Evie Hooper- Olfactory Neuroblastoma

$27,450 of $40,000 goal

Raised by 340 people in 2 months
Created December 29, 2018
Evelyn (Evie) Hooper was first diagnosed with cancer at three weeks of age. Bilateral Retinoblastoma caused tumors to grow in both of her eyes. She lost her right eye to cancer before she could begin treatment in Toronto.  After four rounds of chemo, laser and cryotherapy treatment, and many EUAs (examinations under anesthesia), Evelyn was considered a survivor by the time she was 7.

In August of 2018, Evie noted that her sinuses were bothering her and that her nose wouldn’t stop running. While waiting for the cold or sinus infection to clear up, Evie’s left eye began to swell, and her lymph node in her neck was bothering her as well. After treating her with saline, steroid sprays, and antibiotics and seeing no improvements, Veronica (mom) took her in to the Alberta Children’s Hospital  on November 9 th , where she had a CT scan. The doctors referred her immediately to have an MRI, and a follow up with an ENT as there was something visible in her sinus. The results of the MRI were gutting. Evie had a large mass growing in her sinus, and the doctors had her admitted immediately to perform a biopsy on the mass. The results came back positive, and showed that the tumor had metastasized to the lymph nodes in her neck. After many tense days of waiting, they were finally able to give her tumor a name: Olfactory Neuroblastoma.

Olfactory Neuroblastoma is a rare cancer that is primarily in adults; in other words, they do not see it in children. In adults, the survival rate when the cancer spreads to the lymph nodes is 20%. The Hooper family’s world was turned upside down. Treatment began immediately for Evie after celebrating her 11 th birthday on November 24 th.  Adults with Olfactory Neuroblastoma are not treated with chemotherapy as it does not tend to shrink this very aggressive tumor. Typically, it is treated with surgery and radiation.  As of right now the surgery that needs to be performed would be very invasive due to the size of her tumor, the plan is to use chemotherapy and hope for the best prior to surgery and radiation. With Evie’s history of the genetic form of Retinoblastoma, radiation puts her at a high risk for secondary cancers.

Before Christmas, Evie began chemo, which has yielded some positive results. She still has another 2-3 rounds of chemo to go before they will perform surgery to attempt to remove the mass from her sinus. In all likelihood, they will also remove the large lymph node that was visibly affected by the cancer, but they will not remove the other lymph nodes from her neck. The third course of treatment involves radiation therapy to try to neutralize any cancer cells that are still in her sinus and throughout her lymph nodes. To help improve her chance of survival, the team at the Children’s Hospital are sending her to receive proton radiation therapy, a more precise and less invasive form of radiation that is less likely to trigger secondary cancers post treatment.

Proton radiation therapy is not available in Canada, so Evie and her family will be travelling from Airdrie, Alberta to Jacksonville, Florida as soon as she has recovered from her surgery. Evie’s treatment will be 30 minutes a day, 5 days a week for a minimum of 28 treatments, plus time required to perform scans and tests prior to beginning radiation. The minimum length of time that they will be required to stay in Florida is 2 months, with a strong possibility of needing additional treatments and time spent away. The family hopes to be able to stay together throughout the length of treatment to make the most of the time they are given to be with each other.

The family will require financial support to be able to stay together. Evie has three siblings: Gwen (12), Sully (6), and Celeste (3). Mike and Veronica will be taking time away from work to keep the family together, and the financial burden will be great.

Things they will need to cover in addition to regular monthly expenses include:
- travel expenses for the siblings and Mike
- lodging in Florida
- the cost of food and living at the US exchange rate
- any other incidental costs that arise while treating a critically ill child away from home

The family is very thankful for any and all support they receive, financially or otherwise. Evie is a bright light that deserves all the love she can get while going through a battle that she has already been through.
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Hi Everyone,

Another update on what’s going on right now.
Thank you again for your love and support.

The Hoopers
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I haven’t done an update in awhile. The truth is, the status quo of chemo isn’t much to write about right now. Evie is beginning her 6th course of chemo on Thursday, which we are hoping can be her last. The chemo has had some undesirable side effects this round, including more nausea, mouth sores and gum bleeding which make Evie quite uncomfortable. The MRI still showed some shrinking since last time, but at this point we are not sure if it’s worth the havoc that the chemo is wreaking on her body if surgery is feasible. We would also like to get things going as soon as possible to get the cancer out of her body, and to try to get to Florida sooner than later.
We will be talking to the doctors before chemo begins again on Thursday, so if you are willing to pray, ask for, or put out good thoughts towards the following things, it would be much appreciated!
1) That Evie remains otherwise healthy and chemo is not delayed any further
2) That we can get some answers in terms of next steps, and that those next steps are for surgery and radiation
3) That the side effects are minimal, and that when the time comes for surgery, that Evie is healthy and ready to go!
As always, we are so thankful that we have all made it this far, and continue to live in the here and now and be grateful for time we are given. It’s a fine balance between being ready to go at any time and feeling stuck in a holding pattern. It is just a moment, a feeling, a blip in the grand scheme of things, but we are looking forward to moving towards more healing and getting the cancer out of her body, Lord willing for good.
Love and blessings to all.
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Greetings Friends,

Evie finished her second round of chemo like a true warrior and had her end of round MRI on Monday. Today we found out that she will be doing a third round of chemo starting on the 21st. This isn’t what we wanted to hear, but it’s not a bad thing as the doctors are still confident that she is responding well and it will make a difference in her surgery. It bumps her radiation date back as well, I figure if all goes to plan and we don’t have to do any more chemo that we will be going to Jacksonville in May and June, but we should know more soon.

A giant THANK YOU to everyone who has donated to the campaign- we hit our goal and beyond. I cannot express the difference it has made along this journey, being able to focus on Evie’s treatment right here right now without having to figure out how to stay together during her next steps is an incredible gift for us all.

Stay warm everyone!

The Hoopers
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Hello Everyone,
I am sharing this for those of you who haven’t seen this update on Facebook yet.

The Hooper Family
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$27,450 of $40,000 goal

Raised by 340 people in 2 months
Created December 29, 2018
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