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Saturday, June 28, 2008

H is for HBOT

What is HBOT you ask? Glad you asked! It stands for Hyperbaric Oxygen Therapy. It's something new in the autism community that parents are trying for their children. I am considering this for Ivy. We could buy our own chamber for about $15,000. I am not sure where I could come up with that kind of money, but where there is a will, there is a way, right?

I am going to include this YouTube video showing what HBOT is and how it works for kids with autism. Very interesting indeed.


Tuesday, June 24, 2008

G is for "GEE" and GIFTED

Like my own daughter, you will find that many kids on the spectrum are GIFTED and many fall under another classification called hyperlexia (a precocious ability to recognize written words significantly above an individual's language or cognitive skill level).



BEFORE Ivy was diagnosed with autism, I actually thought at one point she might be a baby genius. Don't laugh....I really did! Here she was just about 15 mths old she couldn't even ask for a drink, but she could read. Weirdly enough, my sister-in-law had given her this old Fisher-Price Electronic Alphabet Board and she LOVED that toy...it was her favorite. She taught herself to push the I and the V buttonson the board...like it was saying her name. She would push the buttons over and over and it was talking to her, I-V, I-V, I-V, I-V.....I thought to myself...what a little smartie she was...then a week later, I was passing through the living room, when I hear the board saying the letters J-D, J-D, J-D, J-D (we call Jade, Jadie for a nickname sometimes). Man, isn't that cute and she is awfully smart!!



Well, that you may think is not so special...even at 15mths....then listen to this. We had a box of alphabet fridge magnets in the garage left over from when Jade was a toddler and thought well, she since seems to like letters, numbers and shapes so much...maybe she would like to arrange them on the fridge like Jade did at this age. So, I send Ed out to hunt them down. Five minutes later, he comes in with the box and says, "Ivy come see what Daddy has for you". Ivy doesn't seem too interested, until he pulls the first letter out which happend to be a "G". Ivy said in her toddler talk, "sa Gee". I thought to myself...did she just say G...and if so then lucky guess little girl. :)



Then Ed pulled out the next letter which was an "S". Ivy said, "sa, Essss". And then Ed & I looked at each other and said, "whoa...how does she know these letters"....and then quickly followed by a "nah...that was just a freak thing". So Ed pulls out a third letter and this time he puls out an "X". Ivy gets excited and says, "es EXXXXXXX". Then I just about choked on my own breath. I said, "Pull another one out, pull another one out!!!" So, Ed continues to pull random letters from the box.....and to add to storyline here....there were actually two sets of magnets in the box...both upper and lower case letters and I want you to know that she guessed every single one of them right except one. When Ed pulled the lower case L out, she said it was a number ONE......not bad and very close IMHO. We had NO CLUE how she learned the letters at such an early age. We had never worked with her on the alphabet either. She had that electronic alphabet board and that was it. SHE MUST HAVE TAUGHT HERSELF!!



So, it started there with the box of refrigerator magnets. A few months after that, while driving down the road, she rattles off....T-A-C-O-B-E-L-L....TACOBELL!! And then stuff like, S-T-O-P....STOP!!! J-A-D-E...JADIE!!! I-V-Y....IVEEEEE!!!! She was so amazing, I really thought she was gifted for her age. I mean her favorite books were What to Expect When Expecting and What to Expect The First Year. She loved those books and would spend hours looking at them intently and turning each page to soak it all in. It didn't surprise me when she starting reading little words in books by age two at all. Dr. Suess was her favorite and she was reading by herself by age three.

After letters came numbers, shapes and colors. She loves them all and her world revolves around numbers, sizes, shapes, calculations etc. Ivy has something called sight counting. She can look at something and know how many there are without even counting. An example of that was when she was four, we went on a field trip with her pre-school class to the Indy Zoo. We walked into the Penguin House and she got all excited and yelled out, "Look!!! It's thirty-seven penguins!!!"

Her teacher and I just looked at eachother and laughed, then I stood there looking at the penguins and started counting the little ones standing on the ledge...and yes, you guessed it...there were thirty seven of those little penguins lined up in a row! Amazing, isn't it? Well, the following July4th, we went to watch the firework show at the local high school football field when she watched she would yell out things like, "oh, it's 200 stars"....."ooooh! It 437 stars"...and this went on through the entire show yelling out numbers every time one went off. We laughed and I can't count that fast, so I will take her word for it that she counted correctly.

Ivy also loves to keep track of people's birthdays ands how old you are. She never meets a person without wanting to know when your birthday is and she will then file it away and tell you if she knows anyone else that has a birthday the same day and who else has one in the same month. She really is amazing when it comes to this. I can't tell you how many birthdays this child has memorized.

She loves the weather and knowing how many degrees it is and if it's sunny, cloudy, windy, rainy, etc. She wants to watch the Weather Channel in the mornings, not cartons. She HAS to know what the temperature is outside now and what it will be today and tomorrow, etc.

I guess as I reflect back now as I type, she really is GIFTED. She is a gift. She is my gift from God and who am I to question that?

Sunday, June 22, 2008

F is for FRIENDS, FAMILY & FAITH

When you have a child that has autism, you will need all three of those things in order to survive in life. I love how Jenny McCarthy described in her book, Louder Than Words when someone's child is diagnosed with cancer, they rally around you and grieve with you and cook for you and hold your hand...but when your child is diagnosed with autism...people stop calling you for play dates, dinner and shopping and they avoid you out in public, lose your phone number and they say things like, "she just looks so normal". Yeah, you're right, she DOES look normal, but you aren't with her 24/7 like we are. You aren't there to see the midnight meltdowns and what happens when you feed her food she isn't supposed to have while she is with you (the after effects which are never while she is with you....it's always hours later when it kicks in and usually lasts for DAYS after).

You aren't there when she is on sensory overload kicking and screaming because she wants to wear a dress and there are none clean and nothing else will do and she has verbal barf and looks like Linda Blair from the Exorcist spewing split pea soup. You aren't there to see her cry when she can't make any friends and no one wants to play with her because she is different. You aren't there to see those little things about autism that no one else except her mom, dad and sister know about. That's the part people do not understand. She seems so normal on the outside, doesn't she? That is the part that makes it so difficult for friends and family to understand.

When it comes to friends and family(aka F&F), you have to have a support network of some kind or you will get sucked into the black hole of autism. Autism rules your life and it dictates how every little thing will happen in your daily life. I don't care how good of a dispostition you have, when autism rears it's ugly, ugly head....you better run for the hills or else it will sweep everyone away in it's wake. After a time living like this, it's starts to chip away at your soul...your spirit...your sense of self. You start to lose faith that things are ever going to get better.

Like I said, what families with ASD kids really need in their lives is a great support network. They need people to take one or more of their children overnight so the parents get some together time (soooooo many ASD families end up divorced due to the stress). They need to offer to cook dinner once in awhile for the exhausted moms. They need someone to offer to help them clean and organize their homes (most ASD mommies are too frazzled to organize anything after a time). They need someone to offer to drop by and watch the kids while you run errands for a couple of hours. That's the kind of support you need. What we need is for you to believe us when we say she can't eat wheat and dairy, that we mean it. We need to be trusted that we know our child better than you do and respect our rules when it comes to food. What we need the very most from our F&F's though, is just a shoulder to lean on. ASD parents need to be able to blow off some steam and get out their frustrations (because there are many). I wish the F&F's of ASD families understood these simple gestures. Reaching out to ASD families is all that is needed....for someone to say, "I see you struggling and I am here....what can I do to help"?

Last that brings me to FAITH. Faith is something I have always had until recently. I think that I am so exhausted, so frazzled, so disorganized, so behind, so lost and so empty from autism sucking the life out of me that it's really hard for me see past the mountain of doubt standing before me. I know the way to get the faith hook-up...I just can't seem to get around that dang mountain. When I feel my faith start to slip away, I always begin to isolate myself. I withdraw within. I hide out and feel sorry for myself and wallow in my own self-pity. I hate being there. I hate that I am that person...but that's just how I feel right now. I feel like I have no faith that things will ever get better for us. I feel helpless and alone. But as a parent of an ASD child, I have had to have FAITH that all that I have done is worth it. All the heartache,sleepless nights and all the sadness is worth it. My faith is what keeps me from completely sinking under. Even though at times I feel like I am white knuckling it...I know that if I just hang on...God's going to send someone out to dig me a tunnel so that I can get through that stupid mountain. So to all the ASD parent's out there...hang in there and have FAITH! That mountain will move, eventually......

Saturday, June 21, 2008

E is for ESSENTIAL FATTY ACIDS

This is another supplement used in the DAN! protocol. Most people that eat the standard American diet (SAD) could benefit from using EFA's since most of today's food is completely depleted of the EFA's. Here is an article written by Deborah Matthew, MD pertaining to the use of EFA's and why they work.


Autism is the fastest-growing developmental disability in the US, currently diagnosed in 1 in every 150 children. It is more common than pediatric cancer, diabetes, and AIDS combined. Despite these statistics, Autism remains poorly understood and often difficult to diagnose. This is partly because Autism is a spectrum disorder, meaning it manifests itself in many different forms. Some children with Autism may rarely speak and have difficulty learning to read or write, while others are so high-functioning that they are able to attend classes in a mainstream school. Unfortunately, there currently is no cure for autism. There are, however, some interesting theories on Autism that lend themselves to dietary interventions that may prove beneficial.

One theory is that Autism may be partly caused by a problem with metabolism of essential fatty acids (EFAs). EFAs are compounds that cannot be made in the body, but are essential for many biochemical processes. For some unknown reason, the brains of individuals with Autism may have problems converting EFAs from foods into the forms necessary for many biochemical reactions. When these biochemical reactions fail to take place, they lead to the signs and symptoms of Autism.

EFAs fall into two major categories: omega-6 and omega-3 fatty acids. Omega-6 fats are found in milk, eggs, meat, grains, processed foods, and many cooking oils, whereas omega-3 fats are found abundantly in flax seed, walnuts, and fish such as salmon, halibut, mackeral, herring and tuna. The relative ratio of omega-6 to omega-3 fats is critical to the health and development of the brain. As the levels of omega-6 fats rise higher and higher, there can be negative effects on cognition, mood, and behavior. As our society has become more dependent on processed foods, levels of omega-6 fats have risen. Many believe that this has helped contribute the increasing prevalence of Autism.

The major omega-3 fatty acids are DHA and EPA. Both DHA and EPA have been found to affect many aspects of brain function. Studies in rats have shown that changing the amount of EPA and DHA in the diet can alter the amounts of certain critical chemicals in the brain. Currently, there have been only a handful of studies on the effectiveness of omega-3 fat supplementation as a treatment for Autism. However, in those studies done so far, there appeared to be an improvement in overall health, cognition, sleep patterns, social interactions, and eye contact in Autistic children given supplemental EPA and DHA. Further studies are needed.

There has been no research on the optimal dose of EFAs for treating children with Autism. The dose range in current studies is 540-2320 mg of omega-3 fats per day. Doses in this range do not appear to cause any significant side effects. As long as EFAs are less than 10% of total dietary intake, they are considered safe. However, it must be noted that fish oil supplements can contain contaminants such as mercury, hormones, dioxins, and PCBs. Thus, care must be taken when purchasing fish oil supplements to find those that have been purified by molecular distillation and are described as pharmaceutical grade.

As the incidence of Autism continues to rise without a definitive cure, novel therapies must be considered. The negligible risks of omega-3 fat supplementation are far outweighed by the potential benefits, so it appears that this treatment should be considered in those suffering from Autism.

We use EFA's for our whole family, not just Ivy. We only use Nordic Naturals. They are by far the best on the market.

Friday, June 20, 2008

D is for DAN!

DAN! stands for Diagnose Autism Now! This is the protocol we have used to recover Ivy from autism. Many people chose this route. It is a biomedical treatment for autism. If your child or someone you know has a child that has recently been diagnosed with autism, I highly recommend you find a DAN! doctor in your area. They specialize in the treatment and recovery of autism.

What Is the DAN! Protocol, and What are DAN! Doctors?

Defeat Autism Now (DAN!) is a project of the Autism Research Institute, founded in the 1960's by Dr. Bernard Rimland. DAN! doctors are trained in the "DAN! Protocol," an approach to autism treatment which starts with the idea that autism is a biomedical disorder. Specifically, DAN! doctors feel that autism is a disorder caused by a combination of lowered immune response, external toxins from vaccines and other sources, and problems caused by certain foods.

What Do DAN! Doctors Prescribe?

Many regular physicians or pediatric physician's do not conduct extensive medical testing for autism, because they believe, incorrectly, that the only useful medical treatments are psychiatric medications to reduce seizures and behavioral problems. Some of the major interventions suggested by DAN! practitioners include:

-Nutritional supplements, including certain vitamins, minerals, amino acids, and essential fatty acids


-Special diets totally free of gluten (from wheat, barley, rye, and possibly oats) and free of dairy (milk, ice cream, yogurt, etc.)


-Testing for hidden food allergies, and avoidance of allergenic foods


-Treatment of intestinal bacterial/yeast overgrowth (with pro-biotics, supplements and other non-pharmaceutical medications)


-Detoxification of heavy metals through chelation, B12 shots, etc

View the list of practitioners who have agreed to assist families with autistic children in pursuing the DAN! approach.

Thursday, June 19, 2008

C is for CHELATION

This is a type of therapy/treatment for the symptoms of autism.

We personally have chosen to NOT use chelation with Ivy. I could have really missed the bus here, but so much controversy has surrounded the treatment that I wasn't convinced it was in her best interest. I was lucky that Ivy responded well to other types of therapies. I had to use my "mommy instinct" and I have just shied away from the treatment thus far. I researched and chose an alternate method in clay baths. They are all natural and holistic. We use these baths here: Kids Clay . But I do want to say that I have read and heard from many a parent that have said, chelation has brought their children out of autism or greatly improved their symptoms. So, to the warrior moms that have tried it and were successful, I stand behind you 100%. You rock!

Because this is such a widely recognized therapy for ASD kids, I felt I had to present it to you. The following is an excerpt from Dana's View web page. Dana has a wealth of information on her website and it has been an invaluable tool to me over the last 4 years.

Several ASD researchers theorize that many ASD children have a genetic predisposition to metal injury, and the metals found in vaccines or other environmental exposures trigger a biological response which is manifesting as autism. There is also some evidence that several other diseases are also a result of metal toxicity, including allergies, asthma, fibromyalgia, memory issues, and depression. For a more complete list, click here.

Removing the metals from your child’s body is called "chelation" [key-LAY-shun]. This process is not without risks, but it has the potential of producing the benefit of your child significantly improving in functioning, even potentially to the point of no longer qualifying as autistic. But because it does have risks, you need to research it and determine for yourself if it is something you would like to consider for your child.

Chelation is a slow process, to make it as "safe" as possible, minimizing the chance of potential risks. Many children do show improvement rather quickly, but it can take as long as two years to realize the full effect of any improvement which will be related to chelation. And, if your child is NOT metal toxic, chelation will have basically no effect.

If you would like to learn more about chelation (because it's not really easy to explain) click here.

Wednesday, June 18, 2008

B is for BEHAVIOR

It took me a long time to understand that behavior is communication with ASD kids. Once I got that through my thick skull though, I was able to use it to my benefit. Now when Ivy gets cranky, irritable or discontent, I know there is an underlying issue at hand and it's up to me to figure out what the "real issue" is, so we can move forward. The following is an excerpt from Ellen Notbohm's TEN THINGS YOUR STUDENT WITH AUTISM WISHES YOU KNEW.


For children with autism:


Behavior is communication. All behavior occurs for a reason. It tells you, even when my words can’t, how I perceive what is happening around me. Negative behavior interferes with my learning process. But merely interrupting these behaviors is not enough; teach me to exchange these behaviors with proper alternatives so that real learning can flow.


Start by believing this: I truly do want to learn to interact appropriately. No child wants the negative feedback we get from “bad” behavior. Negative behavior usually means I am overwhelmed by disordered sensory systems, cannot communicate my wants or needs or don’t understand what is expected of me. Look beyond the behavior to find the source of my resistance. Keep notes as to what happened immediately before the behavior: people involved, time of day, activities, settings. Over time, a pattern may emerge.



**On a side note, we went swimming today and had a little fun. Ivy conned me out of a hot dog on a real wheat bun today...behavior tonight? You betcha!!! Anytime we do dietary infractions, there will be a consequence to that (much to my disadvantage). But sometimes, you just have to let a kid be a kid and swim and have a hot dog on a bun all in the same day! Right now she is happy as a lark and I am happy that she is happy. :)



Tuesday, June 17, 2008

The ABC's of Autism

Many people ask me exactly what IS autism??? I can never really answer that with a simple description. Fact is, autism is very, very COMPLEX. It affects many parts of the body and no two children have the exact same symptoms. My only experience with autism prior to Ivy being diagnosed, was of Dustin Hoffman's portrayal of an autistic man in the movie Rain Man. I do not believe that the 1 in 150 kids being diagnosed today are of the same type of autism. I believe that there is something much more complex about today's autism. I don't buy into the theory that the rise in autism is due to better diagnosing. In fact, I think that is a load of crap. I think the autism of today, is being triggered by outside interferences such as vaccines, exposure to heavy metals, poor diet, nutritional deficiencies, amalgam illness, poisoned water supplies, pitocin overuse, and the list can go on and on.....

So, over the course of the next 26 days I am going to give you autism from A to Z. Each day I will write about something directly related to autism be it an explanation, treatment, therapy, etc. I hope by the end of the alphabet, you will have a much better understanding of autism. Enjoy!

A is for AUTISM

:: Autism is a bio-neurological developmental disability that generally appears before the age of three.

:: Autism impacts the normal development of the brain in the areas of social interaction, communication skills, and cognitive function. Individuals with autism typically have difficulties in verbal and non-verbal communication, social interactions, and leisure or play activities.

:: Individuals with autism often suffer from numerous physical ailments which may include: allergies, asthma, epilepsy, digestive disorders, persistent viral infections, feeding disorders, sensory integration dysfunction, sleeping disorders, and more.

:: Autism is diagnosed four times more often in boys than girls. Its prevalence is not affected by race, region, or socio-economic status. Since autism was first diagnosed in the U.S. the occurrence has climbed to an alarming 1 in 150 people across the country.

:: Autism does not affect life expectancy. Currently there is no cure for autism, though with early intervention and treatment, the diverse symptoms related to autism can be greatly improved.

Monday, June 16, 2008

50 Things I Like About Myself

I recently had the opportunity to meet some fantastic people when we went to DC to the Green Our Vaccines Rally. One such couple was from NW Indiana, named Jacob and Arianne. Arianne is a phenomenal blogger. I have been reading her blogs since we got back from DC and she is such a talented writer and she has 2 boys with autism. I think she is line for Sainthood, only she doesn't know it. So we don't really "know" each other, but we walked together in the march in DC and we just have a common bond with our cause in life and our children, but I feel like I know her better since reading her blogs, ya know? I think she is really cool and I think if we lived closer, we could totally be friends. But, to my point of this whole post...she recently blogged about something and challenged her readers to it as well.

She asked if you can think of 50 things like about yourself. She posted her list and asked her readers to do the same. So, here goes, here is my list and I ask the same of you, make your list, and post the link to your blog in a reply, so we can all see what you like about yourself as well. Good luck, clear your minds and get to typing. I know you can find 50 things if you try hard enough. Every now and then, I think it's good to reminds ourselves, why we love ourselves.

50 Things I Like About Myself

1. I am funny

2. I can take a joke and make one too

3. I love life and all it has to offer

4. I love traveling and love to see the world

5. I like that I am able to see past color, race or sexual orientation in people

6. I love children and think I connect well with them

7. I love music and how it can affect my mood

8. I love God and considered myself one of his "girls"

9. I am crafty when I have time

10. I have good decorating skills

11. I like my sense of style in clothes

12. I am a loyal person

13. I am a good friend

14. I am a good mom to both Jade and Ivy

15. I am a good sibling and look out for them and play the mother hen roll well

16. I am a hard worker

17. I am a good employee and you'll get your money's worth out of me always

18. I love to read and learn new things

19. I am always open minded

20. I am willing to try new things, twice if I like them

21. People fascinate me and I love to meet new people

22. I am a collector of friends, old and young both

23. I am a cat lover

24. I am pretty knowledgeable about autism

25. I am a good advocate for my daughter with ASD

26. I am willing to fight for her

27. I am willing to do whatever it takes to make her life better

28. I am willing to do without so we can have money to treat her

29. I always try to see the good in people

30. I am a pretty positive person and try to spread that around

31. I like the color of my eyes

32. I think I have good taste in men, (ie my husband)

33. I am eccentric and I like being that way

34. I am computer knowledgeable

35. I love living green and am willing to share tips and resources, etc with others

36. I like living simply whenever possible without all the fluff

37. I am content most of the time

38. I would stand up for you if someone was bad mouthing you

39. I despise gossip and usually walk away rather than participate

40. I love taking pictures of my family and do it often

41.
I can dance fairly well and I wanted to be a professional dancer when I was in high school.

42. I am compassionate towards others

43. I have passion for a cause and will go to the ends of the earth to see it through

44. I have really good intuition and use it my advantage

45. I have really good mommy instincts

46. I don't worry about what other's think of me or what the neighbors say

47. I know life is short, I get that

48. I live my life like there is no tomorrow most days

49. I love easily

50. I am not just any Lisa


Saturday, June 14, 2008

~Super Sexy Swingin' Saturdays~

Saturdays ROCK. There is just no other way to describe them. They are my most favorite day of the week, with Friday's trailing a close second place. I live for the weekends.

I just love Saturdays and here are some of the reason's why:

~Sleeping in
~I actually sometimes eat breakfast on Saturday mornings
~Can be used as as excuse to stay in your jammies all day
~Can be used as a NO shower day (come'on admit it, you've done that too)
~HGTV marathon days (and I mean ALL DAY LONG)
~Catching up on the mail from all week (b-o-r-i-n-g)
~Putzing around the house doing nothing
~Cooking out and having friends over
~Swimming at my brother's house
~ Laundry catch-up day
~Yard work and gardening (one of my fave's)
~Honey Do List day (altho my hubby HATES these kind of Saturday's, heh...heh...)
~Project Day (usually something I learned from HGTV marathon day..wink, wink)
~Ordering out for dinner
~Blockbuster Movie Marathon's


Oh heck, I could go on forever, but I think you will agree with me that Saturday's are the most, bestest day of the week!

Hope you enjoy your Super Sexy Swingin' Saturday yourself. We are off the St Michael's Parish Festival where Ed is painting faces, and I am manning the corn on the cob booth! The kids have plenty of carnival tickets to blow...it should be fun for all!

Thursday, June 12, 2008

I love JUNK SALES!!!

I am a professed junk sale junkie. You know what they say, right? One man's trash is another man's treasure? Well, I love to go to trash sales. Love it, love it, love it!! I went today and got lots of goodies to put on eBay. I will be loading my store all next week and I am starting to get excited about it. I think it's the thrill of the hunt that makes me so giddy. I spent $50.00 today and got stuff that will generate about $300.00 - $400.00 in sales. You can beat that people.

So, while I am having trouble focusing on THIS week, I have a clear cut plan for next week. I will be getting my eBay stuff ready this weekend, my postage machine set up, boxes out, etc and I'll create my templates this weekend too and then I will be ready on Monday to shoot photos, upload and send to eBay. By Friday or Saturday, I will be rolling in the Jefferson's. :)

I went to dinner with a girl friend last night. I took her for her birthday, we went to Ritter's after and had something called a Monkey in the Middle. I highly recommend the little Monkey...it was like a little tiny banana split. One scoop of Vanilla or Chocolate ice cream, covered in strawberry syrup, with a slice of banana and whip cream on top if you like. It was yummmmmy!!

I recently became reacquainted with Facebook and I am so addicted to it. I need to step away from the computer and stop playing around on there. Look at this little pretty thing I made while there:



Okay, Happy Thursday to you! Sorry I have nothing more exciting to share with you today.

Tuesday, June 10, 2008

Now What?!?!?!?!?

Well, I have to admit, that since we got back from DC, I have found myself extremely restless and I have been pacing the floors not quite sure what to do with myself yet. I know it's summer vacation and I know I need to get busy and get some stuff listed in my eBay store, but I find myself unable to start anything. I thought maybe I would clean house today, or go to the grocery and get some food, but I accomplished neither today.

What I did do, was call an old friend and went and visited with him. He has been ill for a few years and he just recently moved back into the area and we used to be roomies once upon a time. He recently lost his partner of 13 years and he has been really depressed. I have to say that at times, when you are so full of yourself that you can't stand it, talking to someone else and just listening to them, really helps a lot...it can really get you outside of yourself I mean. You can't be focused on yourself if you are giving someone else 100% of your attention. He needed that today and so did I. I am so glad we were able to catch up and laugh about old times too.

So, I keep pacing, my feet keeping moving and my brain is unable to catch up. I am not sure why I am so restless. I feel like I am doing nothing but walking in circles today. Maybe it's just coming down off the high of being in DC. All, I know is that I need to get focused again and get back on track. I just feel like I am in some sort of funk. Mental exhaustion maybe? I keep going back to YouTube and watching the Rally speeches and trying to decide what I can do to help...to really make a difference. I hate to think that we went through THAT much getting there and spent all that money to go and be a part of it and now it's just over. I feel like I need to do more. Now what????? Hopefully, the universe or God will reveal my purpose in the whole thing to me soon. I don't like not knowing what I should be working on.

I need to thank everyone again that donated to the cause no matter how little you gave or if you gave lots, it was so very much appreciated and I will never forget your generosity. Also, thanks to all who continually prayed for us and kept us in your daily thoughts...also appreciated.

Peace,
Lisa

Monday, June 9, 2008

Doing the Happy Dance we are home!!

After a very hot Saturday morning spent with a friend at the Zoo, we headed to the airport and back to sweet home Indiana. Ivy had the grand daddy of them all meltdowns at BWI Airport before boarding the plane. I had people looking at me and her and staring and for the first time in years I felt the need to explain her behavior. I was mortified. She kicked the poor man sitting directly to our left and the poor lady to my right, just kept looking at her like she was a real brat and the couple behind us was also staring and saying things like, "can you believe the way she is talking" and "omg, what a brat". So, really LOUD, I say, "I'm sorry everyone, she really isn't being bad, she has autism and she has just had a really long and loud week here in DC and she is on system overload, please excuse us". Everyone just shut up and quit staring after that. I think I embarrassed Ed when I did that, but I hate it when people stare at us and assume my child is misbehaving when she can't really help it. Makes my blood boil. I can't NOT say something.

I then proceeded to the counter and begged for a special pre-board pass which they quickly honored. So, we got home in a little over an hours' flight and when we were exiting the plane, Ivy began hopping and flapping like a birdie and dancing and skipping and smiling from ear to ear. She was more than ecstatic to be home. Yeah for you little Ivy, it's so good to see you smile!


Happy Ivy, Happy Jade

video

The Happy Dance

The Rally's over now...so let's vacation!!!

Well, we decided before ever leaving for DC, that we would take the kids and make a family vacation out of it. Can you say "probably not such a good idea"? Washington DC is LOUD, CROWDED, BUSY, NOISY and HOT, HOT, HOT!!! Not the best place for your 7 yr old autistic, sensory overloaded little canary.

Each time we tried something new, Ivy was resistant to that. Her favorite thing was staying in the hotel room, swimming in the hotel pool, eating and the riding the Metro. So, here are some pics of our family trying to have a good time after the Rally.

After the Rally, Jade giving the food 2 thumbs up!!!

I'm exhausted after being in the sun and heat for 4 hours, Ivy is feeling good though!!

Cool shot of Union Station

Love this shot of the Metro Station

The Old National Postal Building, downtown DC

Jade fanning herself At Hard Rock Cafe' with a lettuce leaf...

Me goofing off with my new boyfriend.....

Ivy gets to relax some

The girls being silly together

If we get crowned Miss America, we would strive for World Peace.....

One last shot of horse play in the pool

Riding the Metro...yipppeee!!

I'm so happy on the Metro!!

We had an awesome opportunity to see the Washington Nationals play, thanks to their pitcher Tim Redding who gave us the best seats EVER!!!!! Beautiful night, beautiful ball park, thank you for being SO GENEROUS to our family. There were a couple of people behind the scenes that made this possible for our family, you know who you are and I thank you too!!!

Jade at her first ever professional Baseball Game, she had a BALL!!! (no pun intended, LOL!!)

Ed whistling Dixie....his first ever Pro baseball game as well

Ivy could care less about baseball apparently because it's TOO loud, too hot and too many people at the game. As you can see, she is NOT happy here.
All she wanted was a dang a hot dog!!!

leaving the park

The Smithsonian Castle

Jade in front of the Castle

Loved the gardens and this unusual bush/cactus plant

Jade & Ivy sitting by a pretty fountain in the Botanical Gardens


The Fountain

More flowers, so pretty!

Beautiful Roses in bloom everywhere

The prettiest flowers in the Garden

Ivy riding the Carousel.
It has been there since 1967 and in operation since it was erected.

Jade riding too

I love me some Granny Smith's mom!!

Snacking a little bit and resting a LOT

Please stop whining!! I want to go home!!!

The Museum of Natural Science

The inside of the Museum in the foyer. Ivy had meltdown number FOUR here and she and I left and headed back to the hotel for some much needed decompression time. Ed and Jade stayed on and did some more sight seeing here and at the American Indiana Museum.

Jade sitting pretty by another Fountain, Old Town Alexandria
She is so beautiful here.

Same fountain, me and the girls before dinner with friends


My little yellow canary, she is going to change the world someday...


Jenny Video

My favorite part of the Rally, view this after you have read the update.

Sunday, June 8, 2008

The Final Chapter on the Green Our Vaccines Rally

Well, we are home and we are all completely exhausted. I cannot begin to express the emotions I am feeling at this moment now that I have had time to sleep on it and really, really think about what I have experienced. I think for me, it was one of the most special moments in time for me. Behind getting married and having my children....it was just the most amazing thing to witness and be a part of.

It rained the day before the Rally and the forecast called for 80% change of thunderstorms the day of the march. We were sure we were going to be walking in the rain. Lo and behold after much prayer I am sure...the morning of the Rally, we awoke to partly sunny skies and 85 degree weather, which lasted until after the Rally was over and then we experienced a torrential downpour and a scary tornado warning. Tell me that was not DIVINE INTERVENTION for you.....

Wednesday, Day of the Rally

We ate breakfast and got ready to leave for the Rally and met up with some other local families from Indiana and Donna from Arizona (loved her).


Ivy eating Fruit Loops



Jade doing the same thing



Ivy showing us her sign



Jade's sign


Lisa Fox and Maria Janik founders of IBK (Indiana Biomedical Kids)
Donna from Arizona, Ed and the girls waiting on the shuttle to take us to the Rally

Waiting for the Metro to take us to the Rally:


We took the Metro to the Smithsonian and then started at the Washington Monument:



Washington Monument from across the street



Waiting for the light to change to cross the street, doing ok at this point



Up close



Lining up beside the Monument




A Sea of Green 8400+ people there!



Ed & I waiting to start walking


video


The start of the walk...traffic had to wait on all 8400 of us to file out onto Independence Street



video


Walking with our new friends Jacob and Arianne


video



More walking....with our new friend Donna from Arizona


video


We made the mile and a half walk to Capital Hill...woo hoo!!!!!!!!



Coming on the Capital Lawn



Waiting on the press conference to start


video


More waiting....





More waiting....

A huge bouquet of flowers presents by the MOMS (Moms Against Mercury)
There were 150 white flowers and 1 yellow sunflower to represent
1 in 150 kids diagnosed with autism.



There were several speakers at the Rally including:

Dr. Jay Gordan (Jenny's son Evan's doctor)




Boyd Haley, PhD



Dr. Jerry Kartzinel


Robert F. Kennedy, Jr



Amy Carson from Moms Against Mercury



Jim Carrey



Jenny (Miss Thang) McCarthy:





As I listened to each speaker talk, I decided that I want to be doing more than just flying to DC to attend the Rally. I am not sure exactly what the "more" is yet, but I know with some time to let the whole experience really soak in, I will come up with an answer to that. In the meantime I will just keep on keeping on and hope that one day, our time WILL come. I am going to do as Jim Carrey asked of us and dare to envision that our vaccines are already greener, that there is already a safer vaccine schedule and it is now being spread out and that there is a future generation with no autism because of days like today where we have rallied together to tell our government that we are not going to stop talking until someone listens to us and makes a much needed change.


Loved this guys license plate.

My Video of Jenny