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'Everybody encouraged me to drop out': Woman perseveres through rare illness, getting her diploma

When Keely Pedersen was diagnosed with a rare illness as a teenager, it affected not only her health but also her high school dreams

'Everybody encouraged me to drop out': Woman perseveres through rare illness, getting her diploma

When Keely Pedersen was diagnosed with a rare illness as a teenager, it affected not only her health but also her high school dreams

KEELY PETERSON, LOOKS LIKE YOUR AVERAGE 21 YEAR OLD, BUT SHE LIVES WITH A RARE DISEASE THAT CAN CHANGE HER APPEARANCE DAILY. YOU WAKE UP WITH A DIFFERENT FACE OR BODY EVERY DAY. WHEN KEELY WAS 11, SHE STARTED EXPERIENCING SYMPTOMS THAT SHE KNEW WERE OUT OF THE ORDINARY, BUT HER SYMPTOMS ARRIVED AT THE SAME TIME AS PUBERTY, LEAVING DOCTORS TO BELIEVE THAT WAS THE CAUSE. THEY THOUGHT IT WAS BAD -- PAIN. THEN THEY THOUGHT IT WAS ENDOMETRIOSIS OR OVARIAN CYST. FOR FOUR YEARS, KEELY LIVED UNDIAGNOSED, EXPERIENCING SYMPTOMS LIKE PAINFUL INTERNAL SWELLING AND EXTERNAL SWELLING OF HER HANDS, ABDOMEN AND FACE. SHE FINALLY GOT HER DIAGNOSIS. WHAT WAS IT? IT’S HEREDITARY. ANGIOEDEMA TYPE THREE. NORMAL C1 ESTERASE. FACTOR 12. DEFECT. ESTROGEN DEPENDENT AND DOMINANT. I KNOW IT’S A MOUTHFUL. ALSO CALLED HIGH. KEELY HAS TYPE THREE OF THE DISEASE, AND DOCTORS SAY THAT’S EXTREMELY RARE. THE DISEASE IMPACTED EVERYTHING IN KEELY’S LIFE. YOU WAKE UP TWO HOURS EARLY BECAUSE YOU KNOW THAT YOU’RE NOT GOING TO GET OUT OF BED YET. YOU DON’T REALLY KNOW WHY, BUT IT’S PART OF THE ROUTINE NOW. YOU MOVE MUCH SLOWER. YOU DON’T GET TO DO AS MANY THINGS AS YOU WANTED TO. HER HOSPITAL VISITS WERE FREQUENT. HER MOM SAYS THERE WAS EVEN A DESIGNATED KEELY ROOM. SHE HAD MULTIPLE PAINFUL SWELLS EVERY DAY. BECAUSE OF THIS, SHE COULDN’T KEEP A NORMAL HIGH SCHOOL COURSE SCHEDULE. ALMOST EVERYBODY EXTENDED IN MY LIFE. EVEN TEACHERS ENCOURAGED ME TO JUST DROP OUT, GET AS BETTER AS I CAN, AND JUST GO GET A GED. AND YOU SAID NO. YEAH. AGAIN AND AGAIN AND AGAIN. SHE HAS PERSEVERED IN A WAY THAT IS ABSOLUTELY AMAZING. KEELY STUDIED TO GET HER DIPLOMA THROUGH OMAHA PUBLIC SCHOOLS VIRTUAL SCHOOL, ALL WHILE WORKING WITH DOCTORS TO FIND A TREATMENT PROGRAM THAT WOULD EASE HER SYMPTOMS. WITH THIS LIFELONG DISEASE. IF YOU REALLY WANT SOMETHING THE WAY THAT SHE WANTED IT. I MEAN, SHE JUST WOULD NOT GIVE UP. SHE WAS TIRELESS. KEELY WALKED ACROSS THE STAGE LAST WEEK. IRONICALLY, IT WAS ON NATIONAL HI DAY AND SHE’S STARTING HER CAREER JOURNEY WITH MORE THAN JUST THAT DIPLOMA. I’M A CNA. I DID THAT WHILE GOING TO SCHOOL AND DURING NIGHTS. I’M ALSO A DOULA. A FULL SPECTRUM DOULA. AS FOR WHAT’S NEXT, KEELY SAYS SHE CAN’T WAIT TO LAUNCH HERSELF INTO HER WORK AND FIND HER NI
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'Everybody encouraged me to drop out': Woman perseveres through rare illness, getting her diploma

When Keely Pedersen was diagnosed with a rare illness as a teenager, it affected not only her health but also her high school dreams

When one woman was diagnosed with a rare illness as a teenager, it affected not only her health but also her high school dreams.When sister station KETV spoke with Keely Pedersen, she appeared as a typical 21-year-old.But she lives with a rare disease that can change her appearance daily."You wake up with a different face or body every day," Keely said.When Keely was 11, she started experiencing symptoms that she knew were out of the ordinary.Her symptoms appeared at the same time as puberty, leaving doctors to believe that was the cause."They thought it was bad menstrual pain. Then they thought it was endometriosis or ovarian cysts," Keely said.For four years, Keely lived undiagnosed.She experienced symptoms like painful internal swelling, and external swelling of her hands, abdomen, and face.When she was finally diagnosed, doctors said it's hereditary angioedema type three, estrogen-dependent and dominant."I know, it's a mouthful," Keely said.Doctors say HAE is extremely rare. The disease impacted everything in Keely's life."You wake up two hours early because you know that you're not going to get out of bed yet," Keely said. "You move much slower. You don't get to do that as many things as you wanted to."Her hospital visits were frequent — her mom says there was even a designated "Keely" room.She had multiple painful swells every day. Because of this, she couldn't keep a regular high school course schedule."Almost everybody extended in my life, even teachers, encouraged me to just drop out and just go get a GED," Keely said.But over and over again, Keely said no to that idea.She studied to get her diploma through Omaha Public Schools' Virtual School, all while working with doctors to find a treatment program that would ease her symptoms with this lifelong disease."If you really want something the way that she wanted it, I mean, she just would not give up. She was tireless," Keely's mom, Sharvonna Ballard, said.Keely walked across the stage last week — coincidentally, on National HAE Day.She's starting her career journey with more than just that diploma."I'm a CNA, I did that while going to high school, during nights. I'm also a doula, a full-spectrum doula," Keely said. As for what's next, Keely said she can't wait to launch herself into her work and find her niche.

When one woman was diagnosed with a rare illness as a teenager, it affected not only her health but also her high school dreams.

When sister station KETV spoke with Keely Pedersen, she appeared as a typical 21-year-old.

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But she lives with a rare disease that can change her appearance daily.

"You wake up with a different face or body every day," Keely said.

When Keely was 11, she started experiencing symptoms that she knew were out of the ordinary.

Her symptoms appeared at the same time as puberty, leaving doctors to believe that was the cause.

"They thought it was bad menstrual pain. Then they thought it was endometriosis or ovarian cysts," Keely said.

For four years, Keely lived undiagnosed.

She experienced symptoms like painful internal swelling, and external swelling of her hands, abdomen, and face.

When she was finally diagnosed, doctors said it's hereditary angioedema type three, estrogen-dependent and dominant.

"I know, it's a mouthful," Keely said.

Doctors say HAE is extremely rare. The disease impacted everything in Keely's life.

"You wake up two hours early because you know that you're not going to get out of bed yet," Keely said. "You move much slower. You don't get to do that as many things as you wanted to."

Her hospital visits were frequent — her mom says there was even a designated "Keely" room.

She had multiple painful swells every day. Because of this, she couldn't keep a regular high school course schedule.

"Almost everybody extended in my life, even teachers, encouraged me to just drop out and just go get a GED," Keely said.

But over and over again, Keely said no to that idea.

She studied to get her diploma through Omaha Public Schools' Virtual School, all while working with doctors to find a treatment program that would ease her symptoms with this lifelong disease.

"If you really want something the way that she wanted it, I mean, she just would not give up. She was tireless," Keely's mom, Sharvonna Ballard, said.

Keely walked across the stage last week — coincidentally, on National HAE Day.

She's starting her career journey with more than just that diploma.

"I'm a CNA, I did that while going to high school, during nights. I'm also a doula, a full-spectrum doula," Keely said.

As for what's next, Keely said she can't wait to launch herself into her work and find her niche.