Join me on November 2nd in NYC to celebrate our amazing Rett sweeties

image In my spare time (!), I help raise awareness and funds for Rett Syndrome Research Trust (RSRT), an organization that is near and dear to my heart. Prior to last January, I had never heard of the organization, but since then, they’ve become a crucial part of my life, and my hope for my daughter’s future.

As you all know, Lily was diagnosed early last year with Rett Syndrome. It’s not a high-profile diagnosis, but it is a devastating one. Rett impacts 1 in 10,000 girls and women, and most are wheelchair-bound by the age of 2.

Lily is one of the lucky ones. This year alone, she has lost – and then regained – her ability to swallow and use her hands purposefully. She walks (or runs!), has some hand function, and doesn’t need a feeding tube. She’s also making HUGE progress in her communication skills, with the use of specialized eye gaze technology.  I want to thank you for taking part in this journey with me.  Your support through this blog – both near and far, is indescribable.

I also don’t know what I would do without her army of therapists and doctors (at last count there were over 25). They have become like family to me, as have my friends at RSRT.

Sleeping peacefully during an EEG yesterday at the hospital.

Sleeping peacefully during an EEG yesterday at the hospital.

This organization has made remarkable progress in advancing research on Rett Syndrome. A few years ago, approaches attacking Rett at its genetic root were not possible. Today there is scientific evidence that gene therapy could offer an effective way to treat – or even reverse – the disorder. RSRT is spearheading an ambitious gene therapy project to make this possibility a reality.

But we need your help to continue this scientific momentum and to support more research projects. I hope you can join me this year at the RSRT’s 7th annual Reverse Rett fundraiser to celebrate our girls and help work towards making their fugures even brighter.

Please click here for details. I hope to see you there!  If you can’t make it, please consider making a donation – any amount, small or large, helps us get one step closer to a cure.

Thank you.

Sleep no more

As many of you know, this is the title of a popular, yet confusing and somewhat annoying show here in New York City.  It’s also the title for my life right now, which is somewhat confusing and annoying.

I know this sleeplessness is just a phase.  But it’s going on way too long.  And it’s different from her previous episodes.  Lily’s inability to fall asleep lately is tinged heavily with bouts of hysterical laughter.  Yes, it’s cute.  And a lot of the time I do laugh alongside her because her giggles are infectious.  For those of you who are fortunate enough to have heard her belly laugh, you know what I’m taking about.  But at midnight?  When it’s been going on (and off) for a few hours?  It’s not so funny.  It’s downright alarming.  And annoying.  There, I said it.

So I’ve been researching the laughter.  And it turns out, it’s one of the many facets of Rett syndrome.  Something neurological is going on in this kid’s mind.  And it is likely linked to the increased ‘Rett episodes’ she’s been having.  Yup.  In August, and into September there have been more than a few times that she’s woken up, shortly after falling asleep, with scary shaking and convulsing spells: she’s fully aware of what’s going on and is looking at me with terror in her eyes begging me to make it stop.  That, my friends, is Lily’s version of a Rett episode.  It’s not a full on seizure as she’s present during the convulsing. But something terrifying is going on in her brain.  And it’s terrifying the both of us.

These episodes have also impacted her physical function.  She’s become much more clumsy these past few weeks.

We are going back to the hospital in early October to see the Rett specialist. Likely the doctor’s recommendation will be to give Lily the trazadone she prescribed last year when her last awful sleepless period happened.

For now, I’m keeping an epileptic activity journal, noting all the times Lily has these ‘Rett episodes’.  And, in the meantime, I will do my best to keep laughing alongside my sweetie.

Lily's favorite sleeping position, 'the starfish'

Lily’s favorite sleeping position, ‘the starfish’.

The Master

imageWhile at my yoga retreat this past weekend, I came across the above maxim.  It immediately resonated with me.  And it got me to thinking….

I recently read an article entitled ‘Pity the Parents of Special Needs Children.’  Almost EVERYTHING written in this article was spot on.  But the title?  The use of the word pity?  Well, that most definitely did not resonate.  Empathy, understanding and support – not pity – are what parents of special needs children want.

That article was part one of a series of articles on parenting a child with special needs.  Supposedly the second article is to focus on the positive aspects of it.  Well, that hasn’t been published yet.  I’m impatient.  So I’m going to write it.  Right here.  Right now.  Here goes:

————————————————–

Parenting a special needs child is both heartbreaking and magnificent.  There is so much fear, so many doctors appointments, so much bureaucracy.  But there is also so much beauty, joy and laughter. I try to focus on the magnificence of it.

This is not an exhaustive list of all of the magical things that come with this role, and I’m hopeful that my friends who are on a similar journey will help me add to the below:

  1. You learn to focus on what’s REALLY important.
    I’m completely out of the loop on the latest tv shows, music and fashion trends.  I don’t really care.  Things I once obsessed over (like Ferragamo shoes!) are secondary, or even tertiary in terms of what I think about on a daily basis.  And it saves me money, and time.
  2. You learn to be mindful, and fully present.
    Well, most of the time.  We’re all human after all.  But when you have a child with disabilities, you are so very present – while you’re playing with them, when you’re advocating for them, when you’re at the hospital talking to the doctors, when you’re strapping them in to their equipment.  I try to carry this over into my non-mommy time as well.  When I’m at work, I focus on work.  When I’m doing the dishes, I focus on doing the dishes.  And if I start to worry, I bring myself back to the task at hand.  I’ve not perfected mindfulness outside of my mommabear role, but I’m getting better at it every day.  And I’m becoming a better person because of it.
  3. You recognize that each and every day is full of miracles – small and large.
    Or as Albert Einstein so eloquently stated, “There are only two ways to live your life. One is as though nothing is a miracle. The other is as though everything is a miracle.” Every day that my daughter wakes up and gets out of bed and runs to the kitchen patiently waiting for her breakfast – that is a miracle.  When she communicates with me through her Tobii – that is a miracle.  When she puts her hand out to caress my face and give me kisses – that is a miracle.
  4. You pay attention to your child and help them foster their interests.
    Here, in New York City, I often hear about parents putting their kids in a foreign language class or ballet – all at the ripe old age of 2 – to help them get a competitive edge for their future.  They’re so busy trying to position their kids for their version of success, that they forget about enjoying their child and learning what their kid is actually interested in.  I, and L’s army of therapists celebrate, and encourage, all of the things she shows interest in.  Whether it’s planting and growing blue flowers, playing dress-up, or reading her favorite books.
  5. You are much less judgmental.
    When I see a kid having a meltdown in the grocery store, I don’t immediately go to ‘that parent is raising a spoiled brat’.  I have compassion.  Deep compassion.  And if it seems appropriate, and I’m able, I offer a helping hand.  Because I’ve been there before, and I know what that feels like.  Practicing compassion, moving away from a ‘me vs. them’ mentality’ makes us feel better as human beings and makes us feel more connected to others around us.   And I think that’s pretty cool.

I am the student.   And I continue to learn.

C

L playing dress-up as Doc McStuffins

L, the Master, playing dress-up as Doc McStuffins

A bit of respite

So… Lily is with her dad for 10 days. He’s taken her to Connecticut (where his folks live). I already miss her like crazy (she was picked up yesterday) but I know I need a break. I need to regroup, sleep, remember who else I am (other than mommy and boss). Last night I went out and had a blast.  And today I’m heading out of town for 3 days to go on a yoga retreat (which I try to do every few months).

The rest of the time she’s away, I’m going to work (arrive on time, take a lunch break and go to the gym after work), sleep, and be social (when I’m not sleeping). I feel so lucky that I have some breathing space. But wow. I’m missing my sweetie!!!!!!

The sweetest!

The sweetest!

Screw that

 

Running

Running to the Farmers Market with Mommy

Upon further reflection, I’m going to tell the PTs, OTs and the social worker at Lily’s preschool to stuff it.

My kid is NOT going to arrive at school every day (when she starts kindergarten next year)  in her adaptive stroller. Don’t get me wrong, I’m not in denial that she should have one. But she does not need one for school.

#1 concern: They see her arrive in that and they’ll keep her in it. I’ve heard from numerous parents that this is a REAL issue. And even the Rett specialist agreed when I pressed her on the subject.

#2 concern: How will it make HER feel? I don’t want her to get used to being ushered around. I want her to feel as independent as possible. She’s a strong-willed kid. I want to continue fostering that.

So she might be slower than the average kid, and klutzier (which may or may not have to do with Rett Syndrome – if you know me, you know what a klutz I am), but she walks. And she walks well.  And she will continue to do so.

Now I have to figure out how to get her to and from school every day. But I have a year to figure that out. Wish me luck.

Guess who chose these beauties out at the farmers market?

Guess who picked these beauties out at the farmers market?