Showing posts with label Random. Show all posts
Showing posts with label Random. Show all posts

Wednesday, May 28, 2014

Random baking post


I don't consider myself in any way domesticated. I am one of those accidental housewives, but we happen to bake a lot with the kids, it's something we all really enjoy. 

The 2 older ones were away for a playdate this afternoon (Lia's first in someone else's house, the excitement was unreal!!!) so Fi and I used the time to bake a quick cake that she could mix it all by herself without having to share with anyone else.

 Fi practically spends half of her life sitting on the counter as every meal gets prepared in this house and I just realized I didn't have a single picture of it, so there.  




Wednesday, May 14, 2014

Anxious

I rarely lose hope these days. Today is one of those days. My list of anxieties is endless. Mostly I chose to ignore it.

I worry about Fi's major interest in doctors, she has had so many appointments that she is talking a lot about them. "Which I do I need to patch? Which hospital is the eye doctor at? Where am I going next?"

I wonder what it is like to grow up having so much exposure to the medical profession. If I was a bit more lighthearted I would just say that I hope she will become a doctor, which I hope she will.

Of course I know where my anxiety has popped up from today, I am very aware of the origins of my feelings that I mostly chose to ignore.

I am not talking of a little anxious thought that passes through every mother's mind several times a day. I mean the stomach turning debilitating knot type, which makes me unable to do anything than to think about it and write it out.

We have the follow-up meeting with the endocrinologist in about 2 weeks. Once again I will be prepared with all my print-outs and will be dressed nicely to reinforce the good impression I made last time. I couldn't prepare more for a large business proposal or a master's thesis presentation, but none of those things really matter in the bigger scheme of life, but this does.

I am completely at this woman's mercy, 18 months after I have researched growth hormone treatment and decided to give it a shot, I have met with 5 endocrinologists and I am not 1 step closer to getting her started. OK, this is not true, but it feels like it.

I am in contact with parents of all over the western world, who have managed to pull this off and their kids are benefiting from the treatment. I couldn't feel lonelier than how I feel about this issue.



Sunday, January 5, 2014

This body of mine

There is a lot I could be writing about. Perhaps a lot I should be writing about. But this post is going to be about me. More specifically about my body, which is probably the most neglected part of me. I do a lot with my mind, I read, I write, I think, i work, I speak. And I have a very well analysed and thoroughly exercised emotional life.

Of course I take care of myself, I shower, I floss, I die my hair, I go for a walk every day. But this body hasn't been mine for over 7 years, it is the weirdest feeling that I am quite sure only women can understand. My eldest is turning 7 in March and apart from a short 5 month break I was either pregnant or breastfeeding or both for the last, well, nearly 8 years. I haven't been able to have a drink or take any proper medication for anything for that long. Paracetamol (acetaminophen for my US readers) has taken on a new meaning for me.

I decided to wean Fi just before Christmas. I was done breastfeeding her. I really would have preferred for her to self-wean, but it became obvious that she just wouldn't, she was still nursing at least twice a day. There comes a moment when you are done, so when St Nicholas brought a few gifts on Dec 6, he decided to take my milk supply with him. It has taken a good few weeks of talking about this: "No more milk, Saint Nicholas took it, remember you got some presents instead", but now it's all forgotten about.

Fi is our last biological child, unsurprisingly there is a sense of grief in knowing that I won't be pregnant again or breastfeeding again. Had we started sooner, we would probably have 5-6 children.

I will miss all the intimate moments, but I gave it a good few years of my life and now I can hopefully get rid of the DD cup, go back to a B/C and tackle some of the chronic back-pain. No resolutions as I find the concept utterly ridiculous, nothing ever happens the way I plan it, but this pan has to go and it won't be going on its own... So there will be less walking and some yoga... Happy New Year and I will post pics and write about stuff that dear readers actually care about...


Saturday, August 31, 2013

Person first language

I saw this poster of Down Syndrome Ireland in the library today. I liked it so much that I was thinking about it the whole day. Here is a more detailed explanation of their person first language.

It really-really resonates with me. Especially these parts:


  • "A baby born with Down syndrome is not a “Down’s child” or a “Down syndrome baby.”" 
  • "It is also important to use correct terminology. A person does not “suffer” from Down syndrome, nor are they “afflicted”. It is not a disease. Down syndrome is a chromosomal condition which results in an extra copy of the 21st chromosome. It was discovered by Dr. John Langdon Down." "
  • Person First language emphasises respect for the individual. A child is much more than a label. Help to educate family, friends and professionals about the preferred way to refer to a person with Down syndrome."


Trying to translate these statements into dwarfism terms would be very interesting, wouldn't it...
  • A baby born with dwarfism is not a dwarf or any other label e.g. noun.
  • Dwarfism is not a disease but it is a genetic condition.

Only one question remains, why do members of the dwarfism community promote the use of labels such as "dwarf" and "little person"? 


Monday, January 7, 2013

Murphy should resign...

I think everyone who have kids can relate to this... My life is a chapter in Murphy's book of laws... I am not saying this to complain, I have resigned to the fact by now.

In a few words:
- first day of school and creche
- deadline for assignment submission because jerk FAILED ME by 1 %...
- up all night with Tara vomiting
- nanny still on holiday
- husband not working from home for 1 day
- work calls on my day offs
- and the clingiest toddler in the history of mankind...

Can Mr Murphy please just resign.

Oh wait I have another one... Tomorrow is my first work day and I will start bright and early at ENT with Tara because I had to drug her up every day of the holiday


Monday, November 12, 2012

I came across this fascinating article

while writing my latest assignment for my masters... It was on additional learning needs and I wrote about achondroplasia... And when searching on a historical explanation about society's attitude's to people with short stature, I bumped into this incredibly well-written piece... Enjoy

Monday, November 5, 2012

Got to boast....

We went to see Fi's paediatrician today, we attend her at the busiest maternity hospital in Dublin, but she actually works as a neonatologist at one of the children's hospitals. She asked me if I would be interested in giving a presentation to the registrars at the hospital about hypochondroplasia and about our experience and all the research I have done.
I am not sure if it will actually happen, but I guess this explains why she is our paed, although she is officially a neonatologist, I am not letting go of her, and she is not trying to discharge us either... :-)))

Monday, October 15, 2012

Cognitive dissonance

according to wikipedia is the term used in modern psychology to describe the state of holding two or more conflicting cognitions (e.g., ideas, beliefs, values, emotional reactions) simultaneously. An example of this would be the conflict between wanting to smoke and knowing that smoking is unhealthy.

What I have been wanting to write about is not cognitive dissonance in the true sense of the word, but I can't find a better term for it. How can someone be so imperfect, yet so perfect to me? How can I be so aware most of the time of her condition and how can she not? How can I raise her to believe that she is just like her sisters and has no limitations?
I can't put my head around it. You all know me by now, I need to rationalize until the point of understanding or utter exhaustion.




Sunday, October 7, 2012

It is Sunday night

and I am hectically trying to finish up all work, get the house sorted, do all kids Admin, etc. Before I head off to London for a team meeting for 3 days.
I work every night, it's the price I pay for having the afternoon for my children... Most nights I don't mind, but now as I will be leaving for 2 nights, I would like to snuggle up between them (Tara and Lia share a double bed :-))...

For 3 days, I will be a career woman, I will dress up nicely, have proper make up on, wear business clothes with no food, snot and puke on them. I will be known for me, as the funny and intelligent and humble creature I am... I will wear jewelry without it becoming a choking hazard. I am getting a manicure done tomorrow morning, YAY for business trips...

I will bring 2 books along, I will get tipsy with my colleagues - for my American readers, this is a European thing, we have thins thing, we must get drunk together with the people we work with... Don't ask me why... I won't get very drunk, good Lord, I have been pregnant and/or breastfeeding for 6 years, I take 2 sips of wine and I am done...  Long are the days of my alcohol tolerance gone.

I will be up until the early hours in the morning, chatting with old friends, feeling like a person in my own right. I may even have a bath, I don't think I actually had one since Fi was born.

And then by about Wednesday afternoon, I will start to miss my children terribly, I will look at all my career focused colleagues in the city and know that this self-important life wouldn't satisfy me any longer, I want snot on my clothes... and I am happy to be someone's mummy... This is when I will turn to Louise, she is the only other female on our team on about 20 30 some year olds with kids... We made a pact that we will go to a quiet corner and do the mummy talk when we get really desperate...

So yes, I am all freaked out about leaving Fi for 2 nights, she LOVEs to feed, she comes up to me, and pulls on my top and bra and says milk-milk ever so often... I have no idea, how she will cope, but probably she will be a lot less upset than I am for having to leave them for a few days...

I know that I have an easy life and the vast majority of women need to get up and get dressed and leave their kids every day, and even over night... I do realize how extremely fortunate I am to have such an amazing employer. But still, I will miss them terribly... Maybe one of my work mates will throw up all over my clothes, that may make me feel a bit better...

Tuesday, August 7, 2012

Surviving August

I know I will... Just not sure, how... Here is the set up...
Number of children in the house: 3...
Number of parents working full time: 2 albeit from home and flex hours but still needing to put in 8-10 hours a day...
Number of parent having to complete masters needing lots of help from wife: 1
Number of parents whose client's contract just got renewed and will be mad busy with transition - 1 and it's me...
Parents wanting kids to have a great August - 2...

We will figure it out, we have help for 6 hours every day so we'd better make most of it... Tara will do camp for 1 week, that will help...

I really need to start to share here all my research about the growth hormone treatment and start listing my questions as I will be taking Fi to see the French endocrinologist involved in the interesting study in Sep...

Wednesday, July 25, 2012

Some light holiday reading

I was going to post about our holiday without internet access (YAY) but bumped into this article... I have been wanting to post about the subject of the new genetic testing whereby screening for a multitude f genetic conditions will be possible in the early stages of pregnancy without an invasive test.
I will save my personal thoughts and confused feelings for another post, but for now. Read this truly remarkable article:

Sunday, June 10, 2012

Other parents' blogs

Bloody blogger just deleted all the blogs that I have been following. I will try and recreate the list based on comments, but if you used to be on my blogroll and can't see yourself, please comment here. I do want to follow, I just can't remember everyone's URL... ARGHHHHHH

Friday, May 11, 2012

Rhetorical question of the day:

Why does someone become a pediatric orthopedic consultant if they hardly even look at a patient? I realize hospitals in Ireland suck, they are busy, dirty, a bit like a horrible zoo really, but wouldn't you want to make a difference?
When he reviewed Fi's x-rays he actually said that he wouldn't think that her x-rays belong to someone with HCH as her bones look all normal. Yea, this is why hypo goes undiagnosed until kids are 2 or even older... Can't wait to see him again in 6 months...
I asked him 2 test questions, both answers were incorrect, so none of our ortho questions got answered today. Lucky we will see Dr. Standard in October...

Wednesday, March 14, 2012

Monday, January 9, 2012

Ok so this one made me cry and smile

I am not into this whole thing about finding a meaning why Fi is our child, but this one made me smile and cry at the same time...

http://www.downsyn.com/bombeck.php

Sunday, January 1, 2012

No New Year's resolutions for me

Nope, stopped doing them at 21 or so, not great at following through and way too cynical to even try... Instead I will do a wishlist for each member of the family, not the same thing, not at all :-))

George - I hope that in 2012 he will enjoy his job, he just started a new job and he had 2 horrible bosses in the last few years so he really needs a decent boss and a job that offers enough challenge but allows him to still have a life, I think it looks like he may have found it...  Oh, and I hope he can finish his MA, that's a huge thing for him.
Tara - since she got hear ear tubes her hearing has become so much matter - please may this be the year that her speech will catch up so I can stop worrying myself to death, pretty pretty please... This is a special request to the speech fairy... Please fly by...
Lia - She is perfect the way she is, really, so I just hope that I will somehow have more patience for this 3 year old who is just like ME so drives me up the flipping wall... Please, patience fairy, come by QUICK...
Fiona, - I just hope that her speech will be good, since we are bilingual and she has HCH, please speech fairy, we really need you...
For me... Ok this is a long list, I am a selfish person... OK, I need to stay employed, so I really need our client to extend this contract, pretty please, contract extension fairy... And I need to continue to work on my masters too and it's so BORING.  Oh and I stopped eating sweets for Fiona, because we will need to watch her nutrition, so now is the best time for me to stop as she is starting solids, I can do it for her, easy-peasy, and this is not a resolution, not at all... And last but not least, I have perspective, I really do I just have to remember to focus on it. LOTS.
Oh and we really need to get on with the grandparents this year, can't have any more drama...

Friday, December 23, 2011

We'll celebrate Christmas tomorrow morning

Because I am too excited and because my husband will take the 2 older girls to visit the grandparents on the 27th, so I wanted to have a chance to admire the kids playing with their new toys for a day longer. Fi and I will stay, because I can't stand the cold, I need to work and need to write 2 assignments for this course I am taking, I am doing an MA in Learning and Education, it is a really cool online course...
Tara will be up at like 6... so I hid Lia's present behind the curtain in case we don't hear when she sneaks downstairs, that wouldn't be good... :-)


Saturday, November 19, 2011

This and that

I haven't written for a while, I have so many things that I want to write about, why am I not doing it..?. I guess I have realized that I only have 2 weeks left from my maternity leave, so I am trying to spend it with the kids and I also started a masters, strangely enough I will have more time when I start to work, because I will have a nanny looking after Hannah every morning, so I haven't given up my hopes to make this blog a really informative one...
I also need to start to write more so that I don't freak my poor husband out by oversharing all my worries with him, it's a thing that we, mothers do, and men can't really relate to.
Fi is doing great, she really is the cutest baby ever, so chatty and smiley... I can't wait to see how she will change once she will get her ear tubes in in 2 weeks, it will be so nice to know that she will hear a lot better after that.
She also had a head CT, the local radiologist said that it looked good, but I won't believe anything until Dr. Pauli will have reviewed it next week, as this is the same radiologist who sent us home telling us that there was nothing wrong with her.
Tara has had so many playdates since she started school this September, well, I am sure other kids had much more, but for my standards, having 4 friends that regularly want to get together with her is fantastic, so this week another mum texted me organize something and when I said it to George he said the most painful thing again: He said that he bets noone will want to play with Fiona. He says something like this and I spend 3 weeks  thinking about it, chewing over it. He is such an introvert, he just gets on with it, yet from little comments like this, I can tell that he is always thinking of her condition and how she might be disadvantaged because of it...

Monday, September 26, 2011

This and that

I haven't been writing much lately, I guess the main reason is that I have done most of my research, I think I have done more writing and taking notes than in the last 10 years total... If I would only find the time to at least add all the links here... I will try...
The second reason is that Fiona is doing rather well, so I have stopped worrying all the time, well at least for now... I think both her HC and height are still on the average height chart, but only just about... She is nearly 4 months now and is a real sweetheart, she is interacting so much, full of smiles and chuckles, she is chewing on her little chubby hands and is now properly manipulating her toys. She can hold things now in her hand, just won't grab on her own yet.
The third reason is that I have been quite busy working with Tara on her speech and school stuff...So it has all been very busy, I can't wait for my maternity leave to end, so that I will have the childminder in the house for when I work and will actually have a few minutes to myself, I know this sounds bizarre...
We will go and see Dr Pauli in 2 weeks am very excited about it, not sure what he will say...

Wednesday, August 17, 2011

If I was a radiologist...

If I was a pediatric radiologist, who had sent a woman home with a 3 day old baby assuring her that her child didn't have achondroplasia or hypochondroplasia, telling her that the x-rays were all clear, I think I would want to see the list of radiology findings (if offered to me by the mother) that another specialist could list based on the same x-rays I have reviewed...
I think I would try to get over my pride and my desire to learn from my mistake would be greater than my ego...

Sadly the radiologist where Fi was born doesn't think like me, so only God knows how many children will go un-diagnosed, because they don't have a pathologically information hungry mother who sends their baby's X-rays to the one of the best experts in the world...