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18 CHICAGO TRIBUNE Ô FROM PAGE ONE Ô SECTION 1 Ô SUNDAY, MAY 11, 2008 Varicose veins develop over years. Just like the knowledge of how to treat them. For more than 25 years, Vein Clinics of America has been specializing in treating the entire spectrum of vein disease –from spider veins to varicose veins to leg ulcers –and it shows. Our highly skilled physicians and clinical staff will put you at ease with their extensive knowledge and experience treating varicose vein disease without surgery. Our physicians will answer your questions and explain your diagnosis and non-surgical treatment options, which may even be covered by insurance. Call 1-866-916-VEIN or visit veinclinics.com. Schedule your complimentary consultation today.* Now accepting Blue Cross Blue Shield PPOs and United Healthcare PPOs. We’ll work with you to maximize your insurance benefits. Bourbonnais Buffalo Grove Chicago Gurnee Naperville Oak Brook Orland Park Schaumburg Merrillville, IN *Restrictions May Apply. ® 2008 Vein Clinics of America Oriental Furniture 17 W. Ogden Ave., Westmont, IL - Tel: (630) 515-8851 Subject to Availability Going Out Of Business 60-85% OFF Final Days! All MUST Go! Make an offer! Antique Asian Furniture Oil Paintings Office Furniture Rosewood Furniture 6,000 sq. ft. Showroom 15,000 sq. ft. Warehouse Oriental Furniture 17 W. Ogden Ave., Westmont, IL - Tel: (630) 515-8851 Mon-Wed: 1 1-6pm Thurs-Sun: 1 1-7pm absorbed lectures in calculus or thermodynamics or cir- cuit analysis, Rosa sat not far away, just in case Lucy needed a sip of water or began chok- ing. Lucy, who is 24, was told she had a rare genetic degenera- tive disease, spinal muscular atrophy, when she was 4. SMA is a progressive disease that withers the muscles that con- trol the arms, legs and lungs, and makes breathing a strug- gle. Lucy’s type of SMA usually takes away your ability to walk by the time you’re in your teens—she began using a wheelchair at age 9—but un- like some other types, doesn’t necessarily affect life span. Lucy, who is the oldest of four, has a younger brother, Hugo, who has the same dis- ease. He, too, uses a wheel- chair; he’s a freshman at the University of Illinois at Ur- bana-Champaign, studying architecture. Parental dedication “Lucy’s story is about the sacrifices our mothers make for all of us,” said Pete Nel- son, interim dean of UIC’s en- gineering college. Trevino’s teachers, he said, “were pounding down my door” to ask for some recognition for this mother-daughter feat of unconditional devotion. At UIC, where nearly a third of the students are the first in a family to go to col- lege, Nelson said it’s not un- common to hear tales of par- ents working two or three jobs, sending money from overseas and just plain strug- gling so their kids can get what parents weren’t af- forded. “But this is sort of the pin- nacle in terms of the amount of dedication,” said Nelson. “This is what makes this business worthwhile.” One of the professors pounding on Nelson’s door was Michael Cho, who teach- es mostly graduate courses in cell and tissue engineering, but who has gotten to know— and been amazed by—the ubiquitous mother-daughter duo, so often spotted wending their way up a ramp, on or off an elevator, or tucked away studying in some secluded corner. “The first thing that comes to my mind is this can’t be anything else but a mother’s love,” Cho said. “It goes be- yond commitment. It is sacri- ficial love. And I am just over- whelmed. It’s not just one monthor one semester. It’s ev- ery day for the last four years that I can think of.” In fact, it’s six years, be- cause Lucy had to take time off when she got really sick her junior year; she suddenly couldn’t lift her arms and was quickly losing memory. It took months before a sleep test showed she stopped breathing 30 times an hour when she was asleep. She now sleeps with a machine that helps her breathe, and, with- in a week of using it, she said, she regained her memory, if not her arm strength. “Ever since I was little, I loved science,” said Lucy, who shares her mother’s deep co- coa-colored eyes and rolls around campus in a purple wheelchair with back wheels that sparkle, like fireworks, with tiny neon bits. “Because I went to doctors a lot and had a lot of medical exams, I would always wonder, ‘How do those devices work?’ ” In her senior year at Mor- ton West High School in Ber- wyn, Trevino learned from a counselor about a summer camp in bioengineering at UIC, so she signed up, and found her life’s work. She once dreamed of work- ing to find a cure for her own disease, but decided “it would be too stressful if I couldn’t find it.” The first one in her family to ever go to college, Lucy Tre- vino said she was “too afraid” to venture down to the U. of I. in Urbana-Champaign, where there’s a whole dorm for students with disabilities, and the nation’s oldest col- lege-level disabilities-serv- ices program provides trained personal assistants, physical therapy, even wheel- chair repairs. “I didn’t know if I should risk going all the way down there,” she said. Sticking closer to home seemed like a better plan. But because UIC doesn’t have a personal-assistants program, she was stuck trying to find someone who could help her in a thousand little ways and be there whenever she needed. “In college, you have such a crazy schedule. You stay after to study with other students. You need to talk to a professor. I was like, ‘Oh, my gosh, how am I going to find someone who’s going to put up with all of that?’ “My mom was like, ‘Well, I guess I’ll just go with you.’ “And then it was getting closer to the start of the first semester, and I still hadn’t found anybody. She said, ‘How would you feel if I went with you?’ I was like, ‘Oh, my gosh, would you?’ ” Because Rosa Trevino, who is 47 and moved from Mexico when she was 17, had two chil- dren with special needs, she had long since become a stay- at-home mom, giving up a se- ries of baby-sitting jobs. Rosa’s husband, Hugo, re- tired last year after 32 years as a CTA bus driver. Rosa her- self had never even been to high school. On the day back in 1987 when doctors said her little girl would “someday need a wheelchair,” Rosa recalled, crying at the memory, she promised herself she would do “everything I can.” Mother keeps busy Even if that meant sitting through more than 2,100 hours of 51 classes, countless study sessions and hourlong train rides, back and forth, each day. Most often, Lucy said with a laugh, her mother spends time cutting recipes and coupons, because she gets bored with all the bioen- gineering in a language she doesn’t fully understand. At first, Lucy admitted, go- ing to college with her mother wasn’t exactly with- out its bumps. “I had never spent so much time together with my mom. We would sometimes get on each other’s nerves,” she said, chuckling. “But then we got to know each other really well. We’re like best friends. Now I tell her everything. Be- fore I wouldn’t tell her every- thing that happens when you have a disability. People who aren’t in a wheelchair can’t understand. But now, since we do everything together she knows.” Semester after semester, year after year, Lucy and her mother found a way. She passed 400-level exams. She wrote up labs that took her twice the time of everyone else, simply because the push- ing of a pen on paper is so hard for her. Once, a civil engineering professor noticed that be- cause of Lucy’s wheelchair, she couldn’t write on her desk. He challenged her to de- sign a light-weight writing ta- ble. Then he went and built it. She got an A. Mostly, the Trevinos relied on each other, and on unflag- ging faith. “One time I think in the night, almost for an hour. I cry to on high, ‘Why me? Why me?’ ” Rosa said. “I heard a voice, ‘Why not me?’ ” For those who watched their unswerving per- severance, the simple fact that the Trevinos never stum- bled inscribed a lasting honor on Lucy’s college transcript. “One time last year,” Lucy said, “a student told me she’d felt like ditching class, stay- ing home. But then she looks and says, ‘There’s Lucy, she’s always here. There’s nothing wrong with me. I’m just lazy.’ “Wow, I didn’t even think that anyone noticed me.” Come Mother’s Day week- end, when Nelson tries to make it through his heartfelt salutation to a student and a mother who taught them all a lesson, chances are Lucy and Rosa Trevino will finally understand just how much a whole college noticed. [email protected] Tribune photos by Antonio Perez Lucy Trevino (center), 24, of Cicero checks her e-mail as her mother, Rosa, reads a newspaper in a computer lab on the University of Illinois at Chicago campus. Rosa Trevino (right) presses a button to lift her daughter, Lucy, a UIC engineering student, into their van while Lucy’s father, Hugo, watches outside their Cicero home. For video and photo gallery of Rose and Lucy Trevino, go to chicagotribune.com/lucy IN THE WEB EDITION » LUCY CONTINUED FROM PAGE 1
Transcript
Page 1: Product: CTMAIN PubDate: 05-11-2008 Zone: ALL Edition ...

18 CHICAGO TRIBUNE Ô FROM PAGE ONE Ô SECTION 1 Ô SUNDAY, MAY 11, 2008

Varicose veins develop overyears. Just like the knowledgeof how to treat them.For more than 25 years, Vein Clinics of America

has been specializing in treating the

entire spectrum of vein disease–from

spider veins to varicose veins to leg

ulcers–and it shows.

Our highly skilled physicians and clinical sta0

will put you at ease with their extensive

knowledge and experience treating varicose

vein disease without surgery.

Our physicians will answer your questions and explain your

diagnosis and non-surgical treatment options, which may

even be covered by insurance.

Call 1-866-916-VEIN or visit veinclinics.com.

Schedule your complimentary consultation today.*

Now accepting Blue Cross Blue Shield PPOs and United Healthcare PPOs.We’ll work with you to maximize your insurance bene:ts.

Bourbonnais

Buffalo Grove

Chicago

Gurnee

Naperville

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ay A

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ly. ®

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08

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in C

linic

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f A

me

rica

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Subject to Availability

Going Out Of Business Going Out Of Business 60-85% OFF 60-85% OFF Final Days! Final Days! All MUST Go! All MUST Go! Make an offer! Make an offer!

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Mon-Wed: 1 1-6pm Thurs-Sun: 1 1-7pm

absorbed lectures in calculusor thermodynamics or cir-cuit analysis, Rosa sat not faraway, just in case Lucy neededa sip of water or began chok-ing.

Lucy, who is 24, was told shehad a rare genetic degenera-tive disease, spinal muscularatrophy, when she was 4. SMAis a progressive disease thatwithers the muscles that con-trol the arms, legs and lungs,and makes breathing a strug-gle.

Lucy’s type of SMA usuallytakes away your ability towalk by the time you’re inyour teens—she began usinga wheelchair at age 9—but un-like some other types, doesn’tnecessarily affect life span.

Lucy, who is the oldest offour, has a younger brother,Hugo, who has the same dis-ease. He, too, uses a wheel-chair; he’s a freshman at theUniversity of Illinois at Ur-bana-Champaign, studyingarchitecture.

Parental dedication“Lucy’s story is about the

sacrifices our mothers makefor all of us,” said Pete Nel-son, interim dean of UIC’s en-gineering college. Trevino’steachers, he said, “werepounding down my door” toask for some recognition forthis mother-daughter feat ofunconditional devotion.

At UIC, where nearly athird of the students are thefirst in a family to go to col-lege, Nelson said it’s not un-common to hear tales of par-ents working two or threejobs, sending money fromoverseas and just plain strug-gling so their kids can getwhat parents weren’t af-forded.

“But this is sort of the pin-nacle in terms of the amountof dedication,” said Nelson.“This is what makes thisbusiness worthwhile.”

One of the professorspounding on Nelson’s doorwas Michael Cho, who teach-es mostly graduate courses incell and tissue engineering,but who has gotten to know—and been amazed by—theubiquitous mother-daughterduo, so often spotted wendingtheir way up a ramp, on or offan elevator, or tucked awaystudying in some secludedcorner.

“The first thing that comesto my mind is this can’t beanything else but a mother’s

love,” Cho said. “It goes be-yond commitment. It is sacri-ficial love. And I am just over-whelmed. It’s not just onemonth or one semester. It’s ev-ery day for the last four yearsthat I can think of.”

In fact, it’s six years, be-cause Lucy had to take timeoff when she got really sickher junior year; she suddenlycouldn’t lift her arms and wasquickly losing memory.

It took months before asleep test showed she stoppedbreathing 30 times an hourwhen she was asleep. She nowsleeps with a machine thathelps her breathe, and, with-in a week of using it, she said,she regained her memory, ifnot her arm strength.

“Ever since I was little, Iloved science,” said Lucy, whoshares her mother’s deep co-coa-colored eyes and rollsaround campus in a purplewheelchair with back wheelsthat sparkle, like fireworks,

with tiny neon bits. “BecauseI went to doctors a lot and hada lot of medical exams, Iwould always wonder, ‘Howdo those devices work?’ ”

In her senior year at Mor-ton West High School in Ber-wyn, Trevino learned from acounselor about a summercamp in bioengineering atUIC, so she signed up, andfound her life’s work.

She once dreamed of work-ing to find a cure for her owndisease, but decided “it wouldbe too stressful if I couldn’tfind it.”

The first one in her familyto ever go to college, Lucy Tre-vino said she was “too afraid”to venture down to the U. of I.in Urbana-Champaign,where there’s a whole dormfor students with disabilities,and the nation’s oldest col-lege-level disabilities-serv-ices program providestrained personal assistants,physical therapy, even wheel-chair repairs.

“I didn’t know if I shouldrisk going all the way downthere,” she said.

Sticking closer to homeseemed like a better plan. Butbecause UIC doesn’t have apersonal-assistants program,she was stuck trying to findsomeone who could help herin a thousand little ways andbe there whenever sheneeded.

“In college, you have such acrazy schedule. You stay afterto study with other students.You need to talk to a professor.I was like, ‘Oh, my gosh, howam I going to find someonewho’s going to put up with allof that?’

“My mom was like, ‘Well, Iguess I’ll just go with you.’

“And then it was gettingcloser to the start of the firstsemester, and I still hadn’tfound anybody. She said,‘How would you feel if I wentwith you?’ I was like, ‘Oh, mygosh, would you?’ ”

Because Rosa Trevino, whois 47 and moved from Mexicowhen she was 17, had two chil-dren with special needs, shehad long since become a stay-at-home mom, giving up a se-ries of baby-sitting jobs.Rosa’s husband, Hugo, re-tired last year after 32 yearsas a CTA bus driver. Rosa her-self had never even been tohigh school.

On the day back in 1987when doctors said her littlegirl would “someday need awheelchair,” Rosa recalled,crying at the memory, shepromised herself she woulddo “everything I can.”

Mother keeps busyEven if that meant sitting

through more than 2,100hours of 51 classes, countlessstudy sessions and hourlongtrain rides, back and forth,each day. Most often, Lucysaid with a laugh, her motherspends time cutting recipesand coupons, because shegets bored with all the bioen-gineering in a language shedoesn’t fully understand.

At first, Lucy admitted, go-ing to college with hermother wasn’t exactly with-out its bumps.

“I had never spent so muchtime together with my mom.We would sometimes get oneach other’s nerves,” shesaid, chuckling. “But then wegot to know each other reallywell. We’re like best friends.Now I tell her everything. Be-fore I wouldn’t tell her every-thing that happens when youhave a disability. People whoaren’t in a wheelchair can’tunderstand. But now, sincewe do everything togethershe knows.”

Semester after semester,year after year, Lucy and hermother found a way. Shepassed 400-level exams. Shewrote up labs that took hertwice the time of everyoneelse, simply because the push-ing of a pen on paper is sohard for her.

Once, a civil engineeringprofessor noticed that be-cause of Lucy’s wheelchair,she couldn’t write on herdesk. He challenged her to de-sign a light-weight writing ta-ble. Then he went and built it.She got an A.

Mostly, the Trevinos reliedon each other, and on unflag-ging faith.

“One time I think in thenight, almost for an hour. Icry to on high, ‘Why me? Whyme?’ ” Rosa said. “I heard avoice, ‘Why not me?’ ”

For those who watchedtheir unswerving per-severance, the simple factthat the Trevinos never stum-bled inscribed a lasting honoron Lucy’s college transcript.

“One time last year,” Lucysaid, “a student told me she’dfelt like ditching class, stay-ing home. But then she looksand says, ‘There’s Lucy, she’salways here. There’s nothingwrong with me. I’m just lazy.’

“Wow, I didn’t even thinkthat anyone noticed me.”

Come Mother’s Day week-end, when Nelson tries tomake it through his heartfeltsalutation to a student and amother who taught them all alesson, chances are Lucy andRosa Trevino will finallyunderstand just how much awhole college noticed.

[email protected]

Tribune photos by Antonio Perez

Lucy Trevino (center), 24, of Cicero checks her e-mail as her mother, Rosa, reads a newspaper in a computer lab on the University of Illinois at Chicago campus.

Rosa Trevino (right) presses a button to lift her daughter, Lucy, a UIC engineering student,into their van while Lucy’s father, Hugo, watches outside their Cicero home.

For video andphoto gallery ofRose and LucyTrevino, go to

chicagotribune.com/lucy

IN THE WEB EDITION» LUCYCONTINUED FROM PAGE 1

Product: CTMAIN PubDate: 05-11-2008 Zone: ALL Edition: BDOG Page: 1-18 User: bohap Time: 05-10-2008 02:36 Color: CMK

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