28 THE QUEENS COURIER • HEALTH • APRIL 4, 2019  FOR BREAKING NEWS VISIT WWW.QNS.COM 
  health 
 Baby dolls bring joy to residents at Parker Jewish Institute’s Memory Care Unit 
 A caring daughter’s love is bringing  
 comfort and joy to her mom and fellow  
 residents at Parker Jewish Institute.   
 Th  e  story  began  when  Cassandra  
 Ottaviano, 34, of Bellmore, NY, visited  
 her mother “Marge” (Margaret) Karris  
 in early February 2019.  Marge, at 68  
 years  old,  was  admitted  to  Parker  in  
 August 2018 with a diagnosis of early  
 onset Alzheimer’s disease.  
 Cassandra  had  been  in  touch  with  
 Parker’s  Caregiver  Support  Initiative,  
 while her mother lived alone with home  
 care  in  a  Suff olk  apartment.    Marge  
 participated in their Caregiver Respite  
 Day Program for a short while.  But at  
 some point, Marge needed placement.  
 Cassandra was told about options, given  
 emotional support, counseling and suggestions  
 about long term care, and ultimately  
 support through the transition of  
 placing her mother. 
 During her February visit, Cassandra  
 had her 3-year old Mathew give a baby  
 doll to Marge.  But aft er returning from  
 lunch, Marge’s doll was gone, and another  
 resident was found cradling the doll,  
 like it was her own baby.   
 “I didn’t have the heart to take that  
 doll away and give it back to my Mom,”  
 Cassandra said.  Th  at’s when she got  
 the idea to collect dolls for residents on  
 Parker’s 8th fl oor Memory Care Unit. 
 Cassandra’s brother Peter helped with  
 the fundraising drive.  She posted an  
 appeal on her Facebook page, on the Long  
 Island Preschool and Elementary Moms  
 Group page, and a few Bellmore Civic  
 pages.  Cassandra called it her Dolls for  
 Alzheimer’s Valentine’s Day Fundraiser.   
 “It would mean so much if you could  
 show your support and consider donating  
 a new doll to residents like my Mom,  
 who have Alzheimer’s.  Th  ere are dozens  
 of residents who could benefi t from your  
 generosity,” her appeal stated.  
 When Cassandra visited Parker on Feb.  
 23, she brought her baby dolls and with  
 staff  approval, asked several residents if  
 they’d like one.   
 “Th  eir reactions brought tears of joy  
 to my eyes,” Cassandra said.  “Several  
 residents  began  cradling  the  life-sized  
 dolls, talking to them and making cooing  
 sounds, as if they were their own  
 babies.  We saw a lot of smiles that day,”  
 she added. 
 “We commend eff orts like Cassandra’s.  
 Th  erapy dolls are a helpful, non-pharmaceutical  
 way to calm and soothe seniors  
 with  Alzheimer’s  and  other  dementias,” 
  according to Michael N. Rosenblut,  
 Parker’s President and CEO.  “Gift ing  
 a soft , life-sized baby doll to some residents  
 in our Memory Care Unit, can  
 bring them back to a time in their lives  
 when they had a sense of purpose, joy  
 and comfort.” 
 Aft er  giving  out  dolls  at  Parker,  
 Cassandra, husband Phil and her brother  
 Peter, distributed the rest at local nursing  
 homes.  Th  ey plan another drive for  
 Mother’s Day in the spring.   
 If you’d like to donate, they need new and  
 ethnically diverse dolls.  Please contact her  
 ASAP at: Cassandra.Karris@gmail.com.    
 Photo courtesy of Parker Jewish Institute 
 Some of the baby dolls received by residents at Parker Jewish Institute’s Memory Care Unit. 
 How genetic testing may help to identify your risk for a rare disease 
 Th  ere is no doubt that interest in genetics  
 has exploded in recent years. In fact,  
 genealogy  has  grown  dramatically  to  
 become the second most popular hobby  
 in the United States and the second-most  
 popular internet surfi ng topic. 
 At  the  same  time,  advances  in  our  
 understanding of genetics are broadening  
 our understanding of the role genes  
 play in our overall health and the development  
 of many diseases. Th  is is especially  
 signifi cant for people with inherited  
 conditions, such as hereditary transthyretin 
 mediated (hATTR) amyloidosis. 
  Aff ecting approximately 50,000 people  
 worldwide, hATTR amyloidosis is a  
 life-threatening disease that can impact  
 multiple parts of the body, including the  
 nerves, heart and digestive system. 
 hATTR  amyloidosis  is  passed  down  
 from parent to child in an autosomal  
 dominant fashion, meaning a person only  
 needs to inherit one copy of the aff ected  
 gene from one parent in order to develop  
 the condition. However, inheriting  
 the TTR gene with a mutation does not  
 necessarily mean that you will develop  
 hATTR amyloidosis. Despite its prevalence  
 across generations and the appearance  
 of symptoms, some families may be  
 unaware of their family history or that  
 they are at risk for the condition. 
 Symptoms of hATTR amyloidosis can  
 vary widely from person to person, but  
 oft en include weakness, numbness and  
 tingling in the hands and feet, burning  
 pain, dizziness, shortness of breath and  
 digestive  issues.  Misdiagnosis  is  common  
 with hATTR amyloidosis because  
 the symptoms can resemble those of other  
 more common conditions including carpal  
 tunnel syndrome, diabetic neuropathy  
 and hypertensive heart disease. 
 Th  is is where genetic testing can help. 
 “Making the decision to undergo genetic  
 testing  for  serious  conditions  like  
 hATTR amyloidosis is not easy, especially  
 when it can have implications for your  
 entire family,” said Emily Brown, a genetic  
 counselor. “Knowing you are at risk can  
 allow you to recognize symptoms faster,  
 avoid misdiagnoses and identify a path  
 forward with your doctor.” 
 Genetic counselors can also help to  
 familiarize you with the process of genetic  
 testing and provide support due to the  
 potential implications if you test positive. 
 Th  ere  are  other  resources  available.  
 Companies like Alnylam Pharmaceuticals  
 have made genetic testing and counseling  
 options available to help people make  
 informed decisions about their health.  
 Th  rough Alnylam Act(R), Alnylam sponsors  
 third-party genetic testing and counseling  
 for individuals who may be carrying  
 a gene mutation known to be associated  
 with hATTR amyloidosis at no charge.  
 For more information about the program,  
 visit AlnylamAct.com. 
 Further, if you or someone in your family  
 experience symptoms consistent with  
 those of hATTR amyloidosis, talk to your  
 doctor and visit Alnylam’s hATTRBridge. 
 com for more information and additional  
 resources. 
 Courtesy BPT 
 
				
/AlnylamAct.com
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