Dexter Lawrence Authentic Jersey  Updates

Updates

First things first, NED ( NO EVIDENCE OF DISEASE) people - God has shown us his confirmation of the blessing that occurred May 24, 2010 when God made Nicky CANCER FREE! I was doing ok today but the day started early, 6am to get him ready for 7:15am labs and clearance. Normally you all know we get results quick, after a 9am MRI and recovery at 12:00pm .... the wait started. Our Doctor told us if she could not contact us by 3pm she would be in a meetting until 5pm and call after. So the clock went past 3pm and we thought ok 5pm then ... 6pm went by nothing ... 7pm went by ... nothing ... I want to personally thank Pastor David for this Sundays service where he said that GOD WANTS TO COME IN LAST MINUTE AND SAVE THE DAY so to speak ..... waiting last minute is stressful when you are prepared mentally for a call hours ago. Our doctor had an emergency and called and said everything looks great ...So relieved ... so blessed and so happy to go home tomorrow to decorate that empty Christmas Tree! It was waiting for this news with us ....

So many kids are here .. please pray for our ultrasound on Nickys kidneys, the doctors don't seem worried but they are still picking up contrast. We will be flying home tomorrow afternoon and another 3 month countdown to St Jude begins!!! It was a long day my phone has never blown up like this with so many people worried .... we so felt you love while we too were starting to get worried as the time went by .... BUT ALL IS WELL .....

I SOUGHT THE LORD, AND HE DELIVERED ME FROM ALL MY FEARS. Psalm 34:4

Pray for Brodys scan tomorrow, for Averys scan tomorrow for Reeses on Friday ... Kylies tomorrow ..... wow too many to name ... please say some prayers for great scan for all and for Campbell getting todays results tomorrow.

THANK YOU ALL FOR LOVING US AND YOUR RELENTLESS CONCERN ... all the texts, you worried for us ... : ) We love you !!!!

What a week .... so much undisclosed but this journey is about Nicky ... so on Thanksgiving Eve I find it impossible to not write about how thankful we are for every minute of every day with him.  Yesterday marked that we is now 26 months old ... everyday and every month is a BLESSING .... we do not take for granted. We met locally with the surgical team at Beaumont to close NIckys tummy surigcally because after 5 months of wound care, NOTHING is closing this thing.  The surgeon told me that if it didn't close in a few weeks that is should be done surgically - while relieved it was finally being handled .... another surgery Ughhhh ...  thankfully it's and in and out procedure and we do not have to stay in the hospital, which Dear Lord.... THANK YOU ... I couldn't bear to sit in the hospital he was in after surgery ... I pray we never have to stay there ever.

Our scan is a week away, ... thanksgiving is tomorrow .... ask yourself ... what are you truly grateful for? This is a simple answer for us .... we are greatful for Jesus Christ who allows us sinners a gateway to God .... someone stopped Nick in a store randomly and asked, "are you are Christian?" Nick replied YES .... he said do you know why God sent Moses and the 10 commandments? Nick was a little taken back a stranger grabbed his arm and asked him this ... the mans reply was ... God knew that the 10 commandments no one for be able to find salvation and this is why He sent Jesus Christ..... he looked at Nick and said look around you .... do not be stressed and do not worry .... if you do you take Jesus back to te cross and he already paid that price - don't take him back to the cross again. Profound for a stranger to apporach him in such a way ... he told him to think of others first and to just be happy ... do what Jesus did for us ...

Tonight I post no photos .... but ask you that tomorrow when you sit at your dinner table that you pray for cures, pray for our Nickys scan a week away that it is clear and mostly ... pray for all the families that are in treatment and the ones that we have lost that are soooo missed this year and for the years to follow....

My greatest lesson - is compassion .... give when you have change to give - give when you have dollars to give ... help when you can donate your time to soup kitchens and even your local salvation army ... all volunteers ..... find your way to make a difference this holiday season...because any effort from your heart matters..Find a way to leave an imprint on others hearts .... pay attention to people around you, maybe you need to grab someone, or maybe you need to be grabbed ... either way .. learn from us ...

I am grateful Lord for my boys .... the blessing they are ... I am beyond grateful for every mintue with Nicky .... I am BLESSED beyond measure that my husbnad supports me and all the time I spend volunteering my efforts to aid pediatric cancer. I am blessed because my family is only second to God .... and I am grateful for the lessons, even the ones filled with pain ... I am grateful for my friends - the ones that are truly family ... thank you dear Lord ... for all you have done for us and continue to do .... please allow Nickys scan to be cancer free .... God Bless you all and have a Happy Thanksgiving ...

Please pray for Laine Watkins family as she earned her wings this past week and find myself wishing we just had cures!!!! Lord give researchers PLEASE  Amen ... amen .... AMEN ... Happy Thanksgiving

btw - Colin T is still caner free .. thank God!!! ...   : )

First and most importantly, our next MRI date is Wednesday, November 30, 2011. As you all know I HATE Wednesday scans because getting results right after is really close to impossible because our doctor is in meetings all day. She said she is really going to try to see us in between but that she will at the least give us a call no matter what. Ughhhh .....Please pray for NED ( no evidence of disease)

Seems as posting lately isn't as easy taking a whole month and trying to verbalize and cram it all in a short enough time span that you will still want to read about it. I think I will go back to updating biweekly so that I don't miss important things and email you once a month a notification.

As you all know that follow and read My Nickybear updates - I find ways to advocate, because if I personally can't fight cancer, then I find ways to do it for Nicky and all the children. I want to thank so many of you for signing the petition. On October 21, 2011 not only did the petition meet its goal it surpassed it and people are still signing it! God Bless each of you for signing, re-posting and emailing it out, it truly took an army of people to help and the numbers surpasses the goal! THANK YOU LORD!

On October 20, 2011 my dear friend / sister, Nicole welcomed Baby Jackson Carter B. into the world and I can't be happier for her and her family. I pray for nothing but love, laughter and health to you sweet Jackson! She will always remain a mother of three, two whom will walk and one that soars. We miss you Baby Wade!

Nicky is growing and is being an active 2 yr old and is into everything! He eats like a little piggy and it reminds me of how blessed we are that he can actually eat! a year ago we had switched to baby foods and bolus tube feedings. No more machined feeds and hours of tubes attached to him - finally a little freedom! I think about Jacksonville a lot lately. It was my 2 months alone with Nicky and we watched Toy Story 2 a million times. We cuddled and always slept together, those days will always be precious to me and walking the dock on the St. John's River. Now I get to experience fall here home and I love this time of year. Nicky loves the park and to take him away from a playground is torture!

We are enjoying him and all his spunky attitude. He has become a bit of a Daddies boy lately - Nick can't leave a room without Nicky throwing a fit. I guess he's bored with me since I am with him 24/7 and when he catches Daddy running to another room he runs screaming for him. One of the most stressful things we are dealing with since Nick mainly works from his home office.

It was a rough month in our circle of friends, Lyssie R. gained her wings and within days Drake K. earned his. We were in treatment in Jacksonville shortly with Drake and he would come walking in with his cowboy boots.... both these children and their families need prayers. On a different note, Little Anna Rose whom I have followed since the PICU in Buffalo, NY had a bad scan and there was progression .. some children just capture a part of me and Little Anna has done that, so please pray for her and her family. And since cancer does not discriminate in any way, I ask that you send prayers to Heaven for Flo whom is battling ovarian cancer and Aline also. Please pray for Megan P. in scans, Colin T. and Luca P. both scanning next week.

Nick and I had a chance to go out with friends to ECC and it was fun to be part of the "normal" world, though out of the corner of our eyes at the table next to us was a child, maybe 9 or 10 and he was there with his family - the hallmark signatures of a child that has been treated or in treatment for cancer. Faintly I could see a light scar on his head as I approached them, and he was bald sitting between two siblings and his parents. No stopping me when I see a child, I sprinted over with a Nickybear card in hand and said I have to ask, since my son is local and we just finished a year of treatment at St Jude ... enough said .... he was a boy diagnosed at age 3 PNET tumor and it was removed, they were treated at U of M and he is now 9 years old and cancer free. His hair just never grew back from radiation - but it didn't matter - he pulled off bald beautifully. It shocks me, was I blind before - walking around oblivious to the hallmark signs of pediatric cancer? The normal world goggles that most people wear ... mine were ripped off my face scarring me permanently on May 22, 2010.

I hope that whomever reads this takes those goggles off and sees life and all its beauty and pain and understands what is truly important.

I took this photo while Nicky was sleeping on Oct. 22, 2011 this date marks that he is 25 months old and while I starred at him sleeping and thank God for every minute with him ... I couldn't help but cry looking at the I love St Jude t-shirt he wears. Boy I wish it was a t-shirt we bought in support, but because my little man was a patient. It made me realize that life changes in an instant and nothing is ever the same and that I am suppose to tell all my readers to be grateful for what you have because it can change in a blink of an eye. Pray for CURES! Thank you for always supporting us, loving us, praying for us and reading NickyBears journey ..... God Bless you all .... xoxox

So much to say, I seem to barely have time to write lately. So first things first .... we are still trying to figure out our St Jude stay because since we removed Nickys feeding tube 5 months ago, it simply will not close on its own as expected. That means another surgery for our little guy and while I am not happy about it, it will be closed properly and it will heal now so this is a good thing. 5 months of wound care is no fun at all, for him or for us - so we not only need your prayers for his MRI, but that this procedure is QUICK and HEALS fast! With the holidays approaching so quickly, I find myself getting anxiety to a totally different level when I see Christmas decorations in all the stores with this looming test in my every thought. I just want great results so we can have a great holiday season! Our Heavenly Father has His hands on our boy standing it faith on that!

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So Halloween Christian and Nick love to make the house SPOOKY ... lol all down our long driveway were tiki torches and gates with webs with strobe lights and sound effects... the kids loved it.  Christian and I did our annual carving of the pumpkins and I did one for NickyBear, though I won't lie it was almost just NICKY because it hurt so much to carve the pumpkin. Christian did his this year without any help from me with the double ghosts and the paper ones he won a school contest with. Christian is extremely talented and crreative.

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Nicky would have nothing to do with putting on a costume, however I am still determined to get him in it while sleeping for at least a photo LOL. Nicky and I went to Rose Cancer Center for his port flush last week and he did great. It's either he doesn't care or he's going to scream the whole time and thankfully we got through both monthly flushes with no problems. Below is a photo taken in the lobby there, its really kid friendly so it helps when we need to wait.

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bdaymomSo the 4 of us went to eat at ECC for my birthday and it was a rushed dinner, but it didn't matter to me as long as I have my boys that's all that matters to me.  Thank you all for all the numerous Birthday wishes of FaceBook ... like I will always say ... you already know what this Momma wishes for every single day of my life and always will.

The following night Nick and I got to grab dinner alone and it was again quick but we got a little bit of time alone. Thank you Auntie Kimmy!!! What would we do without you!

On a different note because I always try to update you on the kids I ask you to pray for, Megan P. scan was NED (no evidence of disease), Seth B. and Ian M. too both NED as well as KK with a big fat NED thank you Lord  .... Luca P. may need another surgery - so please keep him in your prayers and Arianna's scan came back and the tumor had shrunk - nothing short of a TRUE MIRACLE.  Colin needed to reschedule so no news there. I ask you to continue to pray for Luca  and Arianna .... all the kids even with NED scans that they remain so. Another new Momma found her way to me and she is a 22 month old named Hallie A. please keep her in your prayers as their journey on SJYC07 protocol just begins. Ryan D. scanned today I believe and Christian S. is a week after us .... all these kids need to be lifted up with our Nicky in prayer PLEASE.

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I can't tell you enough what your prayers mean to us and they continue to strengthen us. We can't imagine this journey without your love, prayers and support ... the Lord took us down this path for a reason and as we continue to find comfort in the Lord, I will always do all I can to help another family .... this is no doubt part of my mission and ministry in life, and as painful as it may be at times to love these children I am reminded that God so loved the world .... that he gave his ONLY son .... for us .... I am reminded this Holiday season what a true blessing each day is, I hope you all see that too.

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pimSo while you shop and rush to put up trees and decorate and spent time wrapping presents and standing in lines to purchase gifts .... think of just one way you can do something to help someone else.  Whether it be a donation, a walk  or doing something for your church .... find someone that needs help and help them ..... it is the GREATEST gift you will ever give yourself.

Dear Lord,

This new year approaching I ask relentlessly request that you gift talented Christ loving researcher with CURES, I beg you to bring healing to not only the children suffering life threatening illnesses but all people of all ages .... I ask you to renew the hearts of anyone reading our posts and that they will be inspired by doing good deeds for others. I have faith in you Lord, my provider, my great physician and strength ... Please hear my prayers and keep Nicky CANCER FREE .... !!!

PS .... Meet Owen and Oliver they are sold this year at J.B. Robinson Jewelers, Gymboree and Kay Jewelers.  Each Bear sells for $12.99 and the profits go to St. Jude Children's Research hospital. So Give the gift of a CURE!!!! God Bless and please please pray for NickyBear's scan Nov 30!!!!

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Its simple, please sign this petition - ask your spouse, boyfriend, girlfriend, Mom, Dad, Grand parents, Aunts, Uncles, Cousins, Kids ... FAMILY and so so many Friends .... cut and paste this - email it, forward it, take the link and facebook it, tweet it - text it please we need 1794 more signature before October 26, 2011.  We need everyone to help - no funds required and no event to be at ... just 5 confusing minutes registering and signing this petition.

PLEASE - For Nicky ... and all the faces I love and have lost .... GOD BLESS!

we petition the obama administration to:
KEEP KIDS ALIVE. Allocate more funds towards CHILDHOOD CANCER RESEARCH.

Children's cancer is the #1 cause of death in children, yet the funding approved by Congress for Childhood Cancer is supremely low when compared to Breast Cancer Research which is the 6th leading cause of death in women. It is not okay that our children are dying because government funding is lacking. Cancer is the leading cause of death in children over all other childhood diseases combined! Children's Cancer Research needs to be at the forefront of funding. These children are our future and need to be taken care, stood up for, and protected, and this includes making them a priority in government funding for cancer prevention research. CHILDREN ARE DYING EVERY SINGLE DAY DUE TO CANCER. IT IS TIME FOR THE GOVERNMENT TO STEP UP AND PROVIDE SUBSTANTIAL FUNDING FOR CHILDREN'S CANCER.


https://wwws.whitehouse.gov/petitions#!/petition/keep-kids-alive-allocate-more-funds-towards-childhood-cancer-research/8ZnnxNgw

wwws.whitehouse.gov
WhiteHouse.gov is the official web site for the White House and President Barack Obama, the 44th President of the United States. This site is a source for information about the President, White House news and policies, White House history, and the federal government.

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