
 
		QUEENS INFANT CELEBRATES MILESTONE BIRTHDAY  
 AMID STRUGGLE WITH RARE GENETIC DISEASE 
 BY JASMINE PALMA 
 From  social  and  physical  
 cues,  parents  can  track  the  
 developmental  milestones  
 their kids pass following their  
 birth.  From a baby’s  first  incoherent  
 gurgle  to  its  fleeting  
 yet  determined  attempt  
 at  their  first  steps,  each  parent  
 earnestly  witnesses  the  
 achievement stages their child  
 undergoes  in  the  transition  
 into toddlerhood. What many  
 parents  do  not  anticipate  is  
 failing to see these milestones  
 take place.  
 Lucy  Gilio  of  Queens  was  
 born  Aug.  16  of  last  year.  
 Barring  a  lack  of  expected  
 frequent  and  energetic  kicking, 
  Lucy  did not exhibit  any  
 worrying  indications  of  any  
 health complications.  
 “At birth, she received the  
 typical  tests  and  checkups  
 at  the  hospital,  such  as  an  
 APGAR  score  and  a  physical  
 performed  by  a  pediatrician.  
 There  were  no  remarks  or  
 concerns  regarding  Lucy’s  
 health,”  Ashley  Gilio,  Lucy’s  
 mother, recalled.  
 Eleven  days  following  
 her  birth,  Lucy’s  pediatrician  
 relayed surprising news  
 —  screening  test  results  
 indicated  that  Lucy  was  afflicted  
 with  spinal  muscular  
 atrophy  (SMA)  type  1,  a  
 neuromuscular  disease  that  
 is  progeny  of  a  rare  genetic  
 mutation  with  a  grim  prognosis  
 of death before a baby’s  
 second birthday.  
 Had  Lucy  not  been  
 screened  at  such  an  early  
 period in her life, Gilio said,  
 even by a mere difference of a  
 few months, the disease could  
 have  progressed  rampantly  
 and  could  have  claimed  Lucy’s  
 life. 
 “When  it  comes  to  SMA,  
 time  is  everything,”  Gilio  
 said.  
 SMA1  —  one  of  the  most  
 aggressive  forms  of  the  disease  
 —  quickly  deteriorates  
 motor  neurons  in  the  brain,  
 consequently  leading  babies  
 to  lose  conviction  over  the  
 mobility of their limbs, grow  
 increasingly weak, and eventually  
 lose  the  ability  to  autonomously  
 swallow,  chew,  
 and ultimately breathe.  
 When  the  body  lacks  the  
 surviving  motor  neuron  1  
 (SMN1) gene,  it relies on  the  
 SMN2  genes  to  pick  up  the  
 slack,  but  these  genes  only  
 compensate  for  a  meager  10  
 percent  of  the  SMN  protein  
 production  in  comparison  
 to  the  SMN1  gene  which  
 leads  to  the  aforementioned  
 complications.  
 Left untreated, this disease  
 can cause death from chronic  
 respiratory  insufficiency  or  
 make  the  need  for  feeding  
 support and permanent ventilation  
 by the age of 2 in more  
 than 90% of cases.  
 Despite  being  largely  unheard  
 of,  SMA  is  estimated  
 to  affect  10,000  to  25,000  children  
 and adults in the United  
 States alone, according to the  
 SMA Foundation. The National  
 Human  Genome  Research  
 Institute reported that one in  
 6,000 to one in 10,000 children  
 are born with SMA. In an oxymoronic  
 manner,  this  makes  
 SMA one of the most common  
 rare diseases.  
 According  to  Cure  SMA,  
 SMA  is  inherited  in  an  autosomal  
 recessive  pattern  
 in  families.  In  other  words,  
 a  baby  diagnosed  with  SMA  
 inherited  two  mutated  nonfunctioning  
 renditions  of  the  
 surviving  motor  neuron  1  
 (SMN1)  gene  from  each  parent. 
   A  DNA  test  can  detect  
 carriers of SMA and other genetic  
 diseases. 
 The  American  College  
 of  Obstetricians  and  Gynecologists  
 states  that  approximately  
 one  in  40  to  one  in  60  
 people are carriers of SMA. If  
 both  parents  are  carriers  of  
 the disease, there is a 50 percent  
 chance  a  child  will  be  a  
 TIMESLEDGER   |   QNS.20     COM   |   SEPT. 25-OCT. 1, 2020 
 carrier,  a  25  percent  chance  
 of  procreating  a  child  with  
 SMA, and a remaining 25 percent  
 chance that the child will  
 not be affected. 
 When  Lucy’s  neurologist  
 gave  Lucy’s  parents  the  rundown  
 of  SMA1  and  the  unfavorable  
 statistics,  Gilio  was  
 shocked at the severity of the  
 disease.  Despite  the  bleak  
 prognosis,  she  and  her  husband  
 continued  to  pursue  
 treatment  with  Lucy’s  care  
 team  as  well  as  conducting  
 their  own  research  to  adequately  
 make informed decisions  
 regarding  Lucy’s  treatment  
 options.  
 The  Gilio’s  said  they  had  
 the unwavering support from  
 family  and  friends  and  that  
 they  received  advice  and  information  
 from organizations  
 such  as  Cure  SMA  and  SMA  
 parent  and  caregiver  Facebook  
 groups. 
 “Seeing  what  other  families  
 are  going  through,  how  
 they  are  making  their  treatment  
 decisions  and  the spirit  
 with  which  they  celebrate  
 their  children  reaching  new  
 milestones  have  brought  my  
 husband and I a lot of comfort  
 and hope,” she said.  
 When it came time to decide  
 on a treatment plan, the Gilio  
 family decided on Zolgensma,  
 a one-time gene therapy treatment  
 option  via  intravenous  
 insertion  for  children  under  
 two years old approved by the  
 Food  and  Drug  Administration  
 (FDA) in 2019. 
 The drug works by  targeting  
 the  genetic  origin  of  the  
 disease and replacing the nonworking  
 or  missing  SMN1  
 gene.  To  learn  more  about  
 SMA and Zolgensma, visit the  
 Zolgensma website here. 
 “We decided on Zolgensma  
 because  it  is  a  one-time-only  
 infusion that has been seeing  
 promising results,” Gilio said.  
 “At the time, my husband and  
 I  were  noticing  the  positive  
 conversations taking place in  
 our Facebook groups around  
 Zolgensma, and that it seemed  
 to be helping SMA kids without  
 too many adverse effects.” 
 Following  her  treatment,  
 Lucy  can  now  be  found  saying  
 words  like  “peekaboo,”  
 and  has  adopted  the  childish  
 inquisition  and  curiosity  
 seen  in many  1-year-olds,  
 asking  questions  about  her  
 surroundings such as “what’s  
 that?”  
 “She  is one happy baby —  
 we’ll  often  catch  her  waving,  
 dancing, and crawling across  
 the  floor.  She  is  now  beginning  
 to stand with assistance  
 and  cruise  along  the  furniture,” 
   Ashley  said.  “Many  
 of  these  milestones  she  is  
 reaching today would’ve been  
 unimaginable,  given  the  progressive  
 nature  of  SMA,  had  
 she  not  received  treatment.  
 As  the  one-year  anniversary  
 of  Lucy’s  treatment  day  approaches, 
 Photos courtesy of Ashley Gilio 
   we’re  thrilled  that  
 she  is  achieving  these  ageappropriate  
 milestones. ” 
 For  parents  whose  children  
 are diagnosed with SMA,  
 Gilio encourages them to seek  
 emotional support and all the  
 resources available to them.  
 “With  SMA  being  a  rare  
 disease, it’s important to have  
 a  community  to  lean  on  at  
 every  stage  of  your  family’s  
 SMA  journey,”  she  said.  “As  
 part  of  that  journey,  it’s  also  
 important  to  celebrate  new  
 milestones  that  your  child  
 has  reached  or  is  working  
 on, no matter how small they  
 seem—each  one  leads  to  big  
 memories  and  even  bigger  
 possibilities  for  your  child’s  
 future.” 
 With  August  being  SMA  
 Awareness Month and September  
 being Newborn Screening  
 Awareness Month in the United  
 States, Gilio would like “to  
 reiterate the potentially monumental  
 benefit  that  testing  
 for SMA as part of the routine  
 newborn screening panel can  
 bring to affected children and  
 their families.” 
 New  York  is  one  of  the  32  
 states that test for SMA with  
 a  routine  newborn  screening  
 panel, and she hopes that Lucy’s  
 story along with those of  
 other  children  who  reside  in  
 states that offer screening will  
 galvanize the 18 states that remain  
 to implement screening  
 to “quickly follow suit.”