Lyme Disease - Share Your Experience

Not ready to share? Read other Patient Comments

Did you or someone you know have Lyme disease? Please share your experience.

Share your story with others:

MedicineNet appreciates your comment. Your comment may be displayed on the site and will always be published anonymously.Patient Comments FAQs

Enter your Comment

Tell us a bit about your background to make your comments more useful to other MedicineNet users. (Optional)

Screen Name: *

Gender of Patient: Male Female

Age Range of Patient:

I am a: Patient Caregiver

* Screen Name will appear next to the published comment. Please do not include your full name or email address.

By submitting your comment, and other materials (collectively referred to as a "Submission") to MedicineNet, you grant MedicineNet permission to use, copy, transmit, publish, display, edit and modify your Submission in connection with its Web site. MedicineNet will not pay you for your Submission. You represent that you have all rights necessary for MedicineNet to use your Submission as set forth above.

Please keep these guidelines in mind when writing your comment:

  • Please make sure you address the question asked.
  • Due to the overwhelming number of comments received, not all comments will be published.
  • When selecting comments to publish, our staff will choose those that are educational and complement the topic. Please try to stay on topic.
  • Your comment may be edited. We would typically edit comments to make them clearer and more readable. We will remove personal information such as last names, email and web addresses, and other potentially harmful information.
  • We will not notify you if your comment has been published. We suggest that you check back on the topic article regularly.
  • We do not provide medical or healthcare advice, treatment, or diagnosis.

Thank you for participating!

I have read and agree to abide by the MedicineNet Terms and Conditions and the MedicineNet Privacy Policy (required).

To prevent our systems from spam, please complete the following prior to submitting your comment.

Please select the black triangle:

What is Lyme disease? What causes Lyme disease?

Lyme disease is a bacterial illness caused by a bacterium called a "spirochete." In the United States, the actual name of the bacterium is Borrelia burgdorferi. In Europe, the bacteria Borrelia afzelii and Borrelia garinii also cause Lyme disease. Certain ticks frequently found on deer from various locations harbor the bacterium in their stomachs. Lyme disease is spread by these ticks when they bite the skin, which permits the bacterium to infect the body. So Lyme disease is a tick-borne disease. Lyme disease is not contagious from an affected person to someone else. Lyme disease can cause abnormalities in the skin, joints, heart, and nervous system.

Return to Lyme Disease

See what others are saying

Comment from: Jeff, 55-64 Male (Patient) Published: May 09

I was working as an IT (information technology) Director and one morning I woke up with one eye swollen almost shut. I went to the emergency room because I wasn"t able to get an appointment with my doctor right away. The emergency room (ER) doctor sent me home with some antibiotic eye drops. This was after I told him that the side of my head was very sore and it hurt to just run my fingers through my hair on that side. Later that night I just thought that something else was wrong because I felt bad. I had fatigue and noticed that I had lost over 20 lb. in the past couple of months. So I googled, "one eye swollen shut", and at the top of the returned list was, "check for tick bites". So I examined the side of my head under the hair and sure enough, I had a black tick about the size of a pencil eraser. I had the tick removed with tweezers and cleaned. They noticed a red bull's eye rash on the back of my head and several bite marks on the side of my head. This thing was on there for quite a while. You can"t feel it because the tick's feet have a chemical that deadens the area. They gave me azithromycin, or a Z-Pak. After the Z-Pak I went back to the doctor because I still felt bad with fatigue and eye pressure like a full time eye headache. They gave me another Z-Pak and after that was gone I felt a bit better, but then got worse after a week or so. My doctor said, "I don"t think you have Lyme disease, but you can go to the ER if you still feel that bad." So I went back to the ER and they admitted me to the hospital and I was diagnosed with Lyme by an infectious disease doctor. She put me on an IV of ceftriaxone and let me go home with a PICC line about a week later. I took the IV ceftriaxone for 6 months. At first it was very hard to function. I had night sweats, headaches, fatigue, and joint pain. After the round of IV treatment she put me on 500 mg azithromycin and doxycycline daily. About 10 months later my doctor suggested that I quit working because the stress and daily activity were making things worse. Now it has been about 3 years and I am still taking 2 antibiotics daily. I have some good days and many bad days. I live with joint pain that seems to move around to various places. I am on disability and had to retire early with chronic Lyme. From the things I have read about other patients, I guess I am lucky that it was diagnosed fairly early and that I got the IV antibiotics for 6 months. I have also been drinking a small amount of silver water each day that seems to help a bit. I understand that silver water used to be a main antibiotic before penicillin. I bought a silver water generator kit for $350 and make it myself out of distilled water. It can be found online. Best wishes to others that have this nasty disease. I lost my high paying corporate job and live with pain every day from it.

Was this comment helpful?Yes
Comment from: Nightingale, 55-64 Female (Patient) Published: May 23

In late May of 1973, I noticed a bull's eye like mark on the inside of my knee. At the age of 22 I didn't give it much thought. Within a day or two I started feeling ill as if I had a cold. Soon after I had a fever of 104 and went to bed. I was exhausted and began sweating profusely. When I awoke the next morning my chest was covered with red blotches. After one week, when I felt good enough I went to see a doctor. He had no idea what was wrong with me accept to say that maybe I had scarlatina. There was no treatment so I went on about my life and never gave it another thought. Over the past forty-two years I have been telling doctors about this incident every time when I've been seen for aches, pains, tiredness, migraines, eye pain, and too many ongoing problems. Back in the 80s when Lyme disease was in the news, the doctors still never thought to test, let alone treat me for it. I finally asked a doctor if she would please test me and her response was a laugh. My eyesight continued to worsen and my pain is so debilitating at times I don't get out of bed. Thank goodness, I get lung or sinus infections often enough that when I'm on antibiotics the pains go away. I still have no idea where to go to be tested, but at 63 it probably doesn't matter.

Was this comment helpful?Yes


Get the latest health and medical information delivered direct to your inbox!