Biggs' Zone

A Geek's Cogitations, Conjectures and other Cortical Experiences

Tag: Leukemia & Lymphoma Society

Let’s Light the Night!

By

On August 27, 2015

In General Cogitation

PrintGreetings friends, family and site patrons.

As some of you know, every year I participate in the Light the Night walk for a cure. It’s a charity event orchestrated by the Leukemia & Lymphoma Society. Participants raise money from donations by folks, like you, to sponsor those of us walking for the ones that survived, are currently battling or in memory of the ones we have lost. This walk means a great deal to me as I walk in memory of my brother-in-laws wife who lost her battle to Sub-cutaneous T-cell lymphoma back in 2013. She left behind a loving husband and two girls, the eldest of which is my goddaughter.

This is Natalie with her girls, a year before she lost her battle with lymphoma

This is Natalie with her girls, a year before she lost her battle with lymphoma

The Leukemia & Lymphoma Society funds research that will one day put an end to blood diseases and cancers. Your donations, which sponsor me in the 2 mile walk on October 15th, will go toward the funding for that research. This is an event I have been participating in for a couple of years, even prior to Natalie’s passing. I would have walked a marathon if it would have made the difference in her prognosis.

Over the next several weeks you will probably see me posting about donations quote often. I will try not to be too obnoxious about it, but I am setting a lofty goal of raising $1,500 this year. I hope that you will be able to help me out this year. You can make a donation on the following web page: http://pages.lightthenight.org/soh/Cinci15/MVleaminck or by clicking on the widget in the top right corner.

Your donation and support means a lot to me!

Thank you.

Lighting the Night 2013

By

On August 9, 2013

In General Cogitation

light_the_night_logoI want to start off by expressing that I work for a wonderful company. Every year my company participates in a charity event called Light the Night. Its a 2 mile walk that raises money for the Leukemia & Lymphoma Society which conducts research for treatments and cures of blood diseases and cancers.

As some of you may know, I recently lost my wonderful sister-in-law to her battle with a rare form of lymphoma. Therefore, not only will I be walking in her memory, but my company’s team has also asked to walk in her memory. It is a great and touching honor that Cardinal Solutions would make such an offer.

The sad and unfortunate passing of Natalie has given me new vigor to raise money for lymphoma research and as such I hope that you will make a donation to our team. On the right hand side of the page you will see a widget that shows my fundraising progress. If you click on the Donate Now button it will take you to my fundraising page where you can make a donation. Any amount can help make a difference in the lives of those battling leukemia and lymphoma.

The walk in Cincinnati is scheduled for October 10th. I’m looking forward to meeting up with all the other folks who are supporters, survivors and those, like me, walking in memory of having lost someone. It is merely a 2 mile walk, so while it won’t be physically arduous, it has the potential to be emotional.

I hope you will be willing to make a donation and if you have any questions, please visit the Light the Night website.

Gone Before Her Time

By

On July 25, 2013

In General Cogitation

Natalie Ungari 1978 - 2013

Natalie Ungari
1978 – 2013

Earlier this week my family and I had to lay to rest our sister-in-law, Natalie. She was 35 years old, married to my wife’s brother and they had two extraordinary daughters (ages 1 and 3). I cannot find the words to express the sorrow and grief all of us are feeling and I can’t even begin to comprehend what my brother-in-law is experiencing. All my prayers go out to him.

Nat always took such good care of herself. I always thought I got up early, but it never failed that before I even had my first cup of coffee she came walking in the door after completing an early morning run. I wish I had that kind of dexterity! I know that was the kind of lifestyle she was encouraging with her daughters as she only allowed treats on rare or special occasions, much to the chagrin of the grandparents 🙂

Nat was diagnosed with a very rare form of lymphoma (called Subcutaneous T-Cell Lymphoma). She’s had it for as long as I’ve known her but it was in remission until about a year ago (just before their second daughter was born). They tried several treatments but ultimately decided to do a bone marrow transplant and during the chemo treatments, to prepare for the transplant, she was taken into the ICU when the doctor’s found fungal pneumonia. She fought it gallantly but ultimately passed away from complications associated with the pneumonia.

When I was reading the beautiful obituary there was a section near the end where a foundation was mentioned called the National Organization for Rare Diseases (NORD – http://www.rarediseases.org/). This organization was formed to research “orphan” diseases to identify, treat and cure rare diseases. Donations in Natalie’s name can be made to NORD.

Just as these organizations are dedicated to finding treatments and cures, the family and friends of Natalie are dedicated to passing on to her daughters just how extraordinary and tremendous of a person she was. We will see to it that her influence on us will pass vicariously to her children.

We love you, Natalie!!
Rest in Peace.

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