Finding Strength in Adversity
It’s not the hand you have been dealt, or even how much the deck is stacked against you. It’s how you play your cards.At least, that’s HollyRobinson Peete’s perspective. Holly and her husband, former NFLquarterback Rodney Peete, have beenblessed with success in their careers. Butcaring for Holly’s father, who wassuffering from Parkinson’s disease, tooka toll on their family, both financiallyand emotionally.Inspired by herpersonal adversities, the actress-turned-philanthropistnow advocates for thecauses dear to her.
Wanting to give back
“It’s such a take, take, take world, and when you give back, you balance outall of the things and the blessings you have received,” Holly says. “It has mademe a less judgmental person and a morepatient person. My desire to live a life ofservice all comes from situations thathave happened to me.”
Holly says she spent years feelingsorry for herself, saying, “Why me?”“Why is this happening to my lovedones?” But shifting the focus fromwhatever is going on in her life to helpingpeople who are suffering has been a verycathartic process.
Drawing strength from family
She and Rodney started theHollyRod Foundation in 1997 to helpthose dealing with Parkinson’s diseaseafford their treatments and medications.And in 2000, their mission expanded toinclude autism when their eldest son,Rodney “RJ” Peete Jr., was diagnosedwith the disorder.
“We try to do a lot ofawareness and alleviate some of theirday-to-day stresses,” she says. “Both themission and the desire to raise funds andadvocate for families came out of twosituations, one with my father and onewith my son.”
Compassionate care
By partnering with the Parkinson’sDisease and other Movement DisordersCenter at the Keck School of Medicineof the University of Southern California,the HollyRod Compassionate CareProgram provides assistance withconsultations, physical therapy,swallowing treatment and ambulationaids. In 2010, the HollyRod Foundation teamed up with nabi tablet creator Fuhu Inc. to launch the Give the Gift of Voicecampaign, offering nonverbal autisticchildren a means to communicate.
“These kids can’t talk, but they havea lot to say,” Holly says. “We have to givethem the tools to be able toexpress themselves.”
Looking toward the future
Holly is trying to bring issues like autistic kids' tendency to wander off, and the transition fromadolescence to adulthood into thediscussion. The same questions andfears she has for her own son, she has forevery child growing up with autism,including, “How is he going to live onhis own?” “Who is going to hire him?”“How will he adjust and become aproductive citizen?”
Holly and RJ were on a flight homeafter a trip to the Super Bowl in NewYork. The seats were small andconfined, and 6-foot-2-inch RJ was fidgety. Midway through the flight, thegentleman in front of RJ turned aroundand scolded him for kicking the backofhis seat.
Putting it in perspective
“There was a time when they wouldhave had to haul me off. As a mom,I would have said, ‘How dare you bedisrespectful,’ ” she says. “Now I say,‘I understand what you are saying,and if I were in your position I wouldfeel this way, too, but here’s the deal.’He moved on, and I could tell he feltbad….I think that is the difference in the15 years we have been dealing with this.”
Because of their experiences, Hollysays she and her family are stronger,more gracious and happier. That’s theirwinning hand.
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