The Amara Campbell Foundation

We - Marnie, Rhiannon (Amara's sisters), Leanne, Madeline and Juliet- will be holding lots of events and fundraising campaigns to assist Amara with her ongoing battle with late-stage neurological Lyme Disease and all the complex and intermingled co-infections and co-conditions. She does not have any specialists nor a specialist GP trained in her complex conditions. Due to her worsening chemical al

lergies (anaphylaxis) she cannot leave her house without taking massive risks. So she is stuck, gravely ill and without help. Amara would not be dying if testing in Australia was more effective. Amara has what is known as Tertiary Lyme Disease or Late Stage Neurological Lyme Disease. It doesn't need to get to this point if caught early. In the last six months she has experienced her second minor stroke, become completely intolerant to light and escalated to having anaphylaxis in reaction to chemicals, has discovered an artefact/mass in her brain and also cerebral atrophy. Amara is deathly ill and without your help we don't stand a chance. So please use this page not only to support Amara, but to learn about Lyme Disease, one of the fastest growing infectious diseases in the world. Share the page, share the posts and hopefully prevent your loved ones, your friends and especially your children from ever having to experience what Amara has. For anyone who would like to donate to Amara's ongoing medical costs we have set up a PayPal account with the email address: [email protected]