Head Pressure and Lyme Disease

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New Member

Date Joined Aug 2008
Total Posts : 1
   Posted 8/5/2008 10:23 AM (GMT -7)   
Oh my gosh, I can't believe so many people have what I have. Where ARE you guys and why haven't we met because every time I mention it to anyone, I get this "what do you mean...head pressure?" question and confused look.
Here's my story....
I've had odd, often unrelated symptoms come and go for years that were all dismissed as "normal" upon further testing.  In 2003, I began having numbness and tingling in the spine with dizziness, especially when standing in one place for more than 5 minutes. Along with the multitudes of other symptoms that came and went,  (usually before I could get in to see a doctor)  I ignored it.
First off, I LOVE to fly and have never had a problem my whole life with elevation problems or pressure until.....In June 2004, not quite 40 years old, after a wonderful vacation in Vermont, we were almost home and I was relaxing with a new cd I'd bought in Vermont when suddenly, without warning, I had the most horrific pain shoot through my head like so much lightning!!  I thought my head was literally exploding and I actually SCREAMED on the plane.  I could not speak, I seemed to have become paralyzed. My husband was panicked, thinking I was having a heart attack. I am not a wimp when it comes to pain and I've dealt with it a lot over the years but this pain made me cry.  People around me "realized" what was happening and handed me gum, water, ice, and the stewardess was giving me tips on dealing with the pressure. When I got OFF the plane, the problems had just begun....my son and daughter picked us up at the airport and I was so completely drained of ANY energy, I felt catatonic. (I wasn't tired at all before all that! I was happy and excited after our trip) I struggled to stay awake till my kids went to their rooms for the night and I went to bed and slept for 16 hours. I was not able to sleep for more than an hour a night for the first 3 weeks so of course, I couldn't stya awake during the day. It was a vicious cycle. I went to the ER after a few days and over the next 2 months, I would have a CT Scan, MRI, and see a neurologist.  During all this, I am suffering headaches  all day and all night. The first month, they were 24/7 with the "almost"  same intensity as on the plane.  The second month they differed in intensity but were still 24/7 with horrible shooting pains at least twice every hour. The 3rd month, they were still horrible but at least I was now sleeping 3 hours at night and this is the time when the neurologist threw up his hands and said, "Well, some people just have headaches their whole life."  Headaches are fine, I told him, I can handle that. But I don't have headaches......I have 1 headache that never goes away. he told me to go home and take Tylenol or something similar....or he could prescribe migraine meds for WHEN i have a headache.  (Apparently he did not hear the part where I said I ALWAYS have a headache 24/7)   Of course, through all this, it wasn't just a headache, it was pressure, primarily  in the back of my head. I couldn't sit back on the couch...too hard. I bought pillow after pillow, even have slept on a balled up blanket because anywhere I laid my head, my eyes felt like they were bulging out of my head!! It feels like something is growing and pressing on my optic nerve. Of course, the scans showed no tumor so I'm "normal", right??
my friend's 14 year old  daughter had just been diagnosed with Lyme Disease after years of searching for answers to this girl's problems....many neurological. (When she'd get a new symptom, I'd often say to myself, "Hmm, I've had THAT for years") Well, when I described my above experience, she said, "you need to be tested for Lyme Disease."  Of course, she'd been bugging me to do it since her daughter was diagnosed in about MArch of that year.
HOWEVER, The trouble with Lyme Disease diagnosis is this....if you just got bit and know it, you go to the doc, he tests you and if you have it, he prescribes 6 weeks of antibiotics. If you get bit and don't know it (which is common) but somehow are "lucky" enough to be diagnosed before the pathogens invade your body systems, again, you'll be given antibiotics and you'll be healed most likely. But when the antibodies to fight off the Lyme Disease start to disappear, there becomes nothing to test. (This is somewhere around a year but may be less for some people) There IS a test though that is probably cutting edge for people who have what they call the desseminated Lyme. My clinical symptoms were already a "given" that I had it, according to a doc I saw in Missouri but the test confirmed it.
In September, 3 months after my initial explosive headache, I drove 5 hours with a raging pressure and headache to see this doctor, as there are few who are truly knowledgable on Desseminated Lyme Disease. He spent 4 hours with me listening to my history while he made notes. His paperwork is extensive as far as questionaires on symptoms and things so he went over the hundred or so symptoms I checked.  When he asked about head pressure (which was an actual symptom of Lyme), I told him the story and he explained the reason (which is confusing and not important here).  He prescribed me Diamox to use as needed but I find it makes me real loopy.  Once I was diagnosed and he created a plan for me, I went home and began a very intensive antibiotic therapy which consisted of 6 weeks on one drug, switch to another and another and another till I went through about  a year and a half's worth.  He also suggested  going off caffeine and sugars (esp. fake sugar like Equal) for the first 2 months of therapy, taking vitamins, and probiotics along with an anti yeast drug to combat all the yeast from the high doses of antibiotics.  Well, barely a month later, I was sleeping 5 hours a night (my normal was 7 hours) and I the headache, though still there had decreased in intensity considerabley! Eventually, they went away completely, as did all my other constant symptoms of pain, nausea, etc. (remember, I had 100 or more symptoms....too many to mention here!) Now it is 2008, and I still have slight pressure in the back of my head still but most of the time, it doesn't bother me. I rarely have headaches and when I do, I wonder what's causing it. It often seems linked to processed foods or fast food hamburgers and such. But I don't know. I am still living with head pressure that sometimes gets worse from time to time but it goes away at least.  I have lived with Lyme Disease since probably around 1992 so I probably wil never completely eradicate it. Not everyone does but they get to a level that is under control.

New Member

Date Joined Aug 2009
Total Posts : 19
   Posted 8/26/2009 5:54 AM (GMT -7)   

My sister has a lot of the same symptoms you describe.  She is in the process of being diagnosed for lyme & feels hopeless that her headaches will go away or diminish.  She is looking for someone to email that is going through the same thing. 




Concerned Sister


Post Edited By Moderator (tysmyboo) : 8/28/2009 8:06:13 PM (GMT-6)

New Member

Date Joined Oct 2011
Total Posts : 2
   Posted 10/9/2011 12:47 PM (GMT -7)   
I have the same symptoms for 5 years now. What doctor did you see for your Lyme test. I have been tested, and it was negative. But my symptoms match. Please help.

New Member

Date Joined Feb 2013
Total Posts : 4
   Posted 2/16/2013 9:38 PM (GMT -7)   
I have constant head pressure as well. I'm still not sure what the cause is, however I have found apple cider vinegar to be an absolute miracle and relieves so much of the pressure that I do not need aspirin every day. I have also found oil of oregano to be greatly helpful as well. Just want to share with everyone I possibly can who also has head pressure and headaches. 2 tablespoons in juice and 2-3 drops of oil of oregano. I find the liquids to be more effective than the pill forms.

New Member

Date Joined Oct 2012
Total Posts : 9
   Posted 3/3/2014 5:31 AM (GMT -7)   

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