Team Caleb - Roth Family Fund

$34,070 of $35,000 goal

Raised by 437 people in 46 months

On July 30, 2015, our world was turned upside down. After some blood work, countless tests and a hospital change, our 2 year old Caleb was diagnosed with stage 4 neuroblastoma. We are still learning what this means for him and how we best fight it. All we need are positive thoughts, prayers and maybe some miracles, but we understand that our wonderful friends and families want to do more. Thank you for your love and support in helping our family fight this rare disease.
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Caleb gained some wings early this morning. It was peaceful and on his terms, as always. There’s a brokenness that can’t be fixed. Fly high, baby boy, you are too good for this world. We love you!
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Our journey always seems to lead us back to Comer. We came in February for some additional treatments but they didn’t seem to do everything we needed. We’ve moved Caleb to hospice to make him more comfortable. We ask for prayers as we continue on this journey.
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After enjoying the past week of beautiful weather, playing outside and even visiting the zoo, we need another push of prayers and positivity for our little Super Hero. We’ve been given the dates for Caleb’s “end of treatment scans”. March 8th and 9th! Clear scans mean “tubies” (central line) can come out!!

Thursday finishes the last round of Acutane. Then a few days off before out patient scans. He’s also begun Physical Therapy and speech therapy. Keep those prayers coming and all the positive energy you can send. It’s been your support, along with Caleb’s hard work, (and a miracle or two) that has helped bring us to this point. Thank you so very much.


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Happy Holidays! Sorry for the lack of updates, truth be told we've been busy being a "normal" family. We were able to celebrate Christmas and the New Year with family (balloon drop included). Caleb is as always a rockstar! Our next steps include physical and speech therapy which should begin next week. We have our hearing aids and have been trying really hard to use them so we only have to shout in excitement! Our future is still uncertain in some ways - over the next few months, further scans and checks are still required to make sure that the medications Caleb was on didn't harm his heart, liver, lungs, etc. (So as always prayers are welcome and encouraged.) His tubies are still needed for the next couple of months but should be out this summer. We are trying to learn how to live as a family of five doing all those things we've missed out on these past 18 months. If you need further updates (because it will be quiet here for a couple months) please follow Stacy on Facebook. Thank you for all your support and Yay for 2017!!
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Mary Fitzpatrick
30 months ago

What a journey all of you have been on and how your lives have changed to a new "normal". It is such wonderful news that he is in REMISSION and I hope that your family can once again find your new "normal" now and enjoy it. P lease know that your entire family have been and will continue to be in my prayers.

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Nikolaus Wagner
32 months ago

$34,070 of $35,000 goal

Raised by 437 people in 46 months
Created August 4, 2015
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$100
Anonymous
1 month ago
RB
$100
RITA BLACKWELL
1 month ago
$25
Anonymous
2 months ago
MF
$100
Matt & Helen Fiore
2 months ago
$50
Anonymous
2 months ago
GS
$50
Glenn Surman
2 months ago
$50
Anonymous
2 months ago
$100
Anonymous
2 months ago
$50
Anonymous
2 months ago
Mary Fitzpatrick
30 months ago

What a journey all of you have been on and how your lives have changed to a new "normal". It is such wonderful news that he is in REMISSION and I hope that your family can once again find your new "normal" now and enjoy it. P lease know that your entire family have been and will continue to be in my prayers.

+ Read More
Nikolaus Wagner
32 months ago
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