Every child is different, every situation, and nothing is universal. That being said, what were some things that helped your child get through? What are/were your strategies for pills, needles, nausea etc?

Goal is to help new/current families have a small bank of ideas to try when nothing seems to help.

Medulloblastoma, started chemo at 2.5, and still recieving chemo from home at 4y.o

Needles

1. Not a choice - we used this phrase back when fighting medical procedures (mostly bloodwork) and gave her lots of choices whenever possible

2. Buzzy bee- can be purchased on Amazon (or tiny massages for significantly cheeper) helps trick the brain

3. "Little pokes" - aka finger pokes. we started requesting finger pokes for when all she needs is a CBC

Nausea

1. Find safe foods - no matter how bad the nausea got (the constant throwing up), vanilla yogurt, apple sauce, milk and chocolate milk were never refused. Creamy pasta and hot dogs were rarely refused. Cheese usually went over good.

2. Normalize, and try not to show disgusted (especially when you get coated in it)

3. Have emisist bags stashed everywhere

Pills

1. Septra, disguise in yogurt, not applesauce

2. Raspberries have a natural pill pocket

3. Spoon with yogurt/apple sauce and pill together

4. Normalize taking meds, talk about you taking meds too (say" time for mommy to take her meds" then take them in front of them)

5. DO NOT LIE. If it tastes bad, have "chase" ready for them. If you do not know, say that and have chase ready.

Other

1. DO NOT LIE,-do not get caught in a lie is more accurate, say idk if you have to, just do not break their trust

2. Comfort items - blankets and photo albums were ours

3.Dr talks outside of room, nurse talks inside the room (drs usually used proper language and was well above her comprehension, nurses were fantastic at simplifying with us for kid language)

1. Universal words, kid language, but not "baby talk"

My youngest has Pleuropulminary Blastoma and is currently going theough treatment. She obviously feels horrible does not want to be put down, is vomiting all of time, won't eat the normal chemo things.

My oldest is 3 and is incredibly jealous of any attention his sister is getting. He is acting out, throwing things, hitting me, hitting her, tantrums etc. I get him a babysitter while we are at chemo he cries and begs to go. I take him he runs around and touches everything so I cant watch her. I pack toys, tablets, and coloring books.

She needs me, and I cant help him transition to sharing when she is actively getting sick. Today she woke up from her nap crying and in the minute it took me tobget to her he dumped a while box of animal crackers just because it would pull my attention back to him.

It's his childhood too, and I am doing my best but Im stressed to the max and I dont know how to do this. How are we dealing with siblings? My kid isnt really old enough to understand cancer.

Hi everyone! I would really appreciate hearing about your experiences.

My nephew was supposed to start the stem cell transplant next week with a Curie score of 1 and bone marrow involvement of <1%.

Today, we had a brain MRI, and this was the result. The MRI was done mostly because I insisted on it, since my child had occasionally complained of headaches. Our doctor initially felt that an MRI wasn’t necessary at this stage because, with such good results after frontline chemotherapy, she didn’t think we would find anything concerning.

After today’s MRI results, however, she recommended extending treatment with 3 rounds of bridge chemotherapy before proceeding with the transplant.

When I asked whether this should be considered a relapse, she said she cannot call it a relapse at this point. She wants to see how it responds to the upcoming treatment first.

Unfortunately, we don’t have a previous brain MRI for comparison, so we don’t know whether these lesions were already present before treatment or if they developed during frontline therapy.

Has anyone been in a similar situation? I would be very grateful if you could share your experience. Thank you.

Good Afternoon, as the title says my son was recently diagnosed with Medulloblastoma and has already undergone surgical removal and biopsy of the tumor. We are now home after spending 3 weeks in the hospital which just started out as an ER visit due to lethargy. We are thankful the doctors discovered the tumor and swiftly removed it and biopsied it to receive the pathology back. We are now scheduled for Chemo starting on the 20th and was hoping for some positivity from other families who have been through similar treatments and diagnosis. I know every kid is different and the last 3 weeks feel like a whirlwind as our world has been flipped upside down. Thank you in advance for any and all support.

Hi everyone,
I’m looking to connect with families whose child has been treated for relapsed neuroblastoma at UCSF Benioff Children’s Hospital, especially with I-131 MIBG therapy.
A family member was treated in Taiwan but recently relapsed. Our doctors have discussed the case with the UCSF team and recommended treatment in the U.S.
If you’ve been through this journey, I’d really appreciate hearing about the treatment timeline, radiation isolation, hospitalization, stem cell rescue, costs, and any advice for international families.
Thank you so much.

Our closest friends have a 19 month old starting chemo/carboplatin next week. They have a good network of friends, but I would like to harness that, possibly even crowdsourcing the purchase of some things that would help them get through chemo.

I thought about getting a tonies box (the newer edition is rated 1y+), but saw there was a disclaimer that the tonies have magnets, which can interfere with programmable shunts (which this little guy now has).

I learned about Port Protect, for applying numbing cream without the use of plastic wrap. These seem pricy--are they worth it?

Mainly:

1. What are comfort items your kid benefited from during and after chemo sessions?

2. If you had a toddler go through chemo--any recommendations on what worked best to keep them as relaxed/entertained/happy as possible?

My son might have neuroblastoma. My husband and I are beyond shocked. He's completely asymptomatic, and his blood work looks completely normal. During a regular doctor's check up, there's nothing indicating it either. It was discovered randomly during an x-ray he had for bacterial bronchitis (which he also had completely unrelated).

​

Everything up until now has given us indicators that the tumor is benign, but today we received his urine tests, which showed moderately heightened levels of catecholamines. We won't know the results of his biopsy or bone marrow test until next week.

​

Have anyone else been in the same situation? Where do we even go from here. How will possible chemo affect him? I've only seen it the affects of it in movies

Just wanted to share briefly our story. Our son in February was diagnosed with High Risk Neuroblastoma at 15 months. We just completed the first phase where we removed the main adrenal gland tumor and completed 5 rounds of chemo. About a month ago they were pleased with how much the soft tissue in the main tumor shrunk - almost 50%. The care team was very encouraged.

unfortunately the MIGB scan showed extensive metastatic bone disease and they are considering this a refractory case. The next phase of Stem cell transplant is now on hold because there is just too much disease left. Skull hip femur all over…Now we will switch to chemo immunotherapy and set of new drugs to try to clear that up. we are beyond devastated because things appeared to be working. now his eyes are black and bruised and protruding , and he is in a lot of pain and discomfort. it is so hard to see this personally. I’ve become a wreck since hearing the news - yesterday. Can’t eat or sleep and am literally just numb from the whole thing. How does everyone keep marching on? just wanted to talk and share our story. it’s not over yet but wow is cancer cruel.

My little girl got rsv at 16 months and we found a cyst the size of an orange on her lung.

They told us they got it all. No chemo.

I just keep getting these phone calls from Dr's actually it is cancer but she won't need chemo, but she needs to be checked for DICER 1.

She has dicer 1 this could happen again.

Actually the pathology results are back we think its type 2 very agressice could spread to her brain. She needs chemo. 6 rounds of chemo.

I can't get my feet under me. The diagnosis keeps changing. It keeps getting worse.

Everyone wants to know how my sweet girl is and the dumb thing is right now. She looks perfectly healthy. You would never know she has cancer.

How is anyone coping?

Is there anything that actually helped you keep track of everything during treatment? Appointments, medications, results, what each doctor said? Or did most of us just figure it out with a notes app and hope for the best?

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NATIONWIDE with fundraiser code 9014094 for 28% of your meal to benefit the kids!

Hi all - very new to this page and space. Unfortunately our 5 month old daughter has just received a diagnosis of MRT in her liver. Unsure yet as to stage, but hoping for any positive stories from those who may have personal familiarity with this condition, particularly with presentation in the liver.

We know prognosis is poor and treatment is brutal - just hoping for any hope.

We have a family friend who's 1 year old has just received the diagnosis of having a wilms tumour,she starts chemo this week and is getting the tumour removed next month, the prognosis seems good and they've caught it early. We live on the other side of the country and although this seems like it's all going well is there anything that I could send up to them to make the next few weeks or months abit more tolerable for them?

My loved one just received a terminal diagnosis. He is only 12 years old, and someone had the audacity to tell me, “Isn’t a short life filled with love better than a long one that isn’t?”
I wanted to scream.

I told them what I actually want: both. A long life and a love-filled one. The two are not mutually exclusive, and the fact that I cannot have both does not make me grateful for only one.

How do you all cope with the platitudes? Every time someone reaches for a tidy phrase instead of sitting with the discomfort— instead of just saying “that sucks, I’m so sorry” — I feel the anger rise a little more. There is something deeply isolating about watching people protect themselves from your pain by repackaging it as a lesson.​​​​​​​​​​​​​​​​

Last week, my 9-month old was diagnosed with an aggressive form of brain cancer (ATRT). This was a very unexpected diagnosis, as he had no symptoms other than a sudden onset of vomiting a week before diagnosis. We've been given a bleak prognosis, and treatment starts in less than two weeks (the majority of which will take place inpatient over the next several months). Has anyone here experienced a similar diagnosis? Or does anyone have tips for things that would be handy to have when staying inpatient for so long with my son?

Hi everyone. I’m an incoming MD student in the US and recently got devastating news about my family, my 3-year-old cousin was diagnosed with B-cell ALL (acute lymphoblastic leukemia). She also currently has malaria, which has complicated things further.

She’s Sudanese, but the family rushed her to Egypt to try to get better care as quickly as possible. From my research, Hospital 57357 in Cairo seems like one of the best options for pediatric oncology in the region, especially since they provide treatment free of charge. However, I’m worried about capacity and wait times because she likely cannot afford major delays in treatment.

Has anyone here navigated pediatric cancer care in Egypt, gotten a child into 57357, or know reputable pediatric oncologists/hematology-oncology centers in Egypt or the surrounding region? Any guidance, contacts, or advice would truly mean a lot. Thank you!

my 6 year old daughter was diagnosed with a pineoblastoma that went to spinal fluid 2 weeks ago and underwent surgery to remove the tumor but unfortunately they couldn’t remove much of it due to it being very vascular. they removed enough for biopsy and installed a temporary shunt because she had a lot of fluid built up. Once biopsy was confirmed they installed a permanent shunt but unfortunately she experienced vision loss which was declining before the surgeries but now the vision is gone. I appreciate any information you can share about it this tumor and would love to hear from others about their experience with the tumor and the vision loss. thank you!

My 10yo starts chemo next week and I'm just looking for some experiences so I can kind of know what to expect. She'll still be in school. Should I be prepared to keep her home on off weeks as well? When do side effects usually start? How quickly did your child lose their hair (if they did)? I'm so sad for my girl and I just want to be best prepared to support her with whatever she needs.

hey

i’m a pediatric cancer survivor, diagnosed at 7 now I’m 17, so it’s kind of always just been part of my life

and i don’t know if this is just me, but as i’ve gotten older i feel like it’s actually gotten harder to relate to people outside of the cancer community. like you can explain things, but it doesn’t really land the same as talking to someone who just gets it

do you guys feel like that too?

what’s helped you with that, if anything?

and what do you wish existed for people our age going through this that you haven’t really found yet

My 2.5 year old just finished her first 3-day hospital stay for chemo (1 day carboplatin, 3 days etoposide), and we’ll check labs Thursday morning to see where her counts are. Her team said there may be a small window where daycare is okay before counts drop, but I’m feeling really torn.

Did you send your child to daycare during treatment?

Would love to hear what others did and what precautions you took. Thank you! 💛