brainthunders.com
Brainthunders — Support, hope and advocacy for those who live each day with epilepsy.Brainthunders is an advocacy and support page for those who live with epilepsy.
http://www.brainthunders.com/
Brainthunders is an advocacy and support page for those who live with epilepsy.
http://www.brainthunders.com/
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Brainthunders — Support, hope and advocacy for those who live each day with epilepsy. | brainthunders.com Reviews
https://brainthunders.com
Brainthunders is an advocacy and support page for those who live with epilepsy.
brainthunders.com
2010 October
http://www.brainthunders.com/2010/10
Support, hope and advocacy for those who live each day with epilepsy. From the monthly archives:. Bias and Stigma…How to Move Forward with Epilepsy Awareness. Revealed…Yet Another Side Effect of Living Life with Epilepsy. Trying to Make it as a Mom without Seizures…. Teaching and Informing the Very Young…when They are the Ones with Epilepsy. 8220;I have Epilepsy and my memory stinks, so please…when you approach me, remind me how I know you! Inspiration and Encouragementof the Equine Kind. E Fact A Day.
2010 December
http://www.brainthunders.com/2010/12
Support, hope and advocacy for those who live each day with epilepsy. From the monthly archives:. New Year’s Resolution Time…What’s Your Story? Courage…and How it Relates to Living Life with Epilepsy. Living with Memory Loss…. Cheryl's Purple Cow. Clayton's Hope Organization. E Fact A Day. Epilepsy Foundation of America. EYC: The Spot for Young People with Epilepsy. More Than Kids, Understanding People Through Photography. Out of the Shadows. PEACE: Parents Educating Arkansas about Children with Epilepsy.
2009 December
http://www.brainthunders.com/2009/12
Support, hope and advocacy for those who live each day with epilepsy. From the monthly archives:. How my dog helps me get through the toughest times with my Epilepsy. To tell or not to tell. Working with Epilepsy. Be truthful to yourself this New Year’s…set some extraordinary resolutions that say, I can take on my Epilepsy! Looking forward to 2010 as someone with Epilepsy…. Epilepsy surgery is a frightening thought, but you are drug resistant, so what are your options? Here’s how…. Larr; Previous Entries.
‘The Doctors’…and the Vagus Nerve Stimulator
http://www.brainthunders.com/new-posts/the-doctors-and-the-vagus-nerve-stimulator
Support, hope and advocacy for those who live each day with epilepsy. 8216;The Doctors’…and the Vagus Nerve Stimulator. I owe a huge thank you to everyone who complimented the segment I participated in on yesterday’s. I was especially fond of Dr. Marie Atkinson’s. Appearance and her interview. For anyone who might be considering the Vagus Nerve Stimulator (VNS). She gave a great explanation of how the device works and how someone living with Epilepsy might live with the device. May 19, 2010. It is true, ...
2010 September
http://www.brainthunders.com/2010/09
Support, hope and advocacy for those who live each day with epilepsy. From the monthly archives:. Protecting our Heads…and Protecting our Lives. Face it…Memory Loss Is and Will Always be Part of this Journey. Tragedy in Texas…Lessons Can Be Learned. Friendship and Life with Epilepsy. Abuse of the Assistance Dog Concept Hurts All of Us. Caregivers…I’m Thankful for Mine! What’s your Story? Cheryl's Purple Cow. Clayton's Hope Organization. E Fact A Day. Epilepsy Foundation of America. Out of the Shadows.
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19
Brain Blips: An Epilepsy Journey: April 2015
http://brainblipjourney.blogspot.com/2015_04_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Thursday, April 16, 2015. Rocking Epilepsy Awareness with Annie Bean. Thank you so much, Annie Bean. For being willing to TALK publicly about having epilepsy. And for not just being willing. To TALK, but actually TALKING! For educating people to the fact all epilepsy doesn't look the same. For being a great role model to my daughter- and others with epilepsy. You Rock, Annie Bean! Friday, April 10, 2015.
Brain Blips: An Epilepsy Journey: August 2016
http://brainblipjourney.blogspot.com/2016_08_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Wednesday, August 17, 2016. Medical Marijuana Journey, Weeks 2-5: Riding the Drug Interaction Roller-Coaster. We've all heard those miraculous stories about kids who become seizure free after a few doses of medical marijuana. By the end of her first week on CBD oil (medical marijuana). In fact, Awesome had as many big seizures in the first 5 weeks on CBD as she'd had in the previous 21 weeks! All the medica...
Brain Blips: An Epilepsy Journey: Thoughts on Living with Epilepsy: #1
http://brainblipjourney.blogspot.com/2016/11/thoughts-on-living-with-epilepsy-1.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Tuesday, November 15, 2016. Thoughts on Living with Epilepsy: #1. Living with epilepsy is:. Knowing that the first appropriately chosen anti-epileptic drug (AED) your child tries has about a 33-60% chance of working to eliminate seizures. Knowing that for about 66% of children,the first or second appropriately chosen AED works to control (eliminate) seizures. Knowing that if one of the dangerous medications...
Brain Blips: An Epilepsy Journey: Medical Marijuana Journey: On Objecting to the Epileptic Child as Lab Rat
http://brainblipjourney.blogspot.com/2016/06/medical-marijuana-journey-on-objecting.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Saturday, June 18, 2016. Medical Marijuana Journey: On Objecting to the Epileptic Child as Lab Rat. On its surface this argument seems reasonable and perhaps even prudent. But is it? My response includes two points:. There's something very perplexing about noting a dearth of studies about a substance which- because of it's classification as a US Federal Schedule I Drug. Think about that for a moment. The tr...
Brain Blips: An Epilepsy Journey: June 2015
http://brainblipjourney.blogspot.com/2015_06_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Saturday, June 13, 2015. Today was not a good day. Awesome had a grand mal (literally "big bad") seizure early this afternoon. The first one in more than five weeks. We had hoped to make it to her next neurology appointment at the end of June without another seizure. It's true that we think we've found patterns and so we've made adjustments, established routines. But who's to say that we're not reading ...
Brain Blips: An Epilepsy Journey: July 2016
http://brainblipjourney.blogspot.com/2016_07_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Wednesday, July 27, 2016. Medical Marijuana Journey: The First Week. Wed, June 1. Awesome declares, "Medical marijuana takes like rotten seaweed.". Her brother sitting nearby asks pointedly, "How do you know what rotten seaweed tastes like? She makes a face at him. Thurs, June 2. In the afternoon Awesome is very tired and nauseated. Despite the fact that she'd eaten very well at both breakfast and lunch...
Brain Blips: An Epilepsy Journey: Medical Marijuana Journey, Weeks 6-12: Distracted
http://brainblipjourney.blogspot.com/2016/10/medical-marijuana-journey-weeks-6-12.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Tuesday, October 4, 2016. Medical Marijuana Journey, Weeks 6-12: Distracted. This is the third blogpost about our daughter Awesome's trial of Medical Marijuana for Intractable Epilepsy. If you want to go back and read the first two blogposts, please click on these links:. First this one: Awesome's First Week on medical marijuana. And second, this one: Weeks 2-5 of Awesome's Trial of Medical Marijuana. 3) Tr...
Brain Blips: An Epilepsy Journey: March 2015
http://brainblipjourney.blogspot.com/2015_03_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Monday, March 30, 2015. Random Thoughts on Epilepsy. What comes to mind when I hear that word? Terrible, Awful, No-good things. Hideous little creatures whose only goal is to ruin my day. I mean seriously, last time, I didn't have the brain power to read a comic that I had been wanting to read all day, and I dropped my favorite stuffed animal in the toilet. But when I hear the words Epilepsy Awareness.
Brain Blips: An Epilepsy Journey: July 2015
http://brainblipjourney.blogspot.com/2015_07_01_archive.html
Brain Blips: An Epilepsy Journey. Learning about and Living with Epilepsy, a Mother/Daughter Blog. Friday, July 3, 2015. Letting Go and Taking Back to Enable Becoming. Today I watched- from the pool deck- as Awesome (10 yrs old) floated on her back from one end of the YMCA pool to the other (the deep end) and back again. This was big- for both Awesome and I- in so many ways. Awesome, just Wow! For me, today was big because of Awesome's accomplishment (what parent wouldn't be proud? No, I won't because, h...
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Brainthunders — Support, hope and advocacy for those who live each day with epilepsy.
Support, hope and advocacy for those who live each day with epilepsy. Email me: brainthunders@gmail.com. Website: www.brainthunders.com. BrainThunders.com is the brainchild, literally, of Alysse Mengason. Alysse returned to her career in corporate communications and began to live life with Epilepsy. Now, 7 years later, 5 brain surgeries later (including a Vagus Nerve Stimulator-VNS implant), a wife (yes, she married that guy she forgot! Comments on this entry are closed. Cheryl's Purple Cow. E Fact A Day.
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