You gotta love Facebook. Thanks to this online community, I am now on a first-name basis with Katherine Southard, Miss North Carolina 2009 .
Turns out Katherine is a fellow scoliosis patient, and she has made a commitment to raise awareness about scoliosis and its treatment during her reign as Miss North Carolina.
Last month, during her July 4 appearance at Fort Bragg, N.C., Katherine met Emily, a 10-year-old-girl who is struggling to adjust to her new Boston Brace.
The diagnosis
Emily was diagnosed with an “S” curve (15 / 17 degrees), as well as a spinal syrinx, at age five. During the past five years, her family has played “watch and wait,” trekking from their home near Fayetteville, N.C., to UNC Hospitals in Chapel Hill, N.C., every four to six months where Emily was subjected to several MRIs under general anesthesia. Finally, on May 5, 2009, they heard the news they’d hoped to avoid. Emily’s curves had progressed to 30 degrees each, thoracic and lumbar – the magical number to warrant bracing.
If you or someone you love has ever received a fateful diagnosis, you’re familiar with the swirl of emotions that follow. Denial, fear, anger, frustration and helplessness are all present and accounted for among Emily, her parents Suzette and Michael, and her brother, Dakota (pictured above, with Emily).
Shortly after the May 5 doctor’s appointment, Emily told Suzette, “Mommy, my having this stupid scoliosis makes me feel like I am going to die.” She’s also had to give up her spot on the pitcher’s mound of her softball team, since she cannot bend or twist quickly enough to catch and grasp the ball. For his part, Dakota is angry about Emily’s scoliosis and wants an answer for the unanswerable: why? “He feels like he’s lost part of his sister because the two of them can’t play and wrestle like they used to,” Suzette said.
The health insurance
Emily’s orthopedist wrote a prescription for a Boston-style TLSO brace to be custom-made for her by Bio-Tech Prosthetics and Orthotics in Durham, N.C. However, since Bio-Tech is an out-of-network provider, Suzette said the family’s health insurance company (United Healthcare) referred her to Orthofix for Emily’s brace. According to Suzette, the Orthofix rep said he did not know why UH had referred Emily to Orthofix. “He said, ‘your daughter needs a custom-made Boston brace. Here, I have small, medium and large.’” Suzette said.
So, Suzette took Emily to Bio-Tech to fill the doctor’s prescription for a Boston Brace and filed a claim with UH. So far, the $2,282.05 claim has been denied three times. Another claim ($1,272) for treating Emily’s brace-induced sleep apnea has also been denied.
In addition to filing several appeals to UH – all of which have, to date, been denied -- Suzette, a tireless advocate for her child, also requested the physician’s reviewer notes to learn who was denying the claim and why. According to Suzette, the physician advising UH about this orthopedic-related health care decision is a plastic surgeon who has not been in active practice since 2003.
Help in the form of clothes
Since receiving her Boston Brace on June 9, Emily has gone from referring to it as “claustrophobic,” to self-consciousness about how others perceive her appearance. She wears the brace 23 hours per day, removing it only to bathe or swim. As the first day of a new school year approaches, Suzette has been scrambling to find stylish clothing that fits over the brace and will help Emily’s self-image.
During her appearance at the Ms. Statesville Pageant, Katherine told her audience about Emily, and asked for clothing donations. Afterwards, a woman from Peebles offered to provide clothes so Emily could go back to school “feeling good about herself.” Emily will receive her new wardrobe at the Peebles store in Lillington, N.C. later this month.
As a mother, I can only imagine what Suzette is going through. Dealing with your child’s scoliosis diagnosis is more than enough to handle, but having to do battle with the health insurance company – and now the mortgage company – is pushing Suzette to the end of her limits.
Health care reform cannot come soon enough for this family. So, if you have any suggestions or offers of assistance, let me know. I will gratefully pass them along.
3 years ago
I am a personal friend of the Schrumps and am seeing the affects of this difficult time on my friend Suzette. She is devoted to Emily and Dakota 110% and is trying her best to kept her families spirits up. I am praying for a resolution to the problem with the insurance claim being denied and of course praying for little Emily , she has been such a trooper through all of this. And I just wanted to say Thank God for people like the WONDERFUL Ms. North Carolina Katherine Southard. There is no doubt in my mind God put her in the Shrumps lives. And thanks for this great blog and the awareness it will hopefully bring to people whom have never heard of scoliosis or have never had to watch loved ones suffering.
ReplyDeleteFind a Clear certified doctor in your area and correct the scoliosis
ReplyDeleteMark, Please explain yourself when you talk about Clear certified doctor?????
ReplyDeleteRespectfully,
Suzette Schrump
My daughter completed the intensive program at CLEAR....happy to answer any questions if you are interested.
DeleteSincerely,
Demetra
Maria, a remarkable post. Your writing skills bring it, unfortunately, all too alive. Keep telling this story and others. All of us who battle the health care system and advocate for our children, other family members and ourselves can relate. Take this to the halls of Congress and send it to the White House. My very best wishes to Emily, Suzette and Dakota and to those who are reaching out to them with tangible help.
ReplyDeleteHi our daughter has congenital scoliosis and just started wearing a brace. We got the brace from Shriners and they were very nice. The services there are generally free of cost after you apply and they accept you. They treat certain conditions.
ReplyDeleteAnon (Aug. 29, 2009): I'm glad your daughter is able to get treatment through the Shriners. Katherine has initiated that process with the National Scoliosis Foundation for Emily, but it does take awhile. Best, Maria
ReplyDeleteWanted to let everyone know that Emily is digging her new clothes. I actually have sewn a hem on her new jeans....Miracles just never cease...:) She has been shown kindness and love, so far, in school. She has a group of little girls in her class who take care of her needs, especially, at PE time, when she now taks her brace off, does stretches and "plays" for 45 minutes, and then puts it back on.They hang her book bag for her, give her big hugs, and of course play with all that beautiful hair...So far, have had a few hug questions..."Why are you so hard?" Emily simply said "I have my back brace on". Little girl says, "You broke your back?" Emily says, "No silly, I have Scoliosis". Sweet, matter of fact and to the point...No more questions asked. If it were not for Katherine, Bria and Peebles, we would not have made it through this rough patch. I cannot express my gratitude enough. Emily feels like a million bucks...Even with her circumstances. It shows in her smile and her positive attitude.
ReplyDeleteHugs to all,
Suzette Schrump
I am a VERY old friend of Suzette and her sister Dianne. I was diagnosed with scoliosis at the old age of 25. Since then I have also been diagnosed with DDD, bone spurs and arthritis. I have been 100% disabled since 2002. I would love to reconnect with Suzette and her family and share "war stories". So glad that her dauther is doing better. Emily sounds like a real fighter! God Bless!
ReplyDeleteLorrie Powell Keyser
(Kelly's little sister)
lokeymom@yahoo.com (preferred email)
Hi, Lorrie:
ReplyDeleteI have passed your message along to Suzette. I hope you're doing well. Btw, what is DDD?
Best,
Maria