Sunday, December 9, 2007
Hiccup in Megan's Journey
I just wanted to let everyone know that Megan had to go into the hospital on Thursday December 6 for monitoring. She started having minor seizures again and the Doctors were afraid she was having ESCS again (continual seizures all night long). The monitoring showed that the ESCS is back and Megan has been put on Valium to help correct this problem. We will see how it goes. Megan is home now and back to her usual funny self.
WADA NEWS
Hurray!Hurray! The WADA test has been scheduled for January 9th. This test involves threading a catheter from Megan's groin to the left side of her brain. Anesteia will be administer through the catheter to put the left side of her brain to sleep and see how she functions without it. We hope she can do everything without the left side this would mean she can have the surgery. Please keep your prayers going we need a positive answer.
Sunday, November 18, 2007
Thanks to Middlesex Sports Club
I can not express in words my gratitude to the Middlesex Sports Club. They chose Megan as the recipient of their Texas Hold'em Tournament this year and they were able to raise over $4,000. Megan is so lucky to have so many Guardian Angels looking over her. Thanks again to the Middlesex Sports Club and all the contestants who turn out to support Megan.
Thursday, October 25, 2007
MEG results
The results from the MEG are back. It is not exactly what we wanted to hear. I guess it is another hiccup in Megan's journey to a healthy life. The MEG showed some speech and language skills on the damaged left side of her brain which means we may not be able to remove the left side. The doctors want to do the WADA test. The WADA involves treading a catheter from Megan's groin up to the left side of her brain so the doctor's can put the left side of Megan's brain to sleep with medication and see how her speech and language is affected. I do not have a date yet for this test. Megan needs your prays and thoughts at this time and so do I. I am really scared for Megan.
Tuesday, October 23, 2007
Just some updates
Hi,
I wish I had test results from the MEG but I guess no news is good news. The "Texas's Holdem" game is this Saturday (10/27). There are few spots still left if anyone is interest. See you there. Also, the Applebee's fundraiser was a huge success. You raised over $700. Thank you so much. Hopefully, I will have news about Megan's MEG test soon.
I wish I had test results from the MEG but I guess no news is good news. The "Texas's Holdem" game is this Saturday (10/27). There are few spots still left if anyone is interest. See you there. Also, the Applebee's fundraiser was a huge success. You raised over $700. Thank you so much. Hopefully, I will have news about Megan's MEG test soon.
Monday, September 24, 2007
Meg in the "MEG"
Mrs. O'Brien took this picture of Megan in the MEG machine. I thought you would like to see what it is like.
Friday, September 21, 2007
Middlesex Sports Club Supports Megan
We are overwhelmed by the support from the town of Middlesex. The Middlesex Sports Club has chosen Megan to be the beneficiary of their Texas Hold'em Tournament. The Tournament will take place on Saturday Oct 27, 2007 at 11:00 am and will start at noon. If anyone would like to enter, the cost is $30.00 and limited to 100 entrants. You can contact Vito LaSala (732) 968-1193. If you are like me and have no idea how to play, the Middlesex Sports Club is looking for volunteers to serve food and beverages to contestants. Please contact me at chemeyn@middlesex.k12.nj.us. The Chemey Family would like to thank the Middlesex Sports Club for their loving support of Megan
Megan's Meg Test
Well, Megan did an outstanding job on this test. We will not know any results from the test for a month. It takes that long to map the information from the MEG onto her MRI of her brain to give a detailed picture of her brain and the locations of speech and language in her brain. This sounds like science fiction or what you would see on the show "House".
I would like to publicly thank Mrs. O'Brien who is Megan's teacher. Mrs. O'Brien went with us Wednesday to help Megan do the MEG test at Children's Hospital.
Mrs. O'Brien is an outstanding example of how teachers impact our children's lives. We all need to thank our children's teachers who help our children reach for the stars.
I would like to publicly thank Mrs. O'Brien who is Megan's teacher. Mrs. O'Brien went with us Wednesday to help Megan do the MEG test at Children's Hospital.
Mrs. O'Brien is an outstanding example of how teachers impact our children's lives. We all need to thank our children's teachers who help our children reach for the stars.
Friday, September 14, 2007
"MEG" Test
GREAT NEWS!!!!!!!!!
Megan has been scheduled for her next pre-surgery test. The "MEG" (I think that is the correct spelling) is schedule for Wed Sept 19. This test uses magnetics to detect magnetic fields in your brain as you are doing some kind of skill such as talking. The theory behind this is the area of the brain giving off the magnetic field is the area of the brain controlling this skill. Hopefully, all the magnetic fields in Megan's brain will be on the right side. Megan likes going to Children's Hospital of Philadelphia (CHOP) because they have great food. A hospital with great food? Go Figure!!! I will hopefully have good news next week.
Megan has been scheduled for her next pre-surgery test. The "MEG" (I think that is the correct spelling) is schedule for Wed Sept 19. This test uses magnetics to detect magnetic fields in your brain as you are doing some kind of skill such as talking. The theory behind this is the area of the brain giving off the magnetic field is the area of the brain controlling this skill. Hopefully, all the magnetic fields in Megan's brain will be on the right side. Megan likes going to Children's Hospital of Philadelphia (CHOP) because they have great food. A hospital with great food? Go Figure!!! I will hopefully have good news next week.
Monday, September 3, 2007
Megan passed her first pre-surgery test. She is now being scheduled for a mag test. This test requires her to do certain activities while wearing a big magnetic helmet so they can locate magnetic fields in her brain. For those of us who are not medically train, the test will show which side of Megan's brain contains speech and language. We need Megan's speech and language to be located on the right side of her brain so the surgeons can remove the entire left side of her brain. I am hoping this test will be schedule sometime in September. Megan has started having continual seizures at night again so the doctors have doubled her steroid dosage which is not good for Megan but this little hiccup in her journey could move the process along faster I hope. Take care.
Saturday, August 25, 2007
Thank You
In our childhood, when ever we experienced a great sadness, hurt, or fright, we would often find comfort from a favorite “blankie” or stuffed animal. This blankie that we clutched tightly in our arms helped to ease our fears and hurts till all would be right with our world once again.
The Chemey Family would like to thank the Community of Middlesex Borough, the Middlesex Public Schools, every private and religious organization, every business, and every individual who has help to form a warm comforting “blankie” for our family to hold on to during Megan’s future surgery and rehabilitation The overwhelming outpouring of caring and concern from everyone for our daughter and sister Megan will never be forgotten.
I thought Megan's journey could be a learning experience for all of us. I will keep everyone informed on her progress with this blogger. Check here for updates on her testing and how she is doing.
The Chemey Family would like to thank the Community of Middlesex Borough, the Middlesex Public Schools, every private and religious organization, every business, and every individual who has help to form a warm comforting “blankie” for our family to hold on to during Megan’s future surgery and rehabilitation The overwhelming outpouring of caring and concern from everyone for our daughter and sister Megan will never be forgotten.
I thought Megan's journey could be a learning experience for all of us. I will keep everyone informed on her progress with this blogger. Check here for updates on her testing and how she is doing.
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