Lyme Disease Support & Resources
Our mission is to find a cure, CA Govt and Health Care acknowledge, accept claims also for chronic illnesses
Our mission is to find a cure, CA Govt and Health Care acknowledge, accept claims also for chronic illnesses
A tick embedding in my inner thigh while in Northern CA set me on a new path, filled with purpose and drive. My journey has involved learning, researching, and coping with chronic illness symptoms to maintain my role as a career woman and world traveler dedicated to sports. Unfortunately, the co-infections have been particularly challenging, leading to a diagnosis of Babesia and Anaplasmosis. For those seeking Lyme support resources and to learn more about my story, I encourage you to visit BayAreaLyme.org, a part of the Lyme Living nonprofit that offers valuable research and support groups for individuals affected by Lyme disease.
Healing is a partnership, a journey and a fight. For those of us living with a chronic illness, like Lyme disease, there is no cure, and we must learn how to navigate life with it. This isn’t the only chronic illness out there, and organizations such as the Lyme Living nonprofit are working tirelessly to raise chronic illness awareness. Many labs and tissue donors are dedicated to research aimed at finding cures, while various Lyme support resources and support groups provide essential help and guidance along the way.
Living with Lyme is a struggle. The symptoms are indescribable, and I don't expect anyone to fully understand the challenges of a chronic illness. What makes it even more difficult is the lack of support from friends and family who choose not to research or engage with Lyme support resources. Over the last eight months, I've experienced PTSD at the sight of a black bug, exposure to mold, loss of appetite, weight loss, chronic fatigue, back problems, numb limbs, paralysis of my hands, anemia, and various neuro-related issues. Raising chronic illness awareness is essential, and connecting with support groups can make a difference.
A tick embedding in my inner thigh while in Northern CA set me on a new path, filled with purpose and drive. My journey has involved learning, researching, and coping with chronic illness symptoms to maintain my role as a career woman and world traveler dedicated to sports. Unfortunately, the co-infections have been particularly challenging, leading to a diagnosis of Babesia and Anaplasmosis. For those seeking Lyme support resources and to learn more about my story, I encourage you to visit BayAreaLyme.org, a part of the Lyme Living nonprofit that offers valuable research and support groups for individuals affected by Lyme disease.
Healing is a partnership, a journey and a fight. For those of us living with a chronic illness, like Lyme disease, there is no cure, and we must learn how to navigate life with it. This isn’t the only chronic illness out there, and organizations such as the Lyme Living nonprofit are working tirelessly to raise chronic illness awareness. Many labs and tissue donors are dedicated to research aimed at finding cures, while various Lyme support resources and support groups provide essential help and guidance along the way.
Living with Lyme is a struggle. The symptoms are indescribable, and I don't expect anyone to fully understand the challenges of a chronic illness. What makes it even more difficult is the lack of support from friends and family who choose not to research or engage with Lyme support resources. Over the last eight months, I've experienced PTSD at the sight of a black bug, exposure to mold, loss of appetite, weight loss, chronic fatigue, back problems, numb limbs, paralysis of my hands, anemia, and various neuro-related issues. Raising chronic illness awareness is essential, and connecting with support groups can make a difference.
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