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No Warranties or Representations
Lyme Disease symptoms vary from person to person. (lymes disease lyme's disease lime disease limes disease)
The data and information presented in this web site are presented in good faith and believed to be accurate regarding Lyme disease (commonly misspelled lymes disease lyme's disease lime disease limes disease) and other related diseases. Any and all liability for the content or any omissions including any inaccuracies, errors, or misstatements in such data or information is expressly disclaimed. The web site is compiled for the sole purpose of informing community members of resources and information pertaining to Lyme Borreliosis Disease and its coinfections. Lyme disease symptoms may vary from person to person.
The Canadian Lyme Disease Foundation, Directors and members are not liable for any direct or indirect damages or any damages whatsoever resulting from loss of use, data or profits, whether in an action of contract, negligence or other tortious action arising out of or in connection with the use or performance of information available from this website.
Consult a qualified Lyme ( Borreliosis ) Disease literate doctor for medical advice if Lyme Disease is suspect to discuss your Lyme Disease Symptoms.
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Gayle's Story - Nova Scotia to Alberta
I am a 52 year old woman from Alberta. In the summer of 2004 my husband and myself vacationed in Nova Scotia. I was at the time an extremely healthy individual with absolutely no health problems other that coping with menopausal "hot flashes".
I was bit by something on my right foot while visiting a relative in a rural area of Nova Scotia. My foot swelled to almost twice its normal size and was very red and hot for several days. I never did get the classic "Bulls-Eye Rash" so never thought about it being a tick bite. The site of the bite bothered me for many weeks and always felt itchy and irritated. About three weeks or so after the bite occurred, I started to get horrible, blinding headaches on the right side of my face, mostly temporal region so my family doctor diagnosed me with Trigeminal Neuralgia. I started taking Tegretol which is the drug of choice to treat the condition.
My condition did not improve, in fact I began having more symptoms, changing on a daily basis. My right arm, leg, fingers, toes started to lose feeling. At times they felt like the were all asleep. Soon after my face was tingling as well as my nose and tongue. My balance was effected so much that when I would try to get out of bed, I often fell over to the right side. My memory (which has always been incredible) was suddenly so bad I couldn't remember the simplest things. I started to stutter and search for words which is really unusual for me. I could hardly make it up a few stairs without sitting down because I was so tired. Suddenly I need to sleep every afternoon because I was exhausted even when I did nothing. The nerve pain was so bad that it felt like an acid cursing through my veins and it would wake me at night.
Needless to say I was very frightened and my family doctor sent me to have a CT Scan of my head. Everything came back normal even though her neurological exam definitely showed marked difference in my reactions from right to left. The next step was an MRI to rule out MS , as well as blood tests to rule out Lupus. Everything came back normal except my C-Reactive Protein came back very high. The neurologist that my family doc sent me to seemed to wash his hands of me and made me feel like I was going crazy. He suggested talking Neurontin for the nerve pain and pretty much told me to go away. I asked him if he thought perhaps this could be Lyme Disease and he said flat out NO! I described the bite, the reaction and where I was at the time (because Nova Scotia has a lot of infected ticks) He did reluctantly order an Eliza test which came back negative, His last words to me were "if you still have symptoms in a year from now, maybe we'll do another MRI".
I was so frustrated and frightened because I KNOW MYSELF. I am not a hypochondriac! How could this come on so soon? I had done lots of research on the internet , entering my symptoms and always Lyme Disease would pop up. I approached my family doc and told her I wanted to contact Dr. Murakami in Hope, B.C. because his name kept showing up and she said "Go for it"
I spoke to Dr. Murakami in January 2005 and decided to go down and see him in February. He sent me for many blood tests and explained that Lyme is clinically diagnosed but he felt that my symptoms were very suspicious. When the tests came back I was positive for Bartonella . One can get this from cats or ticks. I am not a cat person. Have never been scratched or bitten by a cat so we knew it was from a tick. He started me on a 4 month regime of Biaxin and Flagyl. The pharmacists at my local drug store were very concerned about me taking the antibiotics for such a long time and cautioned me to eat yogurt and take acidophilus. I took both of them twice a day and must admit sometimes it was hard because I suffered quite a bit of nausea. I had two or three bouts of Herx reactions which made me feel really bad - almost bad enough to quit but I did not. Dr. Murakami had to me to expect these reactions and I had read about them but I had not expected them to make me feel so bad. They lasted for a week or ten days each time.
Dr. Murakami and I e-mailed back and forth about my symptoms, how I was feeling etc for the whole time. I cannot thank him enough for his patience and understanding.
I am happy to say today I am feeling really good - back to myself with no health complaints at all (other than hot flashes) I saw Dr. Murakami in July in Hope, B.C. again and he explained that this could come back but we will just go back at it again with perhaps different antibiotics. At this point I have no headaches, numbness, dizziness, my memory is back to normal, no stuttering and I have tons of energy!
My family physician is a believer now and has taken quite an interest in Lyme Disease. It was great to have Dr. Murakami and his expertise to guide me through this process and I will stay in contact with him in case my symptoms should re-occur. I encourage anyone who has been bitten by something and becomes ill like I did to check into Lyme Disease. It is not as uncommon as one might think. We need more doctors like Dr. Murakami, who has tirelessly researched this disease and is out there making our doctors more aware of it.
We must be proactive about our own health and don't allow doctors to make you feel like you are crazy. You know your body and mind - and don't let anyone tell you any different.
Dr. Murakami, I thank you for all you did for me and my family is also thankful to you because the have their mother and wife back again.
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