our pad

our pad

Monday, March 16, 2015

Mini Monets



Ella, family sketch, age 6

Here is some recent work from my little artists. If I preserve it on the blog, I am then free to remove it from the fridge and quietly move it to the recycling bin, right? These girls are very prolific colorers...

Avery, gearing up for St. Patrick's Day,Age 6

Avery, always fashionable, and accessorizing with a rainbow kitty
Avery, who forgot to write, "I liked to build a snowman in the winter, like the first time it snowed a foot, but then not so much when the snow got to be 8 feet high."
Ella, hopefully some lamb days commin' soon
Addie, we'll say...experimenting with colors
And how could I forget my sweet, "Abbie's" school work:

Great work Abbie, now if we could spend less time coloring and more time working on your letters...





Friday, March 6, 2015

Well Hello Again...

I realize it has been over a year since I last posted. I needed to take some time off, share a little less, grow a little more, but recently I've been wanting a creative outlet for all my thoughts and ideas. I gave up Facebook for Lent- so here I am. Life has mostly returned to normal if any such thing actually ever existed with seven people under one roof , but I try. I am now working in the corporate world three days a week and back to teaching ballet one afternoon a week. We are crazy busy, but busy is good. We just got back from a great trip to Florida and managed to escape for a week, what promises to be the snowiest winter in history.  We visited with Nanny and Papa in Jupiter, beached and pooled it, then headed up to Disney for a couple days just in time for the first frost Florida has seen all season long. The frigid temps (by souther standards) scared the crowds away from the park the day we visited Animal Kingdom so there were hardly any lines and the kids thought it was the best day we ever spent together as a family. Magic Kingdom the next day was pretty magical too and I hope they all remember this trip for a long time.

Now we are back to the snow- lots of it, and back to grind, but trying to have some fun along the way. So on to what you’ve all been waiting for: The Updates on the kids.

Addie: My little whippersnapper is just as cute and cuddly as ever but boy is she a firecracker. She can be difficult as all get up and knows all my buttons to push although she is a complete mommy’s girl. Lots of transitions for this peanut this year with a move, a new school and full day Pre-K,  and she is not a fan of change so no wonder she has taken to acting out a bit. But she is just the funniest, most affectionate little thing so I can’t hold it against her. She’s taking ballet at the studio where I teach and grew up dancing so seeing her in her ballet leotard melts my heart. She has learned so much in school this year; is sounding out letters, writing numbers up to 100 and is just crazy about her teacher. She loves to play “school” and can still be found talking to herself out in her own imaginary world. She is always playing or trying to play with her big sisters and when they aren’t fighting they get along great-ha! She is smart smart and sassy but can’t pronounce either of those words because of the cutest little lisp you’ve ever heard. Although she will be 5 this spring she is definitely the baby of the family.

Avery: This has been a big year for Avery, in kindergarten and learning by leaps and bounds. She is reading and writing and brings home so much beautiful artwork everyday which reads- From: Avery To: Mom. She has become Miss Independent, as I split her and Ella into separate classes and I think its been good for everyone. She has made some very sweet friends and its nice for each of the girls, as identical twins,  to have their own identity.  Avery is also enjoying dancing and even auditioned and got a part as a mouse in a professional Nutcracker. Both girls did amazing and I was oh so proud.  She is still a girlie-girl and loves fashion and dressing up and make-up. Although she can have a mind of her own at times and is the most vocal of all my kids when things don’t go her way, she is a good listener and a sweetheart. She enjoyed skiing a couple times this winter and is pretty good about trying new things. She is generally willing to compromise and I for one appreciate that in a kid...

Ella: My girl is acing kindergarten, is reading and writing and follows directions and remembers everything. She's got some self confidence and the attitude to go along with it. She knows what she wants and is not the least bit timid in going after it. She has a very tight group of friends,  yet her twin is still her BFF.  Ballet and gymnastics come pretty easily to her so of course it drives me crazy when she says she doesn't want to go to these activities anymore- she can be oh so stubborn! She still loves animals of all sizes and varieties- I think she'll be a vet when she grows up- she has such a big heart.   

Cameron- Cameron is in fifth grade and enjoying switching classes for the first time. I can’t believe my littles boy is almost done with Elementary School. Despite 3 feet of snow on the ground he is gearing up for baseball season and had his first practice last week. He did  swim team this winter and got skiing a few times, just not quite as much as he would have liked. He is proving he is a responsible eleven year old through pet ownership. Santa brought him a guinea pig this christmas and I have been happy with how well he cares for it. He was a Lost Boy in his school play of Peter Pan and has really enjoyed some great after-school clubs. Now we are to the science fair and he loves this kind if thing, me- not so much!

Jameson- My first baby is almost done with middle school. He has had a very busy winter, in addition to playing hockey and on two basketball teams he is applying to high schools which is a very time consuming process for kids an parents alike. So far he has gotten into to both schools he applied to and received prestigious academic scholarships to both- it will be hard to choose. We are so proud of this kid’s accomplishments and can’t wait to see what is in store next. While still sweet and innocent and by far the easiest going kid around, I'm starting too see glimpses of a teenager- texting with friends, shaving that horrible fuzz above the lip, and tuning me out in favor of his phone-he is clearly growing up! This does come with it's perks, however, and with some small kids at home I am reaping the benefits- I have a built in babysitter. I can run an errand here, drive a kid there and not have to load everyone into the car. On the weekends Jim and I can put the girls to bed early then J and Cam watch a movie while we sneak out for dinner. He is more than responsible, has his phone close by and is First- Aid trained . Did I mention he saved Addie's life on a Christmas Eve when she choked on a necklace locket? Although adults were home at the time, he sprang into action and did the Heimlich Manuever until she finally threw up the silver star. Thankful for this kid!!








Monday, January 6, 2014

Out with the old, in with the New!

Good bye 2013! What a year it was. Last year at this time I felt the freshness in the air, a new beginning, the hope for good things to come, a clean slate and the renewed sense of hope and promise. Little did I know what lie ahead, how 2013 would challenge me, what changes it would bring to our family, our routine and everything we took for granted. Little did I know how we would be tested, the pain, fear and anxiety that would be thrust upon is. How blind I was to the life altering diagnosis that was in my future. Last year at this very time, I knew we stood on the verge of change, but had no idea that that change would involve my own battle with cancer. I had no idea I would never look at a New Year, or a new month, week or day the same way again.  I also had no idea that 2013 would bring me closer to my breaking point but bring me closer to God. I had no idea that in challenging everything I once knew I would strengthen my connections with family and friends. I had no idea that my initial feelings of loss and isolation would lead to finding comfort from the warmth of strangers. I had no idea that 2013 was going to be a year I would never forget, but for now goodbye 2013, goodbye..

Hello to 2014, to new beginnings, to health and to happiness. Hello to fresh starts, to hope and to rebirth.

Hello to a New Year, a new month, a new week, and brand new day...



Thursday, November 21, 2013

Clearer Days

The post treatment wait for my scan passed more quickly than I feared. The five week interlude is standard to give the chemo more time to do its job and allow some of the inflammation to subside. Physically, I began to feel a lot better, regained much of my energy, but continued to have some side effects; continuing hair loss, some taste bud damage, peeling skin, strange nail changes, and blufferitis of the eyes, all of which were tolerable.
It was an anxiety filled few weeks but I kept busy and had a lot of pleasant distractions to help take my mind off of the looming tests.  My amazing group of college friends had a get together for me where I received a few wonderful surprises and enjoyed a day catching up with these special ladies.
I had a weekend getaway to Nantucket with another group of wonderful friends where we relaxed, shopped, took walks on the beach, ate out, cooked in, and drank lots and lots of wine (making up for six months of no alcohol consumption). I had a dear friend from high school fly in for a night out in Boston with our other high school bestie, we had dinner at a nice restaurant and stayed overnight in the city. I had a couple of girls' lunch dates and some special family time highlighted by a long weekend trip to the white mountains of New Hampshire.
We hiked and took in the amazing foliage, sat around a cozy fire and enjoyed each other's company away from it all.

I took time to stop in church from time to time over the waiting period and visit a prayer circle where an intention was made in my name. Over this waiting period friends lit candles for me in Rome and relatives made a pilgrimage to Medjagorie, returning with blessed Rosary Beads and Holy Water. Although I had my moments of worry, and one panic when I thought I felt a lump, which thankfully turned out to be nothing, I tried to remain positive and focus on the outcome I wanted. I heard from so many people who told me they were praying for me and so many sending well wishes and positive thoughts my way.  I continued to pray for a full recovery and felt the energy of the prayers around me. I had a few signs leading up to my test which helped me to keep the faith and reminded me to trust in God's plan for me. Perhaps I'm reading to much into it, perhaps they were mere coincidence, perhaps I'm conducting a desperate search for meaning, or perhaps, God really does reveal himself when we need him the most. The first was exactly one week before my test, I happened to step outside in the late afternoon to see the most unusual pink cotton candy sky. I walked to the middle of my road to get a better view and a beautiful double rainbow appeared in the sky above me. I put the kids in the car to drive and try and get a better view and we made it to an opening where we could see the full arc in all its glory.
The kids suggested we should follow the rainbow to the end in hopes of finding a pot of gold. To humor them, I set off driving in the direction of the end of the rainbow, them directing me, "that way, now that way." Soon we were one street away from our house, looking at the rainbow which disappeared into our very own roof line. "I guess we found the end of the rainbow", they exclaimed and we headed home to our own pot of gold. Just that week in school, Cameron had learned the rainbow is a symbol of God's promise to His people. The rainbow leading to our house was a reminder that God's love was all around me and my family during this time and always. More uplifting moments came as I watched John Lester pitch two amazing games helping lead the Red Sox to victory in the World Series. He is a lymphoma survivor and seeing how well he is doing just two years after completing treatment served to give me hope for a full recovery and more good things to come in my future. The afternoon before my scan, I had some time to myself, I did a little retail therapy, then headed to church to say some prayers.  I found the church empty, so I walked in, made my way to front pew and knelt down, resting my head in my hands . The calm was soon interrupted as I opened my eyes to the sound of hammering. A man had quietly entered the church and immediately began working on the alter. He was wearing a tool belt and I noticed that the altar was off balance and he was working to secure it. I grew annoyed as he took out a drill and began screwing in a piece of wood. I only wanted a few moments of peace and quiet, time to myself to pray, and  now there was a full construction zone taking place  on the altar. I closed my eyes and tried to tune out the noise, and when I opened them again I saw the man kneeling at the alter, bowing before the cross. I looked down, burying my face in my hands to give him some privacy in his moment of quiet reflection and when I looked up again he was gone.  My annoyance turned to peace as I realized that this was perhaps another sign. A carpenter, sharing the the same profession as Jesus, appearing out of the blue in the church and leaving as quickly as he came, symbolizing the fact that the Lord was in that moment, right there watching over me.
The last sign came as I headed into Boston for my PET scan. It was slightly overcast, clouds dotted the morning sky; I notice the sky more now than ever before. As we drove I saw beams of light shining down from the clouds. I thought back to riding in  a friend's car when we were young and her pointing to the rays saying that in her family they call those, "God's fingertips". And now when I needed a touch of grace, God stretched his fingertips down from the Heavens, giving me the confidence to enter the Hospital, strength to take the elevator down two levels to radiology and the faith to leave everything else up to Him.
After I had labs drawn and received the injection of the radioactive contrast, I sat in an isolated room for an hour then was brought in for the scan where I could still feel the rays of light shining down. Afterwards, I met Jim in the waiting room and we left together knowing that a long anxiety filled weekend awaited. I tried to put the looming results out of my head and accept that it was no longer in my control. I then focused on making the most of the weekend with my family. We had a family celebration at home for the twins 5th Birthday.
Preparing for this helped to take my mind off of the test and focus on this positive occasion instead; celebrating the fact that my identical twin girls, born prematurely weighing just 4 pounds, were now healthy and happy five year-olds.
They love to perform, sing and dance. They love fashion and puppies and baby dolls. They love to color and paint and pump on the swings. They love to play elaborate imaginary games. They love their family and each other and their mom. And nothing I want more than to be around to see them grow up, see how they maintain their twin bond as they grow, see what kind of strong, independent and compassionate women they become.
Tuesday was there actual birthday and the day I was to receive my results.  To make the morning special for them, Jim and I filled their room with dozens of purple and pink balloons.
We prepared a yummy breakfast, took them to school together then headed into Dana Farber. There we were met by my sister and father in the waiting room.  The wait was nerve wracking and the air felt heavy around me. I could feel my heart beating hard inside my chest and my hand sweating inside Jim's.  We were brought into my Dr.s office and a long wait commenced again.  My doctor finally entered and without hesitation, immediately delivered the good news, the news I had been waiting over six long months to hear; my scan came back clear! There was no longer evidence of the disease. We all cried with joy and what an emotional release it was. There will be a lot of follow-up going forward, I will be closely monitored, the port will stay in place for awhile  until the doctor feels confident that it can be removed, I will have appointments every 3 weeks initially to have the port flushed, a check up in six weeks then scans every six months going forward. The fear of relapse will be ever-present but for now I am thrilled to be celebrating every moment and enjoying every glass of champagne that comes my way.

Thank You for all the prayers, they worked, and there is no better feeling than that.

Monday, September 23, 2013

Update...

Tomorrow I am scheduled for what will hopefully be my last chemotherapy infusion. Almost six months of treatments and, hopefully, my last one is less than 24-hours away! I say "hopefully" because I do not yet know if I am in remission and will not know until I have a PET scan, four weeks later and the course of care going forward weighs heavily upon the results of that scan. The waiting for the test to determine if the cancer is completely gone, will likely be the hardest part of the entire ordeal. My body will slowly recover from the toll that chemo has taken, but my mind will be anxious and fearful of the unknown. Now, during the course of my therapy I feel as though I am doing all I can to destroy the cancer, but after Tuesday when I am no longer receiving active treatment, the fear and worry will set in. "Scan-xiety" is a very real part of recovering from lymphoma as scans are scheduled at regular intervals during remission than gradually spread out until the five year mark- a major milestone, I already have my sights on. During the course of the wait, I plan to combat the worry by staying busy, regaining a normal level of activity, staying positive, enjoying time with family and saying lots of prayers. I have a couple of girls getaway weekends planned, a few dinners out lined up and some fun events to look forward to, but will wait until after a clean, cancer-free scan to let the real celebrating begin...

Thursday, September 19, 2013

2B or Not To Be....


At the time of my diagnosis the cancer was present in two quadrants of my body; it was stage II. It had affected lymph nodes in both sides of my chest, my supra-clavicle region and possibly my neck. During the initial staging, an A or B distinction is also allotted. "A" signifies you are not yet symptomatic, "B" means you are experiencing symptoms of the disease and therefor it is  generally more advanced or aggressive and requires more treatment. I was a B. My cancer was stage IIB. I had cancer and I had symptoms. I was not in denial about these symptoms, I was not afraid to get myself to the doctor, I was not nonchalant about my health. I was concerned, I was proactive, and I was thorough.  Despite all this, it still took over two years to get a diagnosis. Two years that the cancer was growing inside me.  I experienced my first night-sweat in June of 2011. I remember it well, waking in a panic, waking my husband, drenched to the core, having to change the sheets- talking  about it with my neighbors the next morning as we gathered on the street, sipping our coffee and watching the kids play. In perhaps my over-sharing, I was reassured it was normal, many of my friends had night-sweats on occasion. And I was relieved until it happened again. This time, as any concerned mother of five with slightly hypochondriatic tendencies would do, I googled my symptoms on WebMd. I read the ten page list of possible causes, everything from "completely normal part of aging" to "Leprosy",  however the one that jumped out at me was Lymphoma. I shut down the computer and called my primary care physician. She examined me, was not concerned but ordered some tests to help relieve my anxiety. When everything came back normal, I was temporarily relived but as the night-sweats continued at random, so did my concern. I returned to my doctor who, at a loss, suggested it might be hormonal. I went to my OBGYN where I had more tests, then followed back for more tests. With still no answers I went to Endocrinologist, who specializes in tracking the function of all the bodily processes that contribute to sweating. I had several appointments and many tests, blood work, 24 hour fasting tests, and 24 hour urine tests. I checked back in with my primary doctor during this time and had a chest X-ray.  Everything came back "normal." Perhaps it was stress or anxiety I was told time and time again, I did have five kids, including three under 3 years old. Maybe I was stressed, and these sweats were my body's way of working it out? I thought I would tackle the stress, I hired a babysitter more often, worked out five days a week, took yoga classes and even enrolled in a course at MGH on "Utilizing the Relaxation Response." However, I knew my body, knew my mind, knew that something was not right so I pushed on, I got a second opinion from a Primary at a Boston Hospital, a third at a homeopathic practice. When nothing turned up, and still feeling something was not right, I returned to my primary, who at my urging finally sent me to a Hematologist/Oncologist. I thought if a Cancer Doctor says it is not indicative of anything and not to worry then I will I listen and move on, recognizing this is just an unusual, sometimes inconvenient symptom, but something I can definitely live with. I just couldn't live with the worry. Once again everything checked out fine. I thanked God that I did not have cancer and carried on with my life until I soon discovered a hard nodule in my neck. It was small and hard, but after a week when it did not go away, I went to my Doctor. She told me it was certainly not lymphoma and to follow up in a few months time. I went back for the follow-up and mentioned a cough which was waking me up at night. She attributed it to allergies and suggested a humidifier. She recommended yet another follow up and if the node was still present in three months then she would send me to an ENT for a biopsy. Well, like any concerned mother of five with slightly hypochondriatic tendencies, I did not want to wait three months for a biopsy so went ahead and made the appointment with the ENT on my own.  I told him of my symptoms, he examined me but did not find the lump concerning enough to warrant a biopsy. I returned in six weeks for a follow-up with the ENT and the nodule was still there but he was still not concerned so I tried not be either, after all I was feeling fine, working out five days a week, teaching dance classes, chasing around my kids and getting six hours of sleep if I was lucky. Could I do all this if I had cancer? The end of February I had my regular annual physical and was declared "the picture of health". Hard to fathom that at that time, the upper half of my body was filled with cancerous cells. After all those many trips to many different doctors it would only take one trip to the Emergency Room less than two months later, and one CT scan to discover what was hiding on the inside. Alone in hospital bed in the middle of the night I found out about the enlarged lymph nodes pushing on my lungs and heart. I had stage IIB cancer.
I choose not to think about what if it was found earlier?
I choose not to think of how it took two years and managed to reach stage IIB.
Instead I choose To Be.
To be in the moment.
To be happy.
To be positive.
To be forward thinking.
To be here everyday...



Thursday, September 12, 2013

How Cancer Has Changed Me



Cancer has changed me in ways I never imagined.  I think back to the person I was in the spring, navigating an over-scheduled calendar, reconciling baseball practices that overlapped with soccer games, arranging playdates, teaching ballet classes, driving carpools and checking off the grocery list. Overly concerned with keeping the house clean, I nagged the kids to put away their shoes, keep their toys in the playroom and their backpacks out of sight. My biggest complaint; not enough hours in the day to get the laundry put away, my biggest pain; a nagging case of plantar fasciitis which was hindering my running schedule. How quickly that pain in my heel dulled when I awoke from surgery, unable to move, fighting to keep a cough at bay as the pain ripped through the stitches inside my chest. How trivial an immaculate house seemed as I spent a week in a sterile hospital bed not allowed flowers to brighten the room for fear of introducing foreign germs.  How wasted the hours spent cleaning and folding leading up to my hospitalization seemed when torn away for my children for seven days, recovering from surgery while they were out on their school vacation week.  How petty my stress over how my boys had performed in tryouts, and worrying if they would have to miss a soccer tournament to make a hockey game, worrying did the girls have new matching outfits for Easter, and bows and cardigans, worrying if I had completed enough crafts and set out enough decorations to impress at the holiday gathering?  How quickly these stresses fade while waiting to find out what kind of cancer you have.  How quickly the five different colors of ink which marked up our calendar, blurred together while waiting to discover my prognosis and wondering how many more calendar pages I would be able to turn and if I would have a lifetime to celebrate those carefully circled birthdays and highlighted dates of recitals and play-off games.
Cancer has changed me.
There are the physical changes; new scars- one across my ribs, a smaller one on my stomach and this beauty which has left me still without feeling across much of my back, all from my surgery in April.

Then there are the two incisions on my chest from the surgery implanting my portacath and the noticeable bulge under my skin, evidence of the metal disk resting just below the surface.


There is hair loss. I have been slowly shedding since a month into treatment and with the amount of hair left on my pillow in the morning or the amount found in my hair brush after a single use, it's a wonder I have any remaining at all. I now understand why many patients elect to shave their heads before treatment begins to avoid the heartache of watching strands fall to the ground as your part widens and the paleness of your scalp peaks through. My hairline has receded and I never thought I would be the first in my family to inherit my grandfather's male-pattern baldness. My eyebrows are barely visible, elongating my forehead and distorting the familiar proportions on my face. Then there is weight gain. While I thought chemotherapy would lead to weight loss from the nausea, I was surprised to learn that quite the opposite would be true. A twenty pound weight gain is the norm for females my age going through chemotherapy, and unfortunately this has been the case, due to the steroids, the fluids and lack of strenuous exercise (and let's be honest- those delicious meals being delivered every night. If someone spent the time making me and my family a yummy dinner and dessert- damn right I will take the time to enjoy it)!



Being diagnosed with cancer has changed the way I conduct myself as well. I have become inclined to say "yes" more. Yes, we can go out for ice-cream again tonight. Yes, I will watch your dance show in the living room. Yes, I will watch you perform your magic trick which I taught you and yes I will pretend to be astounded as you pick the card I was thinking of. Yes, I will read one extra story. Yes, I will read it again. Yes, you can sleep in our bed. Yes, we can eat dinner outside, yes, we can eat it up in the tree house. Yes, you can wear that, yes, I know it's a costume. Yes, I will come sit and watch the movie with you, and yes, we can eat popcorn in the good room. Yes, I will walk with you to the bus stop.  Yes, we can play Monopoly, yes, I still hate board-games. Yes, I will paint your nails, yes, I will let you paint mine. Yes, I will try and do a cartwheel. Yes, I will pretend to be the baby in your game of house. Yes, I will hold your hand and yes we can skip down the street. Yes, I will wear the painted pasta necklace you made me while I go to the store. Yes, I will join you in the water for a swim, yes I know it's cold and yes I do know how to swim! Yes, you can take the cushions off the couch to make a fort, yes, I will help you make it. Yes, I will lie next to you and hold you until you are fast asleep...

Yes, let's go away someplace we've never been. Yes, let's go to a yoga class together. Yes to a girls weekend away, yes to date-night in. Yes, lets meet for lunch, its been too long...


This diagnosis has given me the strength and perspective to say "no" more often as well. No, I won't be able to make that meeting after all. No, I won't put away all the laundry right now, no I won't bother sweeping all the floors. No, I don't have time to listen to you complain. No, I won't give in to negativity. No we don't have to leave yet. No, no you don't have to go.


Cancer has a way of breaking you down to a point where you finally understand what is truly important.  It has given me a greater appreciation for life; the people around me and the beauty in the everyday.
While chemotherapy can cause vision problems, it has helped to give my eyes new focus.  I notice more around me; the shape of a cloud, the hue of the sky, the call of bird, the delicate perch of a bumble bee on a flower, the sound of the wind whistling through the trees in my yard, the shape of the moon, the texture of a sunflower stalk.
I have become a more perceptive observer of my children, noticing how many times my four year old says "um" in sentence, how her twin moves her fingers in excitement. I note my son's new callouses from climbing and the flecks of green in my oldest's hazel eyes. I notice how my littlest circles her feet like I do when falling asleep and clings to her blanket with the same hand the whole night through.


It has given me a more profound appreciation for all the good around me. I have become the recipient of so much good will from others that it makes me want to be a better person. After constantly bombarded with stories of injustices and all the wrong in the world, it has taken through going through something like this to recognize how much good still exists.
It is truly humbling how many people have reached out to me. How many people were compelled to write, email, call, send help in anyway they could. I have been touched to hear from people I didn't think would remember me after so many years, so many people who are friends of friends, and many I will never get to meet.  I am amazed how the initial outpouring of support has been followed up by continued expressions of concern. Knowing I am in others thoughts and feeling the power of their prayers has given me strength. Having others share their own hardships with me and inspiring me with their stories of victory has given me courage.  
I recognize we all have our battles, many struggling more than I, and we are all just trying to do our best with the circumstances we are given.  
Now, I am more determined than ever to do my best; in fighting this disease,  in being a better wife, daughter, friend, in following through with my dreams, in helping others, in raising my children. I am not a saint, I still look forward to my children's nap time everyday and will be clicking my heals when I can leave them at school for a few hours during the week, but, I will make every attempt to appreciate the time we do have together, thank God for their smiles, the ability to make them laugh, to feel their love. I am not a saint, I still roll my eyes in line, beep my horn at slow drivers, love me some gossip as much as the next gal, but I am more careful when passing judgement, knowing we are all facing our own hardships. I am not a saint, I still want time to myself, make demands on others and like things done my way, but since my diagnosis I'm more ready to help, go out of my way, and to give of myself. 
Just recently, at an outdoor event with my sister and some friends, a young man collapsed before us. A crowd stood around gasping and staring as he began to convulse then lie motionless on the ground.  Without thinking I jumped into action running over to him and his girlfriend who was kneeling at his side. I checked his pulse, when I was informed that he had been stung by a bee just seconds before.  I yelled for an epi-pen, began barking orders, instructing someone to call for help, pleaded for a doctor. Soon a friend produced an epi-pen and handed it to me. Everyone was counting on me to help save this man's life. I removed the cap on the epi-pen then hesitated as I realized he was wearing jeans, obscuring the place on the thigh where the shot of epinephrine is to be administered. Not certain the injection could go through the thick denim, I told his girlfriend to unbuckle his belt. She sat crying and helpless, seemed to be in shock, so I began the task myself. Here's the embarrassing part; just as I got the man's pants unfastened and pulled down revealing his boxers, he suddenly regained consciousness, sat up, out of it, but fine. Turns out he didn't really need to be saved after all.  Although an awkward few moments transpired as the man who had just come to was filled in on what had happened, why I was kneeling beside him and why his pants were undone, he and the girlfriend were most thankful that I was there and more than ready to help. Before my diagnosis I likely would have been sitting on the sidelines with the rest of crowd but now feel a greater urgency and purpose. I am compelled to be that person who goes out of there way, apparently, sometimes whether needed or not... 

Earlier this week while out for a jog, elated to be running again (barely keeping pace with the mailman, who was walking and delivering mail), I came upon a tow truck with a white car bearing a handicap license plate, already loaded up on the platform of the flatbed truck. A woman with two prosthetic legs was attempting to climb up the ladder and get into the passenger seat in the trucks cabin. I saw her struggle as her legs twisted beneath her, missing the step and getting caught under the medal rungs. Using her arms she continued to pull herself up holding on to the handrails. I was tempted  to look the other way as not to 'embarrass' her, justifying to myself that 'she wouldn't want any help', I would 'hurt her pride'. But after a few months with my own health struggle, I know how much those offers mean. I appreciate the smallest gesture, a nod of understanding, anything to lighten the load or help ease the pain. I now know what the right thing to do is and I am more inclined to do it. I walked over and asked how I could help. She was in quite the predicament, legs not able to bend to fit in the truck's compartment and  a seat which couldn't be pushed back. I supported her foot giving her some leverage, and guided her legs as the driver pulled her hands from his seat. She finally made it to the floor of the cab but couldn't lift herself onto the seat from that position, but she was not giving up.  I climbed up onto the steps and helped pull her up and into the seat. I untwisted her legs as she sat back, utterly exhausted- we were both exhausted, it had taken everything we had. She was out of breath as she whispered, "Thank you, I'm not sure what I would have done." I continued on my walk, feeling the fresh autumn air on my face,  I just wanted to scream, I'm alive, I have two legs, and I am walking today- Thank You God.
I am no saint, I loose my patience, I say things I don't mean, but I now take the time to talk to God more and thank Him for the gifts in my life.  And there are so many, and sometimes it takes going through something hard, something sad, something that challenges you, something that makes you question, something scary, something like cancer to make you realize that .