Aug 14 – Sept 11, 2017 |3 Month Check Up

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Lewes, DE (Aug 17-19)

Went down to Lewes for a few days to hang out with my cousins. Had a great time as always. The weather was warm, but overall it was nice. I also outlasted mafia boss by showing her I don’t give in. She demanded I apologize after throwing some tiny rocks at her and she elected to hold/hug me and carry me back to her house from town unless I apologized. Well I played her like a fiddle…not only did I not have to apologize, I didn’t have to walk home. ūüėõ

National Zoo (Aug 28)

Mom and Dad took me to the zoo one morning, before it got too busy. We got there nice and early and saw all sorts of animals. It got warm as the day wore on but overall it was a nice day at the zoo. Mom and Dad carried me around a good amount of the time.

Miscellaneous Fun & Other Milestones Activities

I’ve officially peed in the potty one time to date. Mom and Dad were hoping I would pick this up, but it just hasn’t been a priority of mine. To demonstrate how much I care about using the potty, I

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Texts from Mom to Dad (see dad’s clever pun)

Also got this gnarly shiner one evening hanging out in the living room. Perhaps I should listen to Dad and stop jumping on all the furniture. This thing lingered for at least 3 weeks and there’s still a little indention in my cheek from this thing.

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And for the most part, it’s been business as usual. I hang out with Pop a lot. I work on my tractor. Dad took me to an outdoor movie theater for all of five minutes. Mom and Dad also took me back to Claude Moore Farms in McLean for a quick visit.

Also, I enjoy sleeping in with Mom sometimes, building and painting things and going for ¬†walks in the woods. I also got a new bedroom set and had cousin Hayden over for a sleepover. My new bed has a trundle so friends and family are always welcome and don’t have to share the bed or sleep on the floor anymore.

3 Month Pulmonary Checkup (Sept 11/19) & New Medication ūüė¶

On Sept 11, Mom and Dad took me in for my quarterly checkup. Oh wait, it was rescheduled to Sept 19 and Mom and Dad could not get someone on the phone to let us know when calling to check ahead so they both took off work for nothing.

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Honestly…which way do I go?

After my last Children’s visit (the nasty one I had for staph infection), a weird, very confusing, and inconvenient situation has arose with respect to my health care. Pediatric Specialists of Virginia (PSV) was thrown into the mix. PSV was created in 2003 as part of a collaborative effort between Children’s National Health System ¬†and Invoa Health System, but for some reason something new has taken place which involves me going to both locations and visiting doctors who may/may not have access to my medical records. This makes for longer hospital visits which is not good for me (added exposure of germs, confusion around medical details, etc.) or my parents (trying to schedule work).

Probably worst than juggling through all the scheduling woes was the fact that I have to begin taking a new daily medication – Pulmozyme. The medication must be refrigerated (pain in the ass) and is to be administered through my nebulizer so it’s another breathing treatment to my regiment so add another 20 minutes to life’s breathing treatments. Therefore me, Mom, and Dad have to clean more nebulizer parts and manage yet another prescription. If you’re a glass, half-full type of person, the idea behind this drug is that it is designed to thin the mucus in my lungs so that they are not as sticky and I’m less prone to picking up staph infection/respiratory tract infections. Let’s hope it works!

Naturally like all new medications, this was rejected by insurance, so my doctors have to send information justifying my need for it. It’s been over a week now and I still don’t have my medicine because of the awful medical/insurance industries.

CF Cycle for Life – Oct 8, 2017

Dad’s training is going really well. He biked a total of 16 miles since signing up for this event and has ran a total of 0 miles, played 0 basketball games, and done zero activities/events of cardiovascular health so he should be in pretty top notch shape come the event.

Click here if you want to learn more about the ride or here if you would like to join his team or donate.

Please Get Your Flu Shots

Please go out and get your flu shots. I got mine. It didn’t even hurt. The nurse was so impressed that I didn’t even flinch. Said she’s never seen a 2 year old act so tough.

Outer Banks – Sep 30 – Oct 5, 2017

I’m off to the Outer Banks this weekend with Mom and Dad for our first, real vacation since before I’ve been born. I’m really hoping for some good weather and fishing while down there.

Nationals

Dad and I are going to be out of town for the NLDS (at least first two games) so please make quick work of the Cubs so that I can catch a game of the NLCS and hopefully World Series.

Speaking of baseball, Dad and I have been playing quite a bit of tee-ball in the back yard. I’m getting pretty good at wacking the ball. Dad said he was most proud when he could overhear me telling my cousin how to place hands on the bat – left hand on bottom and right hand on top.¬† I’ll try to throw a video or two up here within the next few days.

Stay safe hurricane victims.

Aug 14 – Sept 11, 2017 |3 Month Check Up

Touch-and-Go & Gender Reveal

Sorry for the delay in posting, but we’ve been busy since getting better. Making up for lost time I guess you could say.

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Saturdays are for the Boys!

Feeling Better

Thank you all for your thoughts and prayers. They must be working!

It’s been nearly eight weeks since I last posted of my staph infection, Dad’s ruptured quad, and Mom’s morning sickness. Basically our house looked like a morgue – I mean, not really, but you know what I’m saying. It was a rough go there for us at the house.

Cross our fingers but we all seem to be doing much better. There was a brief scare for me though. Approximately 72 hours after coming off of antibiotics, I began to have frequent, soft stools – very similar to when I had c.diff so Mom and Dad began to worry. Mom and Dad emailed my pulmonary team (sans Dr. Shukla) and we waited to see what they thought. Naturally, we gathered additional stool samples for testing and waited for what seemed for ever for the results – NEGATIVE!

Lewes, DE – June 21, 2017

As always though, we try and have some fun when we can and we’re all well. We quietly made our way down to Lewes, DE for a weekend, where I got to play with all my cousins and Morgan (who is sort of a cousin by proxy). The only problem with the beach was that it was incredibly hot that weekend and I got a bit overheated…so much so that I was a little disoriented on Friday while there, but I rallied by eating some food an chugging some water. On Saturday we tried again, but I wasn’t having any part of it. We might of stayed down there for 15 minutes tops.

 

Ba-Ba-Mama & Jimmy’s

With Mom and Dad having to take off a few extra hours while I was sick, Mom and Dad had to make up the missed work so Bama and Jimmy stepped up in a big way though Mom thinks I’ve been spending too much time over there because I ask to go over there all the time now.

Bama and I do a lot of painting.

 

Jimmy and I do a lot of racing, but those videos will come next time. In the meantime I’ll leave you with this gem. This is how I ride when at home with Dad.

As a thank you, Mom and Dad took Bama and Pop out to dinner on a nice cool evening in Old Town Alexandria. Naturally I tagged along.

 

Sports Minute

We can all agree this wouldn’t be a good blog post without some discussion on sports or folks stepping up in the fight against CF!

Baseball – I have a little work to do

Baseball – Practice Rain-or-Shine

Loss of a Legend – Don Baylor

This time last week, we lost a great human and ambassador in the fight against cystic fibrosis who lost his own battle with multiple myeloma – Don Baylor.

There were some really great articles that came out as a result of his passing. Here is a link to one of the better stories I found online and here’s another on how he sort of fell into fundraising for the disease.

Bonnie Downing, a 16-year survivor of multiple myeloma, shared her own battle with Baylor after his diagnosis, finally meeting him in person a few years ago in spring training. Yet, while Downing was a spokesman for the disease, Baylor chose to silently fight the battle.

“He was so selfless,’’ Downing said, “that he didn’t want to be a spokesman about his own illness. He wanted to instead talk about his work with Cystic Fibrosis. He said, “I can’t leave these kids.’ He was more concerned about them than himself.

Step Up

Nationals have been stepping up on the field all season long given all the injuries (most recently with Harper going down), maybe one of them could step up off the field and help carry the torch that was first lit by Don Baylor. Just saying..any Nationals player out there want to step up for the cause!?!?!?! Maybe you could help me with my hitting as well.

Speaking of stepping up…if you feel like going for a charity bike ride (20, 40, or 65 miles), join Dad and several of his colleagues and their friends in Leesburg, VA on October 8, 2017. If you fee intimidated, don’t be. Dad’s still recovering from a ruptured quad and has an old mountain bike so chances are you’ll destroy him.

I’m Going to be a Big Brother

To a little girl…

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Saturdays are STILL for the Boys!

Heading back to Aunt Rachel’s beach house this weekend and to see my cousins who’ve been away the whole month of August, so hopefully won’t be too long before I have some more fun stories to share.

Touch-and-Go & Gender Reveal

Two Year Anniversary

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Two Year Anniversary + Checkup with Children’s

At times it’s hard to believe, but today marks the two-year anniversary of being released from the NICU at Children’s National. While Children’s National is a great place in terms of saving lives and treating those in need, I prefer being outside living it up.

My scheduled check up with Children’s was set for Tuesday, March 14, but since there was winter weather in the forecast, the doctors weren’t sure if the clinics would be open, so they asked us to come Monday afternoon to the Fairfax, VA location. Unfortunately, this meant I did not get to see Dr. Shukla (more on this later) or the other members of my team such as Allison and Carol and Beth. That said, I did meet with Dr. Sami and we had a much easier commute than normal and enjoyed a far less busy facility in flu season which was another plus.

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Shoveling Mom and Dad’s¬†Walkway

Dr. Sami listened to my lungs and indicated that they sound really good and clear. That is probably thanks in part to Mom and Dad’s diligent therapy routines where they allow me to do the vest in the morning, but still force me to do manual in the afternoons. Mom and Dad really would love for me to start wearing the nebulizer mask like other kids, but I think I’m grown and fight them on it. For all you other CF parents out there, try to mask train your children as early as possible to avoid this conflict. The vest is second nature to me as Mom and Dad allow me to watch shows during this time and they eased me into the vest when I first was eligible to begin using one. My height and weight are up again from my last visit so that too is encouraging! Per usual, we’ll await on the throat culture before we have a really complete report, but all things are pointing toward a good checkup.

So remember what I said about coming back to Dr. Shukla…he broke it to Dad over email that he’ll be moving on in about three months so if I stay healthy and out of the hospital, I’ll only get to see him one more time before he moves on to a new hospital. Me, Mom, and Dad are going to be sad to see him move on.

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Mom’s response to Dad forwarding along Dr. Shukla’s news

Medications & Therapies

It’s been a while since I’ve spoken about my medications, but not much has changed. I continue to do chest physiotherapy twice daily (one by vest, one by machine) and a nebulizer with albuterol sulfate held close to my face (since I refuse to wear the cute masks). I take four 6,ooo unit Creon (pancreatic enzyme) pills prior to each meal feed. Sometimes I’ll take a snack dose. I take 2mL of vitamins ADEK daily. I also take 1-1.5 tablespoons of Miralax daily to help soften my stool and avoid bowel obstructions. Even though it’s not prescribed, I take a probiotic pill daily in hopes of keeping a healthy guy. The other thing that’s not prescribed which I do an awful lot of is running around and jumping on my trampoline. Those are great workouts for me.

And lastly, daycare for me is still Bama and Jim’s house at Madison Manor park. I don’t go to actual day care and am so lucky to spend each and every day with them. Here, I make them dance.

Lewes, DE (Feb 18-20)

Thanks to climate change, we took advantage of some nice weather and headed to Lewes to Aunt Rachel’s beach house. We enjoyed a really nice weekend¬†at the beach. We saw fire trucks, played at the beach, ran up and down the pier, went on short bike rides.

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While there we stopped by the fire house to look at the tracks.

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Biiiiig Fire Truck

Because it was the offseason, we didn’t have to pay to enter the park so me, Mom, and Dad ran down the ¬†pier at Cape Henlopen. No one was fishing and the tide was extremely low while we were there. There were some folks metal detecting along the beach. Not sure if they were finding anything but apparently some coins from old ship wrecks are found in and ¬†around there.

When I say I ran…I ran when at the pier…I mean I ran! Dad said I’m like Forest Gump.

Bike Ride around DC

Don’t be fooled by the three inches of snow and ice we received in March. Climate change is real and it allowed us to go bicycling in DC to take in some cool sites and see some memorials up close. Some of the cherry blossoms had even begun blooming! With as crazy as the weather has been lately, I’m not expecting much in terms of beautiful blossoms this year.

Maja also came by for a visit and we went to see the owl at the nearby Gulf Branch Nature Center. I also celebrated Mardi Gras in a big way this year. Thanks Pam for the awesome shirt.

 

DC Brewer’s Ball & Bishop O’Connell Superdance

Big thanks to Dad’s employer, IT Concepts, for supporting several employees attendance at the event and providing a great evening. DC Brewer’s Ball raised close $300,000 again this year (it was in the mid-high $200’s last I saw). Dad’s boss even won an autographed Mike Tyson glove (pictured below). Big thanks to all who donated items, their time, etc. to pull off such a nice event.

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Me and Mom shot a video for the the Bishop O’Connell Superdance fundraiser which took place in the first week of March. So far those amazing high school students have raised over $105,000 this year and they’re still going! Keep up the good work!

Here’s one of me and Mom’s outtakes…

Fundraising – Great Strides Walk

As mentioned in my previous post and as we do every year, we’ll be raising money for cystic fibrosis in hopes they find a cure that could one day save my life as well as the more than 70,000 people living worldwide with the disease.

Click here if you wish to see my Dad’s fundraising page. Jack’s Pack¬†has raised nearly $5,000 for this walk already. To everyone who reads the blog and who has donated already…thank you, thank you, thank you so much. I honestly cannot thank you enough.

For those who have nothing better to do or wish to join me and others, the walk details can be found here¬†(or see below for convenience’s sake).

Date: 5/6/2017
Event: 10:00 AM
Distance: Maybe 1-1.5 miles
Event Location: St. Stephen’s & St. Agnes Lower School

Quick Vocabulary Update

So I know I’ve been trying to keep a running list of all the words I say, but it’s hard. I’m probably saying 2-3 new words per week and playing some pretty funny sayings nowadays, so I’ll try to list off one word for each letter, from A-Z.

Alexa (as in Amazon Echo), Black, Cardinal (as in the bird), Digger, Elmo, Funny, Girls, Heavy, I, Jump, Key, Love, No, Owl, Pecker Bird, Q, Roller, Sexy (as in sexy mama), Truck, Up, V, Water, X, Yellow, Zebra

Didn’t think I actually said, “Sexy Mama” did you…well here…take a look. Here’s the safe for work version.

So that’s it for now…well aside from me giving you a DC Sports Update. Bryce leading the Spring Training in HRs (I’m expecting a huge year), Capitals still leading the Metropolitan Division with hopes of a Stanley Cup run. Wizards are doing well, but I’m not much of an NBA fan. Skins are a dumpster fire.

Mom and Dad…who am I kidding…mostly mom and my cousins have become slightly obsessed with SnapChat. Here’s one of my first snaps…

If I don’t see you at the walk, maybe I’ll see you at one of Dad’s ballgames and or around town since flu season is almost out of here :). Until next time.

Two Year Anniversary

It’s Been a While…

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Up to no good

Ugh, where do I start. I’ll start with the medical and then hit the fun I’ve had over the last couple months.

Medical – Sorry to Bore You

As anyone who has CF, cares for someone with CF, or is closely associated to someone with the awful disease knows…it is a roller coaster. Further complicating matters for me is the fact that I contracted Clostridium Difficile Colitis (c-diff). While I thought I was in the clear, I was beginning to feel that maybe the Metronidazole by mouth (Flagyl) only suppressed my symptoms (diarrhea, abdominal pains, etc.) and didn’t fully kill off the c-diff because some similar symptoms resurfaced and doctors were all set to start me out on Vancomycin as the next possible medication to try and kill off the c-diff.

Read the papers nowadays and you’ll constantly find articles warning us of superbugs and our reliance on antibiotics. There’s no doubt I’m going to be on more than my fair share of antibiotics, so Mom voiced her concern to my team of doctors at Children’s.

My team of doctors say the easy thing to do is treat. It’s harder not to treat. Ultimately treating is up to Mom and Dad, but hearing that didn’t make things easier on Mom and Dad to make a decision. And because Mom felt I picked up c-diff from Children’s she was losing more and more trust in the care they provided for me up to this point. The decision wasn’t an easy one, but collectively we elected to hold off on treatment and ride it out a little longer knowing I had already proven that I’m a tough kid. Mom also decided it was time to get a second opinion from Johns Hopkins. I’ll explain that visit and what we thought of it vs.¬†Children’s in a later post for those caretakers out there who also wonder the same thing.

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Showing¬†Dad viral¬†videos on JHU’s network

While I can’t be for certain, we’re pretty sure¬†I picked up parainfluenza while at Hopkins. Very shortly after coming home, I began fussing, crying, coughing, etc. So heavy doses of Tylenol and Motrin for about a week and a visit to Children’s for a throat culture. It must of been a bad strain because half of Team Jack ended up getting it (Dad, Bama, Aunt Rachel, and Hayden).

On to the Fun

We’ve been busy as beavers since Easter – first Nats game, bike rides, weddings, beach, fundraising walks, and visiting Dad’s home from growing up.

May 14 – Nationals vs. Marlins (First Game)

The game sort of stretched into my usual nap schedule so I didn’t make the entire game, but we had fun – 6 strong innings in baseball constitutes a quality start. It was a lot of fun watching the pitchers warm up in the bullpen.

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Nats beat the Marlins 6-4; maybe I’m a good luck charm

Comes at a Cost

Going to the Nats game came at a cost. Dad put me to work.

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Helping Dad in the garage

Apr 30/Jun 04 – Fundraising for cystic fibrosis

I can never thank people enough. It’s so much cooler when family and friends get out and participate in the fundraising walks, runs, bike rides, and hikes. So far this year, Team Jack ¬†(Peden) has participated in four¬†Great Strides walks – Alexandria, VA, St. Michaels, MD, and Annapolis, MD, and New Orleans, LA (sorry for the initial omission Seamus, Jared, Wakemans, Bonuras).

More information on future events can be found at CFF.org.

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Cousins JJ and Killian walking in support of me and 30,000 other Americans fighting

Snapchat

Mom and Dad recently discovered snapchat. You would think they took enough photos of me before. SMH

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#BreakingBad #WalterWhite

Jun 18 – Wedding

Uncle Seamus AKA Tamey married Jared in Alexandria, VA thanks to same sex marriage being legalized in the Commonwealth. So happy they did so I could participate as a ring bearer (well sort of) in the wedding. Had they gotten married in NOLA where they live, I might not have been able to be part of the wedding due in part to Mom and Dad not wanting to expose me to germs commonly found while flying.

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I don’t like when sleeves touch my hands

July 04 – Beach

We decided to head to Lewes for the fourth of July.

The salt air had me feeling good and wanting to go back very soon. I think if it weren’t for the traffic woes getting to and from there, we’d be there every weekend.

Surry, VA AKA “God’s Country”

One of Dad’s friends always refers to Texas as “God’s country” but that’s because he’s never been to Surry, where Dad grew up. Founded in 1652, it’s sort of amazing how its managed to remain underdeveloped and keep its rural charm. It wasn’t for a few years ago that the county finally installed its first stop light.

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Mowing the grass in the hot summer sun

We did so much. We went down to the James River, rode the lawn tractor, swam in backyard, fished, and even dropped in on the new winery that opened up across the street from my grandmother’s house.

Just like Lewes, I can’t wait to get back down south to see the family and spend time on the farm. Just wish they could figure out how to improve the flow of traffic on I-95.

Until next time…

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“Yeah, well that’s just my dream…Baseball needs more stars” — Bryce Harper

 

It’s Been a While…

Father’s Day, 5 Month Old Checkup, and Independence Day

I know, I know…I’m long overdue for posting and I’ve let down many of my readers.¬†I’ll try and do better. Here I am swinging in the new swing Mom installed on my cousins’ new playground set. Probably the best $25 Mom’s spent.

Loving the Swing
Loving the Swing

Father’s Day (June 21) – It was Dad’s first Father’s Day so he and I walked into Georgetown and up the Exorcist stairs to kick things off. We’re able to do this now that the doctor cleared him to remove the boot that was protecting his left calf tear. One of the more important things for Mom and Dad to keep an eye on, is my weight, so Dad purchased a scale which uploads it to his phone. Doctor’s told Dad not to be crazy and track it every day, but since he’s been weighing himself consistently for years with a an adult version of the scale, he figured…what the hell. While I’ve been gaining, Dad has fortunately been maintaining so we’re both meeting our goals!

Exorcist Stairs in Georgetown
Exorcist Stairs in Georgetown

Dad also got to snag some swings in the cage at Nationals Park, so was able to sneak me and Mom into the park since it’s not encouraged to bring me around large crowds. Can’t wait until I get a little older and I get to run around out there.¬†Unfortunately for Dad, Nats GM Mike Rizzo, isn’t going to be calling him up anytime soon.

Me and Mom and Nats Park for Dad's BP
Me and Mom at Nats Park for Dad’s BP

5 Month Checkup (July 1) – All was well on the health front during my 5 month checkup. I’ve demonstrated the ability to gain weight (jumped from 11% to 25%) and doctors are bumping my Creon dosage up to four 3,000 unit¬†pills per feed. Dr. Shukla said my goal should be the 50th percentile for weight. I currently weigh 16 pounds (7.35kg) which is about 200 lbs less than Dad. Dad’s now a “regular” at Walgreen’s.¬†Doctors briefly touched on the additional mutations that were identified and explained to me and my parents that there’s an incredibly high likelihood that I’ll be infertile and that I should use protection. I know kids are starting young these days, but I don’t think¬†that discussion was necessary yet…haha. Dr. Shukla also provided Mom and Dad with a new Cystic Fibrosis Passport which Children’s is trying out as something new for parents.¬†It has¬†some generic medical information (weight, height, head, my CF, allergies, etc).

Children's CF Passport
Children’s CF Passport

Independence Day (July 4) – Heading into the weekend, Mom wasn’t sure what she wanted to do, but as the week wore on, she opted for her sister’s beach house in Lewes, DE which is always a lot of fun and because the wind reports were favorable, Dad would get to go fishing so Dad really lucked out on this mini-vacation. I did fairly well on the drive up Friday morning and slept the entire ride back home on Monday.

Hayden feeding me a morning bottle at the beach
Hayden feeding me a morning bottle at the beach

Once again my cousins demonstrate how awesome they are and how much they care about me by raising $170 for the Cystic Fibrosis Foundation (CFF.org) with their Lemonade stand and some new signs. People’s generosity never seem to amaze me.

Riley, Paige, and Hayden slinging that lemonade for CF
Riley, Paige, and Hayden slinging that lemonade for CF

Spending the Days with Coco and Pop (Ongoing…) – Sometime over the last month, Mom gained more comfortable with her dad helping out some during the week and looking after me so she could focus more on work. Out for summer break, Aunt Coco,¬†has also been around to sing and read to me. I’m no Simon Cowell, but Coco has a much better voice than Pop. It’s been a huge help for both Mom and Dad since Dad’s work is picking up with his customer anxious to begin an upgrade to their PeopleSoft system and Mom’s in the middle of their busy season. Thanks Coco and Pop!

Me and Pop Hanging on Back Deck
Me and Pop Hanging on Back Deck

As I said above, I’ll try to do a better job at getting posts out more frequently – at least biweekly.

Father’s Day, 5 Month Old Checkup, and Independence Day

100 Days Old

I’m officially 100 days old today. I think teachers usually throw parties and stuff when there are only 100 days remaining in the school year. Sort of funny how they count down, while all I want to do is count up and out for many, many years to come, but I get it…who doesn’t like an excuse to party. Did you know a leopard can get pregnant and give birth within 100 days.

Happy Mother's Day
Celebrating 100 Days Old

It’s been 14 days since my last doctor’s appointment so no new news on the clinical front. I did re-up on my Albuterol for 90 days. Mom and Dad say we’re running out of cabinet space with all the meds I’m on. Too bad for them, that number will only grow. :/ My next appointment is on May 26th, following the Memorial Day Weekend.

Hanging at the beach with Dad
Hanging at the beach with Dad

I made my first trip over the Bay Bridge to celebrate Mother’s Day with Mom and Dad this past weekend in Lewes, DE at Aunt Rachel’s “beach house”. I love the way the sand felt between my toes and can’t wait to get back there.

Morning Beach Run
Morning Beach Run

While on my beach run, I stumbled across this bench that had my name on it, so I stopped for a quick photo with Dad.

Jack's Bench (Lewes, DE)
Jack’s Bench (Lewes, DE)

Here I am helping Dad with the Mother’s Day gift for Mom. Needless to say, this didn’t turn out like either of us had hoped, so Mom ended up getting herself a nice little necklace with letter “J” charm at a gift shop in Lewes.

Modern Day Picasso
Modern Day Picasso

You draw, better be picasso, y’know the best — Jay Z

The upcoming weekend is chock full of activity. Uncle Seamus graduates with a degree in Environmental Science this Saturday and on Sunday, friends and family will walk in the Great Strides Walk in Reston, VA. The 5K walk begins at 1:00 PM. So far, my team has raised $6,470 to help find a cure. Thanks to everyone who donated.

Tomorrow I’ll be rooting hard for the Washington Capitals to take care of business in New York against the Rangers in game 7. Let’s go C-A-P-S.

100 Days Old