I created this blog when my 6 year old daughter was diagnosed with Nephrotic Syndrome (NS). As an uncommon and difficult to understand condition I wanted a journal, along with a way to let family know how she was doing, and a way to connect with others experiencing the same thing. This blog chronicals the events, emotions, and more she and we as a family went through. The initial episode begins in March 2008. On the side are pictures as well as links to sites I found helpful.
Monday, January 26, 2009
Wednesday, January 7, 2009
Boring is Good
Does that mean life around here is boring? No Way, not with Ada. She doesn't need prednisone to make her active. She was always one of the kids who got wound up on cold medicine rather than falling asleep. She is having a great time learning and improving her reading and writing. She is a great little scientist, and with the new microscope we got she can now check out her own cells (cool huh)
So with this new year we are hoping for the best for everyone out there. If you are currently on prednisone, we hope you successfully ween off. If you are on a more intensive therapy, we hope it is successful and you will soon be protein and prednisone free. If you are looking at a biopsy, we hope you find the answers you need. And if you are currently in remission, we hope you stay in remission for a long, long time. And if things just are not going well at all, we wish you the strength and courage to carry you through to better times and pray your Drs will be guided to give you the proper care you need.
Love from Ada and a Happy 2009. If all goes well you probably won't get another post here for another month. Thanks for dropping in and checking up on us.
Monday, December 15, 2008
2 months free and still counting


Today marks 2 months being prednisone and protien free. The cytoxan is doing its job.
That first picture is from her last relapse in Aug. The other is her current school pic from Nov. She is certainly doing well. Thank you for all the extra prayers in her behalf. Hopefully she won't relapse, but we'll keep you posted either way.
Monday, November 17, 2008
Mark One Month
Sending our heart felt prayers to those who are in the middle of a relapse.
Friday, November 7, 2008
Kidneys Holding
In all honesty, we expect there will be an occational relaps, but statistically she should respond better to the prednisone now that she has had a cytoxan course. But it would be great if she never had to deal with this again.
For now our instructions are to test for protein once a week, daily if she is spilling proteins, swelling, or sick. But even then we don't need to worry unless she goes beyond a week with higher protein levels.
Thursday, November 6, 2008
1st Test
Saturday, November 1, 2008
Kids are Kids
Friday, October 31, 2008
Another great NS Blog
http://kid-neydisease.blogspot.com/
Tuesday, October 28, 2008
Tuesday, October 21, 2008
Holding on Her Own
As of today she is testing negative for proteins. Hurray!! Here's hoping that Cytoxan did the trick. The Neph said to bring her back in 6 mo for a followup. Hopefully we won't see him before that.
We are suppose to check for proteins once a week. We will probably check more often than that - at least for a while. But even if the proteins are up, as long as it doesn't stay up for more than a week we don't need to worry.
We'll keep you posted.
Thursday, October 16, 2008
Oct Neph Visit





A Medical assistant or PA comes into the exam room and gives her a once over and reviews medical history. Then Ada gets a chance to double check everything.

Friday, October 10, 2008
Stomach Problem identified
I called Ada's NP and we talked about just what sypmtoms she was experiencing, how long etc. She asked if Ada had been having regular bowel movements. (OK, I need to start paying attention to that because medical people are always asking about that :-))
Anyway, I didn't think she had been real regular, but wasn't sure. Her NP suggested that she may be having bowel problems which could include painful gas. (been there, done that, not fun). It seemed to be a good fit with what may be going on - warm baths and back rubs being something that helps and all. She suggested trying miralax to see if that helped, and if Ada wasn't feeling better in the morning to go visit the GP to see if we might be missing something.
So we asked Ada if she had been having normal poops. She said yes, except the other day she had bumpy rock poops. OK, that answers that. At the NP's direction we gave her a dose of miralax (warnings all over the bottle not to use if you have kidney problems without Dr's direction - so "don't try this at home" without Dr approval) and it worked. She slept through the night in her own bed and is feeling much better today.
Don't know if there is any connection between this and the NS, the medications, or if this was just another thing life throws at you and she grabbed it. But glad we have the help we need to get through all this.
Thursday, October 9, 2008
Just not feeling well
She isn't puffy or spilling any proteins, I am just not sure what is up. We have an appt scheduled with the Neph in a week. I guess I will call the clinic and see if she should go in and have her Primary Care Doctor just give her a look over for any obvious problems.
Currently she is on 10mg prednisone every other day, and is also taking the cytoxan (down to the last couple weeks) and previcid (or whatever the insurance is allowing).
Sunday, October 5, 2008
It's a Cold
Wednesday, October 1, 2008
New Milestone
She has been complaining again about stomach aches. Not sure if it is due to the cold/virus she is fighting, or her stomach just being sensitive to the medications. Not too concerned at this point, but I put a call in to the center just to let them know what is going on. Only a few more weeks of the Cytoxan treatment.
Big sister had to have some blood work done Monday. Ada felt pretty brave and important showing her the ropes at the lab :-)
Wednesday, September 24, 2008
Behind the Scenes

Monday when we went to the lab I took all six kids (I know, crazy). But after they were done with the blood draw this WONDERFUL technician showed the kids how she prepares the slides to do a blood count. She told them she would have loved to take them back to look through a microscope with her except there were too many infectious diseases in the back.
Check out the video of the slide prep!
Friday, September 19, 2008
Oops
Something that has helped us keep track of whether or not she has taken her meds is one of those weekly pill packets that your grandparents use to set out their meds each day. It's nice because if I can't tell if I didn't get her meds or if I just failed to record them, we can look in 5h3 weekly med dispenser to see if she has taken that days meds.
Neph Visit
They ran the basic vitals, weight, BP, and listened to her body. Since it was just before lunch they heard plenty from her stomach :-)
The Nurse Practitioner told us that Ada's white blood cell count was down, but not enough to be concerned with at this point, and that they would give us a call if it did drop too much. Otherwise it looked like she was doing well and we could come back in a month.
The Neph dropped in to take a quick look at Ada and then we were on our way.