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lifewithbecca | The life and adventures of a little girl with epilepsyThe life and adventures of a little girl with epilepsy
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The life and adventures of a little girl with epilepsy
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lifewithbecca | The life and adventures of a little girl with epilepsy | lifewithbecca.wordpress.com Reviews
https://lifewithbecca.wordpress.com
The life and adventures of a little girl with epilepsy
lifewithbecca.wordpress.com
Becca’s history | lifewithbecca
https://lifewithbecca.wordpress.com/beccas-history
The life and adventures of a little girl with epilepsy. About us (the short version). These are all of Rebecca’s old Caringbridge updates. In reverse Chronological order. Rebecca Kaylene Kennedy’s. Tuesday, May 3, 2011 11:10 AM, EDT. Things went well at Rebecca’s neuro. We’ve upped her VNS, so both the. Output current and the duty cycle are increased. I know that is Greek to. Most readers – but to those in the Epi/VNS family you’ll understand. Day) If we have to we’ll go back to the original dose. To kno...
Side effects may include… | lifewithbecca
https://lifewithbecca.wordpress.com/2014/09/07/side-effects-may-include
The life and adventures of a little girl with epilepsy. About us (the short version). Side effects may include…. We’ve all been there. You need start on a new medication and read the side effects. Sometimes they sound worse than what you are taking the medication for. Becca has been on more than her share of medications in her lifetime. Most of her seizure medications have similar side effects. After a neurology appointment last month her doctors decided to put her on. She was very uncoordinated (well ev...
Baby got a new set of wheels, and a fresh new battery. | lifewithbecca
https://lifewithbecca.wordpress.com/2014/04/08/baby-got-a-new-set-of-wheels-and-a-fresh-new-battery
The life and adventures of a little girl with epilepsy. About us (the short version). Baby got a new set of wheels, and a fresh new battery. Rebecca got her new wheelchair not long ago. It is so nice to have a new chair that fits her better. Her new wheelchair is a Convaid Rodeo. I am sure any other special needs parent can share in the joy of new equipment! Becca is doing well overall. She had another MRI scan a couple weeks ago. The scans were great! That magical time of night ». Enter your comment here.
That magical time of night | lifewithbecca
https://lifewithbecca.wordpress.com/2014/04/15/that-magical-time-of-night
The life and adventures of a little girl with epilepsy. About us (the short version). That magical time of night. I originally wrote this a year or so ago and just now publishing. Some stuff may be out of date. One of the best things about being a parent of a specials needs child is I am able to spend many magical moments with my child, most parents do not get. I know the time will come in her life when the world will be cruel to her. People will be downright horrible to her, all because of her speci...
Finally – no more stairs! | lifewithbecca
https://lifewithbecca.wordpress.com/2014/07/06/finally-no-more-stairs
The life and adventures of a little girl with epilepsy. About us (the short version). Finally – no more stairs! Becca already has a favorite spot. It is much like her favorite spot at our old house, the sunny spot at the front door. Our dining room, with plenty of space for Becca’s special chair. That is a shot standing from the dining room table, looking across our living room (and yes that is Becca, sitting in front of the door). First night in her new room,. Picture of the house. You are not alone.
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Mission: iPossible: August 2011
http://missionipossible.blogspot.com/2011_08_01_archive.html
Monday, August 29, 2011. Hope everybody had a good weekend. Although I know some of our East Coast neighbors had to dodge Mother Nature, hopefully everyone is safe and secure out there and not dealing with too many obstacles in their path. Wowgetting your tonsils removed hurts more than I thought. In fact, yesterday and today are probably the worst as far as pain and discomfort, and I expected that by today I would be skipping off to work merrily and without incident. Such is NOT the case. I let Romy ope...
Mission: iPossible: February 2012
http://missionipossible.blogspot.com/2012_02_01_archive.html
Wednesday, February 29, 2012. Get That Man Some Pants! Just wanted to get your attention. ;). A long time ago, around these parts, we had our Mission One going, and one of the Recipients (as they came to be called) by the name of Eric Olson (whom I have mentioned before in various places) was here on behalf of his son Liam. Naturally, because of that whole Testosterone and facial hair thing, Eric and I started up a bit of an online friendship. He is a God in the NFL. What exactly does that mean? I'm joki...
Mission: iPossible: WHO WE WERE
http://missionipossible.blogspot.com/p/who-we-are.html
Was comprised of a very special mix of Special Needs parents and other individuals, all working together on various projects to benefit kids in the community with communication-related disabilities. The group was originally co-founded by Heather Needham and Kenneth Lilly, and there were some other contributors, both public and private. These original bios will remain on the site while this site blog is still active. Heather Needham - Co-Founder. As well as follow us over at Little Wonders. I was best kno...
Mission: iPossible: July 2011
http://missionipossible.blogspot.com/2011_07_01_archive.html
Friday, July 29, 2011. Not exactly the title I had planned to post today. No, today's blog was GOING to be titled iLuke, and it was going to feature Luke Lundgren, and the photos of he and his family gathered around the iPad2 that they received yesterday from us. One of our own, one of the families on our list, is struggling now, and we need to divert our attention to them for the moment. And offer your words of encouragement to his family there. All of us here hope that Liam makes a speedy recovery and ...
Mission: iPossible: December 2011
http://missionipossible.blogspot.com/2011_12_01_archive.html
Friday, December 16, 2011. Mission Two Recepients Revealed! Almost from the moment we had decided to do this as a 'Random Sequence' selection process, I think it is safe to say that we had some reservations about it. Not because of the fact that it leaves so many things in the hands of chance (as Special Needs parents I think we all have had just about enough of that thank you very much) but for a much more profound reason. Because after you read people's STORIES, they always have an impact on you. We ca...
Mission: iPossible: Mission 4
http://missionipossible.blogspot.com/2012/03/mission-4.html
Friday, March 16, 2012. Long time no.hey wait a minute. Don't have to say that this time around, cause we are on a ROLL. Mission 3 is in the process of fulfillment. The Recipients have been contacted, it is a matter now of just getting all the Verification worked out. I reached out to all three Parent Contacts today and heard back from everybody, now it is a matter of connecting the Recipients to each of the people who selected them. Taking a different approach this time. Now, regarding Mission 4. You ar...
Mission: iPossible: January 2012
http://missionipossible.blogspot.com/2012_01_01_archive.html
Tuesday, January 31, 2012. Hey everybody. Been a while. Not too long, but we're about ready to get things started on our third Mission. You'll start to notice, if you tend to notice these types of things, some little tweaks and such happening on the pages that are on this site as well as to our Facebook page. It is all some prep we are doing as we get ready to begin Mission 3. And that is never bad news, NATCH! I'll check in again soon with more. Wednesday, January 18, 2012. I think I am beginning to hav...
Mission: iPossible: November 2011
http://missionipossible.blogspot.com/2011_11_01_archive.html
Wednesday, November 23, 2011. As I mentioned Monday, I wanted to make sure I got you all some preliminary info on what we want to do for a small follow-up to our first Mission. Now, I say 'small', though I consider that to be a relative term. Hear me out. Mission Two will be the giving of 2 iPads to 2 families in time for Christmas. But here's the thing. No donations required. We have the iPads already. Also we will, as we are doing this Mission Two: '2 for 2'. And I will go over the details on THAT next...
Mission: iPossible: March 2012
http://missionipossible.blogspot.com/2012_03_01_archive.html
Monday, March 26, 2012. As we wait for some of the iPost materials to trickle in and for some Verification stuff to get sorted out to ship out the last of the M:4 iPads, just want to take a moment to point you in the direction of something that is, without doubt or hesitation, worth a few minutes of your time. Moment of Purity seem so rare sometimes, don't they? Do we not owe it to them, and to ourselves, to stop, turn our heads, and take heed? Special Needs Brothers and Sisters. Thursday, March 22, 2012.
ashleydamonandjames.blogspot.com
The ups and downs of raising 4 amazing kids: Thanksgiving
http://ashleydamonandjames.blogspot.com/2012/10/our-thanksgiving-2012-ashley-is-into.html
The ups and downs of raising 4 amazing kids. Wednesday, 10 October 2012. Ashley is really into eating lately! My Mom and Dad made dinner it was yummy. We even closed the cottage up for the year this past weekend. This summer we painted almost everything all the wood panelling, windows and trim indoors and out. We even had the cottage leveled and put on a new roof. It was a lot of work but we had fun fixing it up and are looking forward to laying down a new floor in the spring. Ashley's Fall 2010 Progress.
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Life With Beamer & Lucy | the adventures of a blind hound & his invisible sidekick, as told by their humans
Life With Beamer and Lucy. The adventures of a blind hound and his invisible sidekick, as told by their humans. Skip to primary content. Skip to secondary content. When Dad’s Away…. March 12, 2014. Dana @ Life With Beamer. Ryan sometimes heads out of town for work, leaving the dogs to. Watch over me for a few days. Here are just a few of the things we get away with when Dad’s away…. The freedom to roll in filth. And our bed goes to the dogs. March 10, 2014. Dana @ Life With Beamer. Thankfully, we came to...
lifewithbeansandweenies.wordpress.com
Life With Beans and Weenies | Opening each can of fun, one day at a time!
Life With Beans and Weenies. Opening each can of fun, one day at a time! As the World Turns. September 16, 2015. Life With Beans And Weenies. It’s awesome to look back things I said … wanting to teach, getting my Bachelor’s and then my Master’s degree. I’m doing all that. Yes, I’m living my dream! I’ve been teaching nursing, this being my fourth year … and I love it. I have my Master’s degree (December 2015), and now I am enrolled and working on my Doctorate of Education. September 16, 2015. No, you prob...
Life with BearBear
The days of a trusted sidekick and his boy(s). Saturday, August 15, 2015. Wish we could stay here all summer. Thursday, August 13, 2015. It's a summer requirement to spend an afternoon at Arnold's Park riding the rides. Jack is getting exponentially more brave about the rides he chooses. He talked his Papa and I into riding the roller coaster with him twice each. So glad they smoothed out the tracks last year! Getting ready to ride the Legend. Climbing to "The Point of No Return". Trying the ski trainer.
life with beauty
Maybelline – Super Stay 10h Tint Gloss – 180 Lasting Pink / Revlon – Colorburst i 006 Strawberry Fraise / NYX – Mega Shine Lip Gloss i La La / NYX – Mega Shine Lip Gloss i Golden Pink / – Chanel – Glossimer i 169 Jalouise. Maybelline – Super Stay 10h Tint Gloss – 180 Lasting Pink / Revlon – Colorburst i 006 Strawberry Fraise / NYX – Mega Shine Lip Gloss i La La / NYX – Mega Shine Lip Gloss i Golden Pink / – Chanel – Glossimer i 169 Jalouise. Veldig dyr for en lipgloss, men den er jo så fin. I går fikk je...
lifewithbecca | The life and adventures of a little girl with epilepsy
The life and adventures of a little girl with epilepsy. About us (the short version). Keeping everyone on their toes. She is into another period where she is babbling more. I really enjoy hearing her “talk”. Her mood has been much better too, ever since we added Zoloft. It seems I made a good choice. Normally a patent (or in Becca’s case, a caregiver) would “swipe” the magnet over the VNS implant in her chest to case it to activate an extra pulse in addition to the normal cycle. The very fabulous Nurse P...
Life's a Beach!
Monday, February 19, 2018. An Hour on Playa Cochorit. I wrote down instructions I found on Trip Advisor to help us find the location. We followed Highway 15 down through Guaymas to Empalme, then started looking for the road that would take us west to Playa Cochorit. After wandering for awhile and dead ending into a port area, I finally decided to turn on my phone data and use Google maps for directions. Lo and behold - it worked! Several fishermen's pangas were pulled up onshore. As far as the eye could ...
BECKIEEE!! x3
Saturday, December 30, 2006. Well, It's almost 2 am My little sister Emily can't fall asleep, which means i can't fall asleep. So now i'm thinking about her. hehe. This girl is my bestestestest friend for LIFE! I love her to death. she's always here for me.and she's always here for you! And this pic is prolly the cutest pic of her.OF MY LIFE! This girl is seriously amazing. Posted by Beckie =] @ 10:34 PM. Tuesday, December 26, 2006. Wellllll yesturday was CHRISTMAS! It was a pretty good day! Well, yestur...
LifewithBeckie | Balancing a full time job, part time school, and coloring books.
Balancing a full time job, part time school, and coloring books. Liebster Award; Discover new blogs. August 17, 2015. August 17, 2015. Thank you to Meesh from MommaMeesh. For nominating my blog for the Liebster award. The answers to the questions asked of me:. How do you rid yourself of stress? Gym life. Nothing life lifting weights to get your blood flowing and help you feeling better. Are you happy with your life choices so far regarding home and career? 5 minutes. I’m totally easy going. 6 What is a h...
