First things first; thank you to everyone who offered to find some boots for my girl. Thank you for the suggestions. We found some. When I say we, I mean my mother found them. She even found them locally. I must get my clever genes from her
Ivy Update
We went back to the dermatologist this morning. Ivy’s bottom is still not great. We thought we would be up for a biopsy today but we have decided to wait it out until after Christmas. The derm reg was fantastic, answered all my questions in detail and helped me to get my head around what might be going on with the little girl. Was empathetic, sympathetic, did not poo poo any of my concerns. Not once. He was interested in my thoughts on the situation of Ivy’s health. It was like he cared and even if he didn’t, he put on a great act. Thank you derm doctor. I can honestly say I feel better knowing we have a plan, at least for her bottom.
We had to go and have more bloods done. I hate that part.
Have you ever had to do it? With your baby, I mean. I have. I have done it alot with Imogen and now I am up to my 6th or 7th time with the Ivy - girl.
I used to cry with Immy until I figured it was distressing her more, having her mother sobbing along with the needle, so I learnt to control it. I’m good at it now. It’s something I have always been able to do when things get a little too stressy but doing it when it involves pain to your baby is a different story.
I vague it out. Go somewhere else. How can I describe it? It’s like not feeling anything, just a dead space inside. It’s weird but effective. It still hurts to see them being hurt, don’t get me wrong and I shake and take a while to collect myself afterwards but at least I can be strong when my baby needs me to be.
And she needed me to be.
After what seemed like forever the pathology tech had a rant in my face about how inconvenient this all was and some of it wouldn’t be back until the new year and then drew 4 vacutainers of blood and two syringes for a couple of serum samples. You know, just in case they didn’t get enough the first time.
She was very brave but Lord did she howl and my heart was smashed into a million trillion tiny pieces all over again. Poor little mite.
As we were walking out we saw the paed and he saw us too, I know he did. First, he tried to cross the road before our paths collided, then, when he figured that was too obvious he cast his eyes downward and walked briskly past us.
That’s when you know you have truly been blacklisted.
We have a follow up in two weeks, with biopsy at that stage if things are still not great.
Can I change my Christmas wish? All I want now is to get to the bottom of this. All I want is to be able to help her.
Posted on December 19th, 2007 by Tiff
Filed under: Health, illness, doctor related posts, family














The bastard of a Paed! What nerve!
I’m glad the Dermatoligist was lovely. Hopefully they will find something soon.
I know what you mean about the ‘other’ place. I go there too. It helps.
Love the new site - it looks fabulous!
So sorry you and your little one are having such a rough time! We went through three years of blood draws and diagnostic junk with our oldest before we finally got her CVS diagnosis… so I completely sympathize with the frustration. Lots of prayers that you will find an answer quickly!
WOW!!! Everyone seems to be getting new digs.
Fabulous by the way.
I know what you mean with the vague dead space. I have to go there a lot. I have even been able to physically lower my blood pressure when Boo is in full meltdown in order to calm him. A doctor didn’t believe me, until he tested it.
We mums are amazing. That is why this stuff is not left up to the blokes
Hoping the bloods shed some answers. Yes it is very emotionally distressing watching your child go through painful procedures. I’ve been there too.{hugs} The Paed is horrid to ignore you like that.
hugs to you… Big hugs..
When we were trying to diagnose Veronicas Headache and her joint pains and nausea and everything else.. I wanted to Scream with frustration.. xxx and we never did get a diagnosis.. *sigh* don’t give up..
and that sucky paed and his useless receptionist.. they are SO GETTING LUMPS OF COAL for christmas…
keep on going.. I am cheering you on..
cheers Kim.xxx
I know what you mean about the vague dead space - I learned to go there when I was teaching special needs kids - I went there when my choice was “vague dead space” or “physcially jump over desk and pummel life out of kid”. Turns out it was good practice for this parenthood kid.
I meant toadd those boots are awesome - your mum rocks .Lil’s socks will be tickled !. I wouldn’t mind a pair myself.