Monday, July 13, 2009

Some Summer Fun

View from the beach at Great Island Common, New Castle, NH


My sister, my neice and nephew were here visiting for the last week, from Kentucky. It was great to see them and spend time.
It was a busy week...we went up to the lake house in Maine for 4th of July, I took them to the beach, we went into Boston and did a Duck Tour, we went shopping, and we spent time hanging out by the pool.

When we were at the beach, Michaela decided she wanted Aaron and my brother to bury her in the sand....


then she wanted them to put chips on her so the seagulls would land on her....it was HYSTERICAL! She loved every minute!


The Duck Tour was fun, even though it poured down rain all day!






The weather has FINALLY started to feel more like summer!!
We're off to the lake house in Maine again this weekend with the WHOLE Spinney family. I have my new Margarita machine all primed and ready to go!

Tuesday, June 30, 2009

We're heading in to Mass General tomorrow for Michaela's brain MRI.
They told us to expect a long day there....I am so dreading this.

Wednesday, June 24, 2009

Another Year Down

I just can't believe the school year is over, and it's the end of June.
It just goes by so darn fast!

Both kids had an amazing year and did really well.

Aaron had his 8th Grade Awards Ceremony on Monday morning. I couldn't have been more proud. He won awards for academics, including the President's Award for Outstanding Academic Excellence and the President's GOLD Award for Volunteer Service...he had 114 hours of community service this year.
The Graduation Ceremony was very nice. There were 300 graduating 8th graders....and that's just in Aaron's school, we have another Middle school, who had their ceremony after ours, that graduated about the same number. He'll have an incoming Freshman class of 750.
The high school he'll go to has close to 4,000 students. It's a private school and looks like a college campus...it's beautiful and has been around for over 200 years (Pinkerton Academy). He's excited to go and is taking all advanced college prep courses. They even let him take the Sophmore level engineering class. I think he'll be busy next year!


Michaela's last day of school was yesterday. She had such a great year. She made Honor Roll again....we're so proud!!! She has grown so much this year, in all areas. And, I've seen SO much progress academically. They got to visit the class they will be in next year and see what kids will be in their class. She has a fabulous teacher and a great class of kids for next year.....I know I'm excited for her!!

So, here we are. The first day of summer vacation, and it's cold and rainy out....feels more like April than the end of June. It had better change real fast...you know, like...hot...humid...80+ degree heat. The kind of heat that makes you sweat even if you're standing still in the shade.....that's what summer is!!! I'm going to start to get really cranky if that sun doesn't come out soon...and no one wants that!!

Sunday, June 14, 2009

Keeping Up

Well, actually, I should say 'not able' to keep up!
I'm checking in on everyone, I just can't seem to find a moment to update the blogs these days. Once the kids are out of school I'm hoping things slow a bit.

Aaron graduates 8th Grade on June 22nd....I still can't believe he'll be in high school! Michaela's last day of school is June 23rd. I'm a little sad to see the year end for them, it's been a great school year for both.

Saturday, May 23, 2009

Whrilwind Week

It's been a crazy week.
On Tuesday, my father-in-law had a stroke. He didn't tell anyone so they didn't get him to the doctors until the next day, at which point he was immediately admitted.
They can't regulate his heart and the right side of his face is effected, he has slurred speech and is hard to understand. No news as to what the treatment plans are.
It's always something.....

I had two big functions at Michaela's school that I was in charge of and had to prepare for, both were yesterday. I left my house at 8:00am and didn't get home until 10:00pm. They both went off without a hitch, a big relief and I'm exhausted! I've been a PTA officer for the last two years and next year I'm President...yikes....what am I thinking?

Michaela was supposed to have an MRI on Wednesday. I re-scheduled for July 1st. I'm second guessing that decision today. She's been having dizzy spells where she's loosing her sight....this is a new one. Does it ever end?

I'm so glad it's a long weekend. We're heading up to the lake in Maine on Monday for the official start of the summer season.

Hope everyone enjoys the long weekend!

Tuesday, May 12, 2009

10 Years Ago Today....

You came into this world, completed our family and changed ours lives. You've shown us the joys of living in your excitement of everyday and the way you happily greet each morning. You've taught us that the appreciation of the small things are just as important as the big.

Happy 10th Birthday, Princess

May you always fly to your heart.....


video

Tuesday, April 28, 2009

Welcome To The Club

My dear friend,

I am so sorry for your pain.

Don’t worry; no one else sees it, I promise. To the rest of the world, you’re fine. But when you’ve been there, you can’t miss it.

I see it in your eyes. That awful, combustible mixture of heart-wrenching pain and abject fear. God, I remember the fear.

I see it in the weight of that invisible cloak that you wear. I remember the coarseness of its fabric on my skin. Like raw wool in the middle of the desert. You see, it was mine for a time.

I never would have wanted to pass it on to you, my friend. I remember so well suffocating under the weight of it, struggling for breath, fighting to throw it off while wrapping myself in its awful warmth, clutching its worn edges for dear life.

I know that it feels like it’s permanent, fixed. But one day down the line you will wake up and find that you’ve left it next to the bed. Eventually, you’ll hang it in the closet. You’ll visit it now and then. You’ll try it on for size. You’ll run your fingers over the fabric and remember when you lived in it, when it was constant, when you couldn’t take it off and leave it behind. But soon days will go by before you wear it again, then weeks, then months.

I know you are staring down what looks an impossibly steep learning curve. I know it looks like an immovable mountain. It is not. I know you don’t believe me, but step by step you will climb until suddenly, without warning, you will look down. You will see how far you’ve come. You’ll breathe. I promise. You might even be able to take in the view.

You will doubt yourself. You won’t trust your instincts right away. You will be afraid that you don’t have the capacity to be what your baby will need you to be. Worse, you’ll think that you don’t even know what she needs you to be. You do. I promise. You will.

When you became a mother, you held that tiny baby girl in your arms and in an instant, she filled your heart. You were overwhelmed with love. The kind of love you never expected. The kind that knocks the wind out of you. The kind of all encompassing love that you think couldn’t possibly leave room for any other. But it did.

When your son was born, you looked into those big eyes and he crawled right into your heart. He made room for himself, didn’t he? He carved out a space all his own. Suddenly your heart was just bigger. And then again when your youngest was born. She made herself right at home there too.

That’s how it happens. When you need capacity you find it. Your heart expands. It just does. It’s elastic. I promise.

You are so much stronger than you think you are. Trust me. I know you. Hell, I am you.

You will find people in your life who get it and some that don’t. You’ll find some that want to get it and some that never will. You’ll find a closeness with people you never thought you had anything in common with. You’ll find comfort and relief with friends who speak your new language. You’ll find your village.

You’ll change. One day you’ll notice a shift. You’ll realize that certain words have dropped out of your lexicon. The ones you hadn’t ever thought could be hurtful...Dude, that's retarded...Never again. You won’t laugh at vulnerability. You’ll see the world through a lens of sensitivity. The people around you will notice. You’ll change them too.

You will learn to ask for help. You’ll have to. It won’t be easy. You’ll forget sometimes. Life will remind you.

You will read more than you can process. You’ll buy books that you can’t handle reading. You’ll feel guilty that they’re sitting by the side of the bed unopened. Take small bites. The information isn’t going anywhere. Let your heart heal. It will. Breathe. You can.

You will blame yourself. You’ll think you missed signs you should have seen. You’ll be convinced that you should have known. That you should have somehow gotten help earlier. You couldn’t have known. Don’t let yourself live there for long.

You will dig deep and find reserves of energy you never would have believed you had. You will run on adrenaline and crash into dreamless sleep. But you will come through it. I swear, you will. You will find a rhythm.

You will neglect yourself. You will suddenly realize that you haven’t stopped moving. You’ve missed the gym. You’ve taken care of everyone but you. You will forget how important it is to take care of yourself. Listen to me. If you hear nothing else, hear this. You MUST take care of yourself. You are no use to anyone unless you are healthy. I mean that holistically, my friend. HEALTHY. Nourished, rested, soul-fed. Your children deserve that example.

A friend will force you to take a walk. You will go outside. You will look at the sky. Follow the clouds upward. Try to find where they end. You’ll need that. You’ll need the air. You’ll need to remember how small we all really are.

You will question your faith. Or find it. Maybe both.

You will never, ever take progress for granted. Every milestone met, no matter what the timing, will be cause for celebration. Every baby step will be a quantum leap. You will find the people who understand that. You will revel in their support and love and shared excitement.

You will encounter people who care for your child in ways that restore your faith in humanity. You will cherish the teachers and therapists and caregivers who see past your child’s challenges and who truly understand her strengths. They will feel like family.

You will examine and re-examine every one of your own insecurities. You will recognize some of your child’s challenges as your own. You will get to know yourself as you get to know your child. You will look to the tools you have used to mitigate your own challenges. You will share them. You will both be better for it.

You will come to understand that there are gifts in all of this. Tolerance, compassion, understanding. Precious, life altering gifts.

You will worry about your other children. You will feel like you’re not giving them enough time. You will find the time. Yes, you will. No, really. You will. You will discover that the time that means something to them is not big. It’s not a trip to the circus. It doesn’t involve planning. It’s free. You will forget the dog and pony shows. Instead, you will find fifteen minutes before bed. You will close the door. You will sit on the floor. You’ll play Barbies with your daughter or Legos with your son (or vice versa). You’ll talk. You’ll listen. You’ll listen some more. You’ll start to believe they’ll be OK. And they will. You will be a better parent for all of it.

You will find the tools that you need. You will take bits and pieces of different theories and practices. You’ll talk to parents and doctors and therapists. You’ll take something from each of them. You’ll even find value in those you don’t agree with at all. Sometimes the most. From the scraps that you gather, you will start to build your child’s quilt. A little of this, a little of that, a lot of love.

You will speak hesitantly at first, but you’ll find your voice. You will come to see that no one knows your child better than you do. You will respectfully listen to the experts in each field. You will value their experience and their knowledge. But you will ultimately remember that while they are the experts in science, you are the expert in your child.

You will think you can’t handle it. You will be wrong.

This is not an easy road, but its rewards are tremendous. It’s joys are the very sweetest of life’s nectar. You will drink them in and taste and smell and feel every last drop of them.

You will be OK.

You will help your sweet child be far better than OK. You will show them boundless love. They will know that they are accepted and cherished and celebrated for every last morsel of who they are. They will know that their Mama’s there at every turn. They will believe in themselves as you believe in them. They will astound you. Over and over and over again. They will teach you far more than you teach them. They will fly.

You will be OK.

And I will be here for you. Every step of the way.

With much love....

Tuesday, April 21, 2009

Join Us

At Brady's Walk....
A Walk For Williams Syndrome


We are walking in honor of Michaela

Sunday, April 26th

DW Field Park ~ 331 Oak Street, Brockton, MA

Be there for 12:30.....Walk starts at 1:00

If you can't make the walk, but would still like to contribute
send me an email at lspinney2006@yahoo.com

Thank You!!!

Friday, April 17, 2009

Wooo Hooo

Michaela made Honor Roll again!!

Thursday, April 9, 2009

Rights Of Passage

We all go through these, sometimes they're a big deal.
Tomorrow my 9 year old daughter will go through one. All 4th grade girls know about "The Movie". They giggle about it at lunch and out at recess, they've heard all the rumors about what they will 'see'. I remember doing that myself, when I was their age.
Tomorrow is the big day where all these young ladies get a taste of womanhood....they get to see the puberty movie....all about the menstrual cycle.
YIKES!
Now, I've already had this talk with Michaela when she started on the Lupron shot to STOP puberty. She got it, she understood, she asked appropriate questions, but this was done in private and she was told to keep it private. Because, at the time, none of the girls her age were having these issues. I'm certainly not against the showing of this movie, it's rather harmless. Corny, yet informative. I went to the Parent viewing so I would know what she was seeing and to anticipate how she would react to what was shown.
I'm not sure if I've ever mentioned that my lovely daughter does not have a filter...she tells it like it is and has a comment for everything. Funny, but THIS is where my small bit of anxiety is, not the topic or content of the movie, she'll be fine with that. OH, but, God only knows what will come out of her mouth....well, actually I have a good guess.
I soooooo wish I could be a fly on the wall!

Friday, April 3, 2009

Thank You.....

Abi and Hannah!!!!!
I love the pictures you made.
Love your friend, Michaela
video

Friday, March 20, 2009

Good Morning Spring

Michaela came rushing down the stairs this morning at 5:00am, came into my room and said "I'm just so excited to say hello to spring!"
Really? 5:00AM?
I was already awake, but that's MY time to ease into the day...you know, hot cup of coffee, peace and quiet...
This is what greeted spring this morning...hehehehehe!!!

Wednesday, March 18, 2009

The Winners

Aaron had his Lego Robotics competition. He was the captain of his team that he named "The Winners" at the beginning of the season.
I am so proud of him. He handled himself so well, stayed calm, cool and collected.

And, of course, they WON!!

video

Thursday, March 12, 2009

If you'd like an invitiation to my private blog, just send me an email lspinney2006@yahoo.com

Wednesday, March 11, 2009

Michaela's Newest Masterpiece

Tuesday, March 10, 2009

For all the things that are not so great about Michaela having Williams Syndrome, there are so many more wonderful things that have come out of it.
For one, all the amazing people we have come to know as friends. People we would never have met otherwise.
I was honored to have been able to spend the weekend with some of those amazing people. There's nothing more inspiring than being in a room with so many who are committed to making life better for their children.....our children.

I was especially thrilled to have been able to hang out with two of our bloggy friends, Heather and Anna. They are both such beautiful people.

Monday, March 9, 2009

A Very L-O-N-G Day

It was a GREAT weekend!
Very productive and informative.....so get ready New England!

I had the best time with some amazing people. Stayed up WAY too late chatting with Heather and Anna. We lost track of time and didn't get to bed til 2:00am, so I started Sunday in a sleepy haze.

We worked until 12:30 then headed to the airport. My flight was scheduled to leave at 2:45 on United...I don't usually fly this airline but they had the best flight times to Detroit. They boared the flight on time, left the gate on time...but then stopped half way on the tarmac due to a computer 'issue'.....interesting considering they had just announced a minute earlier that the plane was less than 2 weeks old! So, we sat there for about 20 minutes....(all the time, I'm freaking out knowing I only had 45minutes in between connecting flights)...before they finally drove back to a gate to see if it could be fixed. We sat on the plane for 2 and 1/2 hours before they announced they couldn't fix it and we had to get off.

Now, I get that these things can happen, it was a pain because I had now missed my connecting flight....I was still calm and not too annoyed until they told all the passengers we then had to go back out to the front check-in and start over by booking other flights.....they made us all go back, get at the end of a very long line at the front check-in, and wait....and wait...and wait. They had 3 people checking in travelers, didn't add anyone knowing they had an entire plane full of people, from their cancelled flight,tring to get out of there. Most of us stood for over an hour and a half waiting our turn, only to be met by an incredibly rude human being behind the counter.

When my turn came, I was rudely told my only 2 options were a flight on US Air at 8:15pm or Monday afternoon. I made my choice to leave on the other airline, was again rudely told to go get my bag and go to the check-in at US Air.
I stood in line to check-in, put my bag up to be checked and was told I had to now pay for it.....Ahhhhhhh, NO, I don't think so...bill United for it.

So, my new flight was scheduled to leave at 8:15pm.....weather delay, we leave at 9:15. Get to Philly with less than 10 minutes before my connecting flight was supposed to leave, run to the gate with several others who are trying to get the heck home, make it, get on the plane ready to collapse and sit and wait...another mechanical issue.....seriously?!
I got home at 1:30am.....was supposed to be home at 6:30pm....tired but safely, thank goodness.

Woke up today to more snow and ANOTHER snowday.....really?

Tuesday, March 3, 2009

Hehehe

While sitting together drawing pictures yesterday, my daughter comes out with this...

Her story about what she drew....'This is me in your tummy, before I hatched'
Never a dull moment with this kid!

You've got to love the curly hair she drew on herself.
What do you think, would it make a good WSA greeting card? Hehehe

Saturday, February 28, 2009

Today Is World Rare Disease Day


The last day of February has been designated as World “Rare Disease Day” to call attention to the public health issues associated with rare diseases. The Project Charity — The Children’s Rare Disease Network has compiled some facts and figures about rare disease that they thought would be of interest.

DID YOU KNOW:

~Approximately 7,000 rare disorders are known to exist and new ones are discovered each year

~Rare disease affects between 25-30 million people in the United States and approximately 30 million people in the European Union

~One in 10 Americans is living with a rare disease

~Children represent the vast majority of those afflicted with rare disease

~Approximately 80 percent of rare diseases are not acquired; they are inherited. They are caused by mutations or defects in genes

~In the United States, rare diseases are defined as those affecting 200,000 or fewer people or about 1 per 1,000

~Rare disease is often referred to as an “orphan” disease

~Orphan or rare diseases are often not pursued by the pharmaceutical industry because they provide little financial incentive for the private sector to make and market new medications to treat or prevent them and because there are not enough patients to make research cost-effective

~Research on rare diseases can often lead to advances in our understanding of common diseases such as cancer, heart disease, diabetes, stroke and other major health problems

~As a whole, rare diseases represent a large medical challenge. Combine this with the lack of financial incentives to treat or cure rare diseases, and a serious public health issue is created

~The US Orphan Drug Act (ODA) of 1983 has been one of the most successful pieces of health related legislation ever enacted in the United States. Through a system of tax credits, government grants, assistance for clinical research, as well as seven years marketing exclusivity, the Orphan Drug Act has resulted in hundreds of approved orphan medicines, treating over millions of patients worldwide. Similar legislation has been adopted in Japan, Australia and the UK

Following are a few examples of rare diseases that afflict children:
Acute Lymphocytic Leukemia, Angelman Syndrome, Apert Syndrome, Aase-Smith Syndrome, Batten Disease, Carpenter Syndrome, Coarctation of the Aorta, Chronic Myelogenous Leukemia (CML), Crouzon Syndrome, Cystic Fibrosis, Duchenne Muscular Dystrophy, Ewing’s Sarcoma, Eisenmenger Syndrome, Fabry Disease, Fragile X, Epidermolysis Bullosa, Gastroschisis, Gaucher Disease, Hirschsprung’s Disease, Hurler Syndrome, Krabbe Disease, Legg-Calve-Perthes Disease, Marfan’s Disease, Microcephaly, Niemann Pick Disease, Neuroblastoma, Neurofibromatosis, Patent Ductus Arteriosus, Pompe Disease, Prune Belly (Eagle-Barrett) Syndrome, Sanfilippo Syndrome, Spina Bifida, Sickle Cell Anemia, Tay-Sachs, Tetralogy of Fallot, Tourette’s syndrome and Williams Syndrome.

In honor of WRDD and Michaela. We had a "Genes" party! We invited friends to wear and bring an extra pair of jeans to decorate!

Friday, February 27, 2009

It's been a great week with the kids.
Michaela's been up and down, just off.

Dr. Pober's office called today. We're heading back down to Boston on the 11th. She wants to give her a thorough check and do an ultrasound of her carotid...this narrowing artery stuff.....BLAHHH!

Thursday, February 26, 2009

Snow Tubing

Yesterday the kids and I went snow tubing with friends. We had a BLAST!!!
It was an amazingly beautiful day, we were actually hot in all our snow gear.

Michaela LOVED it. Stuff like that is just soooo up her alley. She made sure we went on all the trails that gave you 'air time'!

Tuesday, February 24, 2009

We turned this morning's outing to the lab into a good one. It was an interesting one for sure as I saw a side of my darling daughter that I've never seen before. That beautiful, sweet being turned into a devious little comedian at her poor big brother's expense. I just wish I had a video camera rolling.

Let me just say, Aaron is never sick and aside from routine immunizations, there's never a reason for labwork. He's a bit squeamish of it all and will usually hide in his room on Michaela's shot day....big chicken. He really didn't know what to expect today and was asking me questions in the car, on the way there.
The conversation went a bit like this:

Aaron: Will it hurt?

Michaela (who chimed in before I had a chance to open my mouth): Yup, a whole bunch

Aaron: Really?

Michaela: Yup, and then your arm hurts all day.

Aaron(looking horrified): Is she telling the truth?..directed at me

Me: No, it doesn't hurt anymore than a pinch.

Aaron: Will they be taking a lot of blood

Michaela: Yup, tons. And leave the band-aid on or all the blood comes dripping out.
--All said with a completely straight face as her big brother was practically turning green--

We get to the lab, they call his name and she yells to him..."don't be scared and hold your arm up after so it doesn't fall off!"

Hehehehehe.....she has an evil side.

Aaron's Turn

Today it's Aaron's turn for labwork, much to Michaela's relief!! Although she is the ever present cheerleader...."Be brave Aaron"...."It will just be a pinch"...."Do you want me to stay with you?"....she had started to say "Do you want me to hold you hand?" before she remembered he has such sweaty palms, it makes her gag and she won't touch them.....kind of funny.

Aaron went for his yearly physical and we found he has major scoliosis. When bent over, he actually has a hump. Okay, he's never said a word and I feel like such the looser parent for not seeing it til now. The ped. feels it might just get worse as he goes through any major growth spurt.....geesh!
He's having labs for a check on cholesterol, thyroid and diabetes. He's tall for 13 at 5.6 1/2, but for his age his blood pressure was borderline high at 130/76. WTF!! It actually startled me to hear that number considering mine is usually 104/58 and I'm 5.6

So we are off to the lab as soon as the crew gets up.....labs have to be done fasting, so I promised to take them out to breakfast after.
Exciting day 2 of school vacation!

Thursday, February 19, 2009

You Are Cordially Invited

To a Kitty Cat Tea Party.....
I love watching these two....Michaela, age 9yrs old, and Murphy the cat, age 19yrs old....
video

Wednesday, February 18, 2009

"S" Day

SHOT Day.....I'm still not 'used' to doing this. I actually feel so sick to my stomach afterward it makes me dizzy.
She's starting to get angry about having them. I used to get the "You did a great job, mom!" Now I get "I don't want to do this, it hurts!!" Talk about feeling like crap.
Today is going to be a tougher one. I have to go into school and give it to her. She has to have it at 1:30 so labs can be done exactly 2 hours later at the Endo office. She can't stand to miss school, so this was the only way. One good thing, I get to go back to class with her and help them with a project....she's excited about that.

Just to share my anxiety with you all, this is what I have to stab my daughter with every 21 days. The needle has to go all the way in, so it's in the muscle. She limps for 3-4 days after.

New On My iPod

Just thought I'd share some new music I put on my long run playlist





Friday, January 30, 2009

World Rare Disease Day 2009

February 28, 2009

Rare Disease Day 2009



www.RareDiseaseDay.org

Wednesday, January 21, 2009

Award Winning Afternoon

Yesterday was the school Bowling Club pizza party and awards presentation.
Have I mentioned how competitive my darling daughter is?

Her team won the Second Place trophy and she won the medal for the highest average for the season!





Some pictures from this weeks Ski Club....

Friday, January 16, 2009

Our Newest Spinney

Meet my new nephew!!

Owen Robert Spinney
January 16 at 11:16
7lbs 4oz
21 1/2in


What a Day

It was an exhausting day, especially because I wasn't mentally or emotionally prepared. You know when you have a scheduled appointment or procedure you can get yourself 'prepared', I need that. I'm a planner, a scheduler. I don't do surprises.

It was a surprise to Michaela as well, though she wasn't so much upset about where we had to go as she was about missing lunch at school.....hey, priorities of a 9 year old, what can I say. I promised a big chocolate chip cookie from the hospital bakery and McDonald's for dinner, we were good to go....she's easy.

We headed to the lab for bloodwork first. She chose yesterday to be the very first time to sit all by herself in the 'blood' chair (her term). Usually she sits on my lap and I bear hug her for comfort and to keep her from moving. But, not yesterday. She wanted to do it by herself. Of course, that's the day we get the labworker from hell. She sticks the needle in and misses the vein, then starts digging the needle around her little arm until she gets it. I really thought I was going to punch her! Michaela cried a little, but she sat still....amazing.

Then off we went to Radiology for the ultrasound. By then, it was close to 2:00 and Michaela hadn't had anything to eat since 7:00am and she was starving. She couldn't eat or drink anything except for clear fluids until after the ultrasound. We were scheduled to go in for 2:00, they didn't call her until after 3:00. By the time we were done there, it was after 4:00 and we had to head right up to see the doctor. Poor kid was so hungry, I felt so bad.
By the time we left the doctor it was after 5:00. Michaela bounced down the hall to the elevator, thanked me for taking her to the doctor's and asked for a cookie. We made a beeline for the bakery and got a giant chocolate chip cookie and milk for the ride home. We got to the car, she popped in the Mermaidia dvd, set up her milk in the cup holder and her cookie in her lap, we were off.....and as far as she was concerned, life is all good.