This post send by Kendra
Hey my name is kendra and I\\\’m 15 years old I was diagnosed 2 years ago with ALL. When I got diagnosed I was at the end of 7th grade and at a small school with only 10 kids in my class. But not I am a freshman almost sophomore in high schools s I moved to a pubic school where there is more people. Only a few people know what is going on in my life. Lately I\\\’ve been missing a lot of school and when I come back to school after be gone for a while I get all kinds of question like where have you been? Skipping school? Or why do you miss so much school? I also get the question dont you get in trouble for missing school and all I answer is I have a doctor excuse. I am ready to be done with treatment and get back to life like a normal kid. I know I will get through this and one day my story will help someone else. If that person is you and you have question email me I would love to make new friends. Kberschet@yahoo.com ☺ stay strong everyone!
This post send by Savannah
Hey guys it\\\’s Savannah again, just thought I would give all of you the new news. I had scans done last week to check to the chemo and what not. My small tumors that are all over my liver are smaller and the large tumor is showing signs of dying off, also I had a lymph node that was full of cancer and it is now clear. I am at the stage now where I can have a transpant if needed, but my doctor would like to try to salvage my own liver so they are going to do a couple more blocks of chemo and try to get rid of the small tumors. I am super happy about the scan results and hoping for more good news after the next couple of blocks.
Thanks for listening and God Bless ☺
I had the choice to choose treatment or to let the cancer run it’s course, I chose life. Now I feel like I am wasting my life in a hospital because I chose treatment. I have missed so many things because of the cancer and I feel like I am going to miss a lot more. Has anyone else ever felt this way? What am I suppose to do?
I was diagnosed with ALL, a type of Leukemia, nearly 2.5 years ago on June 22, 2010 when I was 18 and a new High School Graduate. I was told it was going to be a three year treatment and I thought I could handle it. I’m 21 now and at college and I’ll be finished when I’m 22. I’m at my 8 month count down (end date is in Oct. 27, 2013) but now I’m getting more and more scared and I don’t know why. I was ok at first, even though the first few months were hell. When I got my first bone marrow biopsy, my parents were much more scared for me than I was. But now that I take daily pills and once a month treatments, it seems like this will never end. I think my support system is going downhill. My parents got divorced last year; it was coming for a while but I think the stress of my treatments helped pushed it over the edge. They both love me and support me, but it seems like the whole structure of my family is gone and that was something I was afraid of ever since I was a kid. I don’t know, I think I just have to man up and take it, but sometimes it’s hard. I know that there are people that have it much, much, worse than me; and seeing others struggles make me grateful for what I have. I think as a survivor I owe it to them to live my life to the fullest and do Gods work. But every time I see those pills in my hand before I go to sleep, it all just seems… wasted. Like I struggled all that time and I’m still not allowed to stop. I shouldn’t feel this way and it’s very frustrating. Does anyone know what to do? Or felt this way as well?
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Hi, my name is Dominique and I am 17, almost 18. I was diagnosed with synovial sarcoma when I was 13. I have only met one other person with synovial sarcoma and he’s a 10 year old boy. Is there anyone else out there?
This past month, I have been dealing with servere issues. I have been dizzy with headaches and passing out, nausea, vomiting, blurred vision, confusion, losing feelings in my legs, just feeling like I am constantly car sick. I was sent for a CT scan and was told I have masses in my brain, and I am going for an MRI this upcoming week, and I can honestly say I’m petrified. Having a brain tumor is scary within itself, having a cancerous brain tumor is a totally different ball game. I am a high school senior with a bright future ahead of me, I can just see it. What will I do if it is cancerous? How will I be able to finish school with my graduating class? How will I get to college on time?
How will I? How will I? How will I?
I just don’t know what to think. I don’t know what to do. And I definitely don’t know where to go for support.
I was also a councellor at a camp for children with Leukemia in Northern Ontario and I know from my own experience that it is sometimes easieer to speak to someone who has been through what your about to go through and knows ways to help other understand and I can also help parents as this can all be a whole new turn in your life…Hope to talk to you soon…
Derek Millington, 3000 Stautw RD. #104 Saanichton BC
V8M 2K5 or Dmillington121@hotmail.ca
Hope to chat with you soon! Derek
I was only 13 when I was told that I have Leukemia and in 1980 the odds were very low on survival and the whole world scared the ___ out of me but I managed to not give in and fought back, taking advantage of the Chemotherapy and radiation and just pushing myself to take the abuse i was recieving and over come it….Well thanks to some great Doc’s at Toronto’s Sick Childrens Hospital, My parents, Ronald Mc Donald House and some great friends I met along the journey, I had three children totally healthy and a great life.
After 32 years Im 100% healthy and you will be too….
if anyone has questons or would like to talk about life with Leukemia feel free to contact me at 250-883-7633 anytime night or day…I hope I can help…Derek