I was once lucky enough not to know anything about Lyme. I found out the hard way that it is one devastating illness, and the real horror comes from the way Lyme disease patients are treated by the medical establishment and government. I'm sure this sounds a little extreme and possibly unbelieveable to anyone who's been lucky enough to not have experienced Lyme, and while I hope they never do, I do hope that awareness of the seriousness of the disease grows tremendously. Always great to see any awareness being promoted.
We have lived it along with you, a Mom and a son. Your words are the exact truth of how it is and not at all over the top, exaggerated at all. The emotional abuse and purposeful harm by others makes survival so much harder!! My son has permanent damage and he's suffering. People are uneducated, dismissive, and that nearly cost him his life! He's still fighting for his life and his own father labels him and refuses to even try to understand or help. The list goes on ... educators, caregivers, family, friends. Then there's the ones who get it and try to help. Have to not quit and be grateful for those that stand by you!
So glad to see public awareness for this disease being presented.....we had a friend who died from complications of Lyme disease. Keep up the good work!
I lived in Binghamton before, deer in backyard, never had a rash, always in woods in vermont too, camping in CT, yosemite, lived in moldy house later on triggered the Lyme I was told
know the neurological effects of lymes. we are fighting for awareness treatment and a cure. stay strong and thank you to all those who dont suffer from this illness who are willing to take a stand with us.
Same here. It took 30 years, three kids with congenital Lyme and serious damage done to my organs, joints, spine and muscles to finally get a test. Positive for Lyme and several co-infections.
I was once lucky enough not to know anything about Lyme. I found out the hard way that it is one devastating illness, and the real horror comes from the way Lyme disease patients are treated by the medical establishment and government. I'm sure this sounds a little extreme and possibly unbelieveable to anyone who's been lucky enough to not have experienced Lyme, and while I hope they never do, I do hope that awareness of the seriousness of the disease grows tremendously. Always great to see any awareness being promoted.
We have lived it along with you, a Mom and a son. Your words are the exact truth of how it is and not at all over the top, exaggerated at all. The emotional abuse and purposeful harm by others makes survival so much harder!! My son has permanent damage and he's suffering. People are uneducated, dismissive, and that nearly cost him his life! He's still fighting for his life and his own father labels him and refuses to even try to understand or help. The list goes on ... educators, caregivers, family, friends. Then there's the ones who get it and try to help. Have to not quit and be grateful for those that stand by you!
So glad to see public awareness for this disease being presented.....we had a friend who died from complications of Lyme disease. Keep up the good work!
Good video. I was ridiculed for having it , no one took me seriously for years, went through pure hell
stay strong, its an epidemic and we are warriors.
I lived in Binghamton before, deer in backyard, never had a rash, always in woods in vermont too, camping in CT, yosemite, lived in moldy house later on triggered the Lyme I was told
know the neurological effects of lymes. we are fighting for awareness treatment and a cure. stay strong and thank you to all those who dont suffer from this illness who are willing to take a stand with us.
My MDs refused to test with a known tick attachment.
Same here. It took 30 years, three kids with congenital Lyme and serious damage done to my organs, joints, spine and muscles to finally get a test. Positive for Lyme and several co-infections.
Only 20% of all patients have a bullseye rash..
the lyme light, lymes warriors
See this page I made years ago help make this reality. 25 years never properly treated made worse and now have identical deadley lyme Carditis