Archives for March 2009

My first “paid” writing gig!

My first paid article has been published 🙂  Hopefully this will be the beginning of a new career for me!  (I know, I have a long way to go, but this is a start!)

Parenting a child with a rare medical diagnosis: Proactive parenting tips
SheKnows, Pregnancy and Baby section

Big Medical Day tomorrow

Would you believe that Hannah is my easiest child to take care of tomorrow (Thursday)? 

Abby has had two ear infections for over a month now.  She had a bloody granuloma in her right ear that had to be suctioned out a few weeks ago.  She did Omnicef for two weeks, and it didn’t help.  Now she is on amoxycillin (same stuff as Hannah).   She is already on her second set of tubes, but her ENT doctor says that they are clogged now.  Also, he is concerned because she should have outgrown her ear infections by now (she is turning 5 next month).

So he did a nasal swab last Thursday, and I found out tonight that she has streptococcus.  But that doesn’t explain her ear infections, however.  But it would explain why she has been acting so uncomfortable for the past couple of weeks.  Tomorrow, I have to take Abby in to get bloodwork done to test for allergies.  We need to figure out what is going on with her now. 

Also, Ethan had another cold sore breakout, and I am on the last of his acyclovir.  Too bad, I didn’t realize that early today when we saw the pediatrician for Hannah (Ethan was at school). 

Like I said, Hannah will be the easy one tomorrow (hopefully!)

Whoo hoo! Gotta love an ear infection!

Hannah just has an ear infection in the left ear.  So it most likely is draining down into the back of her throat while she is sleeping, and that is what is making her cough and wake up.  She has always had a little phlegmy issue at nighttime on her back, so this just exacerbated it.  Thank goodness I took a video of it to show Dr. B. because before he saw that, he was very concerned about this being a GD neuro symptom (swallowing difficulties, etc.)  But once he saw that, he looked so relieved and was like “Oh, this doesn’t really concern me at all!”  Phew 🙂  I was so happy after we found out it was an ear infection likely causing it.  

Just some antibiotics, and we go back in two weeks for a recheck!  Phew 🙂

Nighttime Congestion

Hannah has always had some type of nighttime sleeping issues similar to snoring.  However, over the last few weeks, it has gotten to be more bothersome for her.  Over the last few nights, she has gotten so uncomfortable to the point where she wakes herself up.   The weird thing is that she doesn’t APPEAR to have any congestion during the day…clear nose and all.

Of course I’m all paranoid about sleep apnea and breathing difficulties since those are “on the list” for the neurological issues of GD23. 

I’m going to see if I can take her into the pediatrician this morning to see if he can hear any congestion in her lungs and take it from there.

Sometimes being rare just, well, sucks…

It is so depressing how little support there is for Gaucher’s Disease type 2 and type 3. Seriously.

I have only been able to find about a dozen other families who have had children with GD2 or GD3. Sadly, most of their children have already passed away. I can think of maybe 4 other families that I have been in contact with who are still fighting this disease. Four — in the entire internet, and you know I have tried!

I have so many questions I want ask other parents who are going through this or have gone through it. There aren’t even enough families yet to create a mailing list or message board.

I have found other message boards and mailing lists for other rare diseases. Even though they aren’t hugely active, there are enough members to at least have questions answered and get a few opinions. Not for GD2 and GD3.

I really do feel alone in this…

Hannah’s Blog Makeover

As you can see, I’ve done a bit of redecorating around here. Here is why (and my ultimate goal for Hannah’s blog):

  • To make it easier for friends and family to follow Hannah’s story (Hannah posts on the main page instead of everything like research, etc.)
  • To become a home for other GD23 families to find the latest research and support information
  • To share upcoming fundraisers for all GD23 events all over the country (not just Hannah’s)
  • To help other families of rare disease find support information and share their stories

I have a LOT of work still left to do, so pardon the mess. I wanted to start getting it online, even though I know it will take a few days to get just what I want to get done completed.

If you find any messups, problems, etc., please let me know (just don’t ignore it, I may forget about it!)

Off to play with Hannah and Abby!  Priorities, you know!