Benefit to Help Young Alden Girl Battling Extremely Rare Condition

July 13, 2018

Written By

Mary Friona Celani

Mackenzie Refermat is a vibrant, happy, middle child of a large blended family. She is a happy, loving 9-year-old. She is also going through more than most could even imagine.

Last November, Mackenzie was diagnosed with Parry Romberg Syndrome.  PRS is an extremely rare, progressive, incurable autoimmune disease that causes hemi-facial atrophy; meaning it causes half the face to waste away.

Every case is different and symptoms may include facial atrophy, debilitating migraines, tooth loss on affected side, ADHD, seizures, strokes, loss of vision on affected side and other neurological problems.

Mackenzie has multiple symptoms. Parry Romberg Syndrome is so rare that there are less than 1,000 known cases worldwide. The odds of having PRS are approximately a one in 6,000,000 chance. Research is limited and treatment options vary, with no sure results. PRS is a disease of “unknown origins” and therefore there is no known cure. Some people have had successful results from Methotrexate, a low dose chemotherapy drug, and steroid therapy. Immediately following the diagnosis, Mackenzie started on this protocol but unfortunately; it has not stopped her progression.

In early spring of 2018, Mackenzie’s mother, Cathie, was introduced to Dr. Siebert; the only physician, who does a surgery called Micro Vascular Free Tissue Transfer. Dr. Siebert will take healthy tissue from another part of Mackenzie’s body to replace the diseased tissue in her face. With gene sequencing, the tissue changes back to normal following surgery. Facial growth and soft tissue will become normalized. This gives us hope. This is the only option to save Mackenzie’s face. This is Mackenzie’s Miracle.

Mackenzie’s first surgery has been scheduled for July 23, 2018 in Wisconsin. Even with insurance coverage, Mackenzie’s family will still be responsible for a large portion of cost. There is a minimum three-day hospital stay for the surgery in July and two weeks total to be spent close to the surgical team in Wisconsin.

 

Family and friends are hosting a benefit to help this family with medical, travel and living expenses.

WHEN: Sunday, July 15th from 1-4 p.m.

WHERE: Cowlesville Fire Hall, 361 Clinton St, Cowlesville.

The benefit will include a Chinese auction, silent auction, raffle tickets, 50/50 split along with other kid friendly activities.

The goal is to raise at least $25,000 to cover the out of pocket medical expenses for the initial and follow-up surgeries, travel expenses and loss of wages for Mackenzie’s mother.

Online donations can be made to: https://www.gofundme.com/miracle-for-mackenzie.

More on Mackenzie HERE. 

 

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About Me

 

 

Welcome to Totally Buffalo! A local lifestyle website.

My name is Mary Friona-Celani and I am the creator of this site! I’m a wife, a mom, a grandma, a Buffalo booster, an entrepreneur and a small business owner. I’m so glad you stopped by.  After 20 years in the buffalo media, I went out on my own to tell stories about the people, places, events and all-around fabulousness of this wonderful place we call home. Buffalo is different and so is this site. We are here to share stories, encourage kindness, and help make this a better place to live.

We’ll help those in need when we can through our charity arm, Totally Buffalo Cares.

We help local small businesses, artisans and vendors though our events and our Totally Buffalo Stores.

We’ll do all of this with a little help from friends in our community.

 

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