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39 Posts authored by: Christine Lazzari

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Non-Hodgkin lymphoma survivor, honored patient hero, Light The Night Walk Fundraiser, First Connection volunteer and Survivor mom extraordinaire, Christen Reilert is Giving and Getting. When you participate in Gap's Give and Get program, you're supporting people like Christen, who know the importan

Patient Story: Christen’s little miracle of hope

ce of funding life-saving cancer research.

 

Download your LLS coupon today and use it in any Gap, Old Navy, or Banana Republic store from March 18th -- 21st.

 

Give and Get with Gap and LLS this spring and take advantage of a 30% discount while you support The Leukemia & Lymphoma Society's work to cure cancer and improve the lives of patients.  Christen, we profiled you and your amazing story on an LLS Blog post last fall (see: Patient Story: Christen’s little miracle of hope). How are you doing?

I'm doing very well, thank you -- and so is my 'miracle of hope' Jaden!            


You were diagnosed as a Young Adult with non-Hodgkin lymphoma (NHL) -- how did you get through your treatment regimen?            

I credit my family and friends - but mostly my husband. When I lost my hair and went bald he told me every day how beautiful I was and how much he loved me. And I'm thankful for my Mom who went to every single treatment with me. That got me through!            

 

I'm going to ask you two questions that Gap is using in their Ready, Set Give and Get contest because we think you epitomize what it means to Give and Get. First, what have you done to make an impact on your community?            

The moment I was diagnosed with cancer I knew I had to survive and that became my entire focus. I had a very aggressive treatment that was very difficult at times but I always went in with a smile on my face. But I did survivie -- and as soon as I was well I knew I had to give back. I contacted LLS with the intention of becoming as involved with the mission as possible.            

 

Almost immediately, I began fundraising for the Light The Night Walk program, creating a team (Christy's "Cure"ators) that haa been in existence now for nearly eight years.            

 

Then I began volunteering for First Connection, that's LLS's peer to peer support program. My husband and I volunteer in other ways, as well -- and the folks at the local LLS chapter will tell you that I can always be counted on to speak at an LLS event!            


Now, what results have you seen -- and what impact has that made on your life?           

With every Light The Night Walk, every First Connection support group meeting I'm in contact with, every speaking event --- I'm reminded how powerful my story is and what a source of hope and inspiration it can provide to others. People come up to me all the time that I don't know, people who are in treatment or are caregivers for people in treatment and they thank me for sharing my story. Fundraisers thank me for sharing my story because I remind them that 'Cancer Survivors Have Miracles Too.' That's really become my mottoand the mantra for my life and the hope I want to share with others touched by cancer. The more I give back the more I'm aware of the importance of doing so -- just like Gap!            


What are your thoughts on Gap's Give and Get campaign and the fact that LLS is one of the benefactors!            

I think it's wonderful! It's great of Gap to recognize The Leukemia & Lymphoma Society and the hard work we put forth to find cures.            

 

It's funny because when I was in High School, my friends and I would only shop at Gap. A friend of mine used to say, "if you didn't shop at Gap, you just weren't cool.!" Now, as an adult I still shop at Gap and Old Navy and Banana Republic -- and spend most of my time now at Baby Gap for Jaden!            

Giving back has been huge for me. As soon as I became cancer free I was determined to do something to help others. You can give back too by supporting Gap's Give and Get campaign for LLS!                     

 

Download your LLS coupon today.  The Gap Give and Get Campaign benefiting LLS runs from March 18th -- 21st.

 

Download the LLS coupon to take advantage of the 30% discount available from all Gap, Inc. stores. Then share this post with your family, friends and social networking contacts. Give and Get with Gap and LLS and help save live

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2/24 UPDATE:

The Shavertown Totally Baldacious Event has been cancelled in consideration of the bad weather for forecast.

 

 

 

Next Saturday, February 27th, we'll be holding a Totally Baldacious rally, shaving or coloring hair for everyone who's interested in showing their love and solidarity for cancer patients.

 

The event is planned for 12 to 4 p.m. at Kingston Township Municipal Building, 180 East Center Street, Shavertown, PA 18708. We plan to have participants from local schools, colleges, and busnesses and just people from the community attend. We will have several hair stylists on hand to assist with the shaving and temporary hair color.    Our Honored hero is Shavertown resident, Hunter Wesolowski, 6, a CML survivor.

 

Be a part of the fight against cancer and brave This Totally Baldacious event in Shavertown. Email baldacious@lls.org to confirm your participation so we can plan accordingly.  There's no better way to show cancer patients you care next Saturday.

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Earlier this month we let you know about the launch of a new fundraising campaign, Totally Baldacious, which was designed specifically to show love and solidarity for cancer patients while raising money for life-saving research. The response to this campaign has been terrific, thanks in great part to many of you who've posted comments on the Totally Baldacious Fan Page on Facebook, like this one:


"My son and daughter both shaved their heads in support of their sister after her diagnosis of AML in 2003 which scared their three-year-old niece (worried she'd have to do it too!). We all laugh about it now and the sense of support was so strong! She is 6 years past transplant now and has a huge head of hair! Love this campaign. Love in action!" --Lori Robin Wilson

 

Showing our love is what it's all about and our President and CEO, John Walter, is leading the charge! Last week our John announced his participation in the campaign -- with a bold fundraising goal of $50,000!  (Note: As of 2/25 John is 33% of the way there.)

 

You can help John reach his goal by donating to his campaign today!  Donate to show your solidarity with those currently undergoing treatment.

 

Your contribution will promote advances in treatment that will allow cancer patients to live better, longer lives.   Then visit the @LLS Blog on the 24th to see pics and a video of John 'shaving one for the team.'

 

Show your baldacious support by making a contribution today

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Jadrian, you're currently undergoing treatment, but you didn't lose your hair. Why did you decide to go Totally Baldacious?

When I was diagnosed with CML, I didn't know what to think. The whole process was pretty scary, but as I learned more about my treatment and prognosis, I knew I was one of the lucky ones. There are so many other people who are dealing with cancers or treatments and not responding nearly as well. If shaving my hair helps to raise awareness and money for cancer research and treatment, it's a small price to pay. I hope my story and experience inspire others to help as well.

 

Are you shaving your head for anyone in particular?

A friend of mine, who was diagnosed with CML shortly after I was, has not responded to the same treatment that works for me, and is facing a bone marrow transplant very soon. This is one small way that I can walk beside him and lend him strength on his own journey forward. My dad fought and won his battle with colon cancer a few years ago, and his strength and character throughout my life are also of unending inspiration to me.


How important has the support and solidarity you've received meant to you during your treatment?

It is invaluable. Knowing my friends and family are there with me every step of the way means the world to me. The community of fellow survivors online welcomed me warmly, and the forums provided me with a platform for educating myself about leukemia, its treatment, and new advances.

 

We have a number of support resources available online -- from the Blood Cancer Discussion Boards to online chats. Have you taken advantage of any of these resources?

I delved deep into the community knowledgebase in the online discussion boards immediately following my diagnosis, and am grateful for the outpouring of news and support from its members.

 

What LLS resource have you found the most helpful?

For me, the discussion boards have been the most helpful.

 

You've filmed your hair being shaved! (View Jadrian's video here above).  What a great video! How else are you promoting your participation in Totally Baldacious online?

Via Facebook and Twitter, of course, as well as on the community pages for the LLS   and the Totally Baldacious campaign itself! I'm excited to see response videos on YouTube of other people around the world going Totally Baldacious as well, so if you've got 'em, post 'em!


It's clear this year's Valentine's Day is one you won't soon forget.  Thanks for going Totally Baldacious, Jadrian, and helping emphasize how important it is to show solidarity and support for all cancer patients!

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2/23 UPDATE:

Victory in Iowa! Thirty-one states and the District of Columbia now require insurance companies to cover routine care costs for patients enrolled in a cancer clinical trial!  Today, Tuesday, February 23, blood cancer volunteers from The Leukemia & Lymphoma Society’s Iowa Chapter witnessed Iowa Governor Chet Culver sign House File 2075 into law, officially requiring this coverage for cancer patients in Iowa.  The Leukemia & Lymphoma Society would like to thank the bill’s champions, Reps. Janet Peterson, Tyler Olson and Doug Struyk and Sen. Joe Bolkcom, and Gov. Culver for their support of this vital issue!

 

Today, Wednesday, February 17, blood cancer volunteers from The Leukemia & Lymphoma Society’s Iowa chapter will travel to Des Moines and thank their elected officials for passing legislation that will require insurers in Iowa to cover routine care costs for patients enrolled in a clinical trial.  Volunteers will also be presenting our champions – Reps. Janet Peterson, Tyler Olson and Doug Struyk and Sen. Joe Bolkcom – with awards thanking them for their support of this bill.  But just because you were not able to make the trip to the Capitol building doesn’t mean you can’t still join in the excitement of Iowa’s State Mission Day!

 

For Iowans, there are two ways that you can still participate in the day: 1) Please visit LLS’s Legislative Action Center and send a pre-drafted email to your representatives thanking them for passing House File 2075 unanimously in both the Iowa House and Senate, and 2) you can follow the day online. We will be posting updates, volunteer feedback, photos and video right here on the @LLS Blog and through LLS pages on Facebook, Twitter and Flickr.

 

So check in from time-to-time and be a part of Iowa’s 2010 State Mission Day!

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http://community.lls.org/servlet/JiveServlet/downloadImage/38-1653-5296/baldacious_logo.jpgShow your love and solidarity for cancer patients by promoting Totally Baldacious through your social networks. Whether you fundraise with a Totally Baldacious challenge, donate to support life-saving cancer research or just choose to Totally Baldacious your profile picture --- you'll be making a difference in the lives of cancer patients.

Update your profile image with the Be Baldacious widget or Facebook Application and spread the word about the importance of funding life-saving cancer research.
    
Be Baldacious, pictured below, lets you go bald - virtually.  Just upload your photo, size and position it under the bald cap, match your skin tone, and then share it with your friends.  Dare them to go Totally Baldacious, too!

There's no better way to show you care.

 

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http://community.lls.org/servlet/JiveServlet/downloadImage/38-1653-5296/baldacious_logo.jpgToday at John Allan's in Midtown Manhattan, 12 year NFL veteran Terry Cousin and his pro football colleagues Sheldon Brown and Jyles Tucker will be going Totally Baldacious to show their solidarity for cancer patients and to raise awareness about the importance of funding life-saving cancer research.

Each have registered on www.totallybaldacious.org, where you can donate or use the Be Baldacious widget to share with your friends. Whether you decide to fundraise for Totally Baldacious, donate, or promote the campaign, you'll be making a difference in the lives of cancer patients.

 

Updated:

 

The before picture: Check out Cousin, Brown and Tucker in front of John Allan's Salon in NYC!

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And here's the 'after' shot:

 

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For a complete series of pics -- see the Totally Baldacious Fan Page on Facebook!

 

Be inspired by Terry and his Team, sign up to fundraise at www.totallybaldacious.org, donate to fund life-saving cancer research or just use the Be Baldacious widget/Facebook App to help raise awareness about this important campaign. Do something Totally Baldacious today - you'll be glad you did!

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Do you know someone with cancer? Have you wondered how you can show your support? This Valentine’s Day, we're launching an exciting new fundraising campaign - Totally Baldacious. When you shave or color your hair, you are showing your solidarity with cancer patients, raise awareness about cancer, and help raise money for The Leukemia & Lymphoma Society.

Amy Barlett is the Totally Baldacious Honored Hero.  Amy holds a special place in our heart as a non-Hodgkin lymphoma survivor who’s also a multi-event Team In Training alumna!  When Amy lost her hair during treatment, she found the silver lining...noting that,  “When you’re bald you don’t have to worry about a bad hair day.”

 

Read this Q&A with Amy:

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LLS:  In May you celebrate 3 years in remission. Congratulations! When you began treatment and lost your hair did anyone shave their head to show their solidarity with you?

Amy: Twenty of my male friends all let me shave their heads before my sister shaved mine in front of about 100 of my family and friends.  I shaved mullets, mohawks, tails...you name it.

 

LLS: How did you feel when you realized that they were doing that?

Amy: The day I found out I was going to lose my hair I decided I wanted to throw a party and lose it on my own terms.  Over 100 people showed up to the party.  I was amazed and honored.  When the boys lined up, it was so unexpected yet made the evening more fun.  For us, it was about turning a sad part of cancer in to a happy memory.  When I think of losing my hair, I go back and look at the pictures of the party.  It was seriously one of the best nights of my whole life.

 

LLS: Part of the reason we've launched Totally Baldacious just before Valentine's Day is to spread love to our patients and raise awareness for the importance of showing support for patients. When you were undergoing treatment, how important was your support system to you?

Amy: Having a support system is extremely important.  I am fiercely independent and had a hard time accepting help at first.  Asking for help actually makes you stronger.  It is not a sign of weakness.  Knowing my friends shaved their heads to be "on my team" meant everything to me.

 

LLS: What LLS resources did you take advantage of at the time?

Amy: The night of my party we also accepted donations and had a silent auction with all money raised going to LLS.  We raised over $20,000 that evening.  I joined Team In Training during my treatment to give me a good fitness goal for the end of the chemo and radiation road.  It motivated me to go for walks and stay active even in the darkest days.  Saturdays I knew I would see the team and we inspired each other.  I was so grateful to the other participants for raising money for people like me - with cancer.  And they thanked me for providing them motivation to get up, log the miles, and raise the money.

 

LLS: You have a blog, www.ichoosehope.com and a twitter profile (@amyebartlett)  - how will you be promoting Totally Baldacious online through February?

Amy: While I won't be shaving my head again for the Totally Baldacious month, I would love to connect with patients and hear other inspiring stories of the best parts of being bald.  Like - how fun accessorizing your head can be...big sunglasses, scarves, hoop earrings.  Just decorate it!  Tattoos are super fun, or henna art could also be beautiful.  I wish I would have thought of the artistic things when I was bald.  Turn it in to an opportunity to be creative and put a smile on your face.  And remember, you can't have a bad hair day if you are bald.  That is a bonus.

 

LLS:  Will you be using the Be Baldacious widget to bald yourself and tell your friends?

Amy: Yes, I will share this with my friends and family.

 

LLS:  Amy, one of the most remarkable things about you and your story is your connection to Team In Training. How many times have you participated in Team In Training?

Amy: I had been a participant in TNT four times before I was every diagnosed.  In a strange way, I believe my early involvement could have played a role in my successful treatment.  Perhaps some of the money I raised over the years helped advance research that has given me a second chance at life...  I have participated two times after being a patient, and I am signing up this year, again, for the Nike Women's Marathon in San Francisco.

 

LLS: And how much have you raised to date to fight cancer?

Amy: Somewhere in the $60,000 range which truly boggles my mind.  The dark times in our lives can truly reveal the best qualities in people.  I receive donations when I am not even officially training.  People write a check and say "this is for your next one" which is so amazing.

 

LLS:  I understand you are considering participating again, is that true?

Amy: Yes, I sure am..  I want to eventually do an Olympic distance triathlon, but I haven't worked up the courage for that yet.  For now I am sticking with 1/2 and full marathons.

 

LLS:   What would you say to others who are contemplating Team In Training but have never trained before?

Amy:  It will be one of the best experiences of your life.

 

LLS:  What's the best thing about your Team In Training experience?

Amy:  Knowing that I am making a difference in someone's life.  My dream one day is for us to be able to say "Remember when people used to get cancer?"

 

Learn more about:

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UPDATE: Thank you to everyone who participated in this campaign! The results are in and because of you, more than $650,000 was raised for life-saving cancer resarch. Thanks for shopping!

 

 

Jennifer Donnelly is the mother of Matthew, an acute lymphocytic leukemia patient who's story is featured in the Gap Give & Get Campaign.  Gap Give & Get gives you a 30% off coupon to shop at all Gap, Inc. store, with 5% of the proceeds going to benefit The Leukemia & Lymphoma Society.

 

llsphoto.jpgJennifer shared her story with LLS:

 

How did you find out that Matthew had leukemia?


Matthew was diagnosed on December 11th, 2007, when he was two and a half years old. He hadn't been feeling well and our regular doctor thought he had a double ear infection. In fact he did have a double ear infection, but thankfully our doctor also had blood work done on Matthew, which ultimately determined that he had acute lymphocytic leukemia (ALL).  It was devastating at the time, but in hindsight we were glad he was diagnosed early on.


Before Matthew's diagnosis, had you ever heard of leukemia?


To be honest, no -- but I learned very quickly.  I also found a huge support group of people out there who are willing to help.

 

How has LLS been helpful to you and Matthew?

 

We participate in LLS's finanicial aid program and have also participated in The Light The Night Walk twice.  Matthew was also recently named the 'Boy of the Year' for the local LLS chapter here on Long Island.

 

Your son has an amazing smile.  He looks like he has a very positive outlook.

 

He does!  When he was first diagnosed, going to see the doctors so often was difficult and I would try a number of things to make it a positive experience - like dressing up in costumes. Well now, Matthew actually looks forward to going! Once when we were on vacation in Disneyland, he surprised me with "Lets go to the clinic, Mom!"   There we were, in the "happiest place on earth" and he wants to go to the clinic!

 

How is Matthew doing now?

 

Matthew's doing very well. He's in the second year of his treatment, which will continue through 2011.  We are participating in a trial.

 

A clinical trial?

 

Yes, again, before Matthew had been diagnosed, I didn't realize how important clinical trials could be to treatment options.  I found out as much as I could in advance, especially about the protocol that was suggested for Matthew.  Now, I think of all of the people who participated in trials before us and I'm grateful.  If they hadn't, I wonder where we'd be now.  Thanks to previous trials and the people who participated in them, treatments have improved.

 

Have you participated in any previous Give & Get campaign?

 

We participated in both the spring and summer campaigns.  A coupon was forwarded to me via email.  The 30% discount is terrific and knowing 5% of the sale goes back to LLS - even better!

 

Now, when I know of a business, like Gap, that gives back to LLS -- I think, "They're doing this for research, they're doing this for cures, and they're doing this for my son."  It makes me want to cry because I know the true benefit of this kind of support.


Thank you, Jennifer, for sharing your story with us and allowing us to feature Matthew in this campaign.

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This Thanksgiving, tune into FOX for a new holiday variety show, Kaleidoscope.  The show rounds up Olympic skating champions and GRAMMY Award-winning music artists, like Scott Hamilton, Dorothy Hamill, Olivia Newton-John and David Foster. Also performing are Kristi Yamaguchi, Nancy Kerrigan and Olympic figure skating hopefuls Johnny Weir and Rachael Flatt.

 

But the event isn't only about the entertainment.  Kaleidoscope was designed to recognize women and the key role they play in the battle against cancer - as patients, caregivers, and advocates.

 

In addition to The Leukemia & Lymphoma Society, Kaleidoscope has teamed up with nine other cancer-related advocacy partners.  Together, this team of Cancer Advocacy Partners hopes to shed some light on how we're all touched by cancer and can all make a difference.

 

You can help!  Tune in to FOX on Thanksgiving (November 26th) at 4:00pm (EST), immediately following the Thanksgiving Day football telecast. The event will be pre-recorded on Monday, November 16th at 7:00pm at the Verizon Center in Washington, D.C. If you're in the area, tickets for taped performance are on sale now.

 

Find out more at www.womenandcancer.com, or read the press release.

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Steelers Defensive End, #91, Aaron Smith, was joined by the entire defensive line, more than a dozen players and their families, to make up Team Elijah in this year's Light The Night Walk.   The team was formed in honor of Smith's six-year-old son, Elijah, who was diagnosed with leukemia last year.


“It  was an amazing night,” said Tina Massari, Executive Director of The Leukemia & Lymphoma Society Western Pennsylvania & West Virginia chapter, who said the walk raised $600,000, with Team Elijah as one of the top fundraising teams. “Whenever you have someone like  Aaron Smith saying this can happen to anyone and our family is involved and we  want to be a part of it and join us it’s always a huge call to action. People  think he is a Steeler, he is involved and it can happen to him it can happen to  anyone and we want to help out.”

Read the entire story on Steelers.com, the Official Web Site of The Pittsburgh Steelers.  And view the photo gallery in the "Off The Field" section.




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We are where you are.  Be honest.  How many hours a day do you spend tweeting or updating your Facebook status?  Embrace it.  We have.

 

You may have noticed the recent addition to the community homepage - the "Follow Us" box, which links to many of our social networking pages. 

 

LLS has a major presence on the social networking sites you use regularly.  We're always connected.  Not a day goes by when we're not blogging on this community, chatting with cancer patients and survivors in our discussion boards, tweeting updates to our Twitter followers, or keeping our fans informed on Facebook.  We've cultivated some of our closest relationships online.

 

September is Leukemia, Lymphoma and Myeloma Awareness Month.  In honor of this important time of year, LLS is vowing to be even more connected with our supporters.  We're extremely interested in what our volunteers, supporters and participants across the country - and across the globe - have to say.  Staying connected helps us better understand what we can do for you.

 

Meet Christine Brantley.  Her son, Jake, is a survivor of childhood leukemia. Christine was kind enough to share her family's story with us.  Through our social network, we're able to share the Brantley's tale with hundreds of thousands of people world-wide.  The first step to finding cures for blood cancers is to build awareness about these diseases.

 

 

Christine and Jake know the importance of funding blood cancer research. As Christine shared in our interview, "I know with research there's a brighter future for everyone with blood cancer."

 

Join our network and then consider what you can do to help support our research and LLS help patients like Jake.

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Thanks to our colleagues at Gap and our friends online, our summer Give and Get campaign promotion was another success! Because of you and your efforts sharing this promotion online, The Leukemia & Lymphoma Society will receive nearly $500 thousand to support our life-saving research to find a cure for blood cancers like leukemia, lymphoma, Hodgkin's disease and myeloma. That's an amazing accomplishment for one weekend worth of shopping at Gap, Inc. stores!

As you noticed during the launch of this campaign, we featured Lance Bigelow (see our launch blog post, Lick Leukemia with LLS and Gap), who is living proof that the research we fund has a direct impact on patients. 60 years ago, when LLS was founded, a blood cancer diagnosis was almost always fatal. Since that time, the nearly $1 billion dollars we have invested in innovative research has helped to increase survival rates of some blood cancers by double or even triple. In fact, blood cancer survival rates rose by as much as four-fold from 1960 to 2000.

All of that was possible thanks to partners like the Gap and people like you - who either directly participated  in our fundraising efforts or helped spread the word. Your support makes a difference.

Thank you for helping us serve our mission to find a cure for all blood cancers and help patients and their families live better, longer lives.

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If you're in Manhattan on September 12th, watch out as the city will be stormed with brides and grooms on the hunt for diamonds!  Michael C. Fina and Tacori, leaders in the jewelry and bridal industry, have partnered to host a diamond scavenger hunt. Proceeds from “Diamond Dash: Dash for a Diamond & a Cure” will support The Leukemia & Lymphoma Society (LLS).

 

The dashers will race down the streets of NYC, solving clues sent via SMS, and stopping at various wedding-related destinations throughout the city.  The first couple to reach each destination will be awarded with a prize valued up to $3,500! And, the couple that reaches the final destination first will be awarded an incredible Grand Prize.

 

Grand prize winners of the Diamond Dash will receive a beautiful handcrafted Tacori engagement ring setting, matched with a Tacori Diamond, both valued at approximately $20,000, as well as a honeymoon package to Waikoloa Beach Resort on Hawaii's Big Island, including roundtrip airfare and four nights hotel accommodations at Hilton Waikoloa Village.  The dash will culminate with a once-in-a-lifetime proposal opportunity.

 

Think you know all there is to know about NYC's wedding hot-spots and trivia? Do you and your special someone Want a chance to grab some prizes? Sign up for the event at www.diamondsmakeadifference.com.  We're limited to 1,000 teams, so act fast.

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One of the things that we love about our events is how they enable people to meet others working towards the same goals –trying to help end blood cancers, and having fun while doing it. Every once in a while we hear about a story of how one of our programs has been instrumental in helping people develop an important personal relationship, and I think that following deserves some retelling

 

Michelle Fried has a long history with our National Capital Area chapter (NCA). As a volunteer, participant and Board of Trustees president, Michelle has been a dedicated supporter of LLS for many years.

 

Because of her passion and well-rounded experience with LLS, Michelle was chosen as an ambassador-of-sorts to help encourage participation in LLS events.  Last year, this role brought her face-to-face with Jim Galvanek, a 10-year leukemia survivor.  Not only did this meeting lead to Jim being named NCA’s 2008 Man of the Year, but eventually, to an unexpected romance.

 

The two amazing volunteers quickly became good friends.  Their friendship turned into a lasting connection.

 

This summer, The Light The Night Walk Kick-off was held at National Stadium, home of the Washington Nationals, just before the start of a game. Along with about 500 other people, Jim and Michelle were there showing their support for LLS.  Jim led Michelle to the stadium rooftop, as the game began so the couple could get a bird’s eye view of the field. It was up there that they shared a private moment together and Jim asked her to marry him.

 

After sharing the news with friends and volunteers alike, the two enjoyed a few innings.  Soon after, the Jumbotron lit up naming Jim and Michelle "Fans of the Game.”

 

The NCA Deputy Executive Director, one of the lucky people to see these two lovebirds' relationship evolve, said that it has been really sweet to watch two good friends and amazing volunteers make a lasting connection and remember how LLS has been instrumental in their relationship.

 

Michelle and Jim have not only found each other, but they have also given much of their personal time to LLS – something for which we at LLS are grateful for every day.

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