I want to thank you first of all for all you have done for me and continue to do even though you seem to be tirelessly searching for answers and nothing seems clear.
I know what I have is different and has my family at a loss, I see the way you look at me and my skin lesions and I know it’s got you stumped, I know my parents worry and my brother sometimes finds it tough too. I just want you to know that I also know it’s hard for you.
I am sorry for the times I have been difficult to examine and hitting Dr. Wendy in the face was not my finest hour, not the thanks one would expect for curing my eye from a nasty tumour. Nevertheless this is my experience that I wish to share.
It’s not fair when you don’t let me eat my breakfast to fast me and put me on another machine, and that mum and dad don’t let me eat as much as I would like – the no more sweets rule has offended me deeply. They make me take medicine, and even wake me up when I am sleeping to take it.
I don’t like sleeping without my mum, she sneaks off when I am asleep, I usually wake up a few hours later and call out to her, and dad has to come and get me to take me to mum, every night.
I like to be carried!! My mum won’t carry me very often, because she has hurt her back, this devastates me at times. Even dad has trouble carrying me at times, I like to be carried because I am often tired and need to rest and I love to cuddle.
I am very heavy, when I fall it really hurts and it makes it hard for me to get around. I used to run up the stairs but now I sometimes lose my balance and need to crawl up or hold someone hand to get up and down stairs. I have a new wheelchair pram that helps holds my back up, I like it because I can sit up straight, without it I flop to the side. I remember not long ago I was able to run and jump onto the couch with ease, so it frustrates me now when I get stuck on my back and struggle to get up off the floor.
Why do we keep having to go to the hospital?! Yes, mum I like the meerkats but we just saw them last week. I also find it really tiring sometimes to have to change my nappy which is too small for me and getting dressed can be very exhausting, that’s why I wont lift my legs or arms to help you at those times. And why is it that nothing ever fits me? But most frustrating of all is that being only 2 years old, I cannot tell you how I am feeling.
I love to go swimming lessons with dad, in the water I am always smiling because I am free to move and my weight doesn’t hold me back in the water, I can be like all the other kids, in fact dad told mum I am the best in my class.
I love my childcare sessions and have enjoyed interacting and socializing with other children my age. Mum only lets me stay for a couple of hours because I get very tired.
My favourite things are my friends and family, Leggo, Buzz Lightyear and playing with my brother Jacob.
Seeing mum at my appointments fumbling through her long list of questions, you probably find her a bit over the top, but you can see she is just another mum that cares for her boy and am grateful that you give her your best attention and obviously care for us.
With my loving family I am well armed to battle this mystery illness and I salute you, the generals of my army. To Infinity and beyond! Buzz Lightyear to the rescue.
Where is my dummy?
Thanks from Maxi
6 thoughts on “Letter from Maxi to his doctors”
Dear Maxi everyone that knows you is trying to find the answers for your Mummy and Daddy and especially for you it must be very hard for you to understand people are doing these things to try and find an answer and the right treatment to make you better and it must be frustrating that you cannot run and play like other little boys your age you are allowed to be tired angry and sad at times no one is perfect as Woody and Buzz would certainly tell you so Maxi we all send you and your family love hugs and support and hope and pray for a diagnosis and a cure and really Meerkats are cool love Ax
Just a beautiful letter little Maxi. You have such a Special Mummy and Daddy and a very special big brother too, and I am sure there are also some Very Special Doctors and Researchers out there trying to help find a cure for you sweetheart. Love you all heaps and heaps and more. XOXOXOXO
Beautiful. Must be so difficult for everyone, especially young Maxi. See you July/ Aug in Melbourne Yael x
Maxi, you are a beautiful , unique, strong boy who has a beautiful Mummy and Daddy who love to to infinity and beyond. I wish I could make things better for you all , but I know there are angels who are looking out for you and taking care of Mum and Dad too.
All my love, healing energy and light. Kisses. J.B.
Soldier on little man, soldier on.
Maxi, you are the best, you are the best ranger Like buzz. You Have the best mum, dad and brother. Be happy and strong .