Showing posts with label Liz Martocci Lung Cancer Foundation. Show all posts
Showing posts with label Liz Martocci Lung Cancer Foundation. Show all posts

Tuesday, August 11, 2009

Monday, July 27, 2009

Liz Calling in 7/27

Liz Calling in after they found a mass on her neck.






Press the heart to play

http://www.lmlcf.org stop by and sign the guestbook

Tuesday, May 19, 2009

To realize (The origin of this letter is unknownP

To realize
The value of a sister/brother
Ask someone
Who doesn't have one.

To realize
The value of ten years:
Ask a newly
Divorced couple.

To realize
The value of four years:
Ask a graduate.

To realize
The value of one year:
Ask a student who
Has failed a final exam.

To realize
The value of nine months:
Ask a mother who gave birth to a stillborn.

To realize
The value of one month:
Ask a mother
Who has given birth to
A premature baby.

To realize
The value of one week:
Ask an editor of a weekly newspaper.

To realize
The value of one minute:
Ask a person
Who has missed the train, bus or plane.

To realize
The value of one-second:
Ask a person
Who has survived an accident.

Time waits for no one.

Treasure every moment you have.

You will treasure it even more when
You can share it with someone special.

To realize the value of a friend or family member:

LOSE ONE.

Liz Calling In 5/19 Great News!



Friday, May 15, 2009

Farrah special tonight

Hello Everyone and Thank you for your Support,

If you saw the Farrah special tonight you have an idea of what cancer does to a person. Cancer affects the patient as a person, I often wonder what must go through their mind as they lay their head on their pillow each night. For me personally the Farrah special gave me a new perspective on what those dealing with any kind of cancer must feel. I only know it from a sons perspective. Farrah shed new light for me, and for that I thank her for her courage.

You see I only know it as a son. My mom is fighting, and fighting hard, stage IV lung cancer. It has been almost a year since she has started on her courageous fight. Next week will make the "X-ray" saying she needed more testing. It was not until July when she found out her stage, stage IV, the second to the last stage of cancer.

I want to share something with you that you may already know. In honor of my mom we started a foundation to help those that get that "X-Ray" get the tests they need as fast as possible. We NEED your help. We recent;y became a 501c3, thus you donations are tax free. I understand how tight money is, However if everyone donated just $1 and forwarded this email to everyone they know will be able to help those dealing with this horrible disease
Join us with a dollar ot two. But please pass this email along.

Liz Martocci Lung Cancer Foundation Announces Tax Exempt Status as Official 501 C3 Organization



Phoenix, AZ (PressExposure) April 22, 2009 -- We are pleased to announce that the Liz Martocci Lung Cancer Foundation is now an approved 501(c)(3) tax-deductible charity under US tax law. The IRS grants this coveted status upon organizations who meet specific legal requirements and operate under strict conditions with the goal of providing a public benefit. 501(c)3 status makes the Liz Martocci Lung Cancer Foundation exempt from paying federal taxes and allows any donations to be a tax deduction for the donor. This status is also a requirement by all foundations and government agencies when applying for grants. We started the process in July of 2008 when the Liz Martocci Lung Cancer Foundation was formally organized as a public charity non-profit corporation. After many forms and paperwork, legal fees, government fees, and a lot of effort we were able to surpass this milestone and be granted exempt status.

President Dan Hart was excited about the organization getting the news. “We are pleased to say our dream is finally coming true now that we are tax exempt. We look forward to making a difference in the lives of those faced with lung cancer.” Many people find out that they may have lung cancer through a chest x-ray. Often a CT scan and biopsy are requested to confirm. “Our goal is to help those people without insurance get the tests and treatments they need as quickly as possible” says Hart. One only needs to search the phrase “lung cancer” on the internet to find hundreds of heart-wrenching articles and stories relating to the struggles of those faced with lung cancer and their families.

The Liz Martocci Lung Cancer Foundation had some bold goals in mind as they set to launch this foundation in July 2008. Lung cancer is the NUMBER ONE cancer killer in American men and women of all ethnicities. In 2008, more than 215,000 American men and women will be newly diagnosed with lung cancer. Tragically, approximately 162,000 people will lose their lives to the disease. Lung cancer kills more people in the United States every year than breast, colon, and prostate cancer combined. While lung cancer takes the lives of more people each year it is the most underfunded.

Since our beginning, we have witnessed, first hand, the hopeless need for support in living expenses, doctor referrals, and genuine love. We have devoted ourselves to addressing these issues and are dedicated to helping people living with lung cancer overcome these issues. “We want to help comfort people in the one of the most difficult situation anyone can be faced with” says Hart

Every 2 minutes, worldwide, someone is diagnosed with lung cancer. “We want to help those people and change the statistics” says Hart.

About Liz Martocci Lung Cancer Foundation

The Liz Martocci Lung Cancer Foundation began on July 9, 2008 with one purpose in mind to help those faced with this horrible disease, living without insurance, find and receive the medical treatment they so deserve. Often the middle class hard working are often the ones that can not get the help and support needed during such a tough time. The Liz Martocci Lung Cancer Foundation is here to help those faced with the challenges of the “system” while offering support, resources and compassion. For more information about the Liz Martocci Lung Cancer Foundation or to make a tax deductible donation please visit http://www.LizMartocciLungCancerFoundation.org

Press Release Source: http://PressExposure.com/PR/Liz_Martocci_Lung_Cancer_Foundation.html

--
Dan Hart
www.LizMartocciLungCancerFoundation.org
Every 2 minutes someone is diagnosed with lung cancer
The content of this e-mail message and any attachments are confidential and may be legally privileged, intended solely for the addressee. If you are not the intended recipient, be advised that any use, dissemination, distribution, or copying of this e-mail is strictly prohibited. If you receive this message in error, please notify the sender immediately by reply email and destroy the message and its attachments.

Friday, February 20, 2009

Liz Martocci Calling in 2/2209

Click the Heart to listen






Read more about Liz at

http://www.lizmartoccilungcancerfoundation.org/about.html

Join us March 8th, 2009 for the San Diego Lung Cancer walk


http://events.lungevity.org/goto/lmlcf

Tuesday, February 17, 2009

"Emotions"

Today I sit here at my computer a little lost for words. I feel all the emotions inside. Earlier today I had a conversation with my brother Dan. He told me we need to start thinking about what's going to happen to dad when mom goes. I must be honest and tell you that this is a thought I don't want to ponder. The reality is that mom is going sooner or later. We really should be thinking about what's going to happen to everyone when that time comes. I don't want to think about that. I don't fear much of anything, I mean even death. I have conversations with a girlfriend of mine who says she fears death. I don't think I do really. I do fear losing my mom. How can I continue on without her? Who will I call on the way to work for 15 minutes and talk to every morning. Who will be the first person I call on Saturday & Sunday mornings? I know that statiscally mom's time is short. I can only hope & pray that she will beat the odds. But the reality once again is that mom's body is getting tired. Though emotionally she wants/needs to fight to keep going, how much longer can her weak, frail body continue this fight? I spent Valentines day with my mom & it was great. She actually ate all of her lunch. I was so proud of her! It took a lot out of her though to go to the store & lunch. I am patient with her & tell her to take her time & get what she needs. Well I can't continue much longer the tears are flowing. Until next time, take care all my love, Laura

Monday, February 9, 2009

Liz Martocci Calling in 2/9/09

Liz Martocci Calling in 2/9/09





Click the purple heart to listen


Join us for the San Diego Lung Cancer Walk March 8th http://events.lungevity.org/goto/lmlcf

Thursday, February 5, 2009

Dealing with Cancer

Hello

I am new to this blogging but need to talk, my sister Liz Martocci was diagnosed
with lung cancer about seven months ago and her kids have created a foundation to help her and others dealing with this disease.www.lizmartoccilungcancerfoundation.org

I have watched the site and spoken with the children and see the pain they are going through as I have lived it before you see this is the second sister to be hit by this decease.

We lost our sister Sheryl to Rectal Cancer in 1976, I was 14 at the time and watched this 21 year old woman deteriorate in front of my eyes. She lost her battle after only 6 months, we also lost Sheryl's daughter Kelly to Brain Cancer in 1985.

It has been 23 years since we dealt with this last dealt with this but the fear of losing another has been weighing on my mind. I don't get to see Liz much anymore as we have families of our own that takes up a great deal of our time, there was a time when we were young that we were best friends and I miss that.

I pray that Liz will beat this disease but I know the realty is that she will not.

I need her to know that she is Loved, not only by her children but by her brothers and mother as well.

In closing I ask that anyone who may see this to visit the site and help in anyway you can.


Tim

Tuesday, February 3, 2009

The Meaning of Strong

When you have posted the blogs of your siblings, writing one seems hard.. Getting a text message saying “This is the worst I have ever seen, it reminds me of the video you showed me” “Her face is swollen and she has spots on her arms”. How are you supposed to feel? My brother sent that to me via text. Then my sister in Law Jazmine calls crying telling me how much paid mom is in.
Both my brother and sister have asked what is “strong”. Trust me I ask myself that all the time. Well www.m-w.com says
1: having or marked by great physical power
2: having moral or intellectual power
3: having great resources (as of wealth or talent)
4: of a specified number
5 a: striking or superior of its kind, a strong resemblance, b: effective or efficient especially in a specified direction -strong on watching other people work — A. Alvarez

The only way I know to deal with my own pain is to point out my brother, sister and I, WE all have all of these.
1: having or marked by great physical power, We have god and the Universe Working for us.
2: having moral or intellectual power, We have intellectual power, together we are all smarter
3: having great resources (as of wealth or talent) We have amazing resources, we showed that when the foundation started.
4: of a specified number We have an amazing network of friends, online and off.
5 a: striking or superior of its kind (a strong resemblance) b: effective or efficient especially in a specified direction strong on watching other people work — A. Alvarez

We are working as hard as we know how to, to help those living with lung cancer. www.LizMartocciLungCancerFoundation.org

The last 48 hours have been painful. I sit waiting by the phone. This morning I talked to my mom. I was caught off guard, as mom sounded good. I could tell she was tired but she never let on to the pain. I often wonder if she does it for me, or because she actually feels ok. Then I hang up the phone and wonder if her physical pain is similar or worse to the emotional paid I am feeling. I am a member of inspire.com and I know there are people dealing with lung cancer sometimes say things to make those “not diagnosed” feel better, but the road works both ways. Just Friday I was talking to my mom when I had to pause to compose myself. As much I try to be “strong” in this example maybe #1 works. Its fricken HARD.
It’s hard for so many reasons. Because I am not there for my mom, because I am not there for my family. How does pops feel? This must be crushing him inside. I can only imagine the pressure on his chest is similar to the pressure on my mom’s colon.
In ending this blog, I am going to close with the fact I slept maybe 3 hours last night. Somehow I think my mind will only allow me to do the same tonight. Cancer takes a toll on everyone involved. My roommates feel it, co-workers, my friends (outside of my amazing roommates) my dog, the guy at Fresh and Easy feels it. Cancer is something that once it has touched you in a personal way affects your being. You can do one of two things, let it affect you, or affect it! Kick Cancer in the Rear!!!!!

It's 9:43 Cali time and I text my mom to see if she was up, she said "No have a little pain tried trying to get a little shut i". I text her back and told her "I loved her and sweet dreams."

God Bless,
Dan Hart
Join us March 8th for the First San Diego Lung Cancer Walk

Tuesday, January 27, 2009

Emotions

Today I sit here at my computer lost for words to blog. In my heart & mind I have some many things to say. You see emotions are crazy. I know what I want to say but I can't find the words. Lately I have had so many things going on in my mind. I love my mom more than I can find the words to say. Everyday that goes by I see her weaker than the last time I saw her. Truth is she can barely walk on her own sometimes. Inside I feel like I'm dying sometimes. I find myself reminiscing about the times that we have shared. The moments that she held my hand. The laughs we shared. Why am I feeling all of these emotions? Truth is I am afraid of losing her. I can't imagine life without her. I am having trouble writing this blog right now, it's very hard to talk about it. I know this is short but please remember it is heartfelt. I will blog again soon. Until next time don't be afraid of emotions. Laura Hart