Hi, my name is Taylor, and three days ago, I received one of the worst texts in my entire life. It was from my best friend, who I’ll refer to as lil ducky (Our nicknames for each other are lil ducky and ducky). It read; “I have some bad news, I have leukemia.” She is fifteen. My heart dropped and I went completely numb. I had no idea it was possible to be shaking so hard yet feel nothing. She had been sick for a few weeks, and I had even skipped out on Halloween so we could hangout at her house together.
At this time, I do not know many details, but am terrified. And then I think; :”If I feel like this, how must she feel?” Her family has been through so much already with her brother, who also has countless health issues as well. She is one of the most supportive, possitive and resilient people I have ever met.
All I want to do is see her, but I cannot until her first round of chemo is over.
Anyone have any advice or info? I’m so lost. It would be dearly appreciated.
I’m 16 years old i was diagnosed august 20th with Hodgkin s lymphoma I’m looking for teens my age who know what im going through and can relate to me.
comment if you would like to talk.
It is submitted that my nephew Faisal Ali age 5 years, resident of Wapda Colony G-7/4 Islamabad is patient of “Acute Lymphoblastic Leukemia”. Faisal Ali has been treated in “Al Shifa Internation Hospital Islamabad G-1 Block Isolation Room”. Doctors said that the treatment of this disease is not possible in Pakistan. Parents of the patient are very poor and can’t afford the expenses for proper treatment of this disease. I need help from media to raise an appeal for treatment of this serious disease. You are requested to please make a donation to the patient for his treatment.
I shall be thankful to you for this kind act and will remember you in my prayers for this noble deed.
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My husband is 32 years and was diagnosed with ALL January 9th 2012. It has definitely been a long journey so far for us on chemotherapy but are blessed to say he is in remission. We continue to fight daily! I am proud of my husband, and I admire him even more now. He is putting up a big fight for me & our children. I just want to know what really happens after chemo & maintenance?? Do people with Leukemia really go back to living a normal life?
My name is Samantha and on August 12th, 2012 my life changed forever. I was diagnosed with Acute Myeloid Leukemia. When my family heard the news they broke down and cried. I cried for a minute then realized tears are not going to help me kick this cancer in the bum! My doctors were surprised that I was even there because I looked so healthy and the fact that I had AML since I’m 20 years old. I did one round of chemo (7+3 kind) and a round of consolidation chemo also. I have another 2 days of chemo and 4 days of radiation as part of my Bone Marrow Transplant work up. I’m nervous and excited for my BMT. It will mean that this nightmare will be over, but I’m nervous about the process of healing from the BMT. I would love to hear anyone’s experience with a BMT and radiation.
Also, if anyone would like someone to talk to please email at email@example.com
my name is kate nick my boyfriend that i was with for 3 years since i was 16 he died in june it been like 5m sicne he died he had leukim
i miss him so bad i want to be with him but i cant i just found out i am haveing his baby i know i am 18 but i did love him and i wanted to spend my life with nick but i cant it hurts that i cant see him but i am haveing his baby that makes me to be happy
Hey there! For a project in school, I’m going to write a book for preteens/teens who have friends with cancer, as my best friend has had a brain tumour since she was an infant. I am looking for ANY input anyone has to help me. Do you have cancer? What have your friends done during and after your treatment that has helped you the most? Or, what didn’t they do that you wish they had? And if you are the friend of someone with cancer, how has cancer affected your relationship? How do you deal with your own emotions, and what have you done to try and make your friend feel better? Please share anything you can…the more information the better! Thanks
Hi my name is Aria. For a fundraiser, me and my team are going to make a movie about a teen dealing with his cancer. We still haven’t decided for the kind of cancer. Can an expert give us some choices?
September 26th, 2012, was the day my life changed forever. I was diagnosed with Clear-cell Endocervical Adenocarcinoma. Cervical cancer is literally unheard of in my case: a 17 year old virgin, HPV negative.
It was homecoming week. My LAST homecoming week. I’m a senior in highschool; I was high on life. I was so insanely happy at this point in my life. I really didn’t think anything could knock me down. This story is extremely personal and graphic to say the least, but I want to tell everyone. I want everyone to know that I am strong enough to deal with this. This is my new reality. If I am strong enough to deal with it, then so are all the other teens in the world who have to deal with cancer. It sucks, and it’s scary, and it’s NOT fun. But, even though my journey has just begun, I’ve already had some great experiences and met some amazing people that I wouldn’t have if I hadn’t have been diagnosed.
It all started in summer. I had noticed in the past year that strange things were going on in my feminine area. I had been having excessive discharge for a long time. But, in summer, I was starting to bleed when it wasn’t time for my period. It was happening more and more until it became an everyday thing. I didn’t really think it was a big deal at the time. I am a virgin. So, I mean what could possibly be wrong with me? I was thinking probably just a little infection that would go away. I was wrong.
I figured it was time that I tell my mom what was going on and go to the doctor, but I was so terrified of going to the “girl” doctor. I kept putting it off. I really wish I hadn’t of put it off. When I finally decided to tell my mom, she was concerned and immediately called the doctor and scheduled me an appointment for September 18th. It was two weeks off, so I wasn’t really concerned about it yet.
The day finally came for me to go to the doctor. It was a traumatic experience for me because it was painful. I had to go into the examination room, strip down, and open my legs to someone I had just met, and let them look at my personal area. EW, RIGHT? I was absolutely terrified. The fact that I am virgin made it painful enough, but to add to it, the doctor told me I was abnormally tiny down there. Great. As he was examining me, he spotted an area on my cervix that looked rather questionable. He said that it looked like a cyst. He took a few swabs and was done. He perscribed some antibiotics for me to take and scheduled a follow up a week later. He was assuming it was just infection, but he wanted to do a pelvic ultrasound at the follow up just to make sure. I was relieved that he thought it was just infection.
As we were pulling out of the parking lot, we passed a building with sign on it that said “Cancer Rehabilitation Center.” I stared at the word “cancer.” I had a feeling in the pit of my stomach. Somehow, I knew that this wasn’t just an infection. It was much worse.
I went back to the doctor the next week. It was Tuesday. Homecoming week. The last thing I wanted to be doing was going to the girl doc. My mom drove us back to the doctor, and we passed that cancer rehab center again. I stared at the word again.
I went back to the ultrasound room and the tech squirted the sticky gel you always see on tv on my stomach. I felt like I was pregnant or something. She moved a little wand thing around my abdomen. She asked me what exactly the doctor was looking for. I told her a cyst on my cervix. She replied with, “Oh…I don’t see that.” I felt relieved, but then she called another lady in to have a look. The whispered with each other for a few minutes. I was scared.
Once again, I went into the same examination room to do the dreaded thing all over again. This time the doctor told me he was going to do a pap smear. I bled a lot. This wasn’t normal. They made me and my mom wait for a long time before the doctor came back in and explained what the ultrasound revealed. He said there was a 4cm x 2cm mass on my cervix. My stomach dropped. He said he was going to get the pap smear results rushed so that we would know as soon as possible what kind of cells that it revealed.
It was hard to sleep that night. I knew what was coming. The next day. I was in speech class when my iPad lit up with a text from my mom. It said that the doctor called and wanted us to come in as soon as possible. This was it. The truth would finally be revealed.
When we got to the doctor, the nurse led us back into a big conference type room. We sat down and waited for awhile. I was sitting a coffee table staring at a bookshelf in front of me. My eyes went straight to a book the said in gold letters “CANCER.” The doctor finally came in and sat down and just kind of looked at us very seriously. He said, “I don’t know what this is, but it’s not good.” I looked at him and waited for something else. He said that my pap smear revealed malignant cells. My mom began crying. My throat stung and tears were welling up in my eyes. I cried for a minute, and then dried it up. I was going to fight this. Whatever it was. I was going to kick it in the BUTT. He told us two kinds of cancers that it most likely would be. He said I most likely had Rhabdomyosarcoma. It was more of a childhood cancer. He then said that there was a chance, but it was extremely rare, that I would have Adenocarcinoma.
I went home and began preparing myself for the next day where I would be at St. Jude Research Hospital all day. I was excited to see what the hospital was like since it is considered one of the best children’s cancer research hospital in the world.
Everyone I met there was amazing. Everyone was so nice. I had a MRI while I was there to see if anything looked suspicious in my abdominal area. The results looked pretty good. One of my lymphnodes was a little bit suspicious.
The next Monday I had a PET and a CT scan done. Everything was looking good besides the huge tumor on my cervix. The next step was to get a biopsy of the tumor. It was going to have to be done surgically since I was so tiny down there.
I went in Wednesday and had the surgery done. It went well. I went to another doctor that was specializing in gyno. oncology Friday. The results were back. Clear-cell Endocervical Adenocarcinoma. I was the exception. I was the rare one. I was the one who blew doctors minds. The thing about all types of cervical cancers is that virgins just don’t get it. It evolves from HPV which is a sexually transmitted disease. Once again, I am a virgin. Another thing is that this certain type of cervical cancer is only seen in older women, like 50 years old and up. This was crazy for me to have this, but I do. My doctor told me that they were gonna write books and articles about me. This was a huge deal.
At this point, I didn’t care how rare I was, I just wanted it out of me. I was scheduled for surgery the next week, October 10th. It was a huge surgery. I was having a radical hysterectomy and a lymphadenectomy in addiction to getting the tumor out. A hysterectomy is a surgery to take out your cervix, uterus, and ovaries. This means that I will never be able to have kids. Luckily, I got to keep my ovaries to avoid menopause for as long as possible. But, If I do have to go through chemo and radiation, then I will have to go through menopause, something only 50 year old woman and up have to experience. It’s now October 17th. It’s been a week since my surgery, and now I am just doing my best to recover and get back to myself. I have a follow up next Friday to find out the next step in treatment. I pray that the surgery is enough, but it looks like I will probably have to go through some chemotherapy and radiation to make sure my cancer doesn’t come back and to make sure its all gone.
I just found this website, and I thought it would be cool to reach out to other people my age who are having to deal with cancer this young. It’s a tough experience, but with courage and strength and faith in God, we can do this. I can do this.
Please feel free to talk to me. I’d love to make some friends who are going through cancer too since I’m new to all this.
I’m currently writing a book about a teen with ALL. I was wondering if I could get some help understanding the process and experiences teens have when facing cancer