Family in need

$25,000 goal

Campaign created 8 months ago
Created June 18, 2017

My name is Charles Clark and I am a father of three from Saratoga Springs NY. I am fundraising to gain access to ongoing treatment for chronic Lyme Disease, as unfortunately this treatment isn’t covered by insurance, and after nearly 10 years my family  is still struggling to get better.

      We are a god fearing family overwhelmed by suffering. I am reaching out for help in the hopes to save there lives.  There names are Doreena 40, Nicholas 19, and Kayla 17. I also have two other children.

Doreena mast cell activation syndrome, Lyme, back pain, insomnia, headaches, dizziness, Bartonella, Babesia, Anxiety, chronic fatigue, factor 5 laden, HHV6, chronic migraines  etc.

Nick Lyme,IBS, chronic neck and back pain, insomnia, headaches, dizziness, Bartonella, Anxiety, Hallucinations, chronic fatigue. it affected his entire body, from his brain to his skin, heart, extreme body pain, eyes, shaking, numbness, tingling, kidneys, liver, burning neuropathy, balance issues, weakness in his legs and arms, burning scars all over his body, cold sweets and everything else that you can imagine. He was misdiagnosed for over half of his life and has suffered dearly for it. 

Kayla  Lyme, Bartonella,  chronic fatigue,  Anxiety, HHV6, Moody, Nausea, Scars.

Doreena has been in treatment for over 8 years and has lost everything, her home her savings and her life.  She is currently over $15,000 in debt, can no longer afford acupuncture, Lymphatic Massage, or even therapy.  We drive two hours a week to get her to her LLMD for treatment but other then that she is bed ridden 24 hrs a day.  She can't eat or drink without specialty addictive medications that her resistance builds up to more and more everyday.  She has been debilitated for over 5 years.  The Lyme has activated what is called MCAS or Mast Cell, this is what closes her throat when she takes meds, food, or even water. 

My son Nick has been told for at least 10 years that the marks on his body where stretch marks or they had no clue.  His fatigue was attributed to laziness.  His pain was written off as growth.  He was and is a good person and son and the system failed him.  Nick has time and can still be helped and in time hopefully recover from all of this.  His Bartonella is spreading drastically, he has run through the Doxi, and Lavoxin  and now needs the help of an LLMD as well.

 I am a disabled vet with a crushed deteriorated spine and major neuropathy.  My pain is intense but there is nothing I can do about it.  Mine is a typical broken vet story but if you are willing to help I want you to know I am putting every penny I can into helping my child and my girlfriend as well as her daughter.  I can't do it alone please if you can help please do.  The amount of people this reaches out to the more people may be able to help so please post this.



The LLMD "Lyme Doctor" is running an IV Treatment to kill the Lyme.  She had some bad seizure this time but has had 3 since and has done well.  She gets very weak for days from it.

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$25,000 goal

Campaign created 8 months ago
Created June 18, 2017
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