2020-09-30

158) Day 30 – childhood cancer awareness month

This is is, the last day of childhood cancer awareness month. I hope I’ve gotten the message out, as well shared some information & real-life stories of families affected by childhood cancer.

Today’s I Draw Childhood cancer infographic is Hodgkin’s lymphoma:
 

Today, Childhood cancer Warriors have some final thoughts about childhood cancer:
 

 

2020-09-29

157) Day 29 – childhood cancer awareness month

Today’s fact from Childhood cancer Awareness is actually a fun fact, and it's about what you can do to help the fight against childhood cancer:
 

Today’s I Draw Childhood cancer infographic is non-Hodgkin’s lymphoma:
 

 

2020-09-28

156) Day 28 – childhood cancer awareness month

 Today’s I Draw Childhood cancer infographic is ependymoma:
 

Today’s not-so-fun fact from Childhood cancer Warriors is about retinoblastoma:
 

 

2020-09-27

155) Day 27 – childhood cancer awareness month

 Today’s not-so-fun fact from I Draw Childhood cancer is about Wilms’ tumour:
 

Today’s I Draw Childhood cancer infographic is about neuroblastoma:
 

 

2020-09-26

154) Day 26 – childhood cancer awareness month

Today’s I Draw Childhood cancer infographic is about retinoblastoma:
 

Today’s not-so-fun fact from Childhood cancer Warrior is about neuroblastoma. We met a family whose son, James, had a neuroblastoma diagnosis. James was a happy little man with a great smile, infectious laugh, and his thumbs up. He loved bottle flipping, Camp Ooch, baseball, and cars – both Hot Wheels, and hot rods. He completed his treatment, but relapsed shortly after. Unfortunately neuroblastoma, when it relapses, does not usually have a good outcome, and sadly, James passed away on September 2nd, 2019, forever 5. His funeral was standing room only, packed with friends and family. Spider-man was there, a song from one of James’ favourite movies was played, and a local car club, the Dog Patch Devils. Every year, the Dog Patch Devils host an event named Fenders Day. They raise money to help out families who are going through a difficult time, and the May 2019 Fenders Day was for James. The Dog Patch Devils showed up in spades for James’ funeral, and in a fitting tribute that James would have loved, they left together in single file, all revving their engines as they passed the funeral home entrance. James endured far too much for what any child should have to go through, but he did it with courage, and a great attitude. We could all learn a lot from being more like James. Remember James’ life by visiting his Facebook page, https://www.facebook.com/littletrooperjames/ and sending some love to his mom, Lee-Ann, and his dad, Sam.
  


2020-09-25

153) Day 25 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about brain tumours: 
 
 
Today’s infographic from I Draw Childhood cancer is about osteoblastic osteosarcoma: 
 

 

152) Day 24 – childhood cancer awareness month

Well, I fell asleep putting J to sleep last night, so we'll just have to pretend that I posted this on the 24th. Today’s I Draw Childhood cancer infographic is acute lymphoblastic leukemia, or ALL, which is E’s type of childhood cancer:
 

Today’s not-so-fun facts from Childhood cancer Warriors are about brain & spine tumours:
 

 

2020-09-23

151) Day 23 – childhood cancer awareness month

 Today’s not-so-fun fact from Childhood cancer warriors is about soft tissue sarcomas:
 

Today’s I Draw Childood cancer infographic is Wilms’ tumour. One of my cousin’s sons was diagnosed with Wilms’ tumour in November 2018 at 21 months of age. He ended up having one of his kidneys completely removed, and he has been cancer-free since June 2019. Another little boy we met during treatment, also had Wilms’ tumour, and sadly he was one of the 20% of children who do not survive their cancer diagnosis. Little Sylas was one of the sweetest boys that you ever could meet, and he had a smile like a 100 watt lightbulb. Not a day goes by where I don’t think about him, or his family, and I'm happy to have known him, and to remember him. His mother has a Facebook group, Strength From Sylas, which aims to raise funds for childhood cancer research, and to help local families who have a child undergoing cancer treatment. Strength From Sylas: https://www.facebook.com/groups/1420362524759136/
 

 

2020-09-22

150) Day 22 – childhood cancer awareness month

Today’s I Draw Childhood cancer infographic is acute myeloid leukemia:
 

Today’s not-so-fun fact from Childhood cancer Warriors is about bone cancer:
 

 

2020-09-21

149) Day 21 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is a word that no parent of a child with cancer ever wants to hear – relapse.
 

Today's I Draw Childhood cancer infographic is about a soft tissue cancer, aveolar rhabdomyosarcoma: 
 

 

2020-09-20

148) Day 20 – childhood cancer awareness month

Today’s I Draw Childhood cancer infographic is about atypical teratoid rhabdoid tumour:
 

Today’s not-so-fun-fact from Childhood cancer Warriors is about platelets:
 

 

2020-09-19

147) Day 19 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about blood transfustions. Blood transfusions can be of the types red blood cell, white blood cell, platlet, plasma, or less commonly, cryoprecipitate.
 

Today’s I Draw Childhood cancer infographic shows us medulloblastoma, a brain cancer:
 
 

2020-09-18

146) Day 18 – childhood cancer awareness month

Today’s infographic from I Draw Childhood cancer is Ewing’s sarcoma:
 
 

Today’s not-so-fun fact from Childhood cancer Warriors is about the different groups of cancers that commonly affect children:

 

 

2020-09-17

145) Day 17 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors dives into what might cause cancer in children, and how we still don’t know that much about it:
 
 
Today’s I Draw Childhood cancer infographic is about malignant melanoma:
 

 
 
 

2020-09-16

144) Day 16 – childhood cancer awareness month

 

Today’s I Draw Childhood cancer infographic is about hepatoblastoma, a cancer of the liver:
 

Today’s not-so-fun fact from Childhood cancer Warriors is about cancer treatment protocols:  




2020-09-15

143) Day 15 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about remission. Please remember that remission does not equal cured. Don’t assume that everything is instantly better once someone has a child in remission. There’s still a long road ahead.
 

Today’s I Draw Childhood cancer infographic is about diffuse intrinsic pontine glioma, a brain cancer that’s also known as DIPG. Adults can develop DIPG, but it is mostly a pediatric cancer, with an average onset age of 6 – 7 years old. There is no cure for DIPG, and the median overall survival after a diagnosis is approximately 9 months. DIPG is a prime example of how the lack of research dollars is particularly failing the children affected by this particular cancer.
 

 

2020-09-14

142) Day 14 – childhood cancer awareness month

 Today’s I Draw Childhood cancer infographic is about pineal parenchymal tumours:
 

Today’s not-so-fun fact from Childhood cancer Warriors tells us about intravenous chemotherapy: 
 

 

2020-09-13

141) Day 13 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about stem cells:
 

Today’s I Draw Childhood cancer infographic is about malignant rhabdoid tumours:
 

 

2020-09-12

140) Day 12 – childhood cancer awareness month

 Today’s I Draw Childhood cancer infographic is about germ cell tumours:
 

Today's not-so-fun fact from Childhood cancer Warriors tells us about steroids. I was surprised at the start of E’s treatment to learn that steroids kill cancer cells. They have some not so great side effects though.
 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

2020-09-11

139) Day 11 – childhood cancer awareness month

Today’s not-so-fun facts from Childhood cancer Warriors tells about some of the side effects of treatment:
 

Today’s I Draw Childhood cancer infographic is about primitive neuroectodermal tumours, which is a cancer of the bones and cartilage:
 

 

2020-09-10

138) 27

27. Twenty seven. XXVII. That’s how many days E has left in his treatment. I’m excited, worried, happy, angry, and nervous all at the same time.


I’ll circle back around to that another time.

I haven’t posted an update in a while, and E seems to be doing well. He had bloodwork on July 8th, and it showed his counts were up, so there was a little adjustment in his medication. If I remember correctly, his methotrexate was bumped from 10mg per week to 12.5mg per week. Methotrexate comes in little pills. We dissolve them in water & squirt the methotrexate-yellow water into E’s mouth with a syringe.

On Wednesday July 29th, E had his last lumbar puncture. Thanks to COVID-19, it was also the first ever lumbar puncture he received when I was not there with him. Usually my wife and I go together, but due to COVID-19 restrictions, there is only one parent/guardian allowed with a child at SickKids. Of course, with the problems we’ve been having with his port, there was no blood return, and my wife & him had to wait for the TPA to dissolve some of the clot before they could take him. According to my wife, he put up a bit of a fight when they began to sedate him. He wasn’t happy, and was calling people “stupid” (unfortunately his new favourite word), and it took a bit longer for him to be out. Also according to my wife, he slept pretty much the full hour after, he woke up in a good mood, and just wanted to munch on some cookies. I had driven them down to SickKids to drop them off and returned home, so I again drove down to pick them up.
 
Last lumbar puncture attire

On Tuesday August 11th, I once again drove down to SickKids to take E for a COVID-19 test. Not because we suspected he had it, but because he was supposed to get his port out the next day, which is a minor surgery, which meant he needed a clear COVID-19 test before the anesthesiologists would sedate him. It was a pretty quick down-and-back trip.Later that day, the phone rang, and we were told that E’s surgery for the 12th would have to be bumped to the 13th, because another patient had a higher need. Completely understandable. E’s procedure is technically an elective one, so if someone else needs the spot more than he does, go ahead and bump us. Thankfully, they said they would honour the results from the COVID-19 test on the 13th, and we did not have to come back down for another swab.

On Thursday August 13th, I drove my wife & E downtown to SickKids. I had been debating about staying downtown and finding a park or a café to sit while I waited. We arrived at about 8:30am, and his surgery was scheduled for 12:00 noon. In the end, I decided against staying, not wanting to potentially expose myself to the virus. I drove home & decided to get some hours in on a big project I had been toiling on for work. Literally 10 minutes before E was supposed to go in, my wife was informed that he was again going to be bumped. Not a whole day – just until 4:00pm, because another patient had a higher need. My wife stayed, but if I had have been there, I would have left & asked to be rescheduled for another day. E needed to fast (obviously) before this, and a 4:00pm surgery time would put him at about 20 hours without food. You can’t explain that to a 4 year old, and expect them to understand why you’re not feeding them. My wife told me he just eventually stopped asking her for food. They hooked him up to an IV bag, and started a saline drip, which I believe had a bit of sugar in it to keep his energy levels up. The higher need surgery ended up running a bit long, and they didn’t end up taking E in until almost 5:00pm. His procedure lasted a bit longer than expected because the tube connected to his jugular had some tissue grow around it. I guess normally, they can just make an incision at the site of the port, and pull it out, but they had to make another incision on his neck to get the tube unstuck. That is probably why we’ve been having problems with blood return for the last 8 – 10 months. I had my wife ask, but they wouldn’t let us keep the port. They did however, give him a cool Hot Wheels racetrack for being a good boy about waiting so long. My wife finally got to see him again around 7:00pm. According to her, he had some problems waking up, and when he did wake up, he was C-R-A-N-K-Y. I drove down to pick them up, and made it there by about 9:00pm and we were home by about 9:45pm. All in all, it was an exhausting day all around.
 
E muncing cookies after his port removal

E's port and neck incisions, after about 2 weeks of healing

 

137) Day 10 – childhood cancer awareness month

 Today’s I Draw Childhood cancer infographic is about chondroblastic osteosarcoma:
 
 
Today’s not-so-fun fact from Childhood cancer Warriors is about radiotherapy:
 

 

2020-09-09

136) Day 9 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about chemotherapy, also known as chemo:
 

Today’s infographic from I Draw Childhood cancer is about pilocytic astrocytoma:
 

 

 

2020-09-08

135) Day 8 – childhood cancer awareness month

Today’s I Draw Childhood cancer infographic is langerhans cell histiocytosis:
 
 
Today’s not-so-fun fact from Childhood cancer Warriors is about surgeries childhood cancer patients might face:
 

 

2020-09-07

134) Day 7 – childhood cancer awareness month

Today’s not-so-fun fact from Childhood cancer Warriors is about treatment:
 
 
Today's I Draw Childhood cancer infographic is nasopharyngeal carcinoma: