MRI is Clear!

Not sure why I've been slow on the updates, I guess I've been waiting for this one; her MRI yesterday came back clear. She looks perfect.

Our Super NP, Trish once again went through heroic hoops to get us this news before the weekend (she's not even in town)! This is the first post-treatment MRI . . . 3 whole months with no chemo, does this ever get easier?

It has been just over 1-year since her diagnosis (Nov 14th) and surgery (Nov 16th).

For most likely obvious reasons, this was a difficult milestone (made completely joyous by previously mentioned news!). Our thoughts, daily activities, and small moments are all punctuated with that niggly little feeling in the back of our minds. For now, and especially for this upcoming season of thanksgiving we will rest easy. I went to USCF last Monday to personally thank her neurosurgeon, Dr. Gupta again. I had not anticipated an emotional reunion (and for him I am sure it was not, afterall there are 100s of us and only one of him), but there I was, a puddle holding a bottle of wine and some hand-crafted (by G'pa Walker) wine stops, in the middle of the Neuro surgery waiting room. Wierd. I do remember last year asking him who carved the turkey at his house (he checked in on us on Thansgiving morning in the PICU), and thinking that was an incredibly funny joke...

We've had some great weekends at the cabin, quality time with family and friends - and to save 1,000 words:

Disney with G'ma and G'pa Austin in Oct


Halloween


Cabin Fun with the Trog's


Preparing for Thanksgiving, Gianni's Birthday, AND her "Make-A-Wish" trip to Disneyland (and all this before Christmas)! Kids are both doing great- Gianni started physical therapy this week (finally) and looks like she is in good shape. They will work with her to strengthen her ankles and better her balance but all-in-all she is just a bit behind on some minor milestones.

She's had only one clinic visit and that went well - one of the best accesses yet. Her Magnesium is still low so we've tacked that one supplement back on - but going from the multitude to one small dose usually hidden in a cup of root beer is no sweat.

We are so grateful for all of you everywhere sending her and us your good thoughts and prayers. Thank You.

Feels like fall and Fairy Wings

We've been flirting with normalcy for several weeks now. She has had only one clinic visit in the last three weeks and does not have to go back until next Tuesday. She has had no meds (zero) for three whole days now. Where we used to spend hours a day preparing and administering everything from food to IV antibiotics we now read more stories, take longer baths, and spend way more time than we probably should at the dinner table.

Over the past year I remember fantasizing over what we would do with all the "free" time we'd have together as a family, "once this is all over". I am living with the realization that this is not a situation that just goes back to normal... but flirting with normal is way more than enough. She begins physical therapy next week - took a month to get the insurance straightened out enough so that the therapy won't bankrupt us (they always find a way to get you when you're down to midlin'); from what I remember of PT - it's not fun, however the place we found specializes in children and looks like a giant playgym. The staff are friendly and the kids there seemed to be having fun.

Grandma and Grandpa Austin treated the kids (and me!) to a fun-filled weekend at Disneyland earlier in the month and the two of them were unstoppable (Bruno and Gianni were full of vigor as well!). Big fun. We barely made it out of Tomorrow land ("To infinity and beyond!") and the definite highlights were getting to "meet" some favorite characters and late night fireworks.

We had "Breakfast with the Characters" on Sunday morning and as part of the experience a "cast member" takes a picture of the kids with Tinkerbell (the kids cup their hands for the picture taking and when you collect the photo, Tinkerbell has magically appeared on their palms). Gianni was so enchanted with the idea that Tinkerbell had actually landed in her hand that when she saw the real live Tink "fly" from the Matterhorn to the castle during that evenings firework show she put her hands together the way the photographer at breakfast had shown her and waited for Tink to land in her cupped hands. She waited like that for the entire show.

My grandma (the kids' GG) could use some good thoughts - she broke her foot last July has had to be cared for in a nursing home since. She's not feeling so well. Her birthday is on Monday - 93 years old!

Today we are gearing up for some Halloween fun. Gianni wants to be a "fairy princess"; with wings. This is no surprise, in fact it is the exact same thing she was last year. I even toyed with convincing her to wear the same costume with a few new embellishments but... Halloween is just this one time a year and living in the present makes it so easy to start everything fresh (plus, how cute). Bruno wants to be either Buzz Lightyear or the Grim Reaper... true testament to my little boy - growing up. Tonight we'll make edible eyeballs for his Kindergarten class. After Thanksgiving, Halloween is my favorite holiday.

She gets stronger everyday.

It will be 1-year since her diagnosis and surgery two weeks from Friday. Her 2nd post-treatment MRI is Nov 21.

PICNIC

This has been a weekend of picnics. Yesterday Brisbane held its annual "Day in the Park"; a really fun set up in the main park with bouncy houses (yes plural), carnival games, hay rides, live music, tons of junk food AND the Soap Box Derby. I took the kids and a fun time was had by all. I got the biggest kick out of all the people (big and small) who know Bruno. In the few short weeks since he's started kindergarten the tables have turned - I've gone from being Karen to being "Bruno's Mom".

Today we went to the LPCH NeuroOncology Group's annual picnic. It is a fun-packed day; full of face painting, button making, funny hat decorating, balloon creatures, dog tricks, two pinatas, and really great food. All the invitees were patients (past and present) and neuro oncology team members. A really good time was had by all. I was not sure what to expect - it is a . . . club (for lack of a better word) I never expected to be a part of. . . There were families in all phases of treatment and it was a safe place to share experiences, catch up, and mingle with other kids and parents. It was also fun to see the people who have been taking such good care of us in a more relaxed setting. The kids are exhausted and looking forward to seeing Dad tonight.


We'll have a short week - driving to LA on Friday to hook up with G'ma and G'pa Austin (from Kentucky) for a weekend at Disney Land... woo hoo!

Even more hair, More cabin fun, More baseball, and oh...clinic

Fans

Lots has happened in the past week... I know the title infers just more of the same, and true as that may be, it sure has been fun!

Last Wednesday was The Giant's Game; G'ma and G'pa Walker drove down from Lincoln so that we could all go to the game together. We had the entire experience with hot dogs (carrots and animal crackers for the kids... gotta sneak in those veggies), rootbeer, Margaritas (gotta sneak in those fruits), and of course cotton candy. We arrived early for a quick refreshment at the Acme Chop House and once we settled in, the kid's got to explore all that is AT&T stadium. We played in the "Giant" Coca Cola Superslides (more than 150 ft of slide!) and took batting practice in a miniature replica of the ballpark where they each got to hit balls from a real pitcher!

Cheers! (Note Bruno doing double hat duty)

Jake... or Elwood?

Nutritious AND Delicious

When it was all said and done, the Giants lost to the Rockies (6-15, yikes); we did get to see 5 or 6 pitchers and Bowker hit a homerun in the 6th, but our Giants have had a long season and I bet they were a bit pooped (I can relate). We definitely had more fun than they did.


We all got up (early) Saturday morning for a short and sweet run up to the cabin. Weather was gorgeous - we packed in lots of hiking, bike riding (Bruno's getting good on his 2-wheeler [no training wheels]), music, baseball, 4-wheeling, and my 5-cent popsicle pic.


Monday was clinic. The access of her port was the easiest one yet. Her numbers were pretty good, and I'll let the photos speak for themselves.

As always, we are bolstered by your prayers, good wishes, and warm thoughts. She is getting stronger everyday!

Clinic

Clinic today was just fine. Gianni was a bit apprehensive this morning when I put the numbing cream on her "owie spot" -

G: "Is there going to be a poke today mommy?"
M: "Look me in the eye Gianni; Yes, there will be one poke today, only one and it will be a quick one - and then we can visit with Auntie Trish (our NP). No sleepy time today, just one poke."
G: "Okay, but can I bring my brand new spitty?"

We usually all put the numbing cream on - today she asked me to be sure to cover my very own owie spot (a small mole on my chest)... very sweet.

The access went as well as could be expected, the nurse we got was a 'regular' and she is pregnant, only after not seeing her for a whole month, she is really pregnant. Gianni asked her if she ate too much ice cream.

It was oddly good to see the regular clinic folks again (it has been 1 whole month!). The visit with Trish was great. Gianni's numbers all look good (17.8 kg!!!). We will be cutting her meds to 1x per day (Q day for those of us initiated) AND we will be stopping all her feeds effective tonight. We will go back next Monday for a weight check and a quick blood chemistry to see where she stands, if all goes well - we will remove the NG then. This is a milestone: We have been feeding Gianni every night since Feb 14th of this year using the NG and the pump. The clicking of the pump has become some sort of metronome for my sleep... and the beeping of the "I'm stuck" alarm an immediate wake-up call (sometime 2-3 times a night). I am really hopeful that her appetite will keep up and she can maintain her mass (keep your parts crossed!). She has some weakness and splaying in her ankles from the Vincristine - this is an expected side effect and with physical therapy and the right shoes (potentially braces for a short time - we'll see) should resolve itself.

After clinic we made a brief visit to our friend Emily who has been in 1N lock-down for F&N for the past week or so. It was great seeing her, Gianni reads her blog every night and was excited to be able to bring her a little "get well" gift. She was in one of the rooms where we have spent many a week with Gianni's F&N, weird, but good to see Emily doing so well.

Gianni and I went shopping after clinic to get the "right shoes" - and no shopping trip is complete without a rootbeer stop... big fun.

We had a great family night, wonderful dinner and the kids and I salvaged some old bananas by making banana bread - always good kitchen time.

More later, thank you for checking in.

Vote for Project Brain Child

Project Brain Child is an initiative of the Pediatric Low Grade Glioma Association.

Members Project is a program sponsored by American Express where cardmembers submit innovative ideas for projects that make a difference. Cardmembers vote on the projects, and the winning 5 projects will receive up to $1.5 million in funding from American Express.

The Pediatric Low Grade Glioma Association (PLGA) submitted project idea is to conduct a feasibility study to create a National Pediatric Genomic Brain Tumor Registry. The information collected in this registry would allow scientific researchers and medical experts to target specific genetic abnormalities with existing drugs most effectively.

The registry will embody all brain tumor types, not just low grade gliomas.

Project Brain Child was selected from over 1190 other projects to be in the top 25. As of today, September 22, they are in 9th place.

They need to be in 5th place or better to receive an award. You can vote up until Sept. 29. The winning projects will be announced Oct. 14.

Any American Express cardholder may vote. No donation is required to vote. If you don't have an American Express card, you can still help by spreading the word to your friends.

Brain tumors kill more children every year than all other diseases combined. Please help this effort.

More information:

* Project BRAIN CHILD information from PLGA
* Project BRAIN CHILD information on American Express Members Project site
* How to promote Project BRAIN CHILD on your site

So please consider taking two minutes of your time to vote for this worthy project.


* Thank you Steven's mom for sharing this valuable opportunity.

Jes' B-Day

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More hair, cabin fun, and baseball

It has been a fun week. Last weekend was another beautiful 48-hours at the cabin. The highlight had to be the "camp-out" at the firepit. I've never seen so many marshmallows consumed in one sitting (and that was just Bruno)! Nothing screams good ole fashion fun like fire + sharp metal skewers + sticky, gooey, molten marshmallows. They did us proud.

I sure hope this is enough marshmallow!

No Bruno, you hold the extremely sharp implement with the molten sugar
blobs on it THIS way... here let me show you...

Once back in the Bay area, we've made an attempt to maximize the after work/school hours with the kids by incorporating trips to the pharmacy with a trip to the ice cream store, and extra time at the park before dinner. In addition, my employer was kind enough to offer my entire team seats in a luxury box at the Oakland As game last Wednesday. That was fun - we brought our friend Jessica and all three kids had a blast. Much debauchery in the form of popcorn, hot dogs, and soda was had but the topper was the blue cotton candy (we left just moments after that escapade). We missed the very exciting 7 - 9th innings (As pulled out a victory) but everyone really had a great time.

Note: Bruno's Giants apparel... and don't worry Uncle Timmy, his intentions are pure!

Although the As game was fun, we Gheno's are Giant's fans to the core and are REALLY excited to be going to the Giants vs. Colorado game next Wednesday - courtesy of Mr. Kevin Frandsen. The Walker's are joining us and we plan to make quite an evening of it! No cabin for the kids and me this weekend, we will be whooping it up at Jes's 4th B-day.

Clinic is planned for next Tuesday - I'm hoping for great blood chemistry and enough weight gain to chuck the NG... I'll keep you posted.

For the past week or so, every night when I check in on Gianni,
I find her sleeping in this Minnie Mouse hat - cute.

Many thanks to all of you who keep checking in on and sending your good thoughts to our Gianni.

Hair Fairy

Okay, so this has been some blogging hiatus ...! I will chalk it up to post-treatment bliss/stress. This Tuesday will be 3 weeks, 21 days since Gianni has been to clinic - no owies, no pokes, no nothing! The entire past 10 months is already cloaked in a surreal fog (what happened?!?!?). She still has the NG tube; we give her nightly feeds (but no regime of water) and meds 3 times a day... Although her meds consist only of a few supplements now (Potassium Chloride, K Phos, and Magnesium Gluconoate - most items that could be bought OTC). Her appetite is slowly but surely returning - once she starts to maintain her mass on her own we will be able to remove the NG.

Last day of chemo

The 'hair fairy' is working double time - every morning I swear she wakes up with a few more millimeters of fuzz. It is coming in blond so it is difficult to see, but it feels really soft! I read that hair grows about 1.25 cm (~1/2 in) a month - at that rate I'll be pulling her bangs out of her eyes again in no time!

We have been easing into some semblance of normality at the Gheno residence. We've made our weekly trips to the cabin - shorter for me and the kids now that Bruno is in "real" school - but complete family time. Gianni has had a few play dates at Miss Martha's, a great way to ease her back into "the rules". I even treated the kids to a movie last night, something we have not done since last October.

I've been dreading the call from the clinic to schedule her next labs, check-in with Trish, and the always looming MRI...BUT, since it kept popping up in my mind - I called them today ("Oh, good morning Mrs. Gheno, I was just about to call you"). Not a big deal its just that (even with all that has happened, and the ever present reminder of the NG) every once in a while - usually while I'm listening to the kids playing in the background while I'm occupied with an everyday task or chore - I think I forget or regress to a place where none of this ever happened. I don't come crashing back to reality or anything like that, it's just good to be living with a more even cadence.

Her labs will be on Tues, 23 Sep, she'll have another visit near the end of October and then her 2nd post-treatment MRI on 21 Nov.

The LPCH neuro-oncology service's annual picnic will be the 1st weekend in October - I'm looking forward to bringing the kids.

First trip back to G'Ma and G'Pa Walker's (we had 3 birthday parties!)

Daredevil

Batman

Just one nickel for every one of these pics...just one...!

MRI is Clear!

Just a quick note for those of you who continue to send such positive wishes our little girl's way. Her 26 Aug MRI came back clear - she continues to fight the good fight!

Bruno's begun Kindergarten, and we've had a few great weekends at the cabin . . . I'll follow up soon with lots of pictures and "Funny Gianni".

All done...

Tuesday (05 Aug) was the last chemo - 8 rounds... she did it! Our super NP (a.k.a. "Auntie" Trish) sat and visited with us during the administration, we took pictures, the staff gave Gianni balloons and a stuffed unicorn ("Uni-Corny"). I cried, Gianni did not.

I equate this round to the 9th month of pregnancy. You've hit the milestone, but you still have to do the time... So now we just have to finish out this round (clinic, blood chemistry, transfusions, etc.) with no major bumps.

The plan is to have one (Tuesday) clinic a week until August 26th. Aug 26 will be her post-treatment MRI; after that it's 1 clinic a month. The port has to be flushed a minimum of once a month, plus we'll be able to monitor her electrolytes and perhaps get her off some of the supplements. Once she has had 2 or 3 clear MRIs, we'll take the port out.

So... nerves and fear of the future not withstanding - we are moving forward!

We celebrated last weekend with a trip to G'ma and G'pa Walker's - lots of fun shenanigans (we had lots of catching up to do)!

Last Tuesday's labs yielded "adequate" numbers (RBCs, platelets, etc.) - not great but not low enough to transfuse. We are hoping that she will come up on her own. Her head is getting fuzzy, her appetite is slow but sure, and her energy remains high.

Cycle 8, Day 12

Super Heros

Clinic and day hospital went well, however to quote Gianni, [as we walked in the house at the end of the day] "Whew, what a day! Sometimes I go to the hospital and it makes me sooooo sleepy!"

She's still neutrapenic (read: still needs nightly shot), she needed both RBCs and platelets (read: 6 hour day hospital visit), and for the cherry on top ... her gut infection (C-diff) is back (read: no big deal just more antibiotics and kind of a bummer). But all in all the day was fun. I love having the solid one-on-one time with her and knowing how close we are to the end of this treatment phase makes all the bureaucratic stuff seem just not as frustrating.

Brisbane has "Friday Music Night at the Park" so her and I swung by before we came home. I figured she's about as tanked up as she's gonna get and she had TONS of energy. I had to keep her away from the other kids but we enjoyed walking around the park and just watching all the neighbors "shake their booties!"

The pictures from a few weeks ago, but its a good one.

Cycle 8, Day 11

Gianni's still doing well. Dad and Bruno are up at the cabin and Gianni and I are in for a long, relaxing girls weekend. She does have clinic and (most likely) transfusions scheduled for tomorrow. We'll go in the morning and hopefully be home for a late lunch. Getting blood products while neutrapenic is always a bit iffy. Sometimes getting the blood makes her spike a little fever; fever + neutrapenia is an automatic admit. Trish has been great about letting her be pre-medicated with Tylenol to help alleviate any spikes - keep your fingers, toes, eyes, whatever crossed.

She had a long nap today, woke up around 6:30pm and ate TWO whole pieces of pizza (did I mention that Tony is out of town?)! I could not believe it - she'll be keeping up with Bruno's appetite before we know it. Its late, and we should both be in bed - but she's here with me at the kitchen table painting. She's really great.

Cycle 8, In it to win it

Day 6: She is hanging tough. Really tough, in fact she is looking great and definitely feeling her oats. The chemo is just now starting to kick in, but she seems to be holding her own. We have clinic on Tuesday; that will be the actual, penultimate chemo treatment and also when we will be able to determine when (not so much if) she will need her RBCs and/or platelet transfusion.

Monday (day 1) was the LP (Uhggg - we had a few bumps there). She is so smart, and at the point where nothing can distract her from the "routine". No amount of bubbles, flashlights, movies, or promises of the toy store is going to take her mind off the fact that she's about to have an unpleasant experience. Bummer - and we are so close to the end (of this part). We were unable to access her port at the PACU (after multiple tries) so they ended up just gassing her in the procedure room and accessing her after she was asleep. They tried all kinds of ways to get her to "smell" the anesthesia and go under nicely - creative stories and at least 31 flavors of "gas". We (Tony & I) settled on strawberry - ultimately no avail. It ended up being just me 'hugging' her real tight while they held the mask to her [our] face. Of the four nurses in the procedure room - two of them left with me to make sure I wasn't "under". No fun, but we are bolstered by being near the end. She came out of anesthesia pretty well and we got home in time to celebrate Mr. B's 5th Birthday.

Monday morning - Bruno turns 5! Breakfast of CHAMPIONS
(yes that is whipped cream AND sprinkles!)

July 21, 2003: That's the day we first met our Bruno. He is growing so big, strong, gentle, and fast! He is kind and thoughtful, curious, and generous. He is a good boy. He starts kindergarten in August - I almost can not believe it. I'm certain that this past year has had it's toll on him - we've been pretty wrapped up in Gianni, our own shock, grief, struggles - he just keeps on keeping on. He always has a smile and a brotherly pat of encouragement for Gian, and has been a good friend and companion to her through this ... journey.

The party was fun - I even found time to hang streamers and buy balloons (an 'official' party per Gianni). Auntie Jen and Jessica came over for Blueberry Pie (it is what he asked for - although not such the big hit) and presents.

Balloons AND streamers... its a REAL party now

SURPRISE!

Blueberry Birthday Pie

Tuesday morning Tony and Gianni went to PEC for the 3-day admit. He again got to spend the lion's share of time with her (all day Tues - Wed night, and all day Thur). I was able to visit in the mornings and early evenings and spend Wednesday night with her.

Wednesday night - shenanigans...

Since Thursday was the last in-patient chemo treatment the nurses and staff at PEC had a mini 'graduation' for her. She got a nice certificate with hand written farewell's from her nurses, a big goodie bad of "littlest pets", and a beautiful SpongeBob SquarePants ice cream cake. Tony brought champagne and just after the last push (Etoposide) he let Gianni cut off the 'good luck' arm bands he has worn since she was first diagnosed - last November (peyou!).

After living day to day - this milestone kind of creeped up on us. And it feels great!


We ran out of PEC as soon as the de-access and sub-Q procedures were done and ran straight to Auntie Jen's to celebrate and share SpongeBob.

Now we just wait - we are doing our best to keep her healthy and out of the hospital... from our cycle 6 to cycle 7 break we know that once she's past the nadir hump she will bounce back quickly. I am sure that we have more long hauls in our future but for now .... it's looking so bright I gotta wear shades!

Gearing up for Cycle 8

The words are hard to type... it's really cycle 8! To torture us, the folks at LPCH have had to delay our start date from today (Wednesday) to Monday. Lots of reasons - a small contribution having to do with her health (still trying to clear up the UTI) and a larger contribution due to scheduling. Lots of sick kids at LPCH and PEC this week. So rather than throw the dice and wait for a potentially late Friday night admit; we've decided to start the whole boogy on Monday morning with a guaranteed room at PEC on Tuesday. This will push her "final" chemo administration to the 1st week of August and the official end of cycle 8 just in time for Tony's birthday (now how are we supposed to top that gift!).

She's doing well - well enough to have collected a whole cadre of 'regular' kid bumps, scrapes, and bruises from running too fast, playing too hard, and pushing her limits. Its grand.

More party.... still no streamers!

The GI thing ended up being some nasty bug named Clostridium difficile (C Diff) - treatable with more antibiotics. The antibiotic of choice is named Flagyl; funny to me, because it sounds so similar to flatulence (a real symptom too) . . . I guess you had to be here, or perhaps, had no consistent sleep for many, many days . . . So she gets this one every six hours, four times a day for two weeks (thank goodness for the NG). This infection does not qualify, however, for an "excluding event" and cycle 8 is On. We will start, with the "regular" routine (LP on Wednesday, admit to PEC Thursday - Saturday) next week.

Last Wednesday Gianni was ill during the night (emesis) and she 'lost' her NG tube - she has clinic on Thursdays so I just let her go commando for the rest of that night and the following morning. Although we love the NG (route for all her nourishment, fluid, meds . . . ), she seemed so footloose and fancy free without it. I could not stop kissing her bare little check! Alas, the nurses at LPCH did a great job, and the NG is back doing its thing.

Thursday's clinic netted some really great numbers (very high ANC) so the monthly pre-round cabin trip was on! We've really gotten the 2-day turn around down to a science. We left very early Saturday morning - got to the cabin in time for breakfast. Lots of great cabin stuff.

Bongos and brownies, but no streamers = no party!

Gianni's MJ tounge... pure concentration.

If I had a nickel for every popsicle picture!

We are home now, ready for action.

------------
Funny Gianni

"Cheese doesn't make you fat, cheese makes you happy!"

Cycle 7, Closer to the end than the begining

Quick update; Gianni's hanging tough. We discovered early Sunday morning that she has had a UTI . . . since last Wednesday . . . don't ask. Regardless, we got a prescription for antibiotics ordered and picked up in no time flat and she has been feeling a bit better. Monday's clinic visit uncovered a gastrointestinal (GI) tract infection that has also probably been brewing for a while - this is a bummer because if she does not resolve this one on her own it could mean a long hospital stay (~ 1 week) to "rest" her GI. We are crossing all appendages however because, so far, the antibiotics for the UTI seem to have had some positive effects for this infection too and she is holding her own (at home).

This past weekend Gianni and Bruno spent a lot of quality time at the park; Gianni is proving to be fearless when it comes to slides . . . a real daredevil!

Trish and Dr. Fisher are back in full swing and all seems to be "right" with our little world again.

Glorious Independence Day!

Happy, happy fourth to all. We had a great day with family and BBQ. The kids (all of 'em, including big sis Elly!) ran amok and the grown-ups enjoyed a relaxing and fun afternoon. We had steaks, spaghetti, ball park brats, potato chips, root beer, special anniversary wine, and even a cupcake cake decorated like the American flag (with lots and lots of icing) - oh my! Tony even decorated with flags all abound.

Because Gianni kept insiting that this was her birthday party we put candles in the cupcakes and all sang, "Happy 4th of July to us...Happy 4th of July to us..." and then blew out the candles. She also duly chastised us for not having streamers ("You can't have a party without streamers!" - next time).

Yesterday was also our 7th wedding anniversary - wow, it seems like just yesterday! The 7th anniversary traditional gift is copper or wool - the modern gift is a desk set - - - hmmm romantical. We stuck with the ever more traditional time and family.

Tony snuck up to the cabin early this morning. Bruno and I will take Gianni to the day hospital for a quick set of labs to determine if her counts are high enough to stop giving the shot. Catch 22 really cause she needs a poke to stop giving her the pokes . . . We'll make a day of it - stop off at the park and maybe spend some bucks at the ice cream truck!