Friday, February 26, 2010

MRI Results

Owen had his routine 3-month MRI yesterday. The procedure went very well and the results showed that there has been no change in the tumor - again, we have much to be thankful for! We prepared Owen the day before the MRI by telling him that he was going to the doctor's and he was going to get a "pinch." He woke up on Thursday morning knowing where he was going and having a good idea of what was going to happen.
He's such an amazingly strong boy as when it was time for his IV he didn't even cry. The nurse practitioner, Jeff, is a blessing as he inserted the IV into Owen's foot with one try. Owen flinched but didn't cry... he did cry a few minutes later when they were holding his legs still and then he drifted off to sleep. After the MRI, he slept for 1.5 hours at the hospital, woke up, sat up, and said "all done, yeah" and started to clap for himself - it was like he didn't even miss a beat!
His recovery was much better than last time. The effects of the sedation didn't seem to last as long. He was back to his normal self by 3pm yesterday. We were so thankful that he handled the sedation better and that the results were positive in that the tumor has not grown. Now the MRIs will be every four months for the next year. Thanks for your prayers as they've provided Owen with much strength.

Sunday, February 7, 2010

Our trip to NC

Cousins Alex and Ronnie Jr.

Giving Uncle Ronnie goodbye kisses.

Smiling with Auntie Terry.

Uncle Ronnie and Owen building with Lincoln Logs - actually Uncle Ronnie built houses and Owen knocked them down.

Owen helping Uncle Ronnie cook bread.


The Montecalvo Family.

We recently took a trip to Waxhaw, NC to visit our family - Auntie Terry, Uncle Ronnie, Saverio, Ronnie Jr., & Alex. We were actually supposed to take this trip last year when Owen was hospitalized. It was nice to finally get there one year later. We had a great time visiting. Owen really enjoyed playing with his cousins. While we were visiting, we took Owen to the circus for the first time. He had fun - especially while he was eating popcorn, which he ate plenty of! We had one nice weather day when it was 60 degrees... and we had two trips to the playground, which Owen really enjoyed - he would swing for hours if he could. Here are some photos from the trip.

Sunday, January 17, 2010

Snakes & Cake

We spent this past weekend in RI. Owen went to a Toddler Trek class at Roger Williams Park Zoo where he learned about snakes. He was more afraid of the fake wooden snakes then he was of the real one! It was a great hands on class for toddlers. Below are some photos of Pepere and Owen enjoying class.


We also celebrated Jarred's 23rd birthday - hard to believe that my little brother is 23! Owen enjoyed celebrating Uncle Jarred's birthday. Here's a clip of Owen singing Happy Birthday!

Monday, January 11, 2010

Dana Farber Update

Last Thursday (Jan. 7) we visited with Dr. Mark Kieran at Dana-Farber. We went with the intention of learning more about their Pediatric Low Grade Astrocytoma Program. Luckily, Owen does even qualify for their program because he's not receiving treatment - hopefully he will never qualify! We did visit with Dr. Kieran just about one year ago when Owen was first diagnosed. He does not know much more now then he did then... perhaps he knows even less about Owen's condition... and for the first time in my life I'm thrilled with not knowing!


Let me explain... as long as the "tumor" does not grow, we will not know what type of "tumor" it is because in order to know the type of tumor a biopsy would need to be performed. We don't know the size of the tumor either because the tumor cells are intertwined with his healthy brain cells. We don't know if the tumor is done growing but I'm faithful that it is.

Unlike the opinion that we received from Yale, Dr. Kieran is not convinced that the brain tumor caused the hydrocephalus - perhaps the tumor was just discovered because Owen had the hydrocephalus, which is a common condition in pediatrics. He also said it may not be a "tumor" but rather a collection of cells that "copied" wrong during the multiplying process and then stopped growing at 3 months when the brain stops growing. On the other hand, Yale is convinced that the tumor grew and caused the hydrocephalus.

Regardless, we may never know what Owen has exactly - and that is the hope. We do know that Owen is a strong little boy who is supported in continued prayer. Please know that Owen doesn't just receive prayers either - he's praying too! We pray for family and friends each night before bed as well as read prayers from his favorite prayer books. He now simply says, "God, Amen" and perhaps at times that's all we need to say.

Friday, January 1, 2010

Happy, Healthy New Year!

We celebrated Hanakkuh at Mimi & Papa's house...

Cute cousins!
Owen "O's" face... his truly surprised look!

The Dubois family... the RI bunch... missing about 15 others...

Merry Christmas from the Bernheims!

Wishing everyone a Happy, Healthy New Year! Last night we rang in the New Year with friends, Christa, Jay, and Addie (who is Owen's age). It was great to watch them interact together (as Addie so kindly shared and Owen pulled toys away from her). Amazingly we (not the kids) all made it to midnight and beyond... but Eric and I are a bit overtired today... we're getting old!

This holiday season was a joyous one. We enjoyed spending the holidays with our families and friends. We also celebrated Eric's birthday (he's a Christmas baby). December was a whirlwind of a month, which is why I'm just getting some photos online. I have a resolution to get back to blogging regularly... I'm hopeful anyway... not sure how it will be having two kids! I would also like to encourage more dialogue on my blog... so if you're visiting feel free to leave a comment of vote (I'm going to add some voting polls).

Here are just a few holiday photos... more will be available on our new photo site... The Bernheim Bunch. Please let me know if you need the web address.

Do you have any new year's resolution's for your family? I'm hopeful that I can eat Owen to eat more vegetables, which means I have to eat more veges too? Any helpful hints on getting toddlers to eat veges? He's a fruit addict but not crazy about veges.

Wednesday, December 30, 2009

Ultrasound



Yesterday we had a level II ultrasound... where everything can be seen. The technology is truly amazing. We saw the baby's brain and its healthy ventricles - no swelling. We saw the four chambers of the heart beating so nicely. We also saw the kidneys and the "practice breathing." And no, we did not see what we were having. We still want it to be a surprise... just 21 more weeks to go! Hard to believe that next Thursday I will be 1/2 through the second pregnancy. It's going much quicker then the first. We will have another level II ultrasound toward the end of March... again, they'll check the brain and make sure everything else is working properly. I began to feel the baby kicking this week... it was about 3am on Tuesday morning... the same time Owen was up crying - will I ever sleep through the night again?!

Wednesday, November 25, 2009

Thankful for Stability

As you may have heard Owen's MRI went well last week. We received the best possible news, which is that Owen's tumor is stable. We still send his MRI to Dana Farber for a second opinion.

What does it mean when a tumor is stable? The following is from the Lahey clinic website, When a tumor is referred to as "stable," it means that the tumor cells are in a phase in which they have stopped growing or multiplying. Such stability may be temporary or permanent. When the tumor has actually been destroyed, and the area it occupied in the brain is composed only of dead tissue (necrosis), no new growth will occur. However, if tumor cells remain, it is possible that they will begin growing again at a later date.

The actual sedation process went very well. We were in the very capable and caring hands of Jeff, the nurse practitioner that I previously mentioned. He inserted Owen's IV with just one try - thank goodness... and then Owen was off to sleep. After the MRI he slept for an hour and then we took him home where the challenge of the recovery began. We were told that the effects of the sedation could last the entire day... and they did! He could not walk unassisted, which made him pretty mad! He tried to help him or sit with him but he was not having it... needless to say it was a long day but knowing that sedation is safer than anesthesia makes it bearable.

We have much to be thankful for this Thanksgiving and everyday! Owen is doing well and we have another bundle of joy on the way...