Grace’s wedding

Ok so it wasn’t Grace’s wedding. But it felt like it. On Saturday, Grace was a bridesmaid in our friends Jake & Betsi’s wedding. Getting her ready, I thought this might be the only wedding she will ever be a part of, including her own. So I went all the way. Blush, Chanel perfume, painted nails, curled her hair. She was stunning if I do say so myself and she basked in the admiration all day. I love the photos of her and Betsi together because she looked at Betsi like any little almost-4-year-old girl would look at a beautiful bride.

The photos below all look a bit different because some were taken with my proper camera and others with my iPhone.

The possibility she might die

It’s pretty late. I actually went to bed at 8 but apparently I didn’t tell the mommy fairies that I was punching the clock for the night because they’ve kept me up till midnight with boys in the bed and Grace requiring a much needed yogurt snack at 11. Who doesn’t love yogurt in the middle of the night?

As I type this I can hear her squealing in her bedroom.

Naturally, when I’m awake at night I think too much. Usually about photography and business, but tonight is different. Tonight I’m thinking about death. Cheerful, I know. And strange because I must think about this a lot more than I realise. I think I used to cry when I thought about it. I must have. However tonight, I’m not. It feels like something I must think about every single day.

When I was young -too young to have children- I had this dream. I’d given birth to the most beautiful little girl. I saw her face so vividly in my dream. I wrote about it in my diary in the morning. I remember writing things like “peachy skin”, “the softest cheek” and “the bluest eyes”. But as I stood in this hospital corridor admiring my little girl, someone began to wheel her away and glass doors closed in front of me. I just watched her disappear forever and I woke up with the most painful ache in my arms. It’s not like I had a husband I could turn to in the morning and say “honey I want another baby”. Heck, I probably wasn’t even out of high school when I had this dream. The possibility of ever actually ever being a mother to that dream baby was…well…impossible.

The ache I felt in my heart when I had that dream was never fully resolved until I was handed Grace. Fresh out of my tummy, I sat her up on my chest and felt -ok NOW I’m crying!- I felt like my dream baby had found her way into my arms.

And then, 6 months later, she began.to.disappear.

My dream had turned into my nightmare.

But not really. Because I still have her in my arms. I can still kiss her softest cheek and get lost in her bluest eyes.

But behind all of this happiness that I still have my Grace is the fear -no, not the fear- the possibility that she might die. It’s the thing that hangs between every Rett parent. Between our hellos and our goodbyes, there are the whatifs.

As a Christian, it’s quite taboo to admit that you have a fear. I use the word fear carefully. “Fear” usually brings a “tsk tsk, now now” response. “Just give it to God” they say. “God wouldn’t let that happen” they say. Yea, well God let Rett Syndrome happen. I say that carefully as well. I know that I know that I KNOW that God didn’t MAKE Rett Syndrome happen. And I’m not so sure our family would even be better off if he hadn’t let it happen. Somehow, I appreciate what Rett Syndrome has done to my family. But that’s for a different blog post. Basically, you need to know this: I trust God and I am secure in the fact that he knows what he’s doing. There’s so much more beyond this life. Don’t us humans place the most outrageous importance on what happens in this life? How happy we are, how healthy we are, how rich we are? This is just the most microscopic blip on the meter of eternity.

When we saw the geneticist to find out more about Grace’s mutation (R168X), she said something quickly about it “not being a mutation particularly associated with sudden death”. Sudden WHAT?! Death? Who said anything about death? This stunned me. This realisation that this happens. Rett Syndrome can kill. It’s why Grace is even accepted into the hospice for children to give us respite once in a while. Because she has a technically “life limiting condition”. It’s why girls with Rett get wishes granted by Make a Wish. Because they might actually be dying.

Those on the outside of Rett Syndrome don’t really know the gravity of this possibility. The uncles you see once a year who pat you on the back before going out for a cigarette, muttering something about “don’t worry she’ll get better”. I hope statements like that make people feel better about not actually getting involved. Because genetic mutations don’t just get better.

However, those on the inside of the Rett circle? We see it all the time. All the R.I.P posts about another girl or woman with Rett who has “earned her wings”. It happens. And it’s quite often unexpected. Like sweet little Livvy. Her mum blogs about her and wrote in a letter to Livvy:

“The day your body died, I remember holding you, so peaceful and still. You hadn’t been still. Your body moving no matter how much you didn’t want it to. Now you were still with a beautiful smile on your face. Peace.”

And when we went up north to visit another Rett family last year and the mum revealed to us that her daughter had many of the different elements that add up to sudden death. Steven disappeared moments later and I found him in the caravan crying his eyes out. Crying so hard. I know he was crying for this amazing family we’ve now come to love dearly. And we never talked about it after that, but I think he was also crying at the sheer realisation that this happens. That at any time, any given morning, any one of us Rett parents could go in to get our girls up for the day and she be, as Sara described in this post about Livvy, “so still. so very still.”

There are mornings where I can’t bring myself to go into Grace’s room until I’ve heard her first. And then there are mornings like one morning last week where I find Grace impossibly still. Rigid, even. With her eyes wide open and not moving. Only to find that she’s holding her breath. Or, rather, that her body is not allowing her to breathe. And a few seconds later, she has relaxed back into herself and I can stop holding my breath, too.

This isn’t a fear. It’s a possibility. Grace has Rett Syndrome. This we know. God allowed this to happen and I don’t know why but I have faith in Him. I just don’t know if he will some day also allow her to go to Heaven before we’re ready to say goodbye.

Grace’s new lycra bodysuit

Two days ago, Grace got her DM Orthotics lycra bodysuit delivered. She needs to wear it under her clothes 12 hours a day, every day. It’s extremely specialised with support panels and zippers and holes in all the right places.

The purpose of the suit is to give her muscles the extra support they need to sit up straight. Also, because we reckon she has a hard time judging where her body is in space (imagine feeling like a floating head), the tightness of the suit gives her brain neurological feedback to tell her where her body is. She will have to burn less energy doing simple things like supporting her own body so we anticipate she will have more energy and be less sleepy.

She loves her suit! She smiles massively when I pick her up after squeezing her into it and she sits so strong and tall without the massive effort she used to have to put into sitting.

Embracing the PEG {and banishing guilt}

Yup. That's it. Still scares me a bit.

Just got home from the hospital. Grace got her PEG this week and I thought if I didn’t blog about it, like, right NOW then I knew I probably would never get around to it.

There were so many feelings to get over leading up to this point. It’s like you know how there’s those 7 stages of grief? Well I think there’s also 7 stages in coming to terms with a feeding tube {disclaimer: these scenarios are completely made up *cough cough* I’ve never done any of these things}:

  1. Guilt – guilt that you haven’t fed her enough.
  2. Guilt – guilt that you let your job get in the way of feeding her enough
  3. Guilt – guilt that you let your marriage get in the way of feeding her enough {date nights are for chumps!}
  4. Guilt – guilt that you slept in 10 extra minutes 3 times last week which meant everything was rushed and she missed those last 3 bites of oatmeal when, added together, equals a whole bowl of oatmeal and, thus, you basically forced her to skip a whole meal for your own selfish gain and THAT’S exactly why she hasn’t gained any weight in 2 whole years!
  5. Guilt – guilt that you let her fall asleep before her bottle sometimes and just tiptoe around thinking “if she wakes up, I’ll give it to her. But I’m going to be so quiet that there’s no way she’ll possibly wake up” to make you feel like it isn’t actually your fault that she’s skipping her bottle tonight.
  6. Guilt – guilt that your kids {who you promised yourself you’d homeschool forever} brought yucky viruses home from school {EVIL SCHOOL!} and she got so sick that she vomited for 4 days and lost weight. And THAT’S exactly why she hasn’t gained weight in 2 years!
  7. Denial – and the last step in the process of coming terms with a feeding tube is denial. Whereby you deny any feelings of guilt because -obviously- this has nothing to do with me and everything to do with evil Rett Syndrome {which is actually true. Although the guilt is very real, too}.

So I guess you can tell I’ve been feeling a little guilty leading up to this point. And as much as I’ve taken comfort in the kind words of people telling me otherwise, it’s still really not possible to stop believing that this is completely my fault. That I haven’t fed her enough. Because let’s face it, there are a couple hours left in the day not devoted to cooking food, blending food, cleaning the blender {I HATE washing the blender!} and then coaxing her to open her mouth wide enough to actually get it in. And when you can’t really chew, there are only so many options in this household unless your mum doesn’t have anything to do other than dream up easy-blend recipes for you to sample.

I was kind of getting to the point of acceptance that it wasn’t my fault when the surgeon’s letter summarizing our first appointment came through stating: “Grace’s mother doesn’t feel she can feed her enough”. Great. Thanks lady. I gave you all kinds of fluffy stories about noodles coming out of her nose and gagging and vomiting when she hates what I’ve made and you had to put it in black and white: “Grace is getting a surgically implanted plastic tube ‘cuz her mother doesn’t want to feed her”.

But you know what? In spite of being wracked with made-up guilt, I really REALLY knew that this was the best thing for Grace. And I knew that my over-thinking and self-guilt-tripping was ridiculous. And I knew deep down that this wasn’t my fault. Because you know what? It IS hard to feed Grace enough. Not because I’m self absorbed or because I hate her cute little guts. Because she has Rett Syndrome. And somehow, accepting this operation was like one step further into accepting Rett Syndrome. And somehow, I’m still pretty good at pretending that Rett doesn’t exist most of the time. Kinda hard to deny it when you see that tube sticking outta her guts though.

The hospital thing was great. By far the most amazing hospital experience I’ve ever had {yes, even in America}. The nurses were flipping unbelievable and I’m determined to write each and every one of them a personal thank you card. And Grace’s surgeon was amazing {in spite of her letter} and it’s got to be said that she’s super gorgeous and looks so much like Juliane Moore.

The couple of days after the surgery -quite frankly- were sucky. Seeing Grace cry for a drink for so many hours, staring me right in the eye and crying “Baaaaa baaaaaa” for her bottle and me desperately trying to tell her that it wasn’t mummy’s fault that she couldn’t have a drink. I can only imaging that she was thinking “why are you doing this to me, evil woman?!”

She was {and still is} in pain when the meds start wearing off. But giving her medicine through her tube is simply a dream. I know that at midnight when it’s time for more, I won’t have to wake her up to squirt it in her mouth and then further wake her up by brushing her teeth because I’m worried about rotting them with gooey syrup. I can just squeeze it in her tube and leave her sleeping.

It’s funny. We were in a recovery room with 6 other kids, 3 of whom had also just had the same surgery. And after the nurses came in and trained us how to use it and left us with everything we needed in order to easily feed them lunch and take a much needed nap, we all sat there instead struggling to feed them hospital food. I can’t help but wonder if we were all playing the same game: proving to one another that it wasn’t really our fault that our girls had just gone through a really hellish couple of days. Because we DO feed our kids, dammit! I wonder…

Grace smiling like a loon after her surgery

Note: I’m quite dramatic as you know. And while all of the above is completely true, it’s also true that everything about the last 3 days has been far better than I could have ever dreamed it would be. For example, it took 2 different Drs 4 attempts to get the IV in her hand. And the whole time they were rooting around in her hand looking for a vein, she was laughing her adorable little head off. When I told Steven this, he said he’d just been praying that she would laugh instead of cry. And when she wasn’t groggy from meds or crying for more, she was a super happy little soul that made everyone come and marvel. And at the end of today, I got to share Jesus with a lady and she cried and said I was the 3rd person God sent to her this week and she decided to go back to church. There are silver linings in every cloud! That is the saying, isn’t it? I dunno…I try to avoid cliches as much as possible.

Did Elijah keep quiet all day?

Thank you thank you THANK YOU to everyone who donated to Elijah’s vow of silence for Rett Syndrome. He exceeded his goal by £20 and got some very generous donations.

When I picked him up from school, the headmistress said he had spoken once when he cut his finger. We then went to the park and while Jack and Rosie played afar off, I looked at Elijah next to me and he had tears rolling down his cheeks 🙁 He said “I can’t do it anymore” and felt he’d failed. So he may not have kept quiet for a full 24 hours, but he definitely endured some hardship for his sister!

So thank you everyone for supporting Elijah in his ambitions. He’s so much like me when I was little!

Elijah’s vow of silence {no joke}

On Friday, Elijah’s not going to talk. All day. Seriously. He’s joining some of his friends in a day of silence in honour of their sisters who can’t speak because of Rett Syndrome. Not that they’re silent or anything. Right, Catriona? 🙂 Please go show Elijah your support and donate a few pounds here –> http://www.justgiving.com/elijahhalford

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