Saturday, August 21, 2010
Pinkness
Thursday, August 19, 2010
3-Day video - part 3
Megan did such a good job getting this video. There were thousands of people....thousands...and it was unbelievably loud and chaotic. So, try to hear the words. And try to take me seriously in my outfit.
3-day videos
merged with??? Merry, Katy, Lisa & Rhea...the most AWESOME girls ever. Merry has agreed to be my blog spell checker. You can all thank her. More about them soon.
Monday, August 16, 2010
I walked...60 miles...in 3 days
I walked to heal the wounds her death left. For the life moments she deserved to be a part of. And that we deserved to have her be a part of.
I walked for the friends I have lost to breast cancer.
I walked for my friends who lost loved ones to breast cancer.
I walked for my friends who carried my when I could not walk.
I walked for you, my army of supporters, that still care enough about me to check in on this blog.
And, finally, I walked for my sisters…my sisters, who took the news of my diagnosis with such strength that it took my breath away…and still does. My sisters, who were at my side through my battle. My sisters, who are still by my side. My sisters, who are my heros.
xoxo
p.s. Check back soon for photos and funnies.
Thursday, August 12, 2010
Did I tell you guys?
Getting ready to walk 60 miles...
More soon!
Sunday, August 1, 2010
Feeling so full!
Monday, July 26, 2010
Sunday, July 25, 2010
Wooooooooooooooooooo-we! Stinky!
Wednesday, July 21, 2010
Summer fun...
Click to enlarge (above). Does that work to make it bigger? Anyway, this was hilarious! We thought thumbs up meant "we are doing great"...but oh no....!





Sunday, July 18, 2010
Leah
But I post this morning, as I weep, for one of my friends in Dallas. Leah is in the final days of her battle with breast cancer. My heart is shattered. Please say a prayer for her 3 precious, very young children and husband. I hope God carries her home soon and that her suffering is almost over. She fought her battle bravely.
I had to come here and write. It is where I have come for the past almost 2 years when things were tough and the place I came to cry this morning.

xoxo
Thursday, June 24, 2010
Hot dogs with some brilliant pre-schoolers
I am still giggling...
Sunday, June 20, 2010
Fruit of our labor...
And I am just loving my gardens. They are exploding with blooms and butterflies.


Tuesday, June 1, 2010
Thank you
I have a hard time leaving my children and dogs for an overnight trip. These men and women leave their homes and familys for months and years. How can I ever adequately thank them?
Megan and I went to outdoor mass at a gorgeous cemetary near our houses. They had fields of flags, each in honor of a Michigan soldier that had died in Iraq and Afghanistan wars.
There were too many flags.
Thursday, May 27, 2010
Poor Oddie...
Thursday, May 20, 2010
Couple more...
Volume up...but not too loud if you are at work
This is a sample of the pure joy I experience being with sisters, kids and dogs. There are no kids in the video because they were all in the swampy area looking for frogs. The dogs made brief appearances between getting all muddy too.
Ahhhhhhhhh...bliss!
Saturday, May 15, 2010
Ms. Moons Goes to Washington
I was a "consumer reviewer" at the Department of Defense US Army Medical Research & Materiel Command’s Congressionally Directed Breast Cancer Research Program panel (mouthful!).....to be referred to from now on as DoD BCRP . LOL I was nominated by and proud to represent my HER2 Support group. The Department of Defense paid for my airfare, hotel and meals.
The DoD BCRP has something like $150 million in congressional funds to be specifically applied to breast cancer research. So a panel of scientists and consumers (me and others) reviewed proposals with a goal of allocating funding to support high-risk, high-gain research.
So, what did I do...what did we do...? We would read and evaluate research study proposals, discuss them and then vote on them. My vote counted equally with the scientists!
I was so HONORED to be a part of it. There were just a couple consumers reviewers besides me...and LOTS of scientists. It was like alphabet soup of degrees in the room: PhD, MD, MPH, etc. The critical mass of brain power was incredible!! So many great minds in one place! There were molecular scientists, breast surgeons, surgical oncologist, epidemiologists, biomedical engineers...and a dozen others I have never heard of before. But they were all SO nice and so cool...and most were really fun. There were even a couple cuties so that was enjoyable! :-)
By the way, EVERYONE knew Dr. O'Shaughnessy (my Dallas oncologist).....and hold her in the highest regard. She is famous...in a good way!
As we were reviewing the research proposals, I found it interesting that it wasn't all just "out-of-this-world-can't-get-my-little-brain-around-it" science but also proposals relating to the effects of nutrition and exercise, which I thought was great. I was especially interested in the evidence-based alternative breast cancer therapies. Some even pertained to Native American use of medicinal herbs to treat breast cancer.
We reviewed 48 proposals. There were 49 but 1 got triaged (eliminated before review). In the beginning it took around 40 minutes to complete each review, discussion and vote. Then we picked up the pace. Regardless, we worked hard...really hard...morning 'til night!
Amongst all the talk of T cells, epidemiology, polymorphisms, nanoparticles, immunology and epigenetic something or others, I did get the chuckles a couple times. One of the scientists had a very strong accent and kept saying "toomah"....tooooo ma. Reminded me of Arnold in Kindergarten Cop. LOL
Watch and then hit your back button: http://www.youtube.com/watch?v=OaTO8_KNcuo&feature=related
I also had to bite the inside of my cheek so I wouldn't giggle when they were talking about cleavage. They were not talking about what I used to have peeking out of the top of my shirt but rather splitting cells or something.
One time one of the scientists made a joke about using polymeric nanoparticles for drug delivery...and how that was just like trying to determine genetic factors in a genome wide association study without a symptom cluster. Oh, the eruption of laughter.....! I guess it was a real knee slapper!!!
Seriously, the scientists were GREAT! Some were older, some were younger, some were male, some were female, some were outgoing, some were shy. But they were all lovely...and so grateful for my involvement. Can you imagine?!?! They thanked me. Here are these people that have dedicated their lives to eradicating this disease and they were thanking me! I was weepy with gratitude to them!
I am so glad I was able to do this! It was empowering. It made me feel like I was ACTUALLY doing something. Like it was not all for naught. I was able to represent all of us that have been touched by breast cancer. I am so grateful!
xoxo
Thursday, May 13, 2010
What a long, strange trip it's been...
~~~~~~~~~~~~~~~
Okay...that is as far as we got on Monday. It's me...Maureen again. I am not such a control freak that I took back the blogging from my guest bloggers. It's just that we were very busy celebrating and they did not get farther than the above paragraph. :-) But, for those that have known me a long time, of course I love this post title - loving the Grateful Dead band as I do.
So...yes...I am done. Done. DONE! No more infusions. Thank you, sweet Jesus. I am grateful beyond words. Thank you, Megan and Janice, for being with me Monday and always!
One of the other best parts of my last chemo was also the best part about my first chemo. Michele was with me. Yes, that is right...Michele from Costa Rica via Miami flew in as a surprise to go to me with my last treatment. I was floooooored! And to think I was mad she wouldn't call me back. She couldn't...she was on a plane! ha It was FANTASTIC to have Michele with me in person. I was so grateful!
For those of you that don't remember my sister Michele, you can read more about her here: MICHELE
Megan took a great photo of the infusion pump reading "Volume Remaining: 0.0 / Time Remaining: 00.0".....
Sunday, May 9, 2010
Sweet memories of my mom
Here are some of my favorite memories of my mom:
- She was always nice to people. She smiled and was kind - even when there was no reciprocity.
- She could enjoy the greatest laugh-until-it-hurts-and-you-might-wet-your-pants laughs...serious belly laughs. So contagious!
- Water fights...my mom loved a good water fight!
- She would regularly perform the miracle of the fishes and loaves, with food and clothes, as she raised us on a meager secretary's salary.
- She always had a green corsage for us to wear to school on our national holiday, St. Patrick's Day!
- When Megan and I were young, like 3 or 4 or 5, she used to pin a note to our jackets before we went out to play that said "Please don't feed us. We won't eat our dinner" (we lived in a safe place...the neighborhood behind Brother Rice high school in Birmingham....it was called the Catholic Ghetto)
- She occasionally let us have breakfast for dinner...what a treat!
- She made me take typing for 3 years in high school so I would have a skill to fall back on in case no other career panned out.
- She had incredibly versatile tears. She would cry from sadness, happiness, laughter, joy...or a hallmark commercial. (We all have that in common with my mom. My dad used to laugh that our tear ducts were too close to our bladders. With 7 women in the house, someone always had to pee or was crying)
- She loved her garden
- She talked to me about her impending death as she was dying from breast cancer. She let it be out there...out in the open. It was a gift. And a privilege to be a part of. She was the bravest person I have ever known.
- She hated cats but every cat within a mile ran to her. So funny!
- She would fall asleep while we watched t.v. in her bed with her. She would wake herself up snoring and say "Oh, was I snoring?" Then giggle and go back to sleep.
I could go on for days...
xoxo
Friday, May 7, 2010
News story on my family...I am so HUMBLED!!!
The NICEST folks at WDIV, Karen Drew and her camera man Ted, spent about an hour with me this morning. They are such lovely people...so kind. The story will air at 11:00 est on WDIV, channel 4 here in Detroit tonight (Friday).
Here is the teaser: http://www.clickondetroit.com/video/23491496/index.html
Pay no attention to the date stamp on the above photo. If this was actually taken in 2003, I would only be 19 years old. lol
My sister, Maureen Moons, is a 44 year-old single woman who wanted to be a mom, so she adopted her children from Guatemala. She has a son who is 7 and a daughter who is 4. Her daughter had only been “home” for 10 months in October, 2008 when my sister learned she had Breast Cancer. The news was grim…Stage 3C Invasive Ductal Carcinoma that also invaded her lymph nodes. She was approved to be part of a clinical trial, using new drugs to fight her particular kind of cancer. She went on medical disability from work and began treatments almost immediately.
Maureen (a.k.a. Mimi) is the 5th child in our family of 6 girls. Our parents only planned on having 4 kids, so Mimi and I were “blessings” to them. She moved from Birmingham to Dallas in 1989 after graduating from Walsh College in Troy. In Dallas she made many friends who became her family-away-from-home. They were there for birthdays, sick days, holidays, etc. And when she was diagnosed with cancer, they became her day-to-day caregivers. My other sisters and I would fly to Dallas to be with Mimi for major medical tests, procedures, treatments and to help care for her children, but we are scattered all over the U.S. and couldn’t be there every day.
Being the incredible mom she is, Mimi has always put her children first and tried to insulate them from the torture of cancer. Throughout this journey she has not skipped a beat when it comes to caring for her kids. She still took them to the State Fair, went on vacation, took them fishing, worked in the classroom, attended church, etc. She kept a blog to journal her experience and titled it “Raising Children…Razing Cancer” (http://www.moonsfamily.blogspot.com/). The title says it all.
After 8 months of chemotherapy, Mimi had a double mastectomy and lymph node resection on May 5, 2009. Her recovery was amazing…she was sitting up in bed and chatting with friends only hours after surgery. Within 2 days she was home from the hospital, after a stop at a local Mexican joint for lunch and a margarita! In no time at all she was back on her feet, exceeding doctors’ expectations and amazing everyone who knows her. Her next leg of treatment included 7 weeks of daily radiation, which finished in July, 2009. A combined family reunion & birthday party for Mimi took place at the end of July in Michigan and it was quite a celebration!
Within 2 days of returning to Dallas Mimi called me and shared some great news… she decided to move “home” to Detroit, after being gone for 20 years. She understands the importance of family and raising her children with their cousins, who live close-by. Her employer transferred her sales job to the Detroit market and she moved in September, 2009.
She continued chemotherapy treatments, transferring to the Karmanos Cancer Center in Detroit. Her last session is May 10th. On May 12th she leaves for Washington, D.C. to be part of the Department of Defense Congressionally Directed Medical Research Panel. She was invited to meet with scientists and review proposals for Breast Cancer Research funding.
What I most admire about my sister is her tenacity. She looked cancer in the eye and said, “You picked the WRONG person to mess with!” (see blog post December 27, 2008). Her doctors initially gave her a 60% chance of recurrence upon diagnosis. This percentage has decreased to a possible 10% chance of recurrence because of her positive attitude, sense of humor, dedication to healing and overall refusal to let cancer define her.
Mimi and I will be walking in the Susan G. Komen 3-Day for the Cure (Team Moonwalkers) in August, and I look forward to every step of our 60-mile journey!
I would LOVE to share Mimi’s story with your viewers. Do you have any type of Mother’s Day celebration planned? If there is a “Best Mom” competition…I have your winner! I’m contacting you specifically because I think this is a great home-town story of someone returning to our city and state.
Best regards,
Megan Moons-Grattan
Wednesday, May 5, 2010
another funny memory...
Obviously it was a long day of waiting while I was in surgery. My sister Suzanne and our dear friend Julie were in the waiting area. It was getting later in the day. Well, apparently, at 3:00 all the nurses that cover the big desk in the family waiting area go home. Their day ends at 3:00. Literally, they turn out all the lights behind the desk area and they go home. Well, several patients are still in surgery, like me. And the surgical nurses and doctors call that front area to give updates to the families. So someone has to answer the phones. The nurse came around the desk and, out of the room of people, pointed to Suzanne and Julie and said "YOU...I need you to answer the phone". Suz and Julie look at each other, like what the #*&!? If you knew these girls, and heard them tell this, you would be ROFL like I am to even be typing this. So they jump right in and do as the nurse tells them. They answer the phone, get the patient's families name, and yell it out into the waiting room - just like they were born to do that job. They even divvy up the roles. Suz answers and Julie yells. Hilarious!!
The only thing funnier than all of that was that there was a sweet, delightful mentally handicapped girl that would run towards them flailing her arms at every name that was called saying it was for her.
Not sure if this translates in a blog post. I have tears of laugter just from writing this. If you see Suzanne or Julie, you have to ask them to tell you the story because, damn, it is funny.
xoxo
One year ago today...
Whew..........what a whirlwind!!!
I am the luckiest, most blessed person alive to have had such an army of loving supporters with me every step of the way. And to have His hand on my shoulder every second, before and after this cancer stuff.
When I think about this time last year, what memory stands out the most was playing Scrabble in the hospital waiting room with Megan and Suzanne and lots of laughing. Not nervous laughter, just "you have to let me win" and I have to go to the bathroom AGAIN laughter. Then waking up with my sisters there with me.
All my memories are of the love I received. Not the pain or the fear. Does it get any better than that?!?!?!?!? Seriously!
xoxo