or swelling or tenderness
Stiffness of joints, back, neck
Muscle pain or cramps
Bone pain
Neurological System
Tremors or unexplained shaking (especially at night)
Burning or stabbing sensations in the body
Weakness or partial paralysis/stroke-like symptoms
Pressure in the head
Numbness in body, tingling, pinpricks
Poor balance, dizziness, difficulty walking
Increased motion sickness
Lightheadedness, wooziness
Sudden jerking of fingers or entire limbs
Pain in spinal column
General Well-being
Unexplained weight gain, loss
Extreme fatigue
Swollen glands
Unexplained fevers (high or low grade)
Continual infections (sinus, kidney, eye, etc.)
Symptoms seem to change, come and go
Pain migrates (moves) to different body parts
Early on, experienced a "flu-like" illness, after which you have not since felt well. (If it was mild, you may not even recall this.)
Eyes/Vision
Double, blurry or dim vision
Increased floating spots
Pain in/behind eyes, or swelling around eyes
Over sensitivity to light
Flashing lights
Optic neuritis
Ears/Hearing
Decreased hearing in one or both ears
Buzzing or clicking noises in ears
Pain in ears or sound sensitivity
Ringing in one or both ears
Pressure or feeling of fullness in ears
Digestive and Excretory Systems
Diarrhea, irritable bowel
Constipation
Irritable bladder (trouble starting, stopping)
Frequent urination that is not normal
Upset stomach (nausea or pain)
Respiratory and Circulatory Systems
Shortness of breath, cough
Chest pain or rib soreness
Night sweats or unexplained chills
Heart palpitations or extra beats
Heart blockage
Psychological well-being
Mood swings, irritability, rage
Unusual depression
Disorientation (getting or feeling lost)
Feeling as if you are losing your mind
Overemotional reactions, crying easily
Too much sleep, or insomnia
Difficulty falling or staying asleep
Mental Capability
Memory loss (short or long term)
Confusion, difficulty in thinking, brain fog
Difficulty with concentration or reading
Going to the wrong place
Speech difficulty (slurred or slow)
Stammering speech
Forgetting how to perform simple tasks
Head, Face, Neck
Unexplained hair loss
Headaches, mild or severe
Twitching of facial or other muscles
Facial paralysis (Bell's Palsy)
Tingling of nose, cheek or face
Stiff or painful neck or creaking
Jaw pain or stiffness
TMJ – sudden onset, jaw spasms
Sore throat, hoarseness
Loss of sense of taste
Difficulty swallowing, throat spasms
Females only:
Unexplained menstrual pain, irregularity
Unexplained breast pain, discharge
Males only:
Testicular or pelvic pain
LYME FACTS
1. You do not have to recall a bite or have gotten the target rash to have Lyme disease. Less than 50% of people with Lyme do.
2. The tick that carries Lyme is as small as the period at the end of this sentence and their nymphs are nearly microscopic. Ticks are on the move at 35ş and above. It’s a year-round problem.
3. You do not have to experience ALL of these symptoms to have Lyme disease. It is also typical for many of these symptoms to come and go or occur once and never occur again.
4. It is possible to have Lyme disease and have a negative test result. After Lyme bacteria enters your system, it tricks your immune system into no longer producing antibodies to fight it, hence, a negative test result. There are also other numerous factors that can affect the results.
5. Lyme bacteria hide in the spinal fluid, bone, tendons, muscle and nerve fibers and tissues and in many cases are not “floating” around in the bloodstream where they can be picked up on a test. It is a cousin to the syphilis bacteria and very difficult to eradicate.
6. It takes a LYME SPECIALIST to diagnose, test for and treat Lyme disease and any of its associated co-infections. To find one go to ***************.
or www.ilads.org. Lyme specialists do not require a referral.
NOTE: Everyone may have symptoms that appear on this list; however, it does not mean he/she has Lyme disease. If one has numerous symptoms on this list and no other explanation for them, consider Lyme.
I only wish that during the two years of hell I went through, someone would have intervened and at least given me the idea. I saw a parade of 14 doctors over the course of two years. My symptoms were to say the least, horrifying. One doctor had the audacity to insinuate that perhaps I had been abused by my father as a child.
My Lyme titers were negative and my Western Blot was negative. Lyme is a clinical diagnosis made my history of symptoms and exclusion of other diseases.
My husband also ended up having it and also the co-infection, Babesiosis. It took another year beyond my diagnosis to figure his out. He had a complete mental breakdown from the neuro-psychiatric effects caused by the bacteria in his brain and central nervous system. He had panic attacks, seizures, suicidal thoughts, agoraphobia and the list goes on. He was sleeping 22 hours a day. He lost his job which sent us into a financial tailspin from which we will never recover.
The cost involved to diagnose and treat both of us had been over $100,000. Yes, we have health insurance, but it certainly did not cover all of our expenses. Quite a bit of it has ben out-of-pocket. I would not want another soul on this earth to suffer like we have.
So, isn't that what these forums are for? To help one another?
If I read a post and it sounds like the person could have some manifestation of Lyme disease, then I post. If it doesn't, then I don't post. It's as simple as that.
I have helped literally hundreds of people through the internet, my newspaper articles and as a contact person. People call me at home and at work for referrals to Lyme specialists and questions about the disease. I will continue to do this with a passion.
Carol
This LLD was sure of her diagnosis and the meds began. Heavy antibiotics for weeks. My wife was getting worse. The LLD said, "getting worse" is normal, and continued on the path of more antibiotics. We would force appointments with the Doc because my wife was in a tailspin.
I took the bull by the horns and paid out of my own pocket to go to a regular "non-LLD" that is respected in our community. He looked at all of her records, gave her a physical, and simply said, "she does not have Lyme" and she is feeling poorly because she is being medicated too strongly and for too long by these Antibiotics.
We decided to go with this opinion. By wife got better in days. He blamed her initial symptoms of "head fog", dizziness and a few other symptoms to anxiety. He was absolutely right !
I know when I joined this forum regarding my viral meningitis, someone posted that I probably had Lyme, not viral meningitis It confused the **** out of me, scared me to death, and had my mind racing for days.
The mainstream medical community does not agree with most of those LLD'ers. They blame Lyme as the cause of way too many things, some which are as simple as anxiety and depression.
I know several woman who believed they had Lyme, despite all the negative test, and personally believe the problem is psycological.
Neurological disorders can present themselves in this manner also.Sinse the tinnitus has continued,maybe contacting your ENT again or a neurologist.
I suffer from tinnitus daily its a bother.Mine is auto-immune related
to the original poster: the fact that you are in front of a computer 10 hours a day to me is important. muscular spasm/imbalance can cause headaches and headache related symptoms, especially when the the neck musculature is involved. the delicate/small muscles of the neck are extrememly overtaxed when sitting in fron of a computer. the fact that your symptoms improve with exercise supports this idea--- when the muscles "loosen up" with activity and are no loger in spasm, your symptoms get better.
i'd pick up a book on posture/neck pain. you can also do a search for jole bookspan and read her website.
One day, at my normal eye exam, the optomitrist told me that she believed I had PSEUDOTURMOR CEREBRI and URGED me to get to the opthomologist. After several hours and tests at the opthomoligst, they also agreed w/ her diagnosis and scheduled me for a spinal tap and MRI.
Pseudotumor Cerebri is not a very well known disease. It is caused from the spinal fluid not draining properly and it builds up pressure in your brain, basically its just backing up in your head. That's why after sleeping your waking up with the really bad headaches. I actually see a Neuro Opthomologist. (Never even knew that kind of doctor existed). He put me on Diamox to relieve the pressure, it helped, but it is a HORRIBLE medicine.
Please urge your doctor's to look into the disease. Like I said, not many doctor's know about it. I was misdiagnosed for 3 years by a neurologist. It wasn't until I went to someone that just happened to know about it that it was recognized.
Mine, thankfully was caused by obesity and was able to have a gastric bypass and now all symptoms are gone.
But, if it is pseudo, I truly urge you to get to the doctor and have them test you. The spinal tap is really not that bad, not like everyone made it out to be anyway. Your better off knowing though.
Please let me know what your doctor's say. I'm really hoping I helped you.
Scott
Before the madness for me started I had steady tinnitus for about two months. In that time I was also having sometimes panicky awakenings and some tingling, numbness in my extremities. Then two months from the start of the tinnitus symptom I experienced a few episodes of heavy tremors in my legs and a bit in my arms. After the tremor episodes I was left with twitching, buzzing/vibrations, tremors/spasms, burning sensation, bug crawly feeling in my upper back, cramping, tingling and numbness in the hands and feet, tinnitus, sometimes an awareness of difficulty of walking due to a feeling of imbalance, weightloss, insomnia, aches and pains.
When the tremors started I would get the feeling of the chills like you know when you are catching the flu.
The past couple of months I have noticed a decline in cramping, tingling and numbness in the hands and feet, crawly feeling in upper back, trouble swallowing, and aches and pains and I have gained my weight back though due to less exercise over this period I have put on the wrong kind of poundage.
Testing: CT scan clear but on the EEG test during the hyperventilation part of the test my legs experienced tremors.
MRI showed no intracranial abnormalities but there was fluid around the nose compatible with sinusitis and my right ear area did show fluid compatible with mastoiditis.
The way things started and the fact that after 8 months I have no serious weakness, likely means ALS, is not the reason. My MRI showed no lesions on the brain and my symptoms are not really compatible for MS at this time; though maybe a person does not always need lesions on the brain to experience the disease in the early stages. My doctors are presuming Anxiety which if I did not have before the symptoms arose I probably have acquired by now. The neurologist I saw twice said I did not have ALS, MS or BFS but I think she just saw me as an anxious patient who was wasting her time.
From some of the posts I have read on this website http://www.nextination.com/aboutbfs/ I could have been infected by a virus or less likely I picked up lyme from one of my camping/hiking trips to the Thompson/Okanagan region of B.C.
All the best in your quest for the truth.
Paul
Well here it goes I had pnemonia (pneumonia) baddly 2 years ago and for the past year or 2 My doctor said with tests he has sent me foer that I have Degenerative disc desease and arthritis also the CT Scan come back saying that I have a brused brain I also have TMJ what I am concerned is why am I getting only head sweats at night could it be something in my diet or could it be caused from computer ( I am at the computer somedays about 6 hrs a day off and ondoctor is sending me to a Nero speciallest after christmas but I am scared to death of getting bad colds cause I am going to another province for christmas and its cold there so if I have a head sweat at night the cold will make it worse
I am also dealing with a lot of stress in my life right now Oh I am 60 years old female I get a lot of Aura Migrains too could someone Help me or give me some answers I am going crazy sometimes It feels like a strke coming on when I have the Migrains followed with weekness and tiredness all day long (only sometimes sometimes I dont have weekness just a bit of Zig Zag lines that last for only 20 min.
Although you can't just jump to conclusions and say "hey, I must have Lyme disease, better get tested", it's can sometimes be a possiblity to rule in or out as well as other diseases. As many of you know, these dieasess can mimic each other. I've heard many stories where people were originally diagnosed for MS or ALS and found out later, with more accurate testing, that they had LYME. I hope the initiatives and testing continue to improve for LYME as it should be consider as a valid disease, next to all the maladies that many are afflicted with.