I received a request for a Custom Etsy Order yesterday. I feel honored to be creating pendants for this Fabulous Group of people and just wish I lived near them in Northern California so that I could attend their upcoming performance of the Jungle Book. Please click on "Angels on Stage" above and it will take you over to their site. Thanks so much Nina for choosing me to make these for you.
I think it's amazing how we grow so much as people when we have a child with a disease or dissability. We learn not to "Sweat the Small Stuff" and Learn to Turn negatives in to positives. I have tried to Teach this to Cameron as well and he is an Awesome Student. He tells me from time to time that as much as Diabetes Sucks he is so glad that I don't work outside the home anymore. We are always talking about how if it werent for his Diabetes we would do this or that differently. I am so proud of him and think our family is stronger and closer beacause of him. Don't get me wrong there are bad days with tears and anger but the good definitely outweigh the bad.
Polymer Clay creations, Jewelry, Diabetes Awareness and so much more by Kellee Paschall
Showing posts with label type 1 diabetes. Show all posts
Showing posts with label type 1 diabetes. Show all posts
Sunday, January 31, 2010
Saturday, June 6, 2009
Cameron has Swine Flu
Wednesday Cam woke up and said he was feeling achy all over. I kept him home from school but wasn't to concerned because he didn't seem terribly sick. He sat up all day playing computer games and watching TV. By the afternoon he seemed to be slowing down and started to run a fever. That bothered me a bit knowing that Swine flu causes a fever to come on quick and also knowing that it has not been a big deal for people with "regular" immune systems and that others with underlying problems were the ones having the most problems and even causing deaths.
I gave him some tylenol and told him to lay down and rest, his fever was 100. A couple hours later when I checked him again he was up to 101. I was starting to feel a bit more nervous but kept thinking maybe I was just being paranoid. He got up to 102.5 and I gave him some more tylenol. A couple more hours passed and he was 102.9, I decided I could no longer ignore that nagging feeling of dread in the back of my mind. We left about 10pm for Primary Children's and when we got there the Emergency room was packed with sick kids. My first thought was "we better find a comfortable spot to sit we are going to be here awhile". They called us up quickly to check his vitals and get a bit of info and then we went back to our seats. I was shocked when they called us back after only about 5 min. That scared me ! I know that they see patients in order of importance and they did not take us to an exam room, they put us in a trauma room. Now I was getting worried that my worst fears were coming true.
Before the Dr. even came over nurses were getting an IV ready and putting patches on his chest that hooked up to a machine. Once the Dr. came over he told us they were concerned because of his rapid heartbeat * 145 * which should have been around * 100* They needed to hydrate him and try to get his fever down to try and lower his heart rate. Then what we were afraid of, they were going to test him for swine flu. What an awful test, they put a bunch of saline up his nose and he was sreaming "I can't breathe" then they put tubes up his nose and started sunctioning. He was screaming out of pain and panic as I held his hand and quietly cried and Mike tried to hold his head still. Once that was over they told us we wouldn't get results til tomorrow. Now it was the waiting game. Why do these things always happen at the end of a long day ? By about 2 am his fever was starting to break but now he was vomiting so the Dr. wanted to continue to stay there. He started talking about keeping him for observation. By 3 am he was still vomiting but his fever had not come back so he gave the option to watch him at home and see our Dr later in the day or watch him in the observation area. We decided he would be more comfy at home so we finally left about 3:45. He continued vomiting and his fever came back..... To be continued later.
I gave him some tylenol and told him to lay down and rest, his fever was 100. A couple hours later when I checked him again he was up to 101. I was starting to feel a bit more nervous but kept thinking maybe I was just being paranoid. He got up to 102.5 and I gave him some more tylenol. A couple more hours passed and he was 102.9, I decided I could no longer ignore that nagging feeling of dread in the back of my mind. We left about 10pm for Primary Children's and when we got there the Emergency room was packed with sick kids. My first thought was "we better find a comfortable spot to sit we are going to be here awhile". They called us up quickly to check his vitals and get a bit of info and then we went back to our seats. I was shocked when they called us back after only about 5 min. That scared me ! I know that they see patients in order of importance and they did not take us to an exam room, they put us in a trauma room. Now I was getting worried that my worst fears were coming true.
Before the Dr. even came over nurses were getting an IV ready and putting patches on his chest that hooked up to a machine. Once the Dr. came over he told us they were concerned because of his rapid heartbeat * 145 * which should have been around * 100* They needed to hydrate him and try to get his fever down to try and lower his heart rate. Then what we were afraid of, they were going to test him for swine flu. What an awful test, they put a bunch of saline up his nose and he was sreaming "I can't breathe" then they put tubes up his nose and started sunctioning. He was screaming out of pain and panic as I held his hand and quietly cried and Mike tried to hold his head still. Once that was over they told us we wouldn't get results til tomorrow. Now it was the waiting game. Why do these things always happen at the end of a long day ? By about 2 am his fever was starting to break but now he was vomiting so the Dr. wanted to continue to stay there. He started talking about keeping him for observation. By 3 am he was still vomiting but his fever had not come back so he gave the option to watch him at home and see our Dr later in the day or watch him in the observation area. We decided he would be more comfy at home so we finally left about 3:45. He continued vomiting and his fever came back..... To be continued later.
Friday, April 10, 2009
A bit of info about JDRF
URL: http://www.jdrf.org/index.cfm?fuseaction=home.viewPage&page_id=100903
About JDRF:
JDRF was founded in 1970 by the parents of children with type 1 (juvenile) diabetes -- a disease that strikes children suddenly, makes them insulin dependent for life, and carries the constant threat of devastating complications. Since inception, JDRF has awarded more than $1.16 billion to diabetes research, including more than $137 million in FY2007. More than 85 percent of JDRFs expenditures directly support research and research-related education. In FY2007, the Foundation funded 700 centers, grants and fellowships in 20 countries. JDRF's mission is constant: to find a cure for diabetes and its complications through the support of research.
JDRF continues to make progress toward a cure for type 1 diabetes. Your donation will make a dramatic impact as JDRF moves life altering research out of the lab and into human clinical trials. Typically, more than 85 percent of JDRF's expenditures directly support research and research-related education.
Type 1 diabetes is a disease which strikes children suddenly and requires multiple injections of insulin daily or a continuous infusion of insulin through a pump. By supporting JDRF's mission to find a cure you won't only be saving children, you will be saving childhoods.
For more information about type 1 diabetes and research efforts for the cure, please visit www.jdrf.org.
About JDRF:
JDRF was founded in 1970 by the parents of children with type 1 (juvenile) diabetes -- a disease that strikes children suddenly, makes them insulin dependent for life, and carries the constant threat of devastating complications. Since inception, JDRF has awarded more than $1.16 billion to diabetes research, including more than $137 million in FY2007. More than 85 percent of JDRFs expenditures directly support research and research-related education. In FY2007, the Foundation funded 700 centers, grants and fellowships in 20 countries. JDRF's mission is constant: to find a cure for diabetes and its complications through the support of research.
JDRF continues to make progress toward a cure for type 1 diabetes. Your donation will make a dramatic impact as JDRF moves life altering research out of the lab and into human clinical trials. Typically, more than 85 percent of JDRF's expenditures directly support research and research-related education.
Type 1 diabetes is a disease which strikes children suddenly and requires multiple injections of insulin daily or a continuous infusion of insulin through a pump. By supporting JDRF's mission to find a cure you won't only be saving children, you will be saving childhoods.
For more information about type 1 diabetes and research efforts for the cure, please visit www.jdrf.org.
Wednesday, April 8, 2009
HOPE Bracelet
This is my Juvenile Diabetes Awareness Bracelet.
The Red signifies the blood from the numerous daily finger pokes * The cloudy beads represent the insulin * The clear Crystals represent the many, many tears shed by children and parents because of this horrible disease.
Please contact me if you are interested in purchasing a bracelet like this from me.
The Red signifies the blood from the numerous daily finger pokes * The cloudy beads represent the insulin * The clear Crystals represent the many, many tears shed by children and parents because of this horrible disease.
Please contact me if you are interested in purchasing a bracelet like this from me.
Tuesday, April 7, 2009
Saturday, August 25, 2007
Another Successful Year for JDRF
Walk to Cure
Today is the Walk to Cure Diabetes at Wheeler Historic Farm. It is the 3rd one we have participated in and Cam is really looking forward to it.
Subscribe to:
Posts (Atom)