Showing posts with label factor. Show all posts
Showing posts with label factor. Show all posts

Monday, April 29, 2013

Day 29: #HAWMC: Congratulations!

Ugh!! Today I need to post three things I love about myself, things I'm good at or just want to share. I'd rather talk about my kids because after all...if it weren't for them and their chronic illnesses I sure wouldn't be sitting here blogging away!

Because of them I love:

1. The fact I can talk to anyone about their chronic illness.

2. I can advocate. Meeting with lawmakers? No biggie! That's what they are there for...meeting with us, the voters and wanting to hear our story. Doesn't mean they are going to vote our way but at least we can meet with them.

3. I have learned to not judge a book by its cover. Maybe the kid that's throwing a temper tantrum in public isn't misbehaving...maybe he is having sensory overload. The kid that cries everyday before she goes into school may have anxiety issues.  My son is covered in bruises...I don't beat him...you can't see his hemophilia. The point is don't be so quick to judge. Just because you can't see it doesn't mean it isn't there.

My kids! 

Wednesday, April 24, 2013

Tuesday, April 23, 2013

Day 23: #HAWMC: Technology


Today I am to write about how my life would change if there were no social media.

NO social media.

How did we survive BEFORE social media!?

Wow...I imagine a ton of free time that I would have.

However...

I wouldn't be able to reach to a friend across the US to ask questions about Hemophilia.

I wouldn't be able to talk to other parents who are having the same issues I am with my son.

I wouldn't be able to connect to a community that is united by bleeding disorders.

Who gets it.

Who understands.

Who knows.

Who has walked and is walking in my shoes.

It would be lonely.

Don't get me wrong. I have wonderful people here in my hometown that I connect with. Sometimes I can't always meet up or attend events so it's nice to be able to catch up with them on Facebook. It's comforting to know that if I'm on the way to the ER with my son and a bleed I can communicate with the entire community if I need to.

The bleeding community is our family. We aren't related by blood...well, yeah, we kinda are in a way, and I can't imagine not being able to connect with our family for support.

Thank goodness for social media.

Thank goodness for our bleeding community family.


Saturday, April 6, 2013

Day 6 #HAWMC: Letters



Dear Hemophilia,

Just wanted to drop you a line and let you know I despise you. I hate how I have had to infuse my son, through IV, from the time he was three days, yes, DAYS, old. When most parents were taking their newborn babies home we had to take our son down to Children's Hospital for a diagnosis and three day stay while he was held for medicine dosage, CAT scan and observation.

You've made him endure several pokes from nurses who said they were good with IV access to bypassing them all together and having us request the IV team for his infusions. You made our son feel like a hospital was his second home. That everyone has to go to the hospital. When he sees the logo of Children's Hospital, no matter where we are, he says "there's my factor mommy!".

My son has had to grow up early...that "kid" is wise beyond his years. He knows his medication days. He knows when he has a bleed. He knows what happens when he has a bleed. Even so much to ask if he has to go to the hospital or if we can take care of it at home. He knows that he needs to take it easy if he has a bleed and believe me when I tell you this is NOT fun. He is an active boy who wants nothing more than to be well...active!

I hate that I have to worry about each whimper in the middle of the night...is he in pain? Is he hurt? Does he have a bleed? Or with each bump or fall if it requires a call to the Hematologist. Or each time he says, "this hurts" if it's the start of a bleed. I hate that I have to type bleed so many times in this blog!

You really make me angry because your treatments are expensive. I hate calling and fighting insurance to get the things needed to deal with you. We have FINALLY been able to take an extended vacation because we have learned to self infuse and didn't have to time our vacation based on nurse visits.

But then...

I want to thank you. Yes, I know...it's weird. But thank you. Because of Hemophilia my son understands and notices his body. He is in tune to how things feel and can tell us when things feel funny. You have made our family stronger in being there for each other. You have given us the opportunity to meet some wonderful people in the bleeding community. You  have helped us raise awareness. You have made us thankful for advancements in modern technology. You have made us appreciate life and to make it the best we can.

So try as hard as you can to be a pain (and you do)...but your messing with the wrong family.

Not so fondly yours,

the Loving's

Wednesday, April 3, 2013

Day 3 #HAWMC

Wordless Wednesday...

Post a picture that symbolizes Hemophilia...



This symbolizes freedom, courage and hope for the Hemophiliacs of today.