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Meet Precious Omari Joel Buchanan

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MEET PRECIOUS 
OMARI JOEL BUCHANAN 
PLEASE VISIT HIS WEBPAGE AT:
https://www.gofundme.com/a-desparate-plea?utm_source=internal&utm_medium=email&utm_content=cta_button&utm_campaign=upd_n 
TO OUR READERS: I MET LITTLE OMARI JOEL ABOUT TWO YEARS AGO AND HAVE KEPT IN TOUCH WITH HIS FAMILY EVER SINCE ON A REGULAR BASIS. WHAT YOU WILL SEE AND READ BELOW IS THE STORY OF HIS DAILY LIFE. I CAN PERSONALLY VOUCH FOR THE HONESTY AND LEGITIMACY OF THIS FUND RAISER.  PLEASE!  IF YOU CAN SPARE A FEW DOLLARS TO GIVE A LITTLE BOY AND HIS FAMILY HOPE FOR HIS FUTURE, PLEASE CONSIDER DONATING TO THE GOFUNDME CAMPAIGN AT THE WEBSITE ADDRESS ABOVE!   THANK YOU!
OLIVE OYL 

A Desperate Plea

$1,112 of $15k goalhttps://www.gofundme.com/a-desparate-plea?utm_source=internal&utm_medium=email&utm_content=cta_button&utm_campaign=upd_n 
Raised by 20 people in 1 day
Lekitta Epps  WASHINGTON, DC 
 
Omari Joel Buchanan was born on Monday, December 31, 2012 in Silver Spring, Maryland.   As much as he is an added blessing to our lives, we are faced with the heartache and challenges associated with raising a child with critical medical needs. Omari was diagnosed at 3 months of life with a rare genetic disease,  Zellweger Spectrum Disorder  (ZSD), where the prognosis is terminal.  Upon diagnosis we were given a life expectancy of 6 months to a year of life. God has blessed us.  Omari is now 4 1/2 years old.

As a result of being diagnosed with ZSD, Omari is faced with many challenges.  Some of Omari’s obstacles include but are not limited to chronic respiratory issues that resulted in a tracheostomy, seizures, hypotonia, renal insufficiencies,  multiple neurological deficiencies, intellectual and cognitive delays,  and visual and hearing impairment.

With a terminal and incurable disorder, doctors can only  treat  the symptoms and not the disease. Recently we read the story of a young girl that suffered severe brain damage from drowning  in February of 2016. Scientists were able to reverse the damages sustained using Hyperbaric Oxygen Therapy (HBOT).  After hearing the story we contacted the treating physician and, through that office, we were directed to facilities in the Washington Metropolitan area where Omari resides. However, these facilities could not accommodate him and a recommendation was made to contact a facility in Tucson,  Arizona. It is our hope that with this therapy Omari can continue his journey to a better quality of life. The trip is scheduled for September 10, 2017.
 

Considering the fact insurance does not cover HBOT, we are estimating the cost of this trip to be $15,000.00 to include treatment (roughly $120-$160/session), a portable oxygen concentrator, transportation, a Register Nurse, and room and board for two to three weeks.

This is our story. This is our life. If you can find it in your heart to help us help Omari, it would be greatly appreciated. Thank you and God Bless!

Warmest Regards,
Omar and Jasmine Buchanan
(Omari’s Parents)

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Help spread the word!

$1,112 of $15k goal

Raised by 20 people in 1 day 
 
https://www.gofundme.com/a-desparate-plea/donate

NESARA- Restore America – Galactic News


Source: http://nesaranews.blogspot.com/2017/08/meet-precious-omari-joel-buchanan.html



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