Have you ever have a child of your own that struggled near Cancer or any other similar siituation?
I am writing a story for my up coming book in which one of the central characters is a thirteen year old girl near Cancer. My problem is that I can personally relate to my own health problems and disability, but I know very precious little around how a child with Cancer might feel.
is the perspective of the parents when they are dealing with that problem? What are the situations that both the parents and the child own to deal with?
What is the general message that could be conveyed by such a story as that?
The vigour problem does not necessarily have to be Cancer, but can be any issue that is considered terminal.
Ty!
Answers: I DO NOT KNOW SOMEONE THANK GOD BUT I DO HAVE CHILDREN I AM WORRIED NOW I MAY HAVE OVARIAN CANCER AT 26 I THINK THAT WE ALL FIND HOPE ESPECIALLY PARENTS GETTING SUPPORT FROM OTHER PARENTS AND CHILDREN BEING AROUND OTHER CHILDREN IN THERE SITUATION I THINK THAT MAKES IT ALOT BETTER AND KNOWING THAT THERE ARE OTHER PEOPLE OUT THERE IN THE SAME SITUATIONS. ALSO HAVING A GREAT CARING DOCTOR THAT GOES OUT OF THE WAY TO INFORM THE CHILDREN AND PARENTS TO GET THEM THE BEST CARE THAT THEY CAN HAVE. ALSO PROVIDING COUNCELING FOR THESE PARENTS GOING THROUGH THESE HARD TIMES. I KNOW THAT WE AS HUMANS ARE GOING TO LOSE OUR MOTHERS AND FATHERS ONE DAY BUT THE LOSS OF A CHILD IS THE WORSE. I WATCH ALOT OF DISCOVERY HEALTH AND SEE MANY FAMILIES GOING THREW THESE PROBLEMS. BUT THEY HAVE STRENGTH FROM THE HOME THAT LIVES WITHIN THEM AND LOVE.
Most people in this situation aren't anxious to talk to relatives with a casual interest.
My son E was diagnosed near a Wilms' Tumour as a newborn, won his battle, and was recently diagnosed near Secondary Acute Myelogenous Leukemia (AML). The best thing we can do is educate ourselves and talk next to other parents of little warriors. Just talking with other parents something like similar experiences and what to look for, what to avoid, and what to do that helps comfort kids is more helpful than you could imagine. One great website is call People Against Childhood Cancer (PAC2). There are tons of wonderful people here who have children that survived, have earn their wings, and who are currently fighting their battles. They adjectives have great advise and are all melt and welcoming.
first person I met after my son was diagnosed the first time told me to cause a caringbridge site for him. This was the most wonderful thing I could have be told. We gave the website to family and friends so they could keep up next to E's progress without having to constantly ask us. This gave us more time to spend devoted to war for E and being with our other 7 children. The other thing is that we looked-for to get other children involved in his treatment. Since all of our children are too little to fully read what cancer is, we told them that E isn't home because he's being very brave and fighting a monster right presently. It has helped us both in giving Eli the attention that he wants as well as giving each of our other children the attention they need too. They love to call round him (when he's feeling ok enough) during the time he is in the hospital and we usually take one or two beside us when he has clinic visits. It really gives the other children a sense of pride surrounded by that they're helping E fight his monster and get better.
There are times that he gets anxious, whether it's needles or someone new he just isn't sure about. We freshly have to stay strong for him and make sure he knows it's ok. And yes, my wife and I sure hold had our moments of worrying about the future sobbing but we try our hardest to stay as strong as we possibly can within front of E and our other children. There's no need in worrying them any more than they already are.
This have all has not only have effects on my son but it's had effects on my wife and I as well as our other kids. We have have to take days off work to spend with E and we've spent various nights apart, one with E and one home with our other kids. The verbs and the waiting has been the worst part for us, we hold both definitely lost a lot of sleep over it. Our kids are all pretty youthful (ages 8 years to 16 months) still but my oldest two, to some degree, understand that E is pretty sick. I know they constantly worry almost him, especially when he isn't home.
It's just one of those things, it happens, as unfair as it is, but it happen. We just have to do everything we can for our warrior and hope he can have a long, robust life. If you have any other questions perceive free to IM me (crazycanuckj) or send me an email (crazycanuckj(a)yahoo.ca) Source(s): My 2 year old son is a warrior who beat a Wilms' Tumour and is currently battle Secondary Acute Myelogenous Leukemia.
http://www.caringbridge.com/visit/warrio…
Related Questions:
is the perspective of the parents when they are dealing with that problem? What are the situations that both the parents and the child own to deal with?
What is the general message that could be conveyed by such a story as that?
The vigour problem does not necessarily have to be Cancer, but can be any issue that is considered terminal.
Ty!
Answers: I DO NOT KNOW SOMEONE THANK GOD BUT I DO HAVE CHILDREN I AM WORRIED NOW I MAY HAVE OVARIAN CANCER AT 26 I THINK THAT WE ALL FIND HOPE ESPECIALLY PARENTS GETTING SUPPORT FROM OTHER PARENTS AND CHILDREN BEING AROUND OTHER CHILDREN IN THERE SITUATION I THINK THAT MAKES IT ALOT BETTER AND KNOWING THAT THERE ARE OTHER PEOPLE OUT THERE IN THE SAME SITUATIONS. ALSO HAVING A GREAT CARING DOCTOR THAT GOES OUT OF THE WAY TO INFORM THE CHILDREN AND PARENTS TO GET THEM THE BEST CARE THAT THEY CAN HAVE. ALSO PROVIDING COUNCELING FOR THESE PARENTS GOING THROUGH THESE HARD TIMES. I KNOW THAT WE AS HUMANS ARE GOING TO LOSE OUR MOTHERS AND FATHERS ONE DAY BUT THE LOSS OF A CHILD IS THE WORSE. I WATCH ALOT OF DISCOVERY HEALTH AND SEE MANY FAMILIES GOING THREW THESE PROBLEMS. BUT THEY HAVE STRENGTH FROM THE HOME THAT LIVES WITHIN THEM AND LOVE.
Most people in this situation aren't anxious to talk to relatives with a casual interest.
My son E was diagnosed near a Wilms' Tumour as a newborn, won his battle, and was recently diagnosed near Secondary Acute Myelogenous Leukemia (AML). The best thing we can do is educate ourselves and talk next to other parents of little warriors. Just talking with other parents something like similar experiences and what to look for, what to avoid, and what to do that helps comfort kids is more helpful than you could imagine. One great website is call People Against Childhood Cancer (PAC2). There are tons of wonderful people here who have children that survived, have earn their wings, and who are currently fighting their battles. They adjectives have great advise and are all melt and welcoming.
first person I met after my son was diagnosed the first time told me to cause a caringbridge site for him. This was the most wonderful thing I could have be told. We gave the website to family and friends so they could keep up next to E's progress without having to constantly ask us. This gave us more time to spend devoted to war for E and being with our other 7 children. The other thing is that we looked-for to get other children involved in his treatment. Since all of our children are too little to fully read what cancer is, we told them that E isn't home because he's being very brave and fighting a monster right presently. It has helped us both in giving Eli the attention that he wants as well as giving each of our other children the attention they need too. They love to call round him (when he's feeling ok enough) during the time he is in the hospital and we usually take one or two beside us when he has clinic visits. It really gives the other children a sense of pride surrounded by that they're helping E fight his monster and get better.
There are times that he gets anxious, whether it's needles or someone new he just isn't sure about. We freshly have to stay strong for him and make sure he knows it's ok. And yes, my wife and I sure hold had our moments of worrying about the future sobbing but we try our hardest to stay as strong as we possibly can within front of E and our other children. There's no need in worrying them any more than they already are.
This have all has not only have effects on my son but it's had effects on my wife and I as well as our other kids. We have have to take days off work to spend with E and we've spent various nights apart, one with E and one home with our other kids. The verbs and the waiting has been the worst part for us, we hold both definitely lost a lot of sleep over it. Our kids are all pretty youthful (ages 8 years to 16 months) still but my oldest two, to some degree, understand that E is pretty sick. I know they constantly worry almost him, especially when he isn't home.
It's just one of those things, it happens, as unfair as it is, but it happen. We just have to do everything we can for our warrior and hope he can have a long, robust life. If you have any other questions perceive free to IM me (crazycanuckj) or send me an email (crazycanuckj(a)yahoo.ca) Source(s): My 2 year old son is a warrior who beat a Wilms' Tumour and is currently battle Secondary Acute Myelogenous Leukemia.
http://www.caringbridge.com/visit/warrio…
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