09 December 2010
Updates on Bug
December 09, 2010
It has been so crazy around here the last few weeks. We have had so much going on besides Doctors appointments, and therapy. Trust me it is catching up to me. I could take a nap.
We are now registered with Unique Rare Chromosome and will see what comes out of that. It looks like a really interesting site, I look forward to exploring it now that I am a member.
Bug goes in next month for a video EEG, which means Bug and I will be in the hospital from anywhere from one to five days. This is to make sure she is not having any seizures. All of her EEG have came out normal but, she has too many oddities to rule out no seizures. This should clear up that concern. The neurologist wanted to be aggressive and rule it out completely. I hope and pray it is not the full five days. The thought of being in one room and not being able to leave is daunting. They need an adult with her the whole time to press a button if we see her doing her staring spells. She will be hooked up 24 hours to the EEG but, they want us to press the button when we see her doing her thing that has concerned us. I can leave if daddy or someone else is there to take my place. I will stay at the hospital overnight. I have a feeling that this will be very hard for Bug. I think both of us will feel like a caged animal. They told me to bring along movies, games and toys. I will try to do some school while we are caged in.
Little Man is not so happy about Bug and Mommy being gone. The thought of mommy not being there during the night time is just horrible. I am never away from the kids overnight. I think he has stayed at the Grandparents overnight maybe, three times in his almost 5 years of life. He loves to cuddle at night time in bed with me and we talk about the day and everything in between while he is to winding down to go to sleep. It is one of my most precious times that we spend together.
This post could get longer but, I will fill in the IQ testing results in another post. Many blessings.
We are now registered with Unique Rare Chromosome and will see what comes out of that. It looks like a really interesting site, I look forward to exploring it now that I am a member.
Bug goes in next month for a video EEG, which means Bug and I will be in the hospital from anywhere from one to five days. This is to make sure she is not having any seizures. All of her EEG have came out normal but, she has too many oddities to rule out no seizures. This should clear up that concern. The neurologist wanted to be aggressive and rule it out completely. I hope and pray it is not the full five days. The thought of being in one room and not being able to leave is daunting. They need an adult with her the whole time to press a button if we see her doing her staring spells. She will be hooked up 24 hours to the EEG but, they want us to press the button when we see her doing her thing that has concerned us. I can leave if daddy or someone else is there to take my place. I will stay at the hospital overnight. I have a feeling that this will be very hard for Bug. I think both of us will feel like a caged animal. They told me to bring along movies, games and toys. I will try to do some school while we are caged in.
Little Man is not so happy about Bug and Mommy being gone. The thought of mommy not being there during the night time is just horrible. I am never away from the kids overnight. I think he has stayed at the Grandparents overnight maybe, three times in his almost 5 years of life. He loves to cuddle at night time in bed with me and we talk about the day and everything in between while he is to winding down to go to sleep. It is one of my most precious times that we spend together.
This post could get longer but, I will fill in the IQ testing results in another post. Many blessings.
Labels:Special Needs
Subscribe to:
Post Comments
(Atom)
Search This Blog
Grab my button!
Followers
Powered by Blogger.
Homeschool Planet
HSP Free Offer Email for REVIEWERS!doctype>
Popular Posts
-
After several weeks of hard work on our Native American Teepee Village Diorama we are finally done. This was a fun project. Everyone is rea...
-
We are learning about the Viking in our history studies. What better way the enhance the learning by adding a craft to the mix. With my kid...
-
Over the last few weeks my kids have been using IXL Learning . I received a Full Annual Membership for IXL , it came with the subje...
-
Last week during our study of the Inca culture the kids made an Inca Quipus. If you are not familiar with what a quipus I will try to give...
-
My children are now young adults. Gone are the days of diapers, sleepless nights, toys, and messes all over the house. Honestly, I have ne...
Labels
20p12.1
4-H
About Me
American History
Ancient History
Autism
Beekeeping
Beekeeping 101
Bible
Blog Hop
Blogging
book
Book reviews
Camera Shots
Classroom
Coding
Curriculum
Disclosure Policy
Egypt
Entomology
Experiments
Family
Feast of Tabernacles
Field Trips
Free Printables
Garden
Geography
Giveaway
Giveaways
Hanukkah
Health
Hebrew
High School
History
homemade
Homemade Bread
Homemaking
homeschool
Homeschool crafts
Homeschooling
Honey Products for Sale
Honey Recipes
Horse Therapy
iPad & Apps
Israel
Just For Fun
Juvenile Arthritis
Kids
Lapbooks
Life Cycle
Life in general
Math
Medieval History
My kid said...
Organizing
Organizing/homeschooling
Our curriculum
Our Week Through the Lenses of a Camera
Passover
Photography
Prayer
Purim
Random Pictures from my Kids
Recipes
Review
Review Policy
Reviews
Rosh Hashanah
Science
Scripture
Sensory Processing Disorder
Shabbat
Shavout
Simchat Torah
Sonlight
Special Needs
Special Needs High School
Special Needs Product Reviews
STEAM
STEM
Stuff
Tish B’Av
tos
TOS Crew Reviews
Tu Bishvat
Viking History
Week in Review
Wordless Wednesday
Workboxes
Yom Ha'atzmaut
Yom Hashoah
Yom Hazikaron
Yom Kippur
0 comments:
Post a Comment
Thank you for visiting my blog.