Support Team Reese
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Below is the story of the unthinkable. We never thought our happy, sweet, kindhearted little boy would have a brain tumor. Seven months ago, our lives changed forever.
Your donations will help with the mounting medical bills as well as continuous rehabilitation costs.
Beginning in September 2018, Reese started vomiting in the morning and complaining of stomach pain.
We pushed and pushed to figure out the cause, including a visit to a Pediatric GI specialist. Unfortunately, he was not able to identify anything wrong such as ulcers, acid reflux etc. However, he did prescribe an Upper GI with Barium and said we could get a MRI of the head.
Reese wasn’t feeling well enough to go to school during the last week of October, but was able to gather enough strength to go Trick or Treating on Halloween 2018. He had such a great time running into a few of his friends. He seemed extra tired that night and went to bed early, without eating his candy.
The next day (11/1), we had an MRI of the head scheduled in the afternoon thinking we should just do it to be sure.
The MRI took an hour longer than planned, and when we finally got the MRI results late that night, a 4cm mass at the base of his brain was discovered. The mass turned out to be a malignant tumor blocking the fluid from draining in his brain, ultimately causing his nausea.
We were admitted to Lurie’s that evening and emergency surgery was performed the next morning on 11/2. Surgery resulted in a full resection of a Group 4 Medulloblastoma (an aggressive form of Cancer) from 4th ventricle.
Post-surgery however, resulted in Reese having Posterior Fossa Syndrome. It is a form of mutism and he has had to relearn how to move all of his body, swallow to eat (feeding tube), talk and even open his eyes to see. Other than nausea, Reese seemed and felt perfectly normal in every way prior to surgery.
4-5 days post-surgery Reese stopped all movement and communication. It was 31 days post-surgery until he said his first word. 47 days till he was able to eat his first bite of real food. He is able to walk with maximum assistance, so currently he is in a wheel chair. He has weakness on his right side, his dominant side, so his right arm has limited movement and strength.
A scared little boy went into surgery (to remove a “bump”) with the only symptom being nausea and woke up not being able to see, talk, eat or communicate.
Reese stayed at Ann & Robert H. Lurie Children's Hospital from 11/1/18 until 11/20/18, and was transported to Marion Joy Rehabilitation Hospital. Which was located close to where he was to begin Proton Radiotherapy and Chemotherapy.
While at Marion Joy, from 11/22/18 to 1/9/19, Reese underwent 30 sessions of Proton therapy, each session requiring him to be under anesthesia. During this time, Reese was also administered Chemotherapy regimen.
Reese recently completed his 3rd of 9 rounds of inpatient Chemotherapy, which will last the rest of the year and into 2020. Each round includes a few nights back in Lurie’s to have the Chemotherapy administered, as well as multiple Outpatient sessions in between.
During this time, Reese is also attending Physical, Occupational and Speech therapy at Shriner’s Children’s Hospital in Chicago. Needless to say Reese has a long, long road of recovery ahead of him.
Reese’s goal is to beat this awful “bump in his head” and return to being a kid...walking on his own, playing with his friends and continuing on to the 3rd Grade with his class; even though his treatment has kept him out of the classroom this past academic year.
We are so very thankful for the generous support from our friends, family and community, the amazing team at Amazon, Ann & Robert H. Lurie Children’s Hospital, Marion Joy Rehabilitation Hospital, Shriner’s Hospital for Children, the wonderful support of the Keystone Montessori School and Horace Mann Elementary communities and the countless well wishes over the past several months.
Your donations will help with the mounting medical bills as well as continuous rehabilitation costs.
Beginning in September 2018, Reese started vomiting in the morning and complaining of stomach pain.
We pushed and pushed to figure out the cause, including a visit to a Pediatric GI specialist. Unfortunately, he was not able to identify anything wrong such as ulcers, acid reflux etc. However, he did prescribe an Upper GI with Barium and said we could get a MRI of the head.
Reese wasn’t feeling well enough to go to school during the last week of October, but was able to gather enough strength to go Trick or Treating on Halloween 2018. He had such a great time running into a few of his friends. He seemed extra tired that night and went to bed early, without eating his candy.
The next day (11/1), we had an MRI of the head scheduled in the afternoon thinking we should just do it to be sure.
The MRI took an hour longer than planned, and when we finally got the MRI results late that night, a 4cm mass at the base of his brain was discovered. The mass turned out to be a malignant tumor blocking the fluid from draining in his brain, ultimately causing his nausea.
We were admitted to Lurie’s that evening and emergency surgery was performed the next morning on 11/2. Surgery resulted in a full resection of a Group 4 Medulloblastoma (an aggressive form of Cancer) from 4th ventricle.
Post-surgery however, resulted in Reese having Posterior Fossa Syndrome. It is a form of mutism and he has had to relearn how to move all of his body, swallow to eat (feeding tube), talk and even open his eyes to see. Other than nausea, Reese seemed and felt perfectly normal in every way prior to surgery.
4-5 days post-surgery Reese stopped all movement and communication. It was 31 days post-surgery until he said his first word. 47 days till he was able to eat his first bite of real food. He is able to walk with maximum assistance, so currently he is in a wheel chair. He has weakness on his right side, his dominant side, so his right arm has limited movement and strength.
A scared little boy went into surgery (to remove a “bump”) with the only symptom being nausea and woke up not being able to see, talk, eat or communicate.
Reese stayed at Ann & Robert H. Lurie Children's Hospital from 11/1/18 until 11/20/18, and was transported to Marion Joy Rehabilitation Hospital. Which was located close to where he was to begin Proton Radiotherapy and Chemotherapy.
While at Marion Joy, from 11/22/18 to 1/9/19, Reese underwent 30 sessions of Proton therapy, each session requiring him to be under anesthesia. During this time, Reese was also administered Chemotherapy regimen.
Reese recently completed his 3rd of 9 rounds of inpatient Chemotherapy, which will last the rest of the year and into 2020. Each round includes a few nights back in Lurie’s to have the Chemotherapy administered, as well as multiple Outpatient sessions in between.
During this time, Reese is also attending Physical, Occupational and Speech therapy at Shriner’s Children’s Hospital in Chicago. Needless to say Reese has a long, long road of recovery ahead of him.
Reese’s goal is to beat this awful “bump in his head” and return to being a kid...walking on his own, playing with his friends and continuing on to the 3rd Grade with his class; even though his treatment has kept him out of the classroom this past academic year.
We are so very thankful for the generous support from our friends, family and community, the amazing team at Amazon, Ann & Robert H. Lurie Children’s Hospital, Marion Joy Rehabilitation Hospital, Shriner’s Hospital for Children, the wonderful support of the Keystone Montessori School and Horace Mann Elementary communities and the countless well wishes over the past several months.
Organizer
Anthony Siler
Organizer
Oak Park, IL
