Day 87: July 31st, 2013

It’s a good news sort of day.  I found out recently, that my husband’s deployment will not be 180 days, but I still plan on counting down to 180 days, because it just doesn’t make much sense to me to change the title, now.  We are actually well over 50% complete on this deployment, and I was looking at the calendar, and the next 8 weeks before he comes home are going to be booked!  There are 3 projects I have to complete– the landscaping project which is well over 50% complete, painting my room, and painting the kids’ rooms.  I would like to do a garage sale and get rid of some clothing.  I would very much like to buy some new furniture or something as a treat saying that I got through this relatively unscathed.  Yesterday I booked a golf trip I had won at a local autism event, and we have another kid-free weekend planned over Veteran’s Day weekend.  I have so much to look forward to, even though there are a few things mixed in that I’m not anticipating.  You take the good with the bad.

Day 88: July 30, 2013

Just when you think things are going well, Jeremy Hilton posts a copy of the latest filing from Tricare to the US Supreme Court, and that particular filing explains why they relented.  Sadly, I can understand why this is happening.  I understand that costs need to be cut, and there are some children on the spectrum that really don’t need intensive ABA therapy to survive.  Look at me, I didn’t have any therapy until I was in my 30s, and while some behavioral therapy would have helped me a little bit, I would have been fine without it.  I probably would have gotten more out of going to OT and perhaps some speech therapy.  I even understand the utmost importance of doing parental grading and involvement.  Why should the government spend hundreds of thousands of dollars on a child, when the parent just undoes everything at home?  What bothers me about this whole thing is the underhandedness regarding it.  And the sad fact that no other medical condition requires this.  The outrage would palpable if we were to do this to diabetics– you don’t watch your diet, you don’t get insulin; or people who are morbidly obese.  Yet why autistic kids?  With the cuts in ABA therapy, cuts in respit care for both adults and children on the spectrum, and cuts in compounding pharmacy coverage– it just seems to me like they are attacking families on the spectrum.  I don’t see them attacking my neighbor with cuts– she had breast augmentation surgery after breast cancer, and instead of a traditional implant, she got an expensive experimental implant grown out of her own tissue.  While I think she should get implants, I don’t see her experimental boobies being more medically necessary than a child’s therapy.  The military has an extremely high number of children on the autism spectrum– could be the environment in which they are born into, and the stress of being a military family, could be the type of people who join the military, or could be the stress of being a military wife.  It just seems unfair to take away so much to such a large population when there are other places that desperately need cuts.

Day 89: July 30th, 2013

I worked hard today and went way beyond my comfort zone.  A small surprise project is turning into an expensive, gut wrenching endeavor.  Today, I removed 24- 50 pound concrete blocks from the garden.  I was drenched in the 2 hours I spent doing the task, then I moved the border from inside my van to the end, installed the lighting, and started moving the rock from my car.  Unfortunately, I accidentally left the gate open, and spent another few hours looking for Sadie.  At this point during the day, I’m spent, absolutely physically and emotionally exhausted.  I feel like I just ran a marathon.  I hope tomorrow, I will have the energy enough to move the rock again.  I would very much like to have this project done before I leave for Disney World, next Thursday.

Days 93-90: July 24th-July 28th, 2013

I bid my final farewell to an old life, that I didn’t like anyway.  I mailed off my last Louis Vuitton bag.  It is freeing in a way.  I feel no longer tied to the old feelings towards my former friend.  Letting go of that bag was like letting go of my friendship with her.  I had no hard feelings about the bag, I didn’t care one way or another.  And that’s the same way I feel about her– no hard feelings.  I feel relieved, and I feel like I can move on with my life.  I don’t think she is a bad person, I think that sometimes two people should not be friends because of they bring out the worst in each other.

The last four days, I finished one side of the landscaping project I started a few weeks ago.  The rock is laid, I have new outdoor lighting.  Unfortunately, the hardest part of the job is to come– the other two sides have become overgrown with weeds, and it’s going to be tough to clear it.  Even though my parents have been somewhat of a help, my mom is starting to have negative lupus affects from the heat and sunlight, and cannot be outside more than an hour or so, and certainly not pulling rock or doing difficult landscaping.  My dad can barely stand unassisted, plus he is busy pouting about some slight that I have no idea about.

It’s frustrating sometimes living with an elderly parent, and it is slightly reminiscent of the visit with my mother-in-law.  He often behaves much like a 4-year-old.  A prime example of this is when I make food.  I make plenty of leftovers, which he says he will eat, then he doesn’t eat them the next day, and there’s no way the kids and I will eat all the leftovers, so my fridge is full of left overs that don’t get eaten, and I end up throwing away a good portion of food.  Plus, also like my mother-in-law, he has to have his snacks in order for his world to be complete.  I can offer him a nice variety of nutritious foods, and he goes for the salty snacks, or sweets.  Then complains when he doesn’t feel well.

Day 94: July 23rd, 2013

I did it.  It took days for me to decide, but I listed the last remnants of my former life.  I listed the purse.  I don’t know what I’m going to do with the money, but something more meaningful than a purse.  Maybe a new computer, or some clothing for the kids, or money spent on a home improvement project.  I want this purse to make someone else happy, it doesn’t bring fulfillment to my life anymore.  It never really brought fulfillment to my life.  It was someone else’s love, someone else’s passion– not mine.  I can’t wait until I ship it off to its new home, and I can move on with my life, without the constant reminder of someone else.

Day 99-95: July 19th-July 22, 2013

I have come to a cross roads, and I need to make decision.  It’s not a major life changing decision, yet it somewhat is.  I have to decide if I want to “kill” the old me once and for all.  I have written about my friend, who last year had “dumped” me as a part of a disagreement.  Since the dumping, I have changed my e-mail, blocked her phone number, and have cut off all contact.  There are two things that I still to this day have that are a part of her.  Two Louis Vuittons, one a wallet and the other a purse.  I am grappling with whether, or not, I should get rid of the purse.  I used to like it, but I’m not sure if it’s me anymore.  I’m not 100% certain that it’s me, or the extension of me that was trying to be like her.  I don’t really want it anymore, because it reminds me of our friendship.  Part of me wants to just forget about the friendship, dump the purse, and use the money to buy other, more meaningful things that are more “me.”  Another part of me thinks I should keep the purse, because it does hold some sentimental value, yet I have other things to remind me of my trips overseas (other than a purse).  My lifestyle doesn’t lend itself well to Louis Vuitton anymore.  I’m not a yuppy, I don’t really care about outward appearances.  The purse actually makes me uncomfortable, because I’m afraid it will be stolen.  It’s cute, but it’s not really my style.  The question is should I let my past die, or should I hold onto it as a vague $400 memory?

Day 100: July 18, 2013

Sometimes the smallest voices can make the biggest impact.  The last two weeks families of 23,000 children on the autism spectrum united and fought.  We didn’t fight the war our family members are fighting, or have fought.  We fought a war for our children.  June 25th, Tricare released its new policy, this policy would have nullified the authorizations of 23,000 military children, and made it damn near impossible for them to receive services.  Today, Tricare backed down from its policy.  Instead of affecting active duty families, the policy now only affects families of retirees, and only those retirees with newly diagnosed children on the autism spectrum.  I was one of those voices.  I wrote to congressmen, the President, and even Oprah, everyone I could think of to get our story out there.  I spent hours, if not days at the computer, organizing a response to this growing concern.  Then, without warning it came down from Tricare that we had won.  It wasn’t an out and out victory, where they admitted that they were wrong, it was a kind of sort of victory, where the enemy tries to make you out to look like a pouting child in the corner.  It doesn’t matter to me though, it was still a victory.  In the end, my son will not lose his services, he will not lose his school, and I get the satisfaction knowing that I made a difference.

Now off to teach my daughter the important skill of cross stitching :)!