Chemo Cycle #4 is No More!

Theofanis has done a pretty good job staying on schedule with his Chemo treatments. Despite the two bouts of neutropenia and several blood transfusions, his young body has been fighting hard to quickly recover after every chemo induction. So promptly, 21 days after the start of his last chemo session, he was scheduled to be admitted for Chemo Cycle Four.  Last week, accompanied by his parents and sisters, he went to the SPA (Special Procedures Area) for his pre-chemo physical and blood tests. His nurses were concerned that his platelet counts would not be high enough to start chemo, especially since he had low counts that attributed to his nose bleed the previous week.  But, he checked out ok, so he was checked in to Comer.  His fluids were started, he was transferred to his room, but chemo didn't start until hours later...he was dehydrated so they added a bolus to get his blood to the appropriate level for the chemo.

While the Yianas' waited, they spent some time in the playroom, unpacked for their stay, and they even decorated the window in Theo's room to reflect a "Sizzling Summer" scene. It was, by the way 100 degrees F outside and the heat index was a blistering 110 degrees F. By the way, Theo promptly contacted Child Life Services to ask to borrow the remote Wii system, which he now hopes to claim ownership of at every visit.

There was a heartbreaking event at the hospital that contributed to the minor delays of the day. The doctors, nurses, staff and patients of Comer Children's Hospital were mourning the loss of Dr. James Nachman, professor of oncology and world-reknowned expert in pediatric leukemia. A memorial service was being held that day for the Comer Medical family to honor their colleague who unexpectedly passed away. Dr. Nachman was one of Theofanis' oncologists who was by far, one of the sweetest, kindest, nicest people anyone can ever meet. Theofanis said Dr. Nachman was one of his favorites! He was a baseball fan, so when Theofanis was organizing his baseball cards, Dr. Nachman would spend time with Theo going through his collection. He told us stories of when he met Pope John Paul II (Dr. Nachman was Jewish, so the story was pretty funny!) He even picked up Theo in his arms, giving him a big hug to make him smile. Dr. Nachman was brilliant, made great strides in leukemia research, and helped many, many children battle and win their fight against cancer.  For days, Eleni and Kosta struggled with how to tell Theo that Dr. Nachman had died. Death is a topic that the Yianas' don't want to talk about or think about. They stressed over when and how to tell him. They sought advice from friends and doctors. But, the right time came unexpectedly as they were walking through the halls of the hospital and Theo saw a poster of Dr. Nachman, paying tribute to him.  Deme immediately read the poster.  Theo looked at his parents for an explanation.  Eleni and Dean knelt down and explained that Dr. Nachman now has a special place in heaven. God is taking good care of Dr. Nachman since he took such good care of so many children with cancer.  Deme then asked if Dr. Nachman believed in God. When they heard "yes," all three kids immediately felt better.

THE SPOT

The chemotherapy regimen this time was dissimilar to his previous cycles.  Theo was given three different types of chemo drugs, and all were given in various lengths of time. As always, these medicines are administered intravenously  through his central line. Vincristine was a quick injection.  He was also given Cytoxan again, however, this time he was given a stronger dose which had to be administered over six hours.  His third drug, Doxorubicin, was administered over a 24-hour period.  Once the first bag was complete, his second bag was hung, and so on. 

His chemotherapy schedule for Cycle Four was as follows:

• Chemo Day 1 @ 9:00 pm:  Vincristine (quick injection), Cytoxan (6 hour infusion),  Doxorubicin (24 hour infusion)
• Chemo Day 2 @ 9:00 pm:  Vincristine (quick injection), Cytoxan (6 hour infusion),  Doxorubicin (24 hour infusion)
• Chemo Day 3 @ 9:00 pm: Vincristine (quick injection), Doxorubicin (24 hour infusion)

These three medicines and the constant flow of the chemo through his veins zapped a lot of Theofanis' energy.  He was tired and weaker than during previous rounds. The medications' immediate side effects included nausea, which caused Theo to lose his appetite.  His sense of smell and taste has changed, also.  And if you all recall, Theo has an extreme dislike of hospital food. So when Eleni and Kosta put food (brought from home) on his plate (brought from home), his tummy started rumbling and he immediately did not feel well.  He was a trooper, though, and really did try his best to eat.  He would have a bite here and there and he would try the protein shakes, grimmacing after every sip.

What made him happy and perk up though, despite the lethargy,  were the visits by those who love him...in person and via FaceTime. Theofanis received a FaceTime phone call on Friday from Theio George and Theia Angie (Sophia's Godparents) who, along with their children Filia and Anthony, were entertaining Demetra and Sophia for the day.  On Saturday, he had some extra special visitors from his beloved school, Pythagoras. He had a lot of fun visiting with Miss Jenny, his Greek dance teacher who walked in with gifts and cupcakes for all. And, Miss Evelyn (Sophia's preschool teacher) came by to play several rounds of UNO and make Theo and his sisters laugh.  On Sunday, Theia Tess came by to say hello in the afternoon with a Hexbug toy that Theo had hoped to scare the nurses with.  (It didnt' work, because Marlito wasn't the kind of nurse who gets easily scared.) And an improptu visit from his best buddy Pantelis and his mom Kimberly reenergized Theofanis so much that he ate his entire dinner!  Theo brightens up every time Pantelis walks into that hospital room.  It's precious to see the purity in their friendship!  And, visitors continued to come as Theia Maria and Theio Greg (Demetra's Godparents) came in and stayed until Theo was done with his chemo at 9:30 pm.  They brought with them a very cool Legos set, which would keep Theo busy for several hours.  But, there was no time to even open the box because the doctors said it was ok to go home as soon as he was disconnected from the IV and monitor. So, at around 10 pm, the discharge papers arrived, and the entire Yianas family quickly packed up and went home together!  The 72 hours of continuous chemo was over.

WITH LOVE FAITH AND PRAYER, HE WILL WIN

New battles are created each day. Whether it's getting through the day without nausea, eating a little more than the previous day, fighting off a fever or infection, or holding back the tears that flow at a second's notice, Theofanis has become a warrior.  He is a warrior without anger. He is a warrior who knows what must be done to win. He is a warrior with God on his side. Every day Eleni and Kosta are comforted by knowing that God is on his side. Just like when the kids were comforted by the fact that Dr. Nachman believed in God, the Yianas' trust in God brings them continued strength with each passing day. It is one day at at time, one prayer at at a time, but the power of prayer is immense and will loom large over their continued fight against this cancer.

This weekend, the Yianas family will be attending the Children's Neuroblastoma Cancer Foundation's Annual Parent and Medical Education Conference in Schaumburg, IL. CNCF is a national organization that is the premier source for neuroblastoma information and resources. Comprised of families affected by Neuroblastoma, they are committed to finding a cure for neuroblastoma through research, education, awareness and advocacy. ( http://www.cncfhope.org/ ) At this conference, parents are introduced to researchers who are developing new treatments and therapies to improve survival rates and reduce the long-term effects of treatment. Theofanis' oncologist, Dr. Susan Cohn, will be speaking at this event along with many of her reknowned colleagues from around the country. The Yianas' will meet other families who are fighting the same fight, hold the same fears, and seek the same cure. This conference is also focused on the children...those fighting for their lives, those who are cancer survivors, the siblings, and those children who are now angels. The conference has events planned for the kids. And when we asked Dr. Cohn if she thought that Theofanis would be ok to attend the conference, she said that as long as his counts are ok, its great for kids with neuroblastoma to meet and play together. Eleni and Kosta agree that it's time for Theofanis to meet other kids who understand what he's going through because they are living it, also. (Demetra and Sophia, too, of course.) And with this year's conference being held a mere 10 minutes from home, the Yianas' feel that their attendance is meant to be.

Theofanis' blood test today came back looking ok. Just ok. So, please pray that he is able to go to the CNCF conference and that his body is able to ward off any bugs that may threaten him.  And, please say a prayer for all the brave warriors and their families who are fighting Neuroblastoma and other childhood cancers.

Our continuing thanks and heartfelt regards go out to all of you who have bestowed on us your love, encouragement, hopes and prayers for the health and cure of our Theofanis. - Eleni and Kosta

THE POWER OF FRIENDSHIP

Love and friendship is universal, transcending distance, background, and ethnicity.  The Yianas family is reminded of this daily as the prayers, good wishes, and kind gestures continue to be received and appreciated from all over the world for Theofanis' fight against neuroblastoma. It's truly evident at Eleni's corporate Pentair family, where compassion for Theo has poured in with several amazing expressions of support through individual endeavors by colleagues and their families, both domestically and internationally.

Eleni has worked at Pentair/Everpure for thirteen years. Many of her co-workers have witnessed and shared her most important milestones in her life. They knew her when she was single. They saw her marry Kosta. They threw her a baby shower during her first pregnancy. They held Deme, Theo and Sophia when they were babies. They have watched her and Dean raise their children. And, they cried with her while they tried to comfort her moments after she received that dreadful call from the doctor on May 4th. 

Eleni's home office colleagues in Hanover Park, once Theo was diagnosed, immediately wanted to somehow make life a little easier for Theofanis and the Yianas'. Led by Mike Madsen (Eleni's boss and Dean's fellow political guru), colleagues and friends wanted to pitch in to get Theo an iPad 2. So, with that goal in mind, their creativity led them to design and order  "Support Theo Wristbands." These bright orange (Theo's favorite color) wristbands were offered in exchange for a $5.00 contribution. Through everyone's kindness and generosity, they raised enough money to purchase Theofanis his very own fully-loaded iPad2 with 3G service... and then some. While Theo is in the hospital, he uses "FaceTime," that allows him to speak with and see a live video of his sisters at home. They talk, make faces, act goofy, and share stories of their days. Also, the iPad has plenty of apps and games to keep Theo occupied and engaged throughout his many hours of treatment. The iPad has genuinely provided Theo with a great deal of comfort and happiness throughout his stays at the hospital and has kept his mind and hand-eye coordination very sharp throughout this ordeal. 

Frederick Chang and family have been extremely loving and supportive throughout Theo's journey to victory. Frederick is Eleni's friend and co-worker based out of California. Knowing that Theo is a Presidential buff and has ambitions of someday occupying the White House, Frederick contacted all the living former Presidents and President Obama, informing them of Theo's medical situation and desire to join their rank. Frederick's persistence netted responses from all but President Obama to date.  Presidents Carter and Clinton wrote personally to Theo, with President Carter writing a full letter to him. Frederick presented the responses from the Presidents to Theo in a wonderful binder and the gesture and the kind words are inspirational to him. Theo even displayed the binder in his hospital window during his last chemo cycle over the 4th of July, and he received quite a few "WOWs" from some very impressed doctors and nurses!  

In addition to all the support coming directly from colleagues, it's heartwarming for the Yianas' when expressions of encouragement pour in from co-workers' families.  Spouses, children, and parents of colleagues are praying for Theo. Children who have never met Theo, but have learned about him through their mom or dad and have read about him on this blog, are calling him a friend. When Dave Walczyk, a supervisor at the Hanover Park facility, brought home a flyer about Theo, his eight year old son named Zach decided to raise money for him. A determined young boy, he found three large glass jugs, made his father cut a slit through the cap, and began filling the jar with coins from his home. He took his cause to neighbors, explaining that he was raising money for Theo. When Theo saw the first jar that Eleni brought home with a note from Zach, he thought it was pretty cool! Frederick Chang's son, Travis also rallied his fellow Key Club members in California, where they raised money to send Theo an iPod with Greek children's music.   

Best wishes and prayers are also being sent from international colleagues. In Japan, Everpure employees there began working on hand-folding 1,000 origami paper cranes for Theofanis once they heard the news. They did this with the help of family members in their spare time. According to an ancient Japanese tradition, the folding of the paper cranes will grant a wish by a crane, such as long life or recovery from illness or injury. Along with a Japanese toy, the 1,000 prayers were shipped to Theo while he was in the hospital, and it brought color and life to his room and to the Yianas' hearts. 

Theofanis has received emails, cards, gifts, prayers and best wishes from friends throughout the US....from Minneapolis to Milwaukee, California to New York, and Florida to Seattle. Gifts and prayers have come in from each end of the globe, from Europe to Shanghai, China. Even colleagues from CPT, a newly acquired company in the Netherlands, sent a little something  to help keep Theo safe and healthy while he's immuno-compromised. With prayers coming in from all over the world, it demonstrates that the power of love and faith is strong everywhere!  

More and more bands continue to appear on the wrists of colleagues each day.  And as these friends express that they will wear them until Theo is cured from his cancer, Eleni and Dean feel extremely lucky and blessed to have their Pentair Family walking along side them during this journey. Thank you to all these wonderful people... colleagues, bosses, distributors, suppliers, and their families... for your personal generosity, support, encouragement, and prayers. 

THE SPOT

After Theofanis came home from the hospital on July 5, Eleni and Kosta tried very hard to keep Theo from getting another fever as he did after the first two cycles of chemotherapy. They did not want to go back to the hospital before it was necessary and Theo would be very upset to have another stay in between cycles. However, since the medicine was different for cycle three, they did not really know what to expect.  The doctors indicated that after the administration of the Cisplatin and Etoposide drugs, there would be much more nausea. To curb this, Theo was given round the clock doses of Zofran, Benadryl, and Ativan -- anti-nausea medications-- at various intervals. In addition, another side effect from the chemotherapy medication is lack of appetite. Kosta and Eleni had to ensure not only that Theo eat but that he stayed hydrated as he would need to get IV nutrition if he did not. Thankfully, Theo ate and drank enough to avoid the IV nutrition through much persuasion and explanation, and a touch of coercion. The nausea lingered, however. As Mom and Dad tried to drop one of the anti-nausea medications,  Theo would get sick again.  After about fourteen days, Theo finally was off all of the medications.

Kosta and Eleni were overly cautious during this round of recovery from chemo to protect him against exposure to any viruses or bacteria.  With the exception of a 30 minute outing to accept his baseball trophy, Theo stayed home and did not have visitors. Typically, after the first week to ten days back home after chemotherapy, the white blood cells dip very low and can cause a patient to become neutropenic, as had happened after the first two cycles. Eleni and Kosta awaited the first blood results with anticipation and were shocked to find that Theofanis' White Blood Cell Count and Absolute Neutrophil Count (ANC) were very high when they expected them to be very low. The doctors really had no explanation for this. As the days went by, the counts dropped and were more in line with the other cycles. After fourteen days Theo's WBC count was zero.  

As Mom and Dad were at work last Thursday, Theo's nose started to bleed. Both grandmothers were at home with him, Demetra and Sophia. Although, it was not bleeding profusely, the flow would not stop. After many feverish phone calls back and forth between Eleni, Kosta, home, and the hospital about what to do and where to go, Eleni raced home to take him to the local ER. But thankfully, the bleeding stopped. It was determined that Theo needed a blood transfusion. Kosta took Theofanis to Comer Children's Hospital on Friday for a blood transfusion and a platelet transfusion.  Although, Kosta and Theo spent virtually all day at the hospital, Theofanis felt a whole lot better afterward. Even better, he had no fever, so they were given the thumbs up to leave. So in return, Theo gave them a thumbs up as he left, happy that it was an outpatient day. 

Eleni and Kosta pray and give thanks to God that Theofanis  has been fever-free during this recovery period from Chemo #3. Theofanis' blood counts are being monitored closely. If they continue to increase at good levels, Theo will return to Comer Children's Hospital on Thursday, July 21st for the fourth cycle of chemotherapy. He will be admitted to the hospital for four days of chemo.  

WITH LOVE, FAITH AND PRAYER HE WILL WIN!

Saturday and Sunday were quiet, fun, and almost "normal" days for the Yianas family.  Theofanis was able to attend church and serve in the altar, too. Although still cautious about infection, Theofanis did receive some special visitors on Saturday. Nouna Evy and Nouno George came by the house before their upcoming trip to Greece. Theo was ecstatic to see his Godparents and so were Demetra and Sophia. Arms filled with presents and sweets for all the kids, they spent several hours with Theofanis, helping him complete his new Legos set. But their most precious gift was their news that Nouna will make a special pilgrimage to the island of Tinos. The Greek Isle of Tinos is where the holy place of Panagia's church of the Megalochari is located, as is the Monastery of Agia Pelagia. Tinos is a place of miracles. There, she will pray for her precious Godson. And from there, Nouna will bring back Holy Unction (Efchalio) and Holy Water for Theofanis.  "Kalo Taxidi" Nouna and Nouno, and may the lambada you light in Tinos burn brightly for our Theofanaki.  

When Theofanis is cured and has triumphed over this cancer, Eleni, Kosta, Demetra, Sophia and Theofanis will go to Tinos to echo their personal prayers of thanksgiving.


1 John 4:7, 11-12
Dear friends, let us love one another, for love comes from God... since God so loved us, we also ought to love one another, God lives in us and his love is made complete in us. No one has ever seen God; but if we love one another, God lives in us and his love is made complete in us.


Thanks to all that have shared God's love with Theo!

HOME FREE FROM CHEMO #3

 

It's been a couple of "roller-coaster" weeks for Theofanis and his family with ups & downs, happiness & disappointment, and acceptance that the word "stable" is not entirely bad. 

Following a successful shave-off and lemonade stand party, the Yianas kids spent their week at Vacation Church School. On their first day of VCS, they learned that "Nothing is Impossible with God." They not only sang it throughout the week, but Theofanis kept those words close to his heart during his hospital stay and chemo cycle.  The teachers and students at VCS were nothing short of wonderful. As he headed to the hospital on Friday, they bade him farewell with stacks of cards handmade by each student, and a scrapbook filled with memories of the week.

While his days prior to chemo were filled with stories and learnings about Jesus as a child in Nazareth, his evenings brought him some new experiences as well. He and his family went to their first baseball game together at Wrigley Field. The kind folks at Bear Necessities (organization that supports childhood cancer patients) arranged for Theo to see the Cubs play the Giants (or, rather see the world-champion Giants beat the Cubs). Nonetheless, the Yianas family got to go onto the field before the game, got an autographed ball, saw Theo's name on the scoreboard in the middle of the 5th inning, and even experienced the "bleachers." Theo was a bit overwhelmed at first, but gradually took in all the action around him. Life-long Cubbie fan, Dad loved every minute of sharing his passion for baseball with his son. No worries, the ladies in the Yianas family enjoyed the evening, too.

Theofanis had his first sleep-over with his best friend, Pantelis. They laughed, hung out together and played Wii.Theo was also thrilled that Pantelis cheered on his best buddy during The Angels' last baseball game of the season!  It was heartwarming to watch these two boys--friends since preschool--tell each other that they were having the "best day ever!"  Head to head, they each cuddled in their sleeping bags on the floor, too excited to fall asleep and so excited that they were up the next morning at 6 am!

Theofanis was having "two thumbs up" days...every day! Even though he had to miss VCS on Thursday for his first MIBG scan, he didn't let his disappointment overshadow all the wonderful events of the week. He went into Chemo Round #3 feeling good, feeling happy, and feeling loved!

THE SPOT

Theofanis had his MIBG scans and a CT scan prior to being admitted at Comer Children's Hospital for his third (and most difficult) round of chemo. Eleni and Kosta were anxiously awaiting the results of his tests. On Thursday, they received good news that the bone marrow biopsy showed no signs of neuroblastoma cells. His bone marrow is clear! As their son so bravely sat motionless for a cumulative 3+ hours for the scans, they prayed that they would see a smaller tumor on his adrenal and signs of tumor regression in his arm. When the doctors approached them with the results that the size of the tumor on the adrenal did not change and that the cancer in his ulna was still active, Eleni and Kosta's hearts sank. They so desperately were seeking signs that the tumors were shrinking. There was good news, though, that the doctors delivered and insisted they focus on...the cancer did not spread. It has not progressed. It is stable.  All the doctors told them that because Theofanis' has a relatively low level of disease (relative to those children whose organs and bone marrow have been completely overtaken by cancer) that it is not uncommon that the first two rounds of chemo don't show significant shrinkage. As Dr. Cohn said, Neuroblastoma cells are difficult to kill and that's why the treatment plan is long and aggressive. Every doctor saw the fear in Kosta and Eleni's eyes and all tried to reassure them that they feel good about how Theofanis is responding to treatment. They also wanted them to focus on the clinical signs of improvement, particularly on the fact that Theofanis no longer has pain in his arm.  But, in desperate need of some visual proof that the cancer is going away, Eleni and Kosta asked for another x-ray of his arm. Although an x-ray doesn't show any image of the tumor, they wanted to compare any changes in calcification in the area where the cancer cells are buried. The doctors agreed to their request, and the x-ray did confirm that the bone is showing signs of healing.

They prepared for Chemo #3 with mixed emotions: Relief that the cancer has not spread. Sadness that it's still in their son's body.

• Chemo Day 1 @ 11:00 pm: Etoposide & Cisplatin. 1 hour infusion each. 
• Chemo Day 2 @ 11:00 pm: Etoposide & Cisplatin. 1 hour infusion each.
• Chemo Day 3 @ 11:00 pm: Etoposide & Cisplatin. 1 hour infusion each. 
• Chemo Day 4 @ 8:00 pm:  Cisplatin 1 hour infusion.

Prior to starting chemo, the U of C Hospitals pharmacist met with us to explain the harsh nature of these drugs, particularly Cisplatin, which causes severe nausea and delayed nausea. He suggested to begin controlling vomitting by starting a "three drug cocktail" around the clock:  Zofran, Benadryl and Ativan. The drugs were able to suppress any violent nausea, but he did often need to "get the yuckies out." The Benadryl and the Ativan made Theofanis very drowsy. We could tell he was unstable on his feet when we would go to the playroom for a change of scenery. Because the chemo was administered in the middle of the night, he was able to visit the playroom a couple of times where he played basketball and football on the XBOX system.

Theofanis required extra hydration during this round of chemotherapy. Upon discharge, Eleni and Kosta were told to pay special attention to his fluid intake and nutrition. And, because Cisplatin has the tendancy for intense delayed nausea, the Yianas family left for home on Tuesday with concerns and worry of not only Theofanis getting a nutropenic fever, but also worry that he will not be able to keep down any food or fluids. So, they left with prescriptions that made up the "three drug cocktail."  Not knowing what kind of delayed nausea Theofanis might have, they started out giving him two anti-nausea meds around the clock. When on Wednesday, Theofanis could keep no food or water down, Eleni and Kosta added the third anti-nausea med. Today, Theofanis threw up only once and was able to drink a good amount of Gatorade throughout the day. But, the side-effects and drowsiness concern his parents who are hoping to wean him off the drugs as soon as possible. A slight scare in the shower when Theofanis became dizzy and unstable, raised panic that all these drugs cannot be good for him. Eleni and Kosta's prayers strengthened for Theofanis' treatment and cure quickly follow each other. 

WITH LOVE, FAITH AND PRAYER HE WILL WIN!

Theofanis spent the 4th of July holiday weekend in the hospital. To spruce up his view, he drew pictures of the United States, our flag and fireworks with window markers. His doctors and nurses commented on his window art, and they also mentioned that they read about him in the paper! Demetra and Sophia visited on the 4th of July, and the whole family spent the day together hanging out in his "red, white and blue" patriotically decorated room (thanks to the Guth Family for sending a very special Independence Day care package), doing activities in the playroom, and sharing three simple, but special meals together. Fireworks could be heard outside. But, the celebration was inside because the Yianas family was together.  

Everyone's outpouring support of love and compassion continues to humble the Yianas family. Eleni and Kosta feel deep gratitude to everyone each time they put a smile on their son's and daughters' faces. Every little thing that people do to help lift their spirits is cherished. And every time they are told they are being prayed for they feel comforted. 

So, here are some extra special things some extra special people did for the Yianas family. Each one deserves an extra special thanks, too!

• All the fantastic teachers at St. Demetrios, lead by Presbytera Dimitra, organized and put together a wonderful, memorable and inspiring week of Vacation Church School. Thank you for all your work, dedication, and committment to all the children of our community. Thanks for taking extra special care in protecting Theofanis from germs. (You all did great because his wbc's were at a low 2.2 when he was admitted, but he was able to stay strong throughout his chemo infusions.) Thank you for letting Kosta and Eleni help out in the classroom whenever we could. (Sign us up for full time next year!) Thank you for promoting the Support Theofanis bracelets. Thank you for making Theofanis, Demetra and Sophia feel loved!
• Wishes and prayers from all of Eleni's wonderful friends and co-workers from Pentair has continued to poured in.  From "Theo" bracelets, to an ipad, to 1,000 origami prayers and letters from 4 living U.S. Presidents (1 still pending), the Yianas family's "Pentair Family" throughout the globe has extended an incredible amount of support to Theo. The next blog posting will feature some of the wonderful expressions of compassion and support that have come from co-workers and family members. (There are way too many to write about today, in this already long blog posting)!

• Dimitri Pagonis, our church's parish council president, arranged for Theofanis to have some extra special visitors during his stay at the hospital.  As Theofanis' love of soccer spurred him to mention that he "can't wait for soccer to start in the Fall," the manager of The Chicago Fire surprised Theofanis with an official soccer jersey signed by all the professional soccer players on our hometown team! Frank Klopas and Nick Kounenakis (former Greek league and MLS player) visited Theofanis and spread some cheer. Even though he was a bit groggy from his meds, he thought they were cool and plans to take Frank up on his invitation to go to a game and hang out with the players on the field! Theofanis actually wants to play with them, but it's not certain whether the referees will go for that! A million thanks to Demetri, Frank and Nick!
• Thanks to our other visitors, too! Elaine, Kimberley and Pantelis...thanks for the smiles, the goodies, and food!