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Labels: epilepsy, epilepsy awareness bracelet, epilepsy isn't waterproof, fundraising, Sharon's Ride Run Walk, sharon's ride.run.walk
Labels: epilepsy, epilepsy awareness bracelet, epilepsy isn't waterproof, fundraising, Sharon's Ride Run Walk, sharon's ride.run.walk
Labels: An inspiring true story of healing with the Edgar Cayce remedies, book recommendation, curing epilepsy, epilepsy, Jody's Journey, Linda Caputi
My son Elijah has a mild form of cerebral palsy. He was recently diagnosed with epilepsy in the spring of 2007. We've been treating his condition using natural methods. This blog is a documentation of our experiences. Our goal is to help others who may be going through similar health challenges. Together we can overcome whatever challenges come our way so that we may live full, happy, vibrant, and healthy lives.
Hi. I wanted to share that I was having daily complex partial seizures until I went on a raw foods diet. I started the diet after being partially a raw vegan - but once I went all the way raw I haven't had one seizure now for close to seven weeks.
I just ordered the book by Dr. Graham, the 80-10-10 diet because this is close to what I have been doing on my own already.
I feel close to normal, and my energy level is great, and my brain is healing more all the time. I am able to do things and tolerate a lot more stimulation, and starting to feel like I am supposed to. HEALTHY!
We're currently controlling my son's complex partial seizures with a high-raw diet. He eats mostly fresh, raw fruits, veggies, nuts, and seeds. Occasionally he will have a homemade salad dressing that may contain one or two non-raw ingredients. He may also have a baked sweet potato or steamed veggies (without spices or condiments) once a week or so. He doesn't complain about eating this way. He's not singled out. Our entire family is eating this way as well and we've seen loads of benefits. I just wanted to start this thread to give a place where those of you with questions can feel free to ask them. I also wanted to share this video that I found this morning. Another girl cured her epilepsy and came off medication by changing over to a raw foods diet.These are so exciting. I wish I'd have started learning about the raw food diet years and years ago. But I'm so glad it's catching on, and people are becoming aware that what they eat affects their health in major ways. I feel like a bit of a hypocrite though, since I'm not on a totally raw diet yet. I'd guess I'm at about 20%. Working my way up. I just thank God that I don't have any major illnesses that demand a sudden, drastic change in diet. But I do know that if I want it to stay that way, then I better ease my way into it while it's still voluntary!

Labels: acord d'orsay, acorn slippers, curing epilepsy, epilepsy, organice footwear, raw food diet
Labels: epilepsy, epilepsy awareness bracelet, epilepsy isn't waterproof
Labels: bracelets, donate, epilepsy, epilepsy awareness bracelet, epilepsy isn't waterproof, ozville, ozville.org, Sharon's Ride Run Walk, sharon's ride.run.walk, silicone bracelets

some gummy worms, fruity bears, and gummy swirls. None of them (no, I didn't expect the gummy worms to be sour) ended up quenching my SourPatch Kid craving, but they're darn good candy! They're made by Surf Sweets. I also picked up some organic M&M's. So good. They're called SunDrops, by Sunspire. Mmmmm. I actually really like the almond ones, but the peanut was on sale. You have to get these. They make M&M's taste stale.Labels: epilepsy, make money online, organic, Sundrops, Surf Sweet
Labels: epilepsy, epilepsy isn't waterproof, Green, Sharon's Ride Run Walk
Labels: earth day, epilepsy, epilepsy awareness bracelet, Green, mobile home, news article, ozville, sharon's ride.run.walk
As you probably know, one of this site's main focuses is epilepsy awareness and safety. Today, while I was searching the net for some epilepsy-related news articles, I came across a website that I had somehow missed before. CureEpilepsy.org was started in 1998 by Susan Axelrod, whose daughter Lauren suffers from epilepsy. Citizens United for Research in Epilepsy (CURE) is a nonprofit organization dedicated to finding a cure for epilepsy by raising funds for research and by increasing awareness of the prevalence and devastation of this disease. On their website they state that "Since 1998, the budget for epilepsy-related research has increased 25% at the National Institutes of Health (NIH)." Isn't that great?! They accept donations, which you can give by clicking HERE. I recommend watching a few of the videos they have on their video page. The 2006 video features Hillary Clinton and Barack Obama. I have to say, I like the video I made better, but these are informative, and not terribly long (about 7 minutes each).Labels: CURE, cureepilepsy.org, epilepsy
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