I am a huge fan of the musical, movie, DVD, all that is RENT. I have seen it performed live twice [once with the original members of Adam Pascal and Anthony Rapp], both times taking Ali with me, as it is a favorite of hers as well. The girls and I even went to see the live last performance from seats at our local theatre as the curtains fell in New York and the stage went dark.
I don't know that I would have been a fan when I was Ali's age. AIDS was just becoming known, Reagan was President and it was a scary time as far as the disease was concerned. The movie, And The Band Played On, shows how unknown the disease was for my generation.
But the words, the characters, the music, everything that Jonathan Larson created in RENT was genius. The words and lyrics to his songs are timeless. Everyone knows the song made famous by this work, 525,600 Minutes. Who knew how the year broke down in minutes had it not been for this song? The words that were created are powerful and thought provoking. "How do you measure the life of a woman or a man?" How does anyone?
November 2nd 2013, yesterday, marked one year to the day, 525,600 minutes, since my last chemo treatment. I see my oncologist every three months now instead of bi-weekly, I get up and go through my day as I used to, dragging myself out of bed with the alarm to let the dogs out and then take my morning meds and get ready for work. I go through my usual work day, come home, let the dogs out, prepare dinner and clean up afterwards. I take more meds and watch television or get some reading done, something I had not been able to do for quite awhile, concentration being an issue, and drag myself upstairs to get much needed sleep.
There are a few differences if you were to look at me. My hair being one; it is not shoulder length anymore. It is growing in steadily and I need to get regular haircuts as it begins to look a bit mutton like if I don't, and my hair stylist is helping me to grow it strong and healthy. If you really look there are a bit more differences: my stomach pooch is no longer there, thanks to the TRAM Flap procedure I had for reconstruction. The other difference being that I went from a C to a DD, not by choice but the procedure, I swear. I am still getting used to this difference. I remember telling my surgeon that I didn't want to look much different than I already was and now they tell me I "look more proportionate". Personally, if I was the weight I was when I got married I think I would look more like Barbie. I still have little to no feeling in my breast and abdominal area and likely never will. If I develop an itch, I actually have to concentrate and watch myself scratch or the itch doesnt go away. The look on someones face when they inadvertently bump into me, bumping my chest and apologize and I ask them why is priceless.
I know that there are more subtle differences. I don't have the stamina I used to, I get tired very easily and am easily winded with things that are strenuous. I have permanent neuropathy in my hands and feet. I walk down stairs like a 100 year old woman, clutching the banisters, as I am terrified to fall since I cannot feel my feet touch the stair. My hands are better but, when I get tired, I am unable to grip well and drop things. I have emotional issues, I feel angry and things tend to bother me more. Not to say I was easy going before this journey but I seem to notice it more at least.
There are things I have decided, that I need to do more to help myself. I need to eat better, sleep better and exercise more, although, doesn't everyone? I am slowly trying to do these things in an effort to learn from what happened to me. I guess I felt that this would be a life changing thing for me and yet at times I do not and I think this is what frustrates me. How do you not learn from something like cancer? I wonder this from time to time and I think for most of the journey, all I wanted was my life back. To go from day to day as I used to and yet, this is what I think bothers me. I was not the healthiest, more active person and I know that this is exactly what I need to do to help myself feel better and age better.
Ali and Amanda are great examples of strength for me in this area, as well as Greg. Greg took up running when Amanda joined the ROTC. He felt that he should get in shape while she did. Amanda is always striving for better times and numbers in her PT scores with the ROTC and it pushes her to constantly improve herself. Ali, who suffers from a condition called POTS [Postural Orthostatic Tachycardia Syndrome] needs to exercise to help her condition; the very thing her body does not want to do. Yet, when she called me last week, after having an extremely difficult week of classes and meetings and issues due to her condition, it was 8:30 in the evening and she was in the health club on campus, working out on a recumbent bike.
In an effort to improve myself, for me and my family, I first need to understand that I need to do this for myself. I am going to take better care of myself than I have before. I am going to look into yoga again, meditation, relaxation and healing myself. If this past year has taught me anything it is that while all I wanted to do was to return to normal after the cancer, my normal is not something that I like or is good for me.
So, my question for all of you that are so kind to take time and read my blog posts is, do you like your normal? How do you measure the moments in a year of your life, all 525,600 minutes of them?
525,600 minutes,
525,000 moments so dear.
525,600 minutes - how do you measure, measure a year?
In daylights, in sunsets, in midnights, in cups of coffee.
In inches, in miles, in laughter, in strife.
In 525,600 minutes - how do you measure a year in the life?
How about love?
How about love?
How about love?
Measure in love.
Seasons of love.
SOLOIST 1
525,600 minutes!
525,000 journeys to plan.
525,600 minutes - how can you measure the life of a woman or man?
SOLOIST 2
In truths that she learned, or in times that he cried.
In bridges he burned, or the way that she died.
COMPANY
It's time now to sing out, tho the story never ends
let's celebrate remember a year in the life of friends.
Remember the love!
Remember the love!
Remember
Sunday, November 3, 2013
Thursday, June 13, 2013
Lessons Learned...
Important dates allow us to recall memories, moments and time. Families and friends recall good times and bad through collective memories and it is a wonderful way for family to continue stories from the past and allow their history live on.
Last Tuesday, June 11th, marked one year that I had my cancer surgery. It is amazing to me that it has been only 365 days. Some things are so easy for me to recall from this time, others, most likely due to the morphine, are not so easy to remember and I need to rely on my family for help.
We learn things from our experiences and those of others. The goal when I began this blog was not only to help me get through the experience but, my hope was to help others if, sadly, they had to go through the same type of health crisis. Through this adventure I have learned kindness, goodness, friendship and even sadness. I treasure the time. This may sound strange, but this experience has not only changed me in obvious ways, but I am different and continuing to change, evolve if you will.
Kindness and goodness of others is something that is easy to find at a hospital or oncology office. The staff at Northwestern and my oncologists office were unknown to me when I began what was terrifying to me at the time. Only having the memory of what my mother went through, I was scared and my family, though strong on the outside were scared as well. How they go in day after day and help save lives is remarkable to me. How they helped me, helped others, and how they deal with losing patients, I will never know. Now, I consider these people to be lifesavers and am even more proud that I have one daughter who has chosen to be a nurse and one who is considering surgery.
It may seem peculiar that sadness would be included. Sadness though comes in many forms. There is sadness in losing another part of my body that makes me female. There is sadness in losing what fed my daughters when they were babies. There is sadness in the loss of a few friends. Yet, in the sadness, I find myself learning. I am learning more and more the importance of family. The true security that it brings. We have been put through many tests this past year and have become even stronger. I have learned who true friends are and have found that some are better friends than I may have given them credit for. Those that I have lost, I have learned that they were not true friends to begin with. Does it make me sad? Absolutely, but I have chosen not to dwell on the sadness.
I believe that if we do not learn from our own experiences, we are not taking full advantage of what has happened to us therefore not growing.June 11th will always be a day that I remember. It will continue to bring up memories and emotions, and I expect to continually grow from this experience.
Friday, April 19, 2013
I Am Far From Over
I have always loved Cher. There is something about her voice that has always appealed to me. I can remember as a young girl watching the Sonny and Cher show on Sunday evenings with my family back home in Southern California. Sonny and Cher's antics were silly but I always remember her solos. "Half Breed" was my absolute favorite song. And, who can forget her singing, "If I Could Turn Back Time", on the battleship with all the Marines behind her years later?
Her roles in movies have always been well done. Moonstruck is one of my all time favorites. I can drive Ali crazy within minutes as I speak each characters line; having seen the movie for the umpteenth time. She was wonderful in Witches of Eastwick, Silkwood, Mask and Suspect.
My mother was a fan of Cher as well. I remember watching her smile when we watched Sonny and Cher. I remember one day, before she got ill, walking to the sidewalk to get into our car. My mother was walking in front of me and I said excitedly, "Mommy, you have hips just like Cher!". I meant it as a complete compliment but it took me a few years to understand that it was not a compliment to her.
Today marks the day that I was told a year ago that I had Invasive Ductal Carcinoma of the right breast. Breast Cancer. The idea that I had a disease that I watched take over and kill my mother when I was a child was terrifying to me.
Strange as it seems, I gained strength from Cher. She was in a horrible movie a couple years ago entitled Burlesque. But, in that movie is a song she sings that I have played over and over and over again. It has helped me get through the past year.
The words are below and I know that you will see why I love this ballad and the strength it has given me. I thank Cher for her beautiful voice and, I thank the writer, Diane Warren. Her words are striking.
You Haven't Seen The Last Of Me
Feeling broken
Barely holding on
But there's just something so strong
Somewhere inside me
And I am down but I'll get up again
Don't count me out just yet
I've been brought down to my knees
And I've been pushed way past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
You haven't seen the last of me
You haven't seen the last of me
They can say that
I won't stay around
But I'm gonna stand my ground
You're not gonna stop me
You don't know me
You don't know who I am
Don't count me out so fast
I've been brought down to my knees
And I've been pushed way past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
You haven't seen the last of me
There will be no fade out
This is not the end
I'm down now
But I'll be standing tall again
Times are hard but
I was built tough
I'm gonna show you all what I'm made of
I've been brought down to my knees
And I've been pushed right past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
I am far from over
You haven't seen the last of me
No no
I'm not going nowhere
I'm staying right here
Oh no
You won't see me fade out
I'm not taking my bow
Can't stop me
It's not the end
You haven't seen the last of me
Oh no
You haven't seen the last of me
You haven't seen the last of me
Her roles in movies have always been well done. Moonstruck is one of my all time favorites. I can drive Ali crazy within minutes as I speak each characters line; having seen the movie for the umpteenth time. She was wonderful in Witches of Eastwick, Silkwood, Mask and Suspect.
My mother was a fan of Cher as well. I remember watching her smile when we watched Sonny and Cher. I remember one day, before she got ill, walking to the sidewalk to get into our car. My mother was walking in front of me and I said excitedly, "Mommy, you have hips just like Cher!". I meant it as a complete compliment but it took me a few years to understand that it was not a compliment to her.
Today marks the day that I was told a year ago that I had Invasive Ductal Carcinoma of the right breast. Breast Cancer. The idea that I had a disease that I watched take over and kill my mother when I was a child was terrifying to me.
Strange as it seems, I gained strength from Cher. She was in a horrible movie a couple years ago entitled Burlesque. But, in that movie is a song she sings that I have played over and over and over again. It has helped me get through the past year.
The words are below and I know that you will see why I love this ballad and the strength it has given me. I thank Cher for her beautiful voice and, I thank the writer, Diane Warren. Her words are striking.
You Haven't Seen The Last Of Me
Feeling broken
Barely holding on
But there's just something so strong
Somewhere inside me
And I am down but I'll get up again
Don't count me out just yet
I've been brought down to my knees
And I've been pushed way past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
You haven't seen the last of me
You haven't seen the last of me
They can say that
I won't stay around
But I'm gonna stand my ground
You're not gonna stop me
You don't know me
You don't know who I am
Don't count me out so fast
I've been brought down to my knees
And I've been pushed way past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
You haven't seen the last of me
There will be no fade out
This is not the end
I'm down now
But I'll be standing tall again
Times are hard but
I was built tough
I'm gonna show you all what I'm made of
I've been brought down to my knees
And I've been pushed right past the point of breaking
But I can take it
I'll be back
Back on my feet
This is far from over
I am far from over
You haven't seen the last of me
No no
I'm not going nowhere
I'm staying right here
Oh no
You won't see me fade out
I'm not taking my bow
Can't stop me
It's not the end
You haven't seen the last of me
Oh no
You haven't seen the last of me
You haven't seen the last of me
Tuesday, April 16, 2013
Things We Won't Forget
There are days and times in all of our lives that we will not forget. Yesterday, sadly, is a perfect example. There are memories that we all will deal with in different ways; those big headlines that we will always remember and those on a more personal level that we, and a few close to us, may always recall.
Me? There are a few headlines I remember. I was in the Student Center at my high school when President Reagan was shot. I was coming up the basement stairs with a load of laundry when the news came on that Princess Diana was killed. I was standing at the back door waiting to wave good-bye to my husband as he left for work, something I try and do every day he leaves first, when he yelled to me that we had been attacked and then turning on the t.v. to see a plane fly into the Twin Towers and Pentagon. I will now recall being at work and having a text from CNN beep into my phone to announce the terrorist attack in Boston.
This week though, there are the other kind of memories that are hitting home for me. Tomorrow, the 17th of April, was the day I went to Northwestern for my scheduled biopsy a year ago. I had already had my diagnostic mammogram and an ultrasound a few days before that was questioned I remember having the ultrasound tech tell me that she was going to bring in the radiologist. The radiologist came in and she spent a great deal of time looking at my right breast and then showed me the ultrasound, something they usually do not do. I saw the black circular area that spanned out a bit like a paisley design and I knew. She told me she was concerned. She was very kind and quietly waited outside the changing area to personally walk me to the scheduling area.
A few days later, the 17th of April, I was back for the biopsy. I was not nervous. If you have been to Northwestern you know that it is more like a spa than a hospital, as a friend this morning told me when she was there for the first time. Dr. M. came in and when the resident asked her if she still wanted me to have the biopsy, having seen the screen image, I knew that the results I would get were not good.
This Friday will mark the one year mark that I received the phone call telling me that I had cancer. It is a day that will be forever in my memory, my husbands, daughters and family. It is a marker for me, something to use and look back on. With regret? No.
I pray for those who were killed, maimed and in any way hurt by yesterdays terrorist attack. It is a horrific tragedy for all. Most especially for the families of the three who were murdered.
Sunday, February 3, 2013
Lesson Learned... The Hard Way
I have been feeling better these past few weeks. I thought that the start of the new year was the start of a new me. My hair has been growing on my head slowly but surely, albeit there are days when it itches like crazy, but I take it as a good sign. My eyelashes have come back as well as my eyebrows.
The neuropathy in my hands and feet has been really slow to dissipate The numbness is gone for the most part though. My hands don't tingle although they ache if they are washed in hot water and are painful and swollen in the morning. I have to pay close attention to when I am typing [something I do at work all day long]. If I don't, Iendupwithaparagraphwithoutspaces [I end up with a paragraph without spaces]. I also tend to knock things over when not paying attention, of course, I was a klutz as a kid, maybe it's just returned from childhood.
My feet are another story. When I wake up I feel like my feet are swollen balloons. Walking on them first thing in the morning is really painful, it takes awhile to feel comfortable on them. Sometimes, a water pill is needed to take the puffy feeling away. The great thing is I have been able to wear heels at work. I love high heels. Not the ridiculously high ones, just one inch kitten heels or my favorite pair of Enzo's, never more than three inches high. It makes me feel feminine again. I don't believe there is any correlation with feeling the morning pain and wearing heels the day before. It happens in flats or when I wear my new gym shoes [fluorescent hot pink and black, Amanda is so proud].
I got up this morning and put on my robe and slippers, as usual. I had my book in my hand and started walking down the stairs the way I always do, like an old lady [no offense]. I go one step at a time. I put my left foot down onto the stair and then my right and I proceed down the stairs in this manner until I reach the bottom and hold the handrail the entire time.
Last night though, it snowed. For this California girl, the first morning of a measurable snowfall is always breathtaking; really to me they all are. I love the white stuff. The crisp feel in the air, the clean smell, the way the white of the snow can make the world look new and fresh. I used to wake up Amanda if the first snow began after she had gone to bed. I don't know why, just something we always shared. I think my friends from Chicago think I am nuts about how much I like the snow. When we had the blizzard two years ago I was probably as happy as the neighborhood children who played while I shoveled. It makes a great work out. I find myself upset with weathermen who tell us it is going to snow and then, in the morning or at the end of the day, there is no snow.
I found out the hard way that I still need to pay close attention at all times to my walking. As I came down the stairs my eye caught the whiteness in the window and while my left leg was lifted to go to the next stair, and my eyes were on the snow, in that split second I lost my footing and fell the last four or five stairs down. I landed hard. So hard that Greg, who was in the backroom on the recumbent bike and rocking out to Katy Perry with his headphones, heard the thud. Thankfully he was home, I was freaked. I landed and slid. I am almost positive that I did not hit my head. I joked with a girlfriend that the scar from hip to hip in the front will be paired with a bruise from hip to hip in the back that I am sure to get. My left elbow has suffered the worst of it. Right on the spot that bends I have a lovely gash.
For those who don't know me as others, I don't deal well with blood. My security staff when I was the Assistant Manager at the Chicago Hilton and Towers knew this. If there was a call and there was blood, they shielded me. I have never handled it well. So, as Greg was cleaning up my elbow in the bathroom, he walked out to get the first aid kit and I saw the elbow in the mirror. The room started spinning, the queasiness came on, my eyes went blurry and the cold sweat soaked me. I don't think I have ever been so close to fainting.
I didn't break anything thank God. I am sore as sore can be and know I will be popping Motrin tomorrow.
I also wanted to share with you an amazing thing that a bunch of students and a couple faculty and staff did at Trinity a week ago. They gave of themselves by giving their hair. They donated almost 40 feet of hair to Locks of Love. I was asked to speak to the school [yikes!!] .
You can view it here [copy and paste]:
http://www.youtube.com/watchv=ECwMMgzookQ&list=UUvarpww9kSGsThIG0Gv_KZQ&index=1
or go to trinityhs.org. At the top right you will see the youtube icon. Click on it and I believe it should pop right up.
You can view it here [copy and paste]:
http://www.youtube.com/watchv=ECwMMgzookQ&list=UUvarpww9kSGsThIG0Gv_KZQ&index=1
or go to trinityhs.org. At the top right you will see the youtube icon. Click on it and I believe it should pop right up.
Monday, January 21, 2013
It's a New Year...
I would like to say that 2012 was horrible; the worst year ever, one not to be repeated. Surprisingly, I cannot. I saw a post on Pinterest the other day that helped me to realize something. That although the glass may look half empty [yes, a true pessimist I am], it is really not. That the glass, with the water only filling it halfway, is still full, simply with another form of matter, oxygen. Hence, the glass is always full. It's another way to look at it at least. I have heard this before of course, but it seemed funny to me that on the very day I saw this post, my dear husband and I had a talk and he said virtually the same thing in an anecdotal way.
One would think that a diagnosis of Invasive Ductal Carcinoma would tag 2012 as a horrible year. Of course, April 19th, 2012 will forever be in my mind; the day of my diagnosis. Then there will be June 11th, the day of my very long surgery which I am sure my husband will never let me forget as he, my daughters and family members spent over 16 hours in the waiting room. July 26th, my very first chemotherapy session. I will surely never forget the sickness from the first chemo.
Then, there is Amanda. When she went away to school we all believed that the plan was that she would graduate and return to the Chicago area. A true Chicago sports fan, we knew that she would not want to be far from Soldier and Wrigley Field and the United Center. It was discussed that when she graduated, she would return home for a year or so to save money as she worked as a nurse at one of the many great hospitals in the Chicago area. As most of you know, Amanda joined the Army ROTC. Hence, she will not be coming home. Once she graduates in 2014 she will be sent somewhere, who knows where, but it will not be home.
And, Alexandra. Ali left for her first year out east to Haverford. Greg and I are officially empty nesters. It is so quiet in our home now. What do I miss most? My drive to work. I work where the girls went to high school and every morning for the last two years, Ali and I would drive to school together. It was usually a quiet ride as Ali and I are not what you would call "morning people", but it was nice. The drive home was always a great time to check in with Ali and what was happening at school. She would tell me about her day, her friends and the homework she had or presentations that she was either preparing for or how they had gone. But that does not happen anymore. Ali loves Haverford, of which we could not be happier. The transition has been hard for all of us. She loves the school so we are comforted by that.
I will remember my husband and Ali looking at me, being with me for my first chemo session and trying very hard not to look scared themselves nor trying to look at me with sympathetic eyes. I will remember Amanda, not my daughter but my nurse, who worked so hard to get that first chemo through me and then very sweetly had to tell me that I needed a port, something that I was actually truly grateful for as it made it so much easier all the other visits. I will remember every chemo session, the amazing nurses, my amazing Dr. T.. I will remember November 2nd, my last chemo session and the huge hug my oncologist gave me. I will remember the friends and family that took me to my sessions, lunches at Corner Bakery and how wonderful so many people were to me. My bosses, Sr. Michelle and Chris, so understanding and supportive, full of love and prayers. Dr. B, the principal where I work, who texted me faithfully everyday to see how I was doing, and upon returning to work, made a point of seeing me everyday to check in, lend her support and give me a hug and smile. She is a breast cancer survivor herself and was so full of information and support. My neighbors and friends, who helped me and my family by bringing dinners or brunches and my sister-in-law Kim who organized it all. For all the cards, flowers and fruit, even a yummy jar of bread and butter pickles came my way. I will remember Ali, running through Target to track down the two teenagers who laughed at me and her berating them in the store.
Although I would not recommend cancer to anyone, it does, if you let it, allow you to see all the wonderful people around you. People who in their own way, show their care and concern. I cannot thank my dear Ali enough. She and I have always been close and, if possible, this brought us closer. Her care was 24|7 day after day as Amanda had to leave for ROTC leadership training and Greg had to go back to work.
Although Amanda will not be coming back home after school, and we don't really know where she will end up, she has made me so proud. She is excelling at school and will make an amazing nurse when she is done next year. She has amazed me with her determination and strength of self and character. I know that she will not be coming home but, I also know that she has made the decision that is right for her. She will be serving our country by serving those who go out and protect our country and those that need protection. She will be providing much needed care to those who live to defend others. She truly inspires me.
Ali has just left to go back to school. It is quiet in the house, when the dogs are not barking at anything passing by, when the girls are both gone. I am slowly getting used to it. I miss our mornings but, I also know that she is right where she is supposed to be. She loves where she is, excels in her classes and, has made many great friends around the country..
I love the unexpected phone calls from the girls. I also love the hugs when they come home, I will not forget them. Likewise, I will not forget the shopping excursions, lunches, movies or just sitting and talking. They mean the world to me, and honestly tide me over until I get to see them again.
So, as we are heading to February, I am thankful and grateful for all that I have.
One would think that a diagnosis of Invasive Ductal Carcinoma would tag 2012 as a horrible year. Of course, April 19th, 2012 will forever be in my mind; the day of my diagnosis. Then there will be June 11th, the day of my very long surgery which I am sure my husband will never let me forget as he, my daughters and family members spent over 16 hours in the waiting room. July 26th, my very first chemotherapy session. I will surely never forget the sickness from the first chemo.
Then, there is Amanda. When she went away to school we all believed that the plan was that she would graduate and return to the Chicago area. A true Chicago sports fan, we knew that she would not want to be far from Soldier and Wrigley Field and the United Center. It was discussed that when she graduated, she would return home for a year or so to save money as she worked as a nurse at one of the many great hospitals in the Chicago area. As most of you know, Amanda joined the Army ROTC. Hence, she will not be coming home. Once she graduates in 2014 she will be sent somewhere, who knows where, but it will not be home.
And, Alexandra. Ali left for her first year out east to Haverford. Greg and I are officially empty nesters. It is so quiet in our home now. What do I miss most? My drive to work. I work where the girls went to high school and every morning for the last two years, Ali and I would drive to school together. It was usually a quiet ride as Ali and I are not what you would call "morning people", but it was nice. The drive home was always a great time to check in with Ali and what was happening at school. She would tell me about her day, her friends and the homework she had or presentations that she was either preparing for or how they had gone. But that does not happen anymore. Ali loves Haverford, of which we could not be happier. The transition has been hard for all of us. She loves the school so we are comforted by that.
I will remember my husband and Ali looking at me, being with me for my first chemo session and trying very hard not to look scared themselves nor trying to look at me with sympathetic eyes. I will remember Amanda, not my daughter but my nurse, who worked so hard to get that first chemo through me and then very sweetly had to tell me that I needed a port, something that I was actually truly grateful for as it made it so much easier all the other visits. I will remember every chemo session, the amazing nurses, my amazing Dr. T.. I will remember November 2nd, my last chemo session and the huge hug my oncologist gave me. I will remember the friends and family that took me to my sessions, lunches at Corner Bakery and how wonderful so many people were to me. My bosses, Sr. Michelle and Chris, so understanding and supportive, full of love and prayers. Dr. B, the principal where I work, who texted me faithfully everyday to see how I was doing, and upon returning to work, made a point of seeing me everyday to check in, lend her support and give me a hug and smile. She is a breast cancer survivor herself and was so full of information and support. My neighbors and friends, who helped me and my family by bringing dinners or brunches and my sister-in-law Kim who organized it all. For all the cards, flowers and fruit, even a yummy jar of bread and butter pickles came my way. I will remember Ali, running through Target to track down the two teenagers who laughed at me and her berating them in the store.
Although I would not recommend cancer to anyone, it does, if you let it, allow you to see all the wonderful people around you. People who in their own way, show their care and concern. I cannot thank my dear Ali enough. She and I have always been close and, if possible, this brought us closer. Her care was 24|7 day after day as Amanda had to leave for ROTC leadership training and Greg had to go back to work.
Although Amanda will not be coming back home after school, and we don't really know where she will end up, she has made me so proud. She is excelling at school and will make an amazing nurse when she is done next year. She has amazed me with her determination and strength of self and character. I know that she will not be coming home but, I also know that she has made the decision that is right for her. She will be serving our country by serving those who go out and protect our country and those that need protection. She will be providing much needed care to those who live to defend others. She truly inspires me.
Ali has just left to go back to school. It is quiet in the house, when the dogs are not barking at anything passing by, when the girls are both gone. I am slowly getting used to it. I miss our mornings but, I also know that she is right where she is supposed to be. She loves where she is, excels in her classes and, has made many great friends around the country..
I love the unexpected phone calls from the girls. I also love the hugs when they come home, I will not forget them. Likewise, I will not forget the shopping excursions, lunches, movies or just sitting and talking. They mean the world to me, and honestly tide me over until I get to see them again.
So, as we are heading to February, I am thankful and grateful for all that I have.
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