Logen is DESPERATE for your prayers. Pray blog family, PLEASE pray. Just grab this code and add it to your blog (html gadget) so you can help us spread the word! Thanks! Pray for Logen

A sincere THANK YOU to all of you who have added this to your blog! And, to Anelys for creating such a cute blinkie!!
Showing posts with label Disabilities. Show all posts
Showing posts with label Disabilities. Show all posts

Sunday, January 11, 2009

Geneticist Appt

LOGEN DOES NOT HAVE ANGELMANS!!!!!!!!!!!!!!! Or CP (confirmed by yet another Doctor)

The newest Dr on our 'list', the Geneticist. We really liked him. He was straight forward. We have never had a Dr say that all of Logen's 'weird/abnormal' th ings must be related. Thank you Lord. How do you have a child that is non-verbal, developmentally delayed, begins seizures at 4.5years, and has a lipoblastoma- and some how these things just happen to the same child? No... the lipoblastoma in itself is very rare. We've ruled out Angelmans. We've ruled out CP. The Microarray came back normal. The next round of testing is below. Let me tell you, I tried to research the groups of disorders. There wasn't much info out there. The results will be back in 6-7 weeks. Until then, we just pray.

Prayer warriors- Lets Get Our Prayer On!!!
Testing: Round: Momma's lost count...
1) PTEN Hamartoma Tumor syndrome (PHTS) is a group of disorders caused by alterations in the PTEN gene. This group includes:
Cowden syndrome (CS)
Bannayan-Riley-Ruvalcaba syndrome (BRRS)
Proteus syndrome (PS)
Proteus-like syndrome

2) Aristaless related homeobox, also known as ARX. This can be broken down into sub categories, with rare syndromes, etc- theres not a whole lot of info out there on this (that I was able to find). Partington Syndrome is one name I found.

3) RETT

Monday, January 5, 2009

Fears & Funnies

On Jan 31, 05 Logen was given the Dx of CP at the hospital we are going to tomorrow. I thought long and hard about this today. That Dx followed us around for 3 years and 10ish months. (And, in most everybody's documents hasn't changed.) You get used to something and *think* you accept it, then it's 'gone'. The concept is something that I don't understand... but maybe that's part of our makers plan. Who really knows. I have this little voice that keeps saying, 'it's going to be ok. Maybe it's going to be a 'better' Dx.' Then, it's like a sudden crash- 'Jessica, he doesn't speak at age 5. Somethings not right. He started having seizures at age 4. It cannot be 'better'.' Agg... there's my pessimism kicking in. It gets me. Every time.

I guess my overall thought was... 4 years ago we got a dx I did not want. I cried like no other the entire trip home. I cried until I had no tears left to cry. We go to that same building tomorrow. It's the same month, the same time of year. Am I going to leave there with a Dx for Logen? Will we continue to test or wait? What happens next? What about Logen? What does Logen think about all of this? Is he sick of the testing and sitting in Drs office? Of people talking about him in front of him like he's not there (I think this is rude. I wish Drs would not do this!) Or being poked and prodded like a pin cushion? Or does he even know whats going on?

On a lighter note: Some Parker Funnies & Sicklies! (Mmm... not a word, 'eh?)
* Parker has officially started calling a Bus and Bus. It was a Butt. I liked Butt. It was funny...
* And, he ate bloodworms today. Yum. Not. They were being thawed in the sink for the fish. Parker decided to have a taste. He ate the whole container.
* He also informed me this morning that his ears hurt and he needed to go to the Dr. So, mean mom said- what if they give you a shot? You still wana go? He said, "Es. Ear ur." (We know, he needs speech. And, he qualifies. However, our insurance company doesn't agree) My 2 y/o diagnosed himself! Both ears are indeed infected. Suprax for 10 days. He's also on Pulmicort and Xopinex {breathing treatments, he does great with these... HAHAHAHA}. (P for the remainder of the winter... nothing new, we've done this for the last 2 years and X until the Antibio is finished)

Tuesday, October 21, 2008

An Incomplete Definition

I found this here. Wish I could have said it that well.


Long before I even met Nick, a friend of mine in Maine learned her beautiful blonde daughter’s developmental delays fell into the category of mental retardation. And though I hate to say it now, I felt sorry for her.



A child with special needs.



What a pity.



I wish I knew then that pity is the last thing us parents need.



(And don’t even think about feeling sorry for our children.)



What does it mean to parent a child with disabilities?



It means the reframing of your worldview.



It means taking nothing for granted and spending more time in the present than in future plans

and dreams.



It means endless appointments and paperwork and the introduction of your child to all kinds of

adults who specialize in understanding his or her needs.



It means missing your own six-month dental check-ups and yearly pap smears.



It means growing comfortable with stares, even if your comfort is in knowing that you won’t be comfortable, but it will happen anyways.



It means knowing how to silence a pesky questioner with a single statement:



“His brain was injured at birth.”



“I have two wombs instead of one.”



“Why do you ask?’



“He has Cerebral Palsy.”



“There’s nothing wrong with him.”



“Well, he’s not looking at you because he’s legally blind.”



“What do you mean by Ok?”



It means redefining the words OK, healthy, and childhood.



It means continually adjusting expectations so you neither expect too little or too much but

rather remain open to wherever your child leads.



It means learning to follow.



It means a redefinition of your social life because either your friends don’t understand or because you find yourself with so much less time to devote to cultivating friendships. You want to extend invitations to dinner, you truly mean to return the favor, but months go by and you still haven’t had an extra second to plan a social evening. It means being so grateful to those friends who do understand.



It means working on learning how to scoop with a spoon instead of learning how to chew with your mouth closed, learning how to walk instead of ballet lessons.

Learning to go slow instead of racing. It means letting go of comparisons and bailing out of the My-Kids-More-Advanced-Than-Your-Kid game.




It means becoming almost fluent in medicalese and actually knowing what the following terms mean: IVH-III, C-PAP, Nystagmus, Strabismus, Hydrocephalus…



It means doling out medications--even if you planned on raising all natural kids.



It means joy in the controlled bend of a knee, a flash of eye contact, sunlight on an orange Lilly, the sound of your young son saying, “No.”



It means befriending therapists, multiple adults that not only love your child but remind you when you most need to hear it that your doing a good job. “You’re a good parent,” they tell you-- and you realize that all parents could benefit from hearing this from interested parties and you think how lucky you are. It means always thinking you could do more.


It means wanting time alone as a family, without appointments, professional judgment, and medical advice.



It means multi-tasking, squared, times three.



It means buckling your son into his car seat to drop him off at daycare and then driving straight to work.It means constant surprise. “Did you see what he just did?!?!”



It means never shaking the specter of death.



It means gulping joy like water.



It means questioning whether you can do this again, whether you can conceive and carry another child.



It means wanting to try.



It means not wanting to try.



It means fear.



It means acceptance.



It means hope.



It means never saying, “I don’t care if it’s a boy or a girl, as long as it’s healthy.”



It means…

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