Showing posts with label catching up. Show all posts
Showing posts with label catching up. Show all posts

Wednesday, June 30, 2010

Not Alone

 

2009 04 18_Fish Hatchery_0113

I know I need to do a better job of writing here but I don’t always want to write about bad or sad things.  Lately, my mind just seems consumed by the changes Taylor’s brain is going through & how it is affecting who she has always been & who she might become.

However, after reading  Joyce's blog, I know I’m not alone.  I hope she won’t mind the link to her and her daughter’s blog.  (If so, just let me know & I’ll remove it.)

That day of Taylor leaving me in the grocery store went from bad to worse.  My middle daughter Brandy, who is Taylor’s respite care provider, thought it might give me a break if Taylor went to her house for awhile…something she does a lot.  That day, she was acting so different & out of it that it scared Brandy.  It was like “Invasion of the Body Snatchers” & my Taylor was someone else.  Luckily, days end.  It’s too bad the fears & feelings don’t end with it.

I am happy to say that we have not had anymore of those really horrible days.  Is Taylor different than last month?  Yes, but it’s our new normal.  Just like her birth and subsequent medical problems became our new normal almost 21 years ago.

That’s something about our kids…there is always a “new normal”.  They are never consistent unless you count consistently changing. 

The other day, out of the blue, Taylor packed her things that she always takes to her sister’s house, put them at the end of the couch that looks out the window to the street and sat down. She sat on the end of that couch for several hours.  She had it in her head that she wanted to go to her sister’s house & nothing was going to change her mind.  We hadn’t planned on her going to Brandy’s but when I told Brandy what she did, she said she just had to come and get her when she was done with her other client.   She did come get her & Taylor was as happy & sweet as ever. 

I just have to brag for a minute.  My daughter is a wonderful care provider for those with disabilities.  I’m sure it’s because from the age of 5 years old, she grew up with a sister that had severe problems.  Brandy was the first one to make Taylor laugh & the only one for awhile.  My oldest daughter Courtney has a special bond with Taylor as well.  Unfortunately, she lives in Georgia with her husband & kids.

Brandy & Courtney, never once complained about the time I had to spend with Taylor at the hospital.  Taylor had a bad seizure when they were 11 & 12.  She stopped breathing & her heart stopped.  They did not panic.  I did CPR, Courtney called 911, & Brandy went to the top of the driveway to wait for the ambulance.  I have awesome girls.

I don’t know what I would do if Brandy hadn’t moved here to Oregon from Georgia last year.  Because of lack of  funding, the program that Taylor was going to do after graduation, she can’t do.  They can’t afford a 1 on 1 aide for Taylor and Taylor can’t be left to her own devices because of her health & seizures.  Brandy is sitting down with Taylor’s case worker and going to come up with some activities she can take Taylor to, so at least she will get out of the house.  The program does go out a lot to plays, swimming, movies, & the like so that’s something Brandy can do with her.

I don’t want her life to be reduced to being bored to tears every day.  Taylor is a social butterfly.  She needs interaction with people…lots of people.  So much so that right this very minute, Taylor is standing in the bathroom, looking out the window watching the traffic go by. *laughs*  She’s been standing there for the past 20 minutes.  Whatever makes her happy. 

Thursday, June 17, 2010

Gummi Worms & an Update

Taylor & B gummi worms

        Taylor & her sister enjoying some gummi worms.

Update:  Sorry for using a happy title and then writing a depressing entry.  I put the title and picture in 1st with the expectation of writing a blog on the picture but somehow I got sidetracked.  I guess this needed to come out more than I realized.  Thanks for all the kind words in your comments.  They mean a lot to me.

Taylor graduated last Tuesday so that was her last day of school.  By this past Monday, the summer boredoms had set in.  She went from going to school everyday, to having to stay home.  She doesn’t start her new program at Sunshine Industries until July.

Normally she would have gone to her sister’s house a couple of days this week but my grandson is really sick with some sort of virus.  The last thing we need is for Taylor to get sick.  We are hoping he’s better by tomorrow so she can go over Friday and spend the night.

As far as Taylor’s health is concerned, well there are some issues that are going on with her brain.  We’ve noticed that for the past several months, Taylor’s behaviors have changed quite a bit.  Because she has so many seizure a day, we know that brain tissue is dying and we think that whatever part controls memory might have died.

Normally, if Taylor asked you for something, if you told her to wait, she would…for a limited amount of time.  Now when you tell her wait, she’ll ask again within 5 minutes.  It’s like she forgot she just asked.  Also, we’ve noticed a change in the way she “plays”. 

Now, while Taylor has always had the attention span of a gnat, it’s even worse now.  It’s like she’ll start something and then you see this look on her face like she forgot what she was doing.  It’s hard to explain.

We just know that Taylor is losing more abilities much quicker.  Sometimes I’ll watch her have so many seizures, one after the other and think, I need to call the neurologist.  Then it hits me.  Why bother?  We have exhausted all medicines and medicine combinations.  She takes 4 seizure meds right now.  We’ve also exhausted all surgical options.  Cutting her brain in half didn’t even stop the seizures.

I struggle with am I giving up too soon and do I want what could be her last weeks, months, years to be spent in the hospital.  I know that when she goes, I’ll second guess my decisions, wondering if there was some treatment I missed.  Deep down in my heart, I know I’m making the best decision I can for Taylor.  Right now, she is happy (except for missing school) and for her, the quality of her life is good.

Unfortunately, those second-guessing thoughts come at night, when my brain just keeps replaying every medical decision I’ve made over and over…wondering if somewhere, I made the wrong choice.

I realize that we as parents of special needs kids do what we think is in the best interest of our child based on what information we have at the time and the deep love we have for our children.  I keep telling myself that replaying Taylor’s life and worrying that I did something wrong is a waste of time.  Sometimes, myself doesn’t listen.

 

Sunday, January 3, 2010

I’m Still Among the Living


I really need to catch up with everything. I can't believe it's been so long since I last posted. I just know things have been very hectic here and my blog always seems to be the thing that gets left undone.

I suppose in the scheme of things, that's how it should be but I always have this nagging voice in the back of my mind going…"shouldn't you blog, really, shouldn't you at least say you are alive, really?"

So, here I am, letting my friends know that I am still a blimp on the planet. Things are going as well as they could be with Taylor and life is just a bit topsy turvy right now. I'll share more later, including Christmas pics since I know I'm way behind on that.

I hope this finds everyone having a great start to the New Year.