Sunday, December 27, 2015

so i got to be in the newspaper!

Well it turns out the article came out christmas day, the article covering my medical life going with T.C Thompson's Children's Hospital of Chattanooga Miracle child. Thought Id post the article here for people who may not have access to Chattanooga Times, or the Dalton Daily Citizen as it was also published there a day or two later.
Cameron Watkins looks out of place as he leans back into the chair in Room 2 of the Pediatric Cancer and Blood Disorder Center at the Children's Hospital at Erlanger. Large plastic dinosaurs stand in some of the adjacent rooms, a giraffe towers over one wall and children toddle around a play area filled with plastic balls and a toy kitchen.
But Watkins, 23, is at home.
"I've spent more time here than I've spent in school," he said. "They've known me my whole life."
This is the 51st time he has made the trip from his home in Dalton, Ga., this year, once each week. He has been coming for 10 years, ever since he took part in a clinical trial for a new drug that saved his life.
On this Tuesday morning, his friend Triston Smith, who hopes to one day become a doctor, sprays a numbing anesthetic around the port inserted into Watkins's chest. Nurse Laura Gibson inserts the IV that will slowly drip a drug solution into his body over the next five hours. Then he and Triston settle down for a game of Connect 4, a version of tic-tac-toe on steroids.
"He's an amazing kid," said Dr. Manoo Bhakta, who has helped treat Watkins since he was 5. "People ask, do you believe in miracles — he's simply a miracle."
When Watkins was a young boy his mother, Tressia, thought she saw problems she had not noticed with his older brother. Doctors initially brushed her off as an overprotective mom. She persisted, and found a doctor who realized something really was wrong.
The diagnosis was Hunter syndrome, an extremely rare condition caused by the lack of an enzyme in his body; a genetic defect. It only affects boys — around one in 150,000.
The enzyme helps the body break down and clear out used material. When it is not present, the material builds up in the heart, the tendons and even the brain, causing myriad problems.
Bhakta remembers when he met Watkins.
"He had a massive spleen, and he had an ear infection that had started bleeding and couldn't be stopped," he said. Watkins also had a leaky heart valve and doctors were considering a risky transplant operation.
At the time, Hunter syndrome was a death sentence — most boys diagnosed with it only lived until their midteens.
But Watkins got a lucky break. Bhakta put him in touch with doctors at Duke University to become part of the first clinical study of a new drug, idursulfase, sold by the Shire pharmaceutical company as elaprase. While the drug can't replace his missing enzyme, it does perform many of its functions, keeping the symptoms from becoming worse.
And then Watkins got really lucky. Since this was a test to determine if the drug worked, half of the boys in the test group got nothing, a placebo.
Cameron was one of the fortunate ones who got the drug, and it worked, almost immediately.
"His spleen shrank, his platelet count dropped," Bhakta said. "He would not be with us today if it weren't for this amazing drug."
Doctors decided his heart condition had improved to the point that he didn't need the valve transplant.
He still has problems with his hearing, and his heart can act up unexpectedly. He's had to fight to keep his body in shape to stay out of a wheelchair, but he is able to walk on his own or with a cane.
Sometimes he overreaches and pay the consequences. On a trip with Smith last year to Disney World, he walked on his own with a cane for five hours, but ended up back in his hotel room, exhausted.
"My heart went off," he said, racing out of control. The photo he posted to Facebook from that night shows him on a stretcher as paramedics raced to get him to a nearby hospital.
Given a lifelong history of medical problems, Cameron could be forgiven for feeling a little sorry for himself.
But what is most striking — both in person and in the comments he posts on Facebook and on his blog, Cameron Lives 365 — is his optimism.
"I've always lived with this condition," he said. "We all have to live with something, and this is it for me. I'm happy."
He graduated from high school with honors and took some college classes, although he has yet to graduate. He would like to write fiction for young adults, he said, or be a journalist.
A recent blog post seems to summarize his attitude about his life, a life he once thought he might miss out on.
"Maybe the trials in my life somehow helped people get their own perspective in life, and pushed them to reach for their goals," he wrote. "If in my life I achieve anything, I'd like it to be that my life helped someone else's life, and maybe made an impact." " -written by reporter Steve Jhonson


Tuesday, December 22, 2015

Treatment, Interview, friends oh my!

    I will just start off by saying today was sincerely a good day! A lot happened, and its right in the middle of all the christmas festivities, so it was definitely memorable. Today was treatment day had to have it moved since usual day was christmas eve. Luckily my best bro Triston whom I haven't seen in about a year due to his college life was able to take me. Also I got interviewed for the Chattanooga Times on my life and my weekly treatments. It should be published around Christmas i believe.
    The day started out normal Triston picking me up and got to the hospital, however once we got there the interview started, and basically I just answered about myself. We went over a lot of my life, so I'm curious to see what all gets put in. There was also a photographer there taking shots to go along with the article. Both the reporter and photographer were nice people, and easy to talk to.
    Triston and I played some games, he even won a few rounds i'll admit ha. Then we just took it easy with a movie called The Martian which i have to say was honestly good. Alas though all good times must come to an end as the IV pole so loudly reminded us when I was done. I was glad to see my friend though during the Christmas holiday.

Monday, December 7, 2015

You decide who you will be

    Alright so a subject has brought itself up to me twice within the last twelve hours from two different parts of my life, and honestly the lesson I feel should be shared. At church last night the subject was over the genealogy of Jesus, his family heritage, and how he had a few people down the line who were less than favorable. However despite their sins, or their family troubles they were still used for a greater good. Some didn't let their past define them, while others did. It's easy to to assume people will do things based on their past, but the truth is we always have the choice to choose to become the person we want to be, whether we are scared because of where we come from we aren't worthy, or thats all we will ever be. Or after choosing to change we slip up, and feel like we can't go back to trying.
    After I got home I got to see the Mid-Season finale of Once Upon a Time, and surprisingly it was also tightly focused on that same lesson, showing that no matter how hard we fall, we can still choose to end up choosing the right path despite whatever we have done, or whatever those who have come before us have done. I think it also showed how some people can't let go of who they were so even after redeeming themselves briefly they let themselves slip back to who they were.
    The bottom line is, don't let your past define you. Choose who you want your future to be, and be that person.

Tuesday, December 1, 2015

Tree Lighting ceremony

    So a while back I was nominated for one of T.C Thompson's Miracle children, and looks like I got it. Today got to attend a tree lighting ceremony at the hospital where all of the patients were honored. though to be honest we almost missed the ceremony as both my mother and myself wrote the date down wrong, but we made it just in time! It was kinda nice being in the spotlight I won't lie, even if I do get stage shy haha, plus I nearly tripped off the stage. but it was nice the tree was very festive.
    The miracle children are nominated I think based on their life experiences and attitude. I just try to be myself and enjoy what I can in life. Looking forward to getting to attend more events like this throughout 2016!