Showing posts with label Georgetown. Show all posts
Showing posts with label Georgetown. Show all posts

Saturday, July 21, 2007


The "aunt" is Aunt Jen, and Minneapolis is actually St. Louis, but otherwise, this is a nice snapshot of what happened today. There were parties in St. Louis and Georgetown. Fairview is just giving out the books like they did last time (hopefully on the meal trays) and the Hackensack party is Monday.

We finished up at Georgetown and drove 9 hours up to Massachusetts to pick up Jack at camp. It has been a long day. We see Jack tomorrow. Yea! Love you.

http://www.abcnews.go.com/Health/story?id=3401421&page=1



Harry Potter the Healer
With Book Release Party, a Magical Dose of Medicine in Pediatric Cancer Ward





Theresa Hammann, 6, right, attends the release party with her brother William, 3. Theresa's black curls are returning after recent chemotherapy treatments. (Molly Frances Norris, ABC News)

By MOLLY FRANCES NORRIS
July 21, 2007—

Young patients had their Harry Potter fanaticism nursed for a change at Georgetown University Hospital's Lombardi Cancer Center here in Washington today.

The children gathered in the clinic dripping with Potter-themed decorations. Some wheeled IVs and spoke from behind face masks guarding their weak immune systems -- features that faded when donning thick Harry glasses and Quidditch player capes.

"This party is for children undergoing chemotherapy and other difficult treatments who are missing out on some of the joys of childhood. It's to deliver some fun during what can be a bleak time," said Laurie Strongin, talking with a volunteer.

Strongin's son's passing at the age of seven after a life-long struggle with a genetic disease motivated her and her husband to start a foundation in his memory called Hope for Henry. They shower young patients with the finest tools of distraction -- personal DVD and mp3 players, Ninetendo Game Boys, digital cameras and other consumer electronics.

Pediatrician Brooke Trenton watched some of her patients bounce around eating cake and waving plastic wands at 10 a.m.

"Kids need a break from what they're going through," Trenton said.

She added the three hour party was already making for an easier morning for everyone in the oncology hematology clinic.

Outside of the hospital, some worry about the swell of darker themes embodied in the very title of J.K. Rowling's final installment, "Harry Potter and the Deathly Hallows." Strongin said the sinister undertones speak to children fighting potentially fatal illnesses.

"They understand things that healthy kids don't. Threats and danger lurking goes along with their life experience," said Strongin.

"Harry Potter is a symbol. Harry went through so much adversity," added Strongin. "With determination and courage, and lots of help from friends, he pulls through."

The foundation is a result of bonds forged through Henry's illness. An aunt in Minneapolis, Minn., lined up with the Strongin family to buy copies at midnight for another release party at a hospital where Henry once received a bone marrow transplant.

At four hospitals nationwide, 275 copies of "Deathly Hallows" were bought for patients who may have been to sick to line up at bookstores.

Subhan Jamil, 19, came down from his hospital room for a free copy of "Deathly Hallows." He's spent about a year here after spending one semester at college.
"I never thought I would say this, but I miss school," said Jamil.

He used to major in accounting, but now he wants to work with children, or maybe be a journalist.

When talking about the Sony PSP he received from the Hope for Henry Foundation, he said, "My time passes faster. It's pretty boring usually."

Maybe less so on a day with gummy rats and a few black witches' hats.

Copyright © 2007 ABC News Internet Ventures

Tuesday, June 12, 2007


This is a video from the Super Hero party that we had a few weeks ago at Georgetown. Hackensack and Minnesota had parties too. The party was in the Lombardi clinic, but this movie is from upstairs on the 5th floor. We took the party to the kids who were in isolation and couldn't come to clinic.





"Henry's spirit will live on."

We went out to the cemetery on Sunday. The weather was really nice. We visited Zack Klein, who is so close to you now. I tried to help Zack's mom and dad get something special on his headstone. Unfortunately, it isn't going to happen. I can understand why, but it is still a disappointment.

The next thing that I am trying to make happen is making sure Molly and her mom meet Jon Bon Jovi. That should happen in July. I cannot fail. I'll keep you posted.

I have been spending a lot of time organizing our pictures. There is (are?) a ton. Which is good. I am going to make a big "Henry at St. Michaels" photo book to put out there. I am going to match pictures of you taken in St. Michaels with nice pictures of birds and trees and things that we've taken out there.

Last week was a tough Henry week. Mom and I spent a lot of time thinking of you and crying. Mom rewrote one of the chapters of her book and it is great. It is about you and Bella. All that came from nowhere. I am glad it happened.

Tuesday, May 29, 2007


One idea I had a little while ago is to compile a photo gallery of Team Henry. I am going to post pictures of your doctors. We just got a newsletter from Georgetown and there were two different pictures of Dr. Shad. I think it is an important part of my Digital Henry project. There are people who are documenting every moment of their lives in real time with digital pictures, websites visited, documents written, you name it. I wish we could have done that while you were alive.

Mom said that her memory is failing her a bit when it comes to you. That scares me more than anything.

We went to a barbeque at the home of an old friend of mine and Uncle Bill. Her name is Ellen and we haven't seen her in about 15 years. She would remind me of things that I had completely forgotten, and I remembered things that she didn't remember. It is good to have other people fill in the blanks from the past.

I had people email me their best Henry stories when you were about to die. Unfortunately, I don't think I still have those.

Tuesday, March 06, 2007


I want to take some time in the next few weeks and explain to you my new job. It is kind of "out there." We use fMRI's to look at people's brains while they are watching TV ads. It is a long way from the radio business, but it is another new technology and I like that.

This weekend when we were at Georgetown Hospital, I walked through the Radiology Department and remembered all of the CAT Scans and MRIs that you used to get. They have a pretty thick file on you. Maybe I should go grab all of that film before they toss it. That could become part of my digital Henry project - Henry Inside and Out.

This is a TV commercial that I am in from a long time ago. I was walking down the street in Austin, Texas with my friend Edmond. The people doing the commercial asked me what I though about a McDonalds hamburger being only 49 cents. I thought that was "Excellent." I wonder what people's brains would think about me.



Maybe the best part of the commercial was the "Premiere" party my friends and I had to view the ad for the first time. We catered the party with McDonalds hamburgers, french fries and a keg of beer.

I'll write you more about what I am doing soon.

Sunday, March 04, 2007


Sunday night might be my favorite time of the week. Tonight I got to sit in the bathroom and watch Joe take a shower. I tell him a number, letter or shape and he writes or draws it with his finger in the mist on the shower door. All the while he is humming "Iron Man" by Black Sabbath. Your brothers are interesting pieces of work.

We are going to Zack Klein's funeral tomorrow. He was an incredibly sweet kid. I feel terrible for his parents and his sisters. I called to see if I could sit with his body but they had enough people, which is a good thing. I sat with Grandma or Aunt Ida, and parents from JPDS sat with you. You stay with the body at the funeral home and read psalms so they are never alone.



On Friday, March 2, 2007, of Bethesda, MD. Beloved son of Greg and Cynthia Klein; beloved brother of Janie and Lily; cherished grandson of Marty and Stephanie Klein, Audrey Horowitz and of the late William Horowitz.

He is also survived by many other loving relatives and friends. Funeral services will be held on Monday, March 5 10:30 a.m. at Congregation Beth El of Montgomery County, 8215 Old Georgetown Rd., Bethesda, MD. Interment Judean Memorial Gardens, Olney, MD. Shiva to be annouced at service.

If you would like to make a donation in Zachary's honor please contact A-T Children's Project at: www.atcp.org Arrangments by HINES-RINALDI FUNERAL HOME INC., Under Jewish Funeral Practices Committee of Greater Washington.


From: parents-owner@mail.jpds.org [mailto:parents-owner@mail.jpds.org] On Behalf Of Julie Fisher
Sent: Sunday, March 04, 2007 2:44 PM
To: parents@jpds.org; staff@jpds.org; alumniparents@jpds.org
Subject: [parents] Additional information about Klein Shiva

The funeral for Zachary Klein, son of Cynthia and Greg Klein, brother of Janie and Lily Klein, will be held at Beth El at 10:30AM tomorrow (Monday).

Internment immediately following at Judean Gardens.

Tomorrow (Monday) beginning around 1:30PM and continuing until 7:00PM the Kleins will be receiving visitors at the home of

Stephen and Susan Sherman
8004 Westover Road
Bethesda, MD 20814

Tuesday, shiva will be from 6:30-8:30PM at the home of Cynthia and Greg Klein

8302 Garfield Street
Bethesda, MD 20817
301-986-8662

Also on Friday, Cousin Adam and Lori had a baby. His name is Nathan Goldberg. I wanted to name you Nathan Goldberg, but Mom said "no way." My grandfather was named Nathan. I thought Nathan and Nate are good names. Mom thought otherwise -- so you were Henry.

This has been an incredibly full weekend.

Cousin Ron -- Nathan's uncle -- Diane, Zoe and Mia all came over for brunch on Saturday morning. Bill, Cristina, Sophia, James and Isabel came over too. It was crazy and fun. They all live so close in Virginia, McLean and Arlington, and we hardly see them. We made a deal that we'd all get together for brunch at least once a month at someone's house.

On Friday night, Sid, Linda, Ari, Helaine, Jake, Abby, Susan, Simon and Alex all came over for Shabbat dinner. We are truly one big, funny family. Last night we went to the Megillah reading at Adas Israel for Purim. Everyone got dressed up. I think my favorite was Jake wearing a cheerleader uniform.

Jack is in the sweatshirt, Joe is a Redskin, Max is an IDF soldier and Ari is just looking suave.




Today, after Joe's baseball practice (he has been asked to be the bat boy for the 6th grade JPDS baseball team),



we went to Georgetown for a Hope for Henry Superhero Party. It was in the atrium outside of the outpatient clinic at the Lombardi Center. There were a lot of families there. They came to the hospital on a Sunday which is saying a lot.

Mom did such a wonderful job that she definitely made it worth the trip on a "non-clinic" day for all of the families because the kids had a great time.

Here is a slideshow of the event.



After everything was in full swing, we went up to the 5th floor to bring some of the party to the kids who couldn't leave their rooms. While we were in the hallway, a mom and her son were walking out but stopped to introduce themselves. She said that Hope for Henry had really made a difference for her son. We gave him an XM radio. The mom told us that she and her son had read an article about you. The son was cured of his cancer, and they were leaving the hospital that very moment to go home for good. Talk about timing.

Everyone started crying. It was an incredible moment.

There was another amazing moment right after that. Mom went into the room of a kid who had just come in minutes before by Medstar helicopter. The pilot and the EMT workers were still on the floor filling out paperwork. The kid had brought a Spiderman toy with him on the helicopter, so you can guess how excited he was to get a bunch of other Spiderman and superhero toys and treats.

A nurse was in the boy's room and when he found out that Mom was your mom, he said that "Henry's spirit is truly living on through all of the good work of the Foundation." He said a ton of really nice things about you and about the Foundation.

While I was on the floor I read a quote tacked up on one of the bulletin boards. It was something that Abraham Lincoln said. And that was back when Presidents of the United States actually wrote their own stuff. He said,

"To ease another's heartache is to forget one's own."

Thursday, January 11, 2007



Kabir is a kid who Dr. Shad was treating at Georgetown. The Hope for Henry Foundation gave him the Harry Potter books and Disney videos. I also loaded up for him a video iPod with some Disney movies and Harry Potter audio books. I hope he is using that on his flight back to India.

I have a lot of pictures of him. I will put some up on here.

This is a very sad story.



Teen Leaves 'His Only Hope' Behind in U.S.

After 20 Months, 14-Year-Old With Leukemia Returns Home, Saying No More Chemotherapy or Bone Marrow Transplants

By Susan Levine
Washington Post Staff Writer
Thursday, January 11, 2007; B01

They had spent a tiring weekend boxing up his Harry Potter books, his Disney videos, the games that had helped sustain 14-year-old Kabir Sekhri in this foreign land. And as his mother and father checked off their final packing details, so did Kabir's doctor. Her list included sterile dressing kits and needles, gamma globulin and antibiotics, methadone for pain -- enough to last him until spring, she had decided.

If only she could guarantee that his cancer would allow him that much time.

These were not the preparations anyone had envisioned when Kabir and his parents, Vikram and Sonia Sekhri, came to Washington from New Delhi almost 20 months ago. They had hoped for a triumphant return to India, a declaration of victory marked by the full recovery of Kabir's health, animated smile and thick, dark hair.

Instead, when the family arrived at Dulles International Airport late Tuesday afternoon, a frail-looking Kabir rode in a wheelchair. A navy knit cap concealed the damage wrought by chemotherapy. His leukemia had kept coming back with more and more vengeance until he unequivocally declared that he was done.

It was a wrenching decision, not only for his parents but for his oncologist, Aziza Shad, who had led his care at Georgetown University Hospital. Yet it was a decision they all felt compelled to honor.

The victory now was simply that he was there at the airport, stable enough medically to endure two long flights halfway around the world. Shad bent low to ask Kabir how he was feeling. She would be traveling the more than 9,000 miles with him.

"I made a promise I would get him home, and I need to stick to my promise," she said.

The journey on which they had embarked was not all that different from the journey many families take. Still, something about Kabir's gentle, uncomplaining manner and his extraordinary distance from home prompted the hospital staff and other patients and parents to embrace him in a singular way. The Sekhris reciprocated. And somehow, despite all the heartache, his mother found blessings. "God's been very kind," she'd say.

Kabir was 11 when he first became ill, and the doctors initially attributed his aches, fatigue and swollen lymph nodes to an infection. When his symptoms didn't respond to the usual medicine, they looked further. The correct diagnosis -- of T-cell acute lymphoblastic leukemia -- came the same week that Kabir's grandfather succumbed to throat cancer after years of grueling treatment. "That was a tender moment for us because we had seen all the treatment fail," Kabir's father recalled. "We thought, 'How can a child go through this?' "

The Sekhris quickly learned. Kabir's particular disease assaults children more than adults, especially older boys, and it carries a poorer prognosis than other pediatric cancers. Though his body responded well enough to the early chemotherapy to put him in remission, he had not completed the full regimen when he relapsed.

"If you really want to do something for him, take him to America," their oncologist in India advised. The newest drugs were available in the United States, as were the best centers for the bone marrow transplant that probably would be needed to save his life. As his mother remembers, "We were told this was his only hope."

They boarded a plane in May 2005, leaving behind Vikram's leather goods business and everything Kabir knew: his beloved sister and the aunts, uncles and cousins who make up the Sekhris' close-knit extended family, the friends he had played with his entire childhood, the dusty, teeming city of Delhi. A relative in Falls Church had contacted Shad, head of the pediatric oncology division at Georgetown's Lombardi Cancer Center. Would she evaluate his case? Did she think he had a chance?

Yes, she did.

Four months of highly aggressive chemotherapy drugs ravaged Kabir but pushed his body into a second remission that made him a candidate for a bone marrow transplant. The perfect donor: his 16-year-old sister, Ridhima. She flew from India, and the family traveled to Duke University Medical Center for the procedure. The graft took well enough that when Kabir returned to Washington in early 2006, he was out of the hospital far more than in it, giving him a chance at memories not integrally tied to pain.

He went to New York, visiting the Statue of Liberty and gawking at Times Square. He also became an enthusiastic camper at a National Institutes of Health program for children battling cancer, canoeing and riding horses and even trying fencing.

"I want to come back from India every year for this camp!" he exclaimed upon his return.

The Sekhris started counting the days to the first anniversary of Kabir's transplant. By September, it seemed likely that they would make it, which would mean that Kabir would be able to be fly to India in time for a cousin's wedding celebration. He'd already bought new clothes.

He never wore them, however. The one-year checkup at Duke revealed a second relapse. The news was shattering. "Everything came to a standstill," his father said. In an instant, wedding travel became impossible, as did his son's greatest hope: to tell everyone back home that he at last was well.

Kabir was readmitted to Georgetown, and the weeks that followed deteriorated in a horrific downward spiral. He rejected any talk of another transplant but acquiesced to Shad's entreaties for one final attempt at chemo. She tried different toxins and combinations as her patient grew ever weaker, wracked by days of extreme fevers, numbness and bleeding. He stopped eating and virtually stopped communicating. When he did talk, he'd say plaintively, in a wispy voice made almost childlike by the drugs: "I just want to go home." Shad feared he'd never leave the hospital.

But just after Christmas, after the final drug in Western medicine's arsenal, a bone marrow biopsy showed the unexpected -- a partial remission. No matter, Kabir reminded her; he'd said he was finished. But Shad, who has a son just one year younger, still is struggling with that. "All I know is that this child gave it his best," she reflected late last week. "He gave it again and again and again and again."

On the afternoon of his departure, the staff at the Lombardi Center threw the Sekhris a cake-and-tears send-off. Then the family and Shad headed to Dulles. Kabir might have wished he'd seen more of America. "I would have liked to have gone to Disney World," he admitted. Not this trip.

His small entourage proceeded to a secluded alcove of an airport lounge. Kabir snacked on french fries, glimpsed at long last the swirling white magic of a brief snow shower and fell asleep under the handmade quilt given to him at the hospital.

"It's time," his mother quietly roused him. The teenager sat up in an instant and readjusted his navy knit cap. And as his parents followed close behind, an attendant wheeled him the final distance down the corridor to gate 32, through the last checkpoint and onto the plane.

He never looked back.

Tuesday, January 09, 2007


On Sunday we had a big Hope for Henry event at the AFI Silver Theatre in Silver Spring, which is near where Aunt Tracey and Uncle Andrew live. We showed superhero cartoons and Batman, Superman and Wonderwoman were there. Kenny Curtis, who I worked with at XM, was with us too. He and Jack did a superhero trivia contest and we had a costume parade. I think it was a lot of fun for the parents and the kids.

Since most of the kids came in costume it made me think of the superhero party we had when we all left for Minnesota and your transplant.

People brought superhero toys for us to give to the kids in the hospital. We also raised a lot of money for the Foundation. One of the young people we helped spoke to everyone. She was a patient at Georgetown and now is more than a year out.

It was very emotional.

We will probably do this every year. Mom did a great job on this event. She is amazing.

Our buddy Hugh is who drew this great Hope for Henry superhero. We got a letter from DC Comics because they didn't like that we were using the word "superhero" because they own it. Crazy, huh, especially since everyone bought so many DC Comics action figures for the kids in the hospital.

















Sunday, December 03, 2006


Had a perfect morning. We let Mom sleep really late. Jack watched cartoons and read the Sunday comics. Joe and I played on the couch under a blanket. It was nice. It was also the only way to keep Joe quiet. He continues to be/play really loud. I wish I had his energy. What I need to do is get up and get him out of the house so he can run around. He really is like a puppy.

I really appreciate any quiet moments with him. I ended up going upstairs to take a shower and he laid down on the bathroom floor with my clothes as a pillow and the towel as a blanket. We had a nice conversation as I took my shower. He is super cute.

When we went back downstairs I showed him this video of you. I took this video the day he was born. You were in the hospital at Georgetown and Mom was in the hospital down the road at Sibley. Before this clip of you is video of him being born. I showed that to him and he said "disgusting." He has an excellent vocabulary.

Joe smiled the whole time he watched you. He wanted to watch it over and over.

After I filmed you I filmed Jack doing the same thing --saying hello to his new brother. In the video Jack says he is going to take care of Joe, his new brother.

When I showed that to Joe this morning he said he wanted to make sure that I would show it to Jack. When I showed it to Jack later on today he said that he broke that promise to take care of Joe. I told him that he has plenty of time to make good. It isn't too late.

I have been having a lot of trouble getting pictures and video on here lately. Strange. I went back and put on a few pictures of Thanksgiving.

Henry TV!



This video doesn't look so good, but it helped me figure out a way to make them better. I will try to go back and fix all of the others, but it will take a lot of time.

The rest of the day was pretty great except the Redskins lost. After the game Joe, Jack and I went out and played football at Stoddert until it got too dark. We needed you out there. We always have to play two men on offense and one on defense. I try and get Jack to go easy on Joe but I have a sense that he would like to put a good lick on him if he had the chance. Just a little payback for Joe being an annoying little brother.

Jack, to his credit, does show great restraint, which means he doesn't wallop Joe. I wonder what it would be like if you were around.

Tonight a Maryland basketball game is on TV. You were such a big Juan Dixon fan. Hopefully they'll be that good again this year.

I got to let Mom sleep late and play football with the boys. If the Redskins had only won... and if Maryland were to win.... well, then I would have to put this day in the perfect category. Of course if you were here then it would be a dream.

Love you.

Monday, October 30, 2006


I was cleaning the basement yesterday and I came across this letter. That was your last birthday.



I saw a story on the news while we were waiting for our plane in St. Louis about a young guy, Jeff Newbauer, who had cancer and was visiting every ballpark with his dad. He was scheduled to come to see the World Series in St. Louis last Wednesday, October 24, but got too sick to make it. He died on your birthday, October 25. He'll be buried today.

The Cardinals ended up winning the World Series. On Friday night I snuck upstairs at Aunt Tracy's birthday and watched the final game. The Tigers lost but the people up there do have the University of Michigan to cheer for now. I am very excited for the game next week.

On Saturday night we all went to Cousin Rachel's birthday dinner. Jack and Joe ended up spending the night with Michael and Joshua.

Let me tell you a little story about your Cousin Michael. Michael, Rachel and Joshua went to the doctor the other day for their annual checkup. Michael and Rachel were clear to get their flu "shot" in a nasal spray, but because of his asthma, Joshua had to get his in a shot with a needle.

Michael didn't want Joshua to be scared so he said he took the shot with the needle. That says a lot about Michael. With Michael's help, Josh was very brave and had no problem with his shot. They are all such good kids.

Yesterday we went to Joe's last baseball game of the year.





It was also the 31st Marine Corps Marathon. They run through Georgetown. Uncle Andy went down to watch a friend of his run. It is marathon season. Richard just ran the Baltimore Marathon and is thinking about running in the London Marathon. We had your heart surgery in Boston when they were running the Boston Marathon. That one is in the spring, though. I get kinda bored running though I like the idea of the challenge.

Mom and I were talking about how we went to watch Bill run in the Marine Corps Marathon the morning after I asked her to marry me. The marathon was October 25, 1992, so I asked Mom on October 24. It would have been neat had we got engaged three years to the day before you were born. Close enough.

Bill gave you his medal that he got from a later Marine Corps Marathon that he ran. You really liked it. It is in my top drawer with your teeth and some other stuff. You know he also got a medal for being brave in war. Maybe we need to make Hope for Henry medals for kids in the hospital.

Sunday, October 22, 2006


It is the start of the Henry Birthday Pageant. All of your doctors came into town for it.

Actually, there is a meeting of the Fanconi Anemia Research Fund in Bethesda that they have all come to attend. On Thursday night we went out there with Joe and Jack to say hello. We saw Dr. McMillan, Dr. Auerbach and Lynn and Dave Frohnmayer.

There were a few other "Fanconi Families" there. One family is the McQueen's of Richmond. I wonder if they know about Jared DeMarco. The McQueen's are super nice. They are raising a lot of money for research. I met the kids for the first time. There is a daughter and the little boy, Casey, has Fanconi.



He is 7 years old. Very handsome guy. I had the usual feeling of just wanting to hug him tight.

It was especially nice seeing Lynn and Dave. I was remembering when Dave had a heart attack when he was here in Washington years ago. You were still around and must have been well. We lent Lynn our car and tried to help them out as much as possible. Luckily he was in a room full of doctors when he started to have trouble. He came through it all okay.

Lynn and Dave lost 2 daughters to Fanconi and their other daughter, Amy, has FA too. She is in college. There are two sons as well. Honestly, I do not know how they do it. On top of running the Fanconi Anemia Research Fund and being a parent, Dave is the president of a college. That is a huge job.

Last night we went out for dinner with Dr. Auerbach. It is always nice spending time with Dr. Auerbach. She said that Dr. Gillio was here for just a little bit and then headed out. After dinner we met up with Dr. Wagner and his wife. We talked a lot about you -- one of my most favorite things to do. Dr. Wagner remembered how he used to see you at hotels and Georgetown when he came to DC. Mom and I learned a lot more about you and what happened, and how Fanconi transplants are going now. They are going much better. Timing. Timing. Timing.

Dr. Wagner is an amazing man. You and Fanconi Anemia let me and Mom meet really remarkable people -- people who we probably would never meet otherwise.

We talked about the fact that you've been dead four years. To me that is officially way too long. I can't say, "he died a year or so ago," anymore. I think I wrote "dead" here because it is harsher than "gone." I feel like you've been dead, not gone.

Dr. Wagner, Dr. Auerbach, Dr. Hughes, Lynn and Dave are Tzaddikim. A Tzaddik is a righteous person. I feel fortunate to know them. I feel fortunate to know there are people like them who devote themselves to saving lives. It makes me feel hopeful.

Yesterday during the day we went to a farm with Susan, Simon and Alex. I asked Mom about the pictures we took of you and Jack at Butler's Orchard. She is going to find them for me.







Today we went to a book signing at Politics & Prose. Jeffrey Goldberg wrote a book. Mom just read it and I will read it when she is finished. I think it will be weird to read about someone you know. Maybe that is why I haven't read all of the book that Mom has written about you and her.

I remember buying Harry Potter CDs at Politics & Prose with you and Jack. Jack was psyched he went with us today because some of his Gan buddies were there, Sam Shoyer and Jacob Stern. Both of you made the best friends there. Mom and I are a little worried that Joe doesn't have any close friends like you and Jack have.

We are going to go with Simon to Cactus Cantina on Wednesday night for your birthday. Ari and Jake, are coming too. Today I was looking at the picture of the four of you -- Henry, Simon, Ari, Jake -- that I have in my Henry memory box. That made me sad. Mom is really sad right now too.

Twice in the past few days someone has asked me, "Do you know what the worst day is?" One was a friend from work and he answered his own question, "the day we start daylight savings time." The other person was Jack. He said the worst day is the day before school starts.

I didn't say anything when they asked that question, but my mind was shouting "October 25!" I think that is the worst day until December comes around and then it is definitely December 11.

The Cardinals are in the World Series. We are pulling for them. I hope Aunt Jen gets to go to some games. She went to one of the Championship games. I don't know if Cousin Hannah and Uncle Dan got to go.

Hey, I wanted to tell you a funny story. We were telling Papa Teddy about Jack's saxophone lessons and he told us how we came to have the instrument. Your great-grandfather was a used car dealer in Brooklyn. He bought a car from someone or someone traded in a car and guess what they found in the trunk.

Friday, September 15, 2006


We had our 5% day at Whole Foods yesterday.



What an awesome balloon, huh. I like Whole Foods 'cause they give away balloons to kids. I'll shop anywhere that gives away balloons and lollipops. In high school when I worked at Sears at Montgomery Mall I would suck on the helium tank we used for balloons. I'd answer the phones with my voice sounding like the Mayor of Munchkinland. That was a great job.

The 5% fundraiser was a lot of fun for everyone. Jack and Joe ran around the store a lot. They gave out these stickers to all of the people buying food.



They are great salespeople.



The people working at Whole Foods were great, too and a lot of our friends came by and shopped. The money we made goes to Hope for Henry.

Nana and Papa Sy helped out and Pop Pop Teddy and his friend Jeri helped too.





--------------------------------------------------------------
From: Fadia Jawdat (MA GTN)
Sent: Friday, September 15, 2006 1:35 PM
To: Goldberg, Allen
Subject: RE: Thank you!

Mr. Goldberg,

The pleasure was ours. Please see below the content of the email I wrote Laurie this morning.

You and your family were amazing, and yes of course you boosted sales. We were happy to see so many of your friends and family members in the store.

I can only compare to last week’s Thursday sales and in that we saw a 9% increase for the day, even though last week was a little unusual in that it started off with Labor Day Monday. I think the work you all did in putting the word out, the ad, the stickers and above all your presence was outstanding. It felt like one big party and we were so thrilled we could present you with that opportunity.

I will strongly recommend you try our Rockville or Kentlands stores for next year for their consideration.

We love Katie and Mamadou too. I will forward your appreciations.

Warm regards from us all at WFM GTN.

Fadia


“Laurie,

Thank you all for being such an amazing presence and bringing in so many wonderful people.

It was a joy to host Hope for Henry Foundation. You will be receiving a check for $4,557.40.

Please email or call me with your FED ID # so I can put the check request through immediately.Also let me know if we should have a photo op with us presenting the check.

As for the real thing, would you like to pick it up at the store or would you like my regional office to mail it out.
Awaiting your reply.”


Fadia Jawdat
Marketing Specialist/Community Liaison
Whole Foods Market Georgetown
2323 Wisconsin Avenue NW
Washington, DC 20007
202-333-5393
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Friday, June 30, 2006


This morning I dropped off a computer we bought for a kid at Georgetown. He is sick. His mom, sister and aunt have all died from the same thing he has. He really wanted a computer. Hopefully this will help him some how.