Dog & Cat Tips : Symptoms of Lyme Disease in Dogs

Posted on May 31st, 2010 by admin

Lyme disease in dogs often causes several symptoms, including depression, fever, decreased appetite, weight loss and joint stiffness. Look for chronic stiffness as an indication of a dog that has Lyme disease with help from a veterinarian in this free video on dog health.

Expert: James Talbott
Bio: Dr. James R. Talbott is a staff veterinarian at Belle Forest Animal Hospital and Kennel in Nashville, Tenn.
Filmmaker: Dimitri LaBarge

Duration : 0:1:56

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Lyme Disease: Victoria’s Victory 2009

Posted on May 27th, 2010 by admin

This is a short film I made about my very ill cousin, she has been sick with Lyme disease for over 3 years. Please show your support by sharing this video with everyone you can, and raise their awareness about the seriousness of this disease.

music: in order of film

Life in Technicolor: Cold Play
Life in Technicolor II: Cold Play
Fix You: Cold Play
Hoppipolla: Sigur Ros

Duration : 0:10:3

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Aug 3, 2009 Lyme Disease Rates Rise

Posted on May 22nd, 2010 by admin

Public health officials say the number of areas where ticks are found is expanding, raising the risk of lyme disease.

Property of Global TV News: Archived here only to raise awareness of Lyme disease

Global TV Ontario Canada

Duration : 0:3:16

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what type of tick bit me, can i get limes?

Posted on May 20th, 2010 by admin

i got bit by some ttype of tick. its really really tiny and its brown. what kind isit and can iget limes disease

Sounds like a deer tick….if you have a "bulls eye" rash around the bite go to the doc right away…that is the most tell tale sign.

This is Lyme Disease

Posted on May 17th, 2010 by admin

Update 2
Thanks to my lovely lyme disease I have had 6 brain/spine surgeries in 18 months to treat Intracranial Hypertension. I will be making a video soon to explain my condition from lyme more. It’s very rare and there are only a few reported cases of kids getting it from lyme. I got the luck of the draw! My lyme is virtually gone, and besides the IH and thyroid problems I have no other symptoms. I am off all antiobiotics. My IH is here to stay, however. I do continue to fight for the rights of both my lyme friends and IH friends (we are treated very similarly to the way lyme patients get treated. no one understands it.) I hope you are all doing well.

UPDATE:
I’ve had 2 months of IV rocephin and 2 picc lines, along with brain surgery to put a shunt from my brain to stomach to continuously drain the fluid. I’m feeling a lot better and am back to school. I’ve also tested positive for coinfections rocky mountain spotted fever and q-fever, along with cat-scratch fever, but am still awaiting a positive lyme disease test. It’s getting there. While I’m feeling better, I still have some lyme symptoms, and always will. For all those people out there with chronic lyme disease- this video is for you.

Ok, So this is unlike any video I have uploaded onto this account. This disease has been affecting me and my family for 2 years, and I need to get the word out about it. Yes, I’m sure many viewers have heard of this, and probably think it’s not very serious. Truth is, that this disease can kill. I was left undiagnosed by 10 doctors, and told by one I was making myself see double and was told to go back to school, I could concentrate because I could count back from 10. Unless you have lyme, you may not understand how hurtful that was. Lyme disease gave me a condition which causes fluid to build up in my brain, it requires spinal taps to drain the fluid, and if we had not figured out why I had pressure in my brain I may have gone blind. It’s called pseudotumor cerebri, and causes debilitating headaches. I have been on 4 different oral antibiotics and I am IV for a couple of months.

PLEASE tell people about this video. I will be posting more informative videos on lyme disease in the near future. This disease is not acknowledged by so many doctors for so many different reasons, I had a rash from lyme disease, and I had so many symptoms, yet so many doctors said “you don’t have this” and now I am at the point where I am out of school.

Duration : 0:3:55

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MORGELLONS DISEASE is what I think I have aquired somewhere in my travels/life experiences. Your p?

Posted on May 17th, 2010 by admin

I live in Ottawa, Ontario CANADA and have only very recently come to this very interesting deduction. I think I need to see a Dr. specializing in lime disease; but I am most interested in sharing and hearing your experience and knowledge. It is actually quite interesting and fascinating. I think "WE" could make excellent use of an at least on line chat group.

I really don’t think Morgellon’s Syndrome is that common, and is completely different than Lyme Disease.

http://www.associatedcontent.com/article/12659/what_is_morgellons_disease.html

http://en.wikipedia.org/wiki/Lyme_disease

Filed under limes disease | 1 Comment »

What are the symtoms of lime disease?

Posted on May 14th, 2010 by admin


Lyme disease is now an epidemic in several US states.4 Estimates are now at 3 million cases of lyme disease in the US in 3 decades. Most of these cases are from states that border Canada yet Canada reports it has only had a few hundred cases…? See an epidemiological map of what is immediately across our border. Canada has no such info – yet where we look we find lyme.

Lyme borreliosis is now acknowledged as the most highly prevalent arthropod-borne human disease in northern temperate regions of the world5. Canadian medicine and science, due to the lack of recognition of the clinical diagnoses, combined with lack of surveillance and research, places us at the bottom of the scale in dealing with this serious disease. We are years behind.

Many Lyme patients were firstly diagnosed with other illnesses such as Juvenile Arthritis, Rheumatoid Arthritis, Reactive Arthritis, Psoriatic Arthritis, Infectious Arthritis, Osteoarthritis, Fibromyalgia, Raynaud’s Syndrome, Chronic Fatigue Syndrome, Interstitial Cystis, Gastroesophageal Reflux Disease, Fifth’s Fisease, Multiple Sclerosis, scleroderma, lupus, early ALS, early Alzheimers Disease, crohn’s disease, ménières syndrome, reynaud’s syndrome, sjogren’s syndrome, irritable bowel syndrome, colitis, prostatitis, psychiatric disorders (bipolar, depression, etc.), encephalitis, sleep disorders, thyroid disease and various other illnesses.
If you have received one of these diagnoses please go to our symptoms page and see if you recognize a broader range of symptoms.

If you are a doctor please re-examine these diagnoses, incorporating Lyme in the differential diagnoses.

If you feel you may have Lyme Disease you are encouraged to contact us. If you have a rash please photograph it (a close-up) and send it to us with as much detail about date/time, place, any tick bite noticed. Please include your name and phone number for our records in trying to track this disease. All information is confidential and shall never be released to anyone without your written consent.

Read this from 1993… where are we now – no better?

Ronald S. Ferris, Calgary, Alberta, deceased (1945-2000), made many a profound statement about Lyme Disease in Canada prior to his death. Read more about Ron and the impact he had on others and take the time to read that interesting and informative web site.

Lyme Disease….A vector borne disease (ticks are one known vector) which has caused controversy in the past decades because of its difficult diagnosis and treatment. The organism is highly fastidious, growing extremely slowly in tissue culture (not bacteriological) media. The vast majority of body fluid or tissue samples from patients with Lyme disease do not yield spirochetes on culture. Lyme disease is thus usually clinically diagnosed. Possible detection of serum antibodies to burgdorferi may only augment the clinical diagnosis. However, acutely antibodies may not occur in detectable titer, making early diagnosis difficult. Many later stage seronegative patients are very symptomatic and treatment intervention has been shown to be very effective. The tick O.hermsii has been implicated as a possible vector and some Canadian cases are reviewed. Lyme mimics many other diseases but clearly an educated doctor will recognize lyme symptoms and include lyme in the possible diagnoses.

The first documented case of Lyme disease to have originated in Canada (Journal details here) was a 51-year old French female nurse visited Quebec, Canada from 20 July to 5 August, 1984 and contracted Lyme disease. She reported an insect bite on 3 August 1984 on the back of her knee with erythema chronicum migrans appearing at the site of the bite on 5 August 1984. The patient presented with meningeal lymphocytic reaction near the end of September, 1984. Total Ig serum titers in indirect immunofluorescence tests on 1 October 1984, 10 October 1984, and 10 January 1985 were 1/512, 1/2048 and 1/16,384, respectively.

Lyme Disease is not the only tick borne disease in Canada but can be complicated by multiple tick-borne co-infections such as Ehrlichiosis, Babesiosis, and Bartonella. Other tick borne diseases include Tularemia, Tick Paralysis and Rocky Mountain Spotted Fever.

Lyme Disease is determined by clinicians, not labs
…no lab has a gold standard test to date, some labs are just better than others.

The only treatment available to date is antibiotic. If caught early and treatment given in sufficient dosage over sufficient time all is well in most cases. There remains a significant number of treatment failures usually as a result of insufficient dose/time of treatment and/or late diagnoses.

These treatment failures have proven to benefit significantly from longer term antibiotic treatment and patients sometimes have to be very demanding to receive such treatment.

One has to be realistic…not being able to find something by available methods in science means nothing to the sick patient who recovers after many weeks/months of appropriate treatment.

Therein lies the difficulty and undermining of appropriate treatment. The cost of treating lyme disease with antibiotics can be expensive in the relative short term so without a doubt business/politics become involved. Without a definitive test the door is left open for money to rule over health. However, the cost of not treating lyme, or treating it inadequately, is infinitely more expensive.

The majority of research is funded/lobbied by 1. Insurers (motivated to keep treatment costs/duration to a minimum). 2. Governments (heavily lobbied by private/public insurers as well as tourism dollars). 3. Drug manufacturers (motivated to peddle drugs).

The results of this heavily influenced research are what we educate our medical students with, who then become our doctors with a bias.

Therefore it takes the wise front line physician to wade through the swamp and treat the patient using good sound judgment. The better doctors learned early on that some of what they were taught just didn’t add up when they encountered their real world patients. Common sense still applies…even in science.

Symptoms may show up fast, with a bang, or very slowly and innocuously. They may creep into ones life over weeks, months or even years.

While antibiotic treatment carries risk, it pales in comparison to the serious danger and cost (in productivity, income and family) of developing late stage illness that may develop within weeks even before the first lyme tests have returned.

My dog has lime disease, will he be okay?

Posted on May 13th, 2010 by admin

We got him medicine, and he just got it

My dog has Lyme disease too. Despite taking his anti-tick medicine regularly he still managed to get it a few years ago after playing in the woods. We caught it quick and the vet gave him meds. He now gets tested regularly for antibodies and takes meds/steroids as needed(which is not often at all). He seems to be doing pretty well, only difference he has is that he snores a lot more since he got it. So I would not worry too much about it, just keep him happy and healthy and he should be fine.

Lyme Disease Treatment Controversy

Posted on May 11th, 2010 by admin

Dr. Raphael Stricker talks about the controversy over chronic Lyme, the pros and cons of the existing Lyme tests, and the IDSA’s argument against long-term use of antibiotics, on April 23, 2008 as part of the Lyme Disease Expert Interview Audio Series.

http://www.lyme-disease-research-database.com/lyme_expert_interview_series.html

Duration : 0:1:27

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Filed under limes disease | 1 Comment »

I’ve been diagnosed with Lyme Disease and am wondering how to properly cope? Please see details?

Posted on May 8th, 2010 by admin

I am tired all the time, get random spells of exhaustion and nausea, can’t think properly, have major neck pain and stiffness, and have sore joints and muscles. I was diagnosed for Lyme Disease the day after getting a check up – at first they thought it was some kind of virus but after consulting other doctors they called me back in a rush stating that they are pretty sure it’s Lyme Disease and that they’ve caught it in it’s earlier stage (I was camping 1 1/2 weeks ago).

Anyways, I am wondering if any of you out there have had Lime Disease and how you coped. I have missed 2 1/2 days of work already and I don’t know what to do. Should I go to work and do my best? Is rest important? Does Lime Disease recurr without another bite? Heck, I didn’t even know I was bite in the first place.

Any and all advice would be greatly appreciated.

Thanks.
I’m mostly concerned with the missing-work part. I mean, at times I feel alright (I am taking amoxicillin, and ibuprofen and tylenol). Like, I’ll be decently feeling then out of nowhere I’ll get exhausted. I’m not too sure how much work I should miss or what. I’m pretty confused about this whole circumstance – I just recently started this job.

You should have been seen immediately if they are sure you have Lyme disease. You need treatment, and yes you need rest

http://health.yahoo.com/ency/healthwise/hw77226/aa10154;_ylt=Am_gVrfwJHfXRtSQlLYcvNXogrMF

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