Help MayaTheDragon Fight Leukemia

$50,865 of $50,000 goal

Raised by 536 people in 26 months
Megan Francoeur Johnson
on behalf of Maya, Sara, Scott, Lincoln Morrison
 CARSON CITY, NV
Calling all supportive, loving, caring people to help Princess Maya and the Morrisons fight! 

Maya is a sweet, smart, bright, beautiful three year old who needs our help! On Thursday night, Sara and Scott, Maya's mom and dad, noticed some unusual bruising on her and decided to take her to the doctor. They went in next morning and the doctor had them go to the hospital immediately, where tests were done. The shocking news came back that Maya has leukemia. Within an hour, Maya and her family left for Oakland Children's Hospital where she is receiving blood and platelet transfusions. She is waiting for a bone marrow biopsy so that a course of action can be taken.

Maya and her family need our support to help them through this difficult time.  One way YOU can help Princess Maya fight is to donate to Go Fund Me.  Any amount, large or small, will make a difference and be greatly appreciated.  We will keep you informed through Caring Bridge as new information becomes available. Keep sending love, prayers, and positive energy for Princess Maya and the Morrisons!
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Sara will brave the shave for St Baldricks at the Fox in Carson City today at 4. If you’re around, come on down and support Sara and childhood cancer research. Link to donate to St Baldricks: https://www.stbaldricks.org/participants/mypage/949201/2018/donors#content
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Hi everyone. I just wanted to give you an update on Maya and share some details of the end of her treatment. I would also like to inform you of a few events that are planned in the upcoming months.

Maya had a pretty bad cough for the past couple months. Recently she was given immune proteins collected from 200 individuals from all over the world in hopes that at least one would provide antibodies for Maya’s bug. It seems as though this was successful as Maya’s cough has improved significantly! Hurray!!

As of today, Maya is in the middle of the second to last week of steroids. She has one more vincristin infusion, one more lumbar puncture, seven more doses of methotrexate, and 51 more days of 6mp (oral chemo). This puts Maya’s last day of treatment on.... APRIL 21!!!!!

There are a few events coming up in honor of cancer research, shedding, healing, and celebrating, so SAVE THE DATES!!

ST. BALDRICKS EVENT
March 17, Saturday, 3pm-6pm, at the Fox Brewpub.
Sara will be shaving her head for childhood cancer research, for Maya, for women, and for SARA. I will post an update on Sara’s shave/shed time when I get more details. Please come out to support Sara, the Morrison family, and all kids and families who are fighting cancer. If you would like more information or would like to donate, here is the link.
https://www.stbaldricks.org/participants/mypage/949201/2018

ALOHA CHEMO EVENT (LOCAL)
May 26, Saturday, Time TBA, at the Shoe Tree Brewing Company.
This will be a local celebration. All are welcome. More details will be available soon, and updates will be posted.

ALOHA CHEMO EVENT (KAUAI)
June 24, Sunday, Kauai
There will be a healing ceremony followed by a celebration party. The Morrisons will be in Kauai with friends and family June 21-July 5. All are welcome.

As always, thank you for the continued support, love, prayers, etc. The countdown continues... we are almost there!!

To find additional updates and information on Maya and the events, please go to mayathedragon.com




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I'm THRILLED to post a very exciting update! Two of the last three times Maya's labs have been taken, the numbers have come back looking great! The last time they were taken, the numbers were high, specifically her ANC. Depending on the next round of labs, there may be some more adjustments made in the dosage of oral chemo-6mp...... But!! Maya was given the OK by her doctor to go back to school!!! This comes a few weeks after Sara and Scott decided to start Lincoln at school too! So today, brother and sister got to attend school TOGETHER!!!

Maya is still in the maintenance phase, taking daily oral chemo, going in for monthly IV chemo treatments, lumbar punctures, taking rounds of steroids, among other things. But she is doing great and the END is in sight!!! As always, thank you for your love, prayers, support, positive thoughts, .... Love is Life.
SUPERGIRL AND SUPERBOY!
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Maya has been off of her oral chemo for 16 days. This was to allow her body to get strong again after being low for quite awhile. Two weeks ago she got a bad tummy bug and spent two nights in the hospital, Sara by her side and Scott visiting when he could. Maya had a pretty high temperature and had maxed out her Tylenol dosage, causing Sara to make the decision to try to keep her cool by placing cold clothes on Mayas body. She changed these every 20 minutes throughout the night. Finally the temperature broke in the morning, and they were able to go home later that afternoon. During this time, Sara's brother was visiting. She missed most of the visit but was able to make it home in time to spend one evening with him. The maintenance phase continues to be challenging and stressful, but Maya just had her labs drawn and the numbers look good. The Morrisons are hoping to get Maya back on the oral chemo, find the right dose for her, and enjoy some less stressful days ahead. For a more detailed update please go to MayaTheDragon.com.
Thank you for all of the love and continued prayers. Love is life.
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Read a Previous Update
Sara Moore-ison
26 months ago
7
7

Dear family, friends, new friends, old friends, long-lost friends, friends like family, friends of friends, friends of family, colleagues, strangers, supporters, lovers, prayers, and the anonymous. Your support and love is tangible and overwhelmingly beautiful. We have found ourselves in some dark times but the light shining upon us from the people of our world (near and far) has lit the way and made this whole experience manageable. Results are back and Maya has been diagnosed with B cell acute lymphoblastic leukemia. She has an amazingly long road ahead of her filled with chemotherapy, steroids, lumbar punctures, body changes, immunity concerns, and other life changes. Even with all this, it is the most wonderful awful news we could ask for as it is the most treatable and curable type of childhood leukemia. She is due to get her first dose of chemo via lumbar puncture tomorrow along with a power port placement which will stay with her for the next 2.5 years of treatment. She has been amazing and her strength humbles me. She is trying out "strong and calm" as her motto. Scott and I are holding up and very thankful for my parents who have been essential with taking care of Lincoln, playing as much as possible with Maya, and keeping us sane. We are trying to be as present as possible while with the kids so please visit Caring Bridge for updates. Thank you all so much for your love and support. There is not a big enough thank you card in the word to express our gratitude. Love is life.

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Kelly Smith Johnson
26 months ago

Please have the family reach out to Northern Nevada Children's Cancer Foundation in Reno. They will be able to support the family both financially and otherwise!

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$50,865 of $50,000 goal

Raised by 536 people in 26 months
Created February 13, 2016
Megan Francoeur Johnson
on behalf of Maya, Sara, Scott, Lincoln Morrison
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$200
Anonymous
1 month ago
$100
Zeina and Dom Sinnott
6 months ago

We love you Maya!

$5
Anonymous
7 months ago
$5
Anonymous
8 months ago
$5
Anonymous
8 months ago
$50
Anonymous
8 months ago
WH
$200
Wendy Haig
8 months ago

Hang tough and never give up!

EH
$200
Ed & Patty Horgan
9 months ago

What a strong little lady! We love you, Maya!!

$50
Anonymous
9 months ago
Sara Moore-ison
26 months ago
7
7

Dear family, friends, new friends, old friends, long-lost friends, friends like family, friends of friends, friends of family, colleagues, strangers, supporters, lovers, prayers, and the anonymous. Your support and love is tangible and overwhelmingly beautiful. We have found ourselves in some dark times but the light shining upon us from the people of our world (near and far) has lit the way and made this whole experience manageable. Results are back and Maya has been diagnosed with B cell acute lymphoblastic leukemia. She has an amazingly long road ahead of her filled with chemotherapy, steroids, lumbar punctures, body changes, immunity concerns, and other life changes. Even with all this, it is the most wonderful awful news we could ask for as it is the most treatable and curable type of childhood leukemia. She is due to get her first dose of chemo via lumbar puncture tomorrow along with a power port placement which will stay with her for the next 2.5 years of treatment. She has been amazing and her strength humbles me. She is trying out "strong and calm" as her motto. Scott and I are holding up and very thankful for my parents who have been essential with taking care of Lincoln, playing as much as possible with Maya, and keeping us sane. We are trying to be as present as possible while with the kids so please visit Caring Bridge for updates. Thank you all so much for your love and support. There is not a big enough thank you card in the word to express our gratitude. Love is life.

+ Read More
Kelly Smith Johnson
26 months ago

Please have the family reach out to Northern Nevada Children's Cancer Foundation in Reno. They will be able to support the family both financially and otherwise!

+ Read More
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