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Welcome to Katelyn Benson's website! This has been created to keep family and friends up to date with the latest news regarding our brave daughter.

At the age of three, Katelyn was diagnosed with Neuroblastoma Stage 4, a rare childhood cancer for which there is no cure. She was diagnosed on Monday 16th May 2005 and since then has undergone 8 rounds of chemotherapy, a 5 hour tumour resection surgery, further high-dose chemotherapy followed by a stem cell transplant, radiotherapy and 6 rounds of Accutane (Retinoic Acid). In September 2006, we discovered that Katie had relapsed and so the battle begins again.

Despite the devastating prognosis, we have great faith that our precious daughter will be granted her miracle cure. Thank you for joining us on our rollercoaster journey. Words cannot express the uplifting joy we feel to know we have such a wonderful "team" standing behind us every step of the way. We thank each and every one of you for the endless love, support and prayers.

We are praying for a miracle!!

Children with cancer are like candles in the wind who accept the possibility that they are in danger of being extinguished by a gust of wind from nowhere; and yet, as they flicker and dance to remain alive, their brilliance challenges the darkness and dazzle those of us who watch their light.

Wednesday, December 12, 2007

Our princess is now resting peacefully in heaven

Katelyn Grace Benson
28th February 2002 - 6th December 2007
Thank you, precious little princess for sharing your love with us. Until we are reunited as a family in heaven, we shall be missing you and we will never forget you. We love you more than words could say.

Wednesday, July 04, 2007

Homeward bound

After I get platelets, I'm going home tomorrow! Hip hip hooray. I am off all painkillers and I'm doing really well. The portacath is a big step up from mr wiggly woo the worm. I can't wait to get home and spend time with my little fishies. I'm having a week or two of treatment and it is a welcome break. With any luck, I will spend minimal time in the hospital and doctor's surgery.

Katie, xox

P.S. Can you believe it's July already???

Thursday, June 28, 2007

Back in hospital

I'm in hospital with a Hickman line infection. I am on antibiotics, paracetamol and I am very miserable. Daddy got me some lovely stickers but even happy smiley faces couldn't cheer me up. Due to the problems I've been having, we are going to pull the line and have a portacath placed (under the skin). I will keep you updated.

Sunday, June 24, 2007

Good times

I'm doing very well. The femoral line was placed without hitch. I am superwoman! My stem cells were collected over 3 days. I am generally feeling well. A proper update is coming soon.

Love you all,
Katie x

P.S. I have 2 fish, one is called Fill and the other is called Fiona!!

Monday, May 28, 2007

Monday monday

It's bank holiday Monday so I am lucky enough to have both Mummy and Daddy at home. The weather is grim so we haven't gone out. We recently got a giant trampoline in our garden. It was from ebay! Josh and I stayed up till 9 pm waiting to see if we won the bid and we did, yay! I am having a femoral line placed tomorrow in preparation for the stem cell harvest. Think of me as we have to get up at 5am! My haemoglobin was down to 7.9 so I had a blood tranfusion yesterday...my first in a while. I'm keeping well and looking good. Sally, our new nextdoor neighbour has promised us a little fishy. I can't wait to have my very own pet. I am going to call him Fill with an 'F'!!

Saturday, May 26, 2007

I'm a little ballerina

I spent the week with Mema and Mummy at Mema's house! That's why we didn't get a chance to update. I've been having GCSF injections in my leg to prepare for the stem cell harvest. Sandra is taking me to see Lilly's ballet show this afternoon. I am so excited. I had my ballet lessson this morning so I'm still in my leotard which I'm going to wear to Lilly's show! Then, we are going out for pizza.

Wednesday, May 16, 2007

More fabulous news

Mummy and Daddy met with Dr. Ainsel on Monday and there was some very good news. My bone marrow and trephine are neuroblastoma free!!! For the next stage in my treatment, I'll be having my stem cells harvested. I will keep you updated. :-)

Sunday, May 13, 2007

Fabulous news

My hair is growing and I am gaining weight. I look and feel awesome (if I do say so myself). I had my CT scan and MIBG scan. I am stable which is great news. The preliminary results from the bone marrow tests look pretty good but we'll know tomorrow when Mummy and Daddy meet with Dr. Ainsel to discuss the plan of action. My attendance at school has been really good and I am thriving. All is welll with the Benson family. Thank you for checking in!!

Thursday, May 03, 2007

School days

Dr. Marcus said my ultrasound scan looked good, my bladder is fine. I will be having a kidney function scan soon. We should know, by next week, the official results from the scan and x-ray. I got a Bob the builder sticker for being such a brave girl. I wanted a Barbie one but Nurse Kathy said they'd run out. I really like Nurse Kathy. I remember her from the first time I was in hospital when I got diagnosed with neuroblastoma.

I am eating really well. I had a bowl of weetabix for breakfast before school. I always meet Maddie in the playground and we go into school together. Miss Elsie tells Mummy that we always sit next to each other at lunchtime and we play together at breaktime.

I am a busy bee!

Tuesday, May 01, 2007

Katie's morning sunshine

Good morning! I slept really well last night, so subsequently I am feeling very chirpy. I am off for my pelvic and renal ultrasound scan and an abdominal x-ray. I have told Mummy and Daddy that I am going to be a doctor when I'm older so it's very important for me to be specific with the medical lingo. :-) Fortunately for me, my Daddy will be taking lots of books to read to me. Joshy is at school, Mummy and Sophie are staying at home. After the hospital, they'll take me to school and Daddy will go back to work. Have I bored you enough??!! Love, Katie XOX