Showing posts with label Cameron. Show all posts
Showing posts with label Cameron. Show all posts

Sunday, January 31, 2010

Angels on Stage

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.

Saturday, July 4, 2009

Happy 4th - 2009


Happy 4th of July !

I am so grateful for all our Brave Men and Women serving in Iraq as well as other areas in the world ~ Thank you for protecting our FREEDOM !

The kids are out of school now as of last Thursday. Lacey will be starting Junior High as a 7th grader at Hunter Jr. High when she goes back to school in August and Cam will return at the end of this month as a 5th Grader. He is looking forward to being the only Paschall at Valley Crest at not having all of Lacey's friends scream out his name and give him hugs. Honestly I think he will miss them.

Mike got the boat out yesterday, checked out everything, made a couple of small repairs and cleaned it up. We are hoping to have it in the water in a couple of weeks.

Lacey will be at Girls camp all next week and Cam and I have plans to see movies, go to Hollywood Connection and the Centennial Park pool.

Next Month is Cruefest 2 and the Walk to Cure Diabetes at Wheeler Farm.
If you have made a Donation to JDRF ~ Thank you very much. I have had so much going on that I have not gotten Thank you cards out, but please know that we are very grateful !
I have tons of inventory and plan to have a fundraiser ~ I just need to set a date.

I hope you all have a fun and safe 4th of July !

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.

Saturday, May 9, 2009

My New Walk Team pendants turned out so cute !





I am just loving the way these turned out so I am offering them on ETSY with customized team names. Cam snatched the first one I finished and put it on right away. I am only charging 3.50ea for them to cover supplies and anything left over will be donated to JDRF.

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.

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.

Thursday, December 13, 2007

Happy Holidays !



It's been awhile since I have had time to post, this is such a crazy time of year !
The Saturday after Thanksgiving I participated in a Holiday open house/Sale at Jana's house. Our turnout was not as big as we hoped but still a great time and always fun to be with my claymates ! It seems like I have been going non stop since then creating Holiday items and loving every minute of it. It is so cold here right now I can't think of a better way to spend my time. My crochet hooks and pens have been especially popular.

Cameron has finally started to give his own shots, I am so proud of him !! He knew the nurses would be asking him at his appt. on Monday so he tried it on Sunday night. The nurses and Dr. Donaldson showered him with praise and even a few gifts as a reward. The order was placed for his pump and he will be getting started with it at the end of January. We are all excited about that !