Monday, December 17, 2012

No School Today- Thinking of the children lost

Skipping work and school today in memory of the kids and teachers that lost their lives at Sandy Brook Elementary.  The pain those parents and family members must be going through... it's incomprehensible.

I worry about Jonah everyday, how long will he live?  Will he be in pain?  Will he be part of a clinical trial?  Will that trial be invasive and dangerous?  Will a treatment come in time?  Then I worry about him getting hit by a car. Now a bullet....

When I was 11 my Grandma was diagnosed with a terminal brain tumor.  We lived with her at the time, I watched my brilliant and talented Grandmother wither away.  When my Dad shot himself. I contemplated the only two deaths of my loved ones. I thought that I would rather have someone that I loved go fast rather then watch them slowly demise. My Grandma didn't know who I was at the end.  The last few months of her life she said every day: "I wish I would just die."

My Dad didn't want to live anymore, he didn't want his family to see him depressed or be a burdened on them.  Dad had a gun, Grandma didn't.

Where am I going with this?

When Jonah was diagnosed with a fatal disease. I took back my decision- that I'd rather have a loved one go fast so that I didn't have to watch them die.  I want to be by Jonah's side for every laugh and tear.  Is that selfish?

My heart goes out to those parents that had their children's lives snatched away from them.  I wish I could do more.  Today Jonah and I will goof off all day. We'll play tag and laugh.  Make Christmas cookies and eat cookie dough until we have belly aches.  My little cookie eater is up now, time to get busy goofing off.

Wednesday, December 12, 2012

Stop trying to sell crazy here, we’re all stocked up.

Stop trying to sell crazy here, we’re all stocked up.

Seriously, it’s time to take a break.  It has finally sunk in that Jonah isn’t going to die tomorrow and that he’s in the prime of his life right now.  I might loose my mind working at this pace.  One of my clinicians told me right at the start: “Ally yourself with the medical professionals who can advise you, so that you don’t look like the crazy lady trying to cure Sanfilippo by herself.”

It has been brought to my attention that I do come off as crazy.  Last week I had an appointment with an art director, my friend introduced us and came to the appointment.  I dove into my agenda and needs, never pausing.  When I did finally stop, my friend told the ad exec: “Sorry, Jill’s always like this, I run into her on the street and ask her how she’s doing and she just brain dumps on me.”

I run into friends on the street all the time and give them an update that is way more then they had bargained for.  One friend told me: “Geez Jill, everything in your life is a matter of life or death.”

Last week I was walking Jonah to school along with another parent and his son, Jonah’s classmate.  Jonah started running down the street.  I ran after him.  When the Dad caught up to me, he asked if Jonah always took off like that, I said yes.  He told me that he has a down syndrome nephew that used to be like that, but he grew out of it. He told me Jonah will eventually slow down too. I told him: “Yeah, because the disease that Jonah has is fatal.” He was dumbfounded, not knowing what to say he walked along dazed.  I felt bad, why did I have to say that? 

Seeing myself through the eyes of my peers has helped.  The constant panic attacks that I’m not going fast enough, is going to put me into an early grave.  The icing on the cake Roy’s recorded testimony.I attached the video of  Roy’s testimony on capital hill, a speech that he made to congress leaders, FDA and heads of Biopharmaceutical companies. Watch the video, it might bring you to tears but it will give you a good sense of what it is that families like ours are up against.  For me... It really hit home on a more personal level, enjoy Jonah now.  Reed was diagnosed with type A about 10 months after Jonah’s DX.  During that time, Reed has gone from using his words to express his needs to having to rely on gestures to communicate.

Without a treatment in Jonah’s near future this will happen to my family too.  I don’t want to have missed the good times, panicking. It's a fine line that I live.

The past 6 months have been really rough, Jonah has entered the ‘hyper’ stage of the disease.  I have been racking my brain as to how to deal with it.   I can’t control  Jonah in public settings.  He’s gone in a blink of an eye.  Nothing I can do or say will divert him.  He has no sense of fear, traffic doesn’t bother him, in fact he likes the traffic so much he’ll attempt to get in a car stopped at a red light.

I have given great consideration to getting a service dog, but a big dog in our 600 square foot apartment... A few weeks ago I had to take Jonah out on an errand.  As soon as we got off the bus Jonah saw some older kids running, it was getting dark out and the sidewalk was packed with people.  Jonah took off after the kids, I wasn’t even off the bus yet.  I ran after him, but I couldn’t get the people out of my way fast enough.  Jonah was a few feet away from the curb when a teen aged boy rose to the occasion and caught him just as he stepped into the street.  That’s when I thought of a service dog, the dog could get through the people and grab Jonah by the tail of his coat. People passing by might actually pay more attention to a service dog and try to stop Jonah.


"Hey, I'm a pet."
Eating, chalk.

My Mom designed us vests that we can attach a leash to.  I used it for the first time yesterday.  We were way uptown at the Presbyterian Hospital it’s a HUGE hospital with several connecting buildings, lots of emergency vehicles coming in and out.  The leash was awesome. Jonah stayed within a couple of feet of me.  He still climbed up on the retaining walls and jumped in all the mud puddles available, but he didn’t run into the street, nor did he mind the leash.  He said: “Hey I’m a pet.”

When Jonah ran into the gift shop and tossed the stuffed animals to the floor, the other shoppers politely smiled and picked them up.  When Jonah drop kicked the life sized stuffed dog across the store, the shop keeper smiled and said: “That’s ok.”

I could get used to this kind of understanding attitude, but we were in the Neurological disorders department of a pediatric hospital.  I have yet to use it in my neighborhood, not sure what my community might think.  But like Grandma said they probably will be envious that they didn’t have the nerve to do the same.

It’s been very difficult to absorb the mental changes happening with Jonah.  I broke down and took him to a psychiatrist to discuss meds that might help control Jonah’s impulsivity. I can’t deny that this is happening and it’s only the beginning stages.  Some of the horror stories that parents have of their Sanfilippo kids hyperactivity and fearlessness would make you loose sleep at night.

One child ran into the street and was hit by a car, broke several bones in his body, amazingly he survived.   Another child liked to jump on the oven door. His Mom started to use a bungee cord to hold it shut, one day the system failed and her son jumped on the oven door and pulled the whole oven out from the wall. 

Many families have created safe rooms in their homes.  Our families post pictures of the modifications they have done to their homes to damage control their kids.  Double dutch doors to keep them in one room but within visibility, plexi glass over all book shelves and entertainment centers, one family built a corral around their open kitchen so their kid couldn’t access anything dangerous. Many Sanfilippo children are compelled to push anything and everything off shelves, tables or counters.  These precautions go above and beyond baby proofing.

Anyhow... I’m just trying to paint a picture of what the behavior is like. Now imagine living in Urban New York, where you have to walk everywhere.  The streets and sidewalks are dangerous for those without disabilities.  Walking to school is a nightmare.  Jonah climbs up every ones stairs, tries to open peoples doors, looks into their windows. Jumps in every puddle, runs into every store.  Lays down rolls on the filthy sidewalk.  If he has to pee, he pulls his pants down and pees right there.  When Jeremy or I try to drag him home, Jonah screams: “HELH HELP, somebody save me, anybody.... come save me.”

When not in public Jonah is brilliant and is the sweetest loving kid.  Always happy and friendly.  The Psychiatrist mentioned several times, that Jonah’s disposition was wonderful, he was impressed with how polite and attentive he was.  Jonah sat down and introduced himself, shook his hand and asked the doctor what his name was.  He wasn’t in the least bit stubborn, he answered all the doctors questions.  He drew for him, counted and wrote his name.  I was so proud of him. My sweet little boy. 

Just now Jonah’s speech therapist popped out to tell me how excited she was.  Jonah had just validated her theory of children with auditory issues had problems drawing and describing pictures.  She proclaimed that Jonah did not have auditory issues!  She asked Jonah to draw a couple of different things and to tell her about it.  Jonah drew a car with wheels, a seat and a passenger.  He made the front and back license plate and told her that those were the #’s and letters.  He drew a picture of himself using a different color for his hair and eyes.  His speech therapist was thrilled, his comprehension and attention to detail and ability to express everything he drew and saw was spot on.  He even drew a side walk with a kid playing with his toy.  I tell yeah if it wasn’t for this forsaken disease, Jonah could be anything he wanted to be. 

Normally praise like this would make me want to run straight home and get back to work.  Not today, Jonah and I are going to go home and draw Christmas Trees.  I’ll post this tomorrow.

People are always giving me advice some say, enjoy Jonah while you can, I want to punch those people.  Other frantic parents will literally put the fear of God in you.  “Jill your son is dying before your very eye’s, what are you doing about it?!”  To those I say: “Stop trying to sell crazy here, I’m all stocked up.”  I know what I need to do, find balance.

Wednesday, November 21, 2012

My Heroes





Ryan Dant
Abbey Meyers
My Heroes

Last week I went to the Rare Voice Award Gala in DC. I was honored to be nominated for the ‘Abbey’ award, for my work in championing the ULTRA/TREAT acts.  The Abbey award was a beautiful marble statue of a Mother protecting and standing up for her child. Inspired after Abbey Myers a mother of a son with Turrets Syndrome.  Abbey was the inspiration for the Orphan Drug Act, her story is quite amazing if not serendipitous.  I encourage you to read the history of the Orphan Drug Act.http://archive.eurordis.org/article.php3?id_article=1751 

After helping to establish the act she went on to found NORD, the National Organization of Rare Diseases.  Abbey spoke at the award ceremony, once again I was moved and inspired by what the power of one Mom can do.  I had the pleasure of meeting Abbey later, this women is a force to be reckoned with, lets just say I would NOT get in her way.

I didn’t win the award and yes it stand’s true it was an honor to have been nominated. I was so proud to be standing with the group of incredible parent advocates and I’m thrilled that my associate, friend and fellow Sanfilippo dad  Roy Zeighami won for his role in driving the ULTRA/TREAT acts.

The event for me was priceless, It was a lovely intimate gala.  Relaxed and small enough to finally get the chance to meet some of my idols face to face.  Ryan Dant.  I tear up just thinking about this young man.  The Dant family embarked on their crusade to save their son Ryan in 1994, Ryan was diagnosed with MPS I at the age of 3, the average life span for MPS I is 10.  Ryan is now in his early 20’s attending college and living a normal happy life.  I crashed his table after having a few glasses to many of wine, I gushed. The poor kid is probably still reeling from the crazy mom, blubbering over him. 

It was so beautiful to sit next to him and talk to him.  Ryan is handsome, charming, bright and happy.  He looks a lot like Jonah but with dark hair and eyes. The MPS features, make our kids look a lot a like. The likeness to Jonah just added to my emotions. Ryan is the first kid to survive MPS I, I told Ryan that I wanted Jonah to grow up to be just like him.  Ryan has no idea how much I cherish him, he gives me immense hope. 

I asked Ryan if he knew how special he was and if his friends new?  He said:  “no, I just want to live a normal life, there are just a few people that I have shared my story with.” 

I pictured Jonah someday saying the same thing.
Here is an expert from an article about the Kakkis and Dant success story. 
http://www.pomona.edu/news/2011/02/09-magazine-hero.aspx

AS KAKKIS WAS STRUGGLING with drug development on a tight budget, a family in Carrollton, Texas, was facing tragedy. Ryan Dant was an energetic three-year-old when his mother, Jeanne Dant, took him to the doctor for a checkup. The pediatrician noticed Ryan’s head and liver were unusually large. “He had this disease no one had ever heard of, called MPS,” his father, Mark Dant, remembers.
There was no treatment. Severe MPS I kills children before the age of 10; people with milder forms may survive to young adulthood. By first grade, Ryan suffered overpowering headaches and nausea. His liver and spleen swelled to twice their normal sizes. His fingers curled up as the GAG stiffened his joints. He stopped talking about what car he would drive, or anything else related to his future, because he knew he wouldn’t have one.


As in many families faced with rare diseases, it fell to the Dants to seek their own cure. In 1992, they started the Ryan Foundation for MPS Children, eventually raising thousands of dollars through bake sales and golf tournaments. But they weren’t sure what to do with the money.


Emil Kakkis is to the Dant family as Alexey Pshezhetsky is to my family.
I also got to finally have some face time with another Hero father John Crowley, the Crowley family have two children with Pompee disease, another one of the lysosomal storage diseases. After driving a treatment for Pompee this dad went on to form Amiccus a biotech that focus’s on chaperone therapies.  A chaperone has been one of the treatment options that Alexey has been perusing for us. I told John about this and he promised to reach out to Alexey and share his expertise.  Alexey was happy to hear about the connection, wanting to speak with Amicus for some time.  John reached out to Alexey yesterday, it’s always nice to know the CEO.  Check out the movie Extrardinary Measures, based on the true story of the Crowley family.

Speaking of Alexey, I may have not won the Abbey, but Alexey did win the award he was nominated for, The Champion of Genetics award for 2013! 

The nominees must meet this criteria: For the purposes of this call for nominations, translational research is defined as a way of thinking about and conducting research that moves basic research more efficiently into medical practice, with meaningful health outcomes. It is about harnessing the knowledge from basic science to produce new options for the prevention or treatment of disease, be that through drugs, diagnostics, or devices.

Alexey received the award based on his work in rare genetic diseases affecting children, including MPSIIIC.  I’m sure Alexey will be winning a lot more awards for his work.

Have a wonderful Thanksgiving!

Monday, November 5, 2012

The Hurricane VS Halloween.

We had so much fun at our Halloween events.  We celebrated party #1, the eve of Hurricane Sandy, despite or inspite of the pending Hurricane we packed the house at the Ceol bar .  Our friend Channon planned the whole party and our friend Loretta, proprietor of the Ceol Bar and Pub, donated her dining area at Ceol for our use. 

There were several awesome kids vendors that came out.  Joanna of Cheeky Monkey Party, came with her bag of goods- tons of kids party games and crafts.  Jonah had a blast playing with the home made robots from the Brooklyn Robot Foundry, this place is so cool.  They make robots out of repurposed motors, batteries and recycled materials.  They came with a big table and a bunch of little robots, Jonah was memorized.  Our favorite kids musician Pete from the Hootenanny Art House came out and brought down the house.  We had bobbing for apples and face painting.  On the way out the parents told me it was the best Halloween party that they had ever been to!  One family said to me we had so much fun, we owe you more money, can I make a larger donation??


It felt good to do something domestic and celebrate a holiday.  I baked, made goody bags and planned costumes.  I haven’t done anything like that since diagnosis.  I’m very much indebted to our community for initiating benefits for JJB.  Thank you Channon & Loretta from Ceol,  Jane and Kenzie from Work Space, for party #2!

On Halloween we had a benefit at Work Space, Jonah’s Physical and speech therapy studio.  Jane and Kenzie our therapists, set up a Spooky Maze, an obstacle course for the kids.  I was very touched to see our friends come out to support JJB.  It was really cute to see Jonah come up with his sitter all dressed up and ready to go Trick or Treating for the first time.  He loved the maze, crawling through tunnels balancing as he walked over a ‘rickety bridge’ over the mote and seeing old friends.

The events leading up to the Work Space event did not go as planned.  I had left a lot of loose ends to tie up on Wednesday, thinking Jonah would be back to school, by then.  Which he wasn’t, trying to pull everything together, was difficult with Jonah wanting to ‘help’.  Then I couldn’t get a ride to Work Space, all the car services were tied up because of Sandy.  I was stressed and late to our own benefit.   Jonah’s sitter Gabby, ran outside for me to try and hail a cab, while I called every car service in town.  Gabby actually caught one for me.


My volunteers couldn’t make it, no transit. Again Jonah’s sitter Gabby came through for us. Gabby had a house guest Rebecca, staying with her.  Rebecca was touched by our story and wanted to come help, she hopped on her bike and sped over. She helped set up, passed out goody bags and helped the kids through the maze.  On the way out I realized I had for gotten my coat, it was freezing out, no way to get a ride home.  Randomly enough Rebecca had two coats on her.  Here’s this stranger I had never met, coming to our rescue spending 3 hours helping and then she literally gives me the coat off her back. To top it off I get home and Gabby refuses to take payment for the evening, her way of donating to JJB.  It’s people like Gabby and Rebecca, that make the World a better place.  You know I know what it’s like to benefit over and over from the kindness of strangers. I hope that I can pay it forward for someone else in need.  Hence my next story.

I’m ashamed to admit that I was completely clueless of the destruction that the hurricane had caused and the ramifications that we’d feel for a long time to come.
We don’t have a T.V., when Jeremy told me the storm was coming, I didn’t take it seriously.  To many other things on my mind, I live in a Sanfilippo fog.  After the storm Jonah was out of school all week. I didn’t get a chance to check out the news reports online until the weekend.  I was horrified to see what had happened to Staten Island, Long Island, NJ, Red-hook...  Mass destruction and loss of life.  It’s such a shock.

Imagine closing on your first home, moving in and decorating the nursery for the baby your expecting in a few weeks.  A new home with a yard for your eldest to play, while she waits for her baby sister to join her.  The American dream, then a hurricane comes along and completely destroys your home. This is what has happened to friends of ours.   Their plight has forced me out of my Sanfilippo fog and reminded me that unfathomable tragedy comes in many forms. I feel guilty for shrugging off the storm, we could have purchased a home in any one of the areas that got hit.  Instead we landed on a hill, far enough away from the water, to have sustained any serious damage.

For those that have wanted to help and just don’t know where to give, here is a wonderful family that needs our help.  A family that has been very supportive of JJB.  To help, click here.

Election day is tomorrow! Much of what JJB and our rare disease community have been working so hard for, has a lot riding on this election.  My mind would be at ease to know that people like Jonah who are dependent on expensive and life long treatments will be protected.  Knowing that we have a president that believes in and understands the value of science would be a huge stress relief.  Our rare disease community works extremely hard at improving public policy in regards to rare disease legislation.  It would be nice if we had a government that appreciated the work that we’re doing.  With all do respect, on Thursday I’d love to go back to my Sanfilippo fog for another four years, with a peace of mind that we have a president that has our back.

Hope for the best prepare for the worse.  My new motto.
Cheers, Jill

Thursday, October 4, 2012

Rebel with a Cause

I’m very much relieved that we won $20,000!  Thanks to all the begging and the harassing of our friends, family and community.  This was a grassroots effort, thank you all for helping.  We could not have done it without you.  There were 30,000 charities nominated and we placed 63rd. Not bad.

The contest just about broke me.  Pounding the streets soliciting votes from my neighbors, stalking the playgrounds passing out flyers to the parents and nanny’s. Having to tell them: “My son Jonah, has a fatal genetic disease, would you please be so kind to vote for him on facebook.”

I’m glad the contest is over, It’s hard to even write this re-cap.  But I need and want to say thanks to all of those who went above and beyond to help JJB win this.  Many of you stood by me passing out flyers, making phone calls, licking stamps and relentlessly harassing your FB friends to vote and for that I can’t thank you enough!

A friend of mine had a brilliant idea.  The last day of voting marked the first year anniversary of Occupy Wall Street.  Vanessa suggested that we take our cause to Wall Street.  What could be more appropriate??  JJB is in existence because our government doesn’t have the funding to help further the science.   Big pharma isn’t interested in producing a treatment for a rare disease. 

So here Chase is offering to give 196 charities a cut of five million dollars. A popularity contest... who can get the most votes on facebook. In return Chase gets to see your age, race and sex and they get good PR props.  I get to promote Chase and in return win $$.  The price you pay to save your child... Obviously I’d do it again in a heart beat.

So I made up some sandwich board signs. ‘Citizen Scientist’ a rebel with a cause.  Our government has turned their backs on our children.  Big Pharma doesn’t see the profit margin and Chase is using us for marketing.  It would have been brilliant, but occupy wall st had ended the day before.  So we hit Union Square instead.  We raised lots of eyebrows and got a lot of questions.  Hopefully it brought us a lot of votes too, but more importantly we made people think.

Jonah and I just got home from a whirl wind trip to CA, where we met up with my mom and Jennifer.  Jennifer hung out with Jonah, while Mom and I attended the RARE | Global Genes Project- Summit and Gala. I’ll give a better re-cap about the brilliant and amazing conference when I have more time.  I want to mention one thing  that has really hit home for me over the last month.

I along with 4 other parent advocates were asked to speak on the summit panels.  We each had different topics to touch on, but we all mentioned that we raise funds for medical research, everyone also mentioned that they have never received any federal aid.  These 5 groups have raised millions for medical research. 

Here we are driving the science and creating our own biotech’s.  We’re all on the verge of saving millions of children’s lives.  Meanwhile we’re creating jobs and saving our government millions.  So I ask... Where is our government bail out?  I guess the CHASE grant was it.

Tuesday, September 18, 2012

Treading Water-2 Days left


Treading Water!

We’re hanging in there by the skin of our teeth.  Please hang in there with us.  Just 2 more days of voting and this contest will be over!

We may have lost hold of our $50,000 grant but we’re hanging tight on a $20,000 grant.  That money is already spent.  We made our September first payment to our gene therapy scientist in Manchester, but we still owe Alexey $35,000.

I had really hoped to win at least $100,000.  There is a Genistein trial that is shovel ready in the UK.  All they need is 600,000 pounds to make it happen.  Lots of people have mixed feelings about Genistein.  Jeremy and I had Jonah on it for about 6months when Jonah was first diagnosed.  It was expensive and honestly I was afraid of giving my baby something that I knew nothing about. 

Two years later, Jonah is slightly showing the traits of Sanfilippo. His hair is changing texture.  He’s more aggressive and very impulsive, he has no fear when it comes to cars.   His sinus’s have gotten  bad, last winter was horrific.  So we put Jonah back on Genistein.  We could see an immediate difference, Jonah is more pleasant and less combative and his sinus’s have been good.  The thing is we’re really just guessing on the dosage.  We don’t have clinical data on the storage accumulation, is it lowering??? We won’t know until we get a trial and really look at the data.

Yesterday I purchased 6mo of Genistein for $2,600! This was for my French friends they have 2 MPSIIIC kids.  That’s another problem the pure form of Genistein is considered a food supplement in the US so the Americans can get it.  Meanwhile I’m shipping it to my friends in Europe who in turn have to pay taxes to get it out of customs. If we had a trial we could get it approved in other countries, insurance would pay for it and the overall cost would go down.  600,000 pounds doesn’t sound like much for a treatment that quite possibly will slow the progression of the disease.

Back to the contest.  It was a lot more work then I had imagined, but the idea of winning big $$$ drove me to give it my all.  I hit the streets soliciting votes from strangers for days.  Tomorrow I’m going to wall street and pitch my case that we need to win back some of the money that CHASE stole from us.  So that we can pay for research and clinical trials that our government ignores and big pharma turns their back on.  With a patient population of 1/1.4 million we are the underdogs, no one see’s the benefit of creating a drug for us.  This will be my grand finale for the contest.

The most wonderful part about the contest was the help that I received from our community and friends abroad.  We raised so much awareness!  We made several new friends, friends of friends just learning about Jonah and the disease. I was really touched to see children in the neighborhood asking for votes at their schools and playground. We even had helpers set up a lemonade stand so that they could spread the word.   I didn’t feel alone, new friends and old friends had our back.

With that said if you could all just rally the votes one more time, we’re in the home stretch. Wednesday at midnight is the last of it. We’re so close to making our last payment to Alexey and it cost the fb holder nothing, just a moment of your time.

For CHASE account holder you get 2 more votes, click here.

To earn a bonus point cut and past this link to your timeline.  https://apps.facebook.com/chasecommunitygiving/charity/view/ein/27-2957730?ref=251d5b64cd
Don’t forget to check back to JJB’s CHASE profile to see if you got it.



and remember to use your second vote for our friends the Sanfilippo Research Foundation.

Monday, September 10, 2012

What an awesome day!

What an awesome day.

Fall is in the air, it’s cool outside.  Dropped Jonah off to hie first day back at school.  He has a new classroom and teacher.  8 of the 12 kids from LY are in his class.  He was a bit apprehensive at first, but he ran in and said hi to all of his friends.  He gave me a great kiss and hug goodbye.

I woke up to a ton of votes on our CHASE Community Giving.  We had the highest voting day so far. Yesterday I went from parent to parent at the playground, passing out flyers and asking for votes.  I tell yeah, having to tell a stranger that your child has a fatal genetic disease is gut wrenching-tear jerking stuff.  I had to take a deep breath and leave the park.  I gave myself a pep talk and headed back in.  It worked though we got a bunch of votes.

If anyone wants to help me out with our guerrilla campaign- passing out flyers on the street and asking for votes... Let me know and I’ll get you a bunch of take away flyers.
We’re struggling to keep our $50,000 payout rank.  We need to be placed at #46 to win $50,000.  The top prize is $250,000 and the following 9 are $100,000 payouts.  We could get into the top ten if everyone voted and spread the word.

In other good news.  Jonah and I will be going to California at the end of the month.  I have been invited to the Global Genes gala and summit.  I’ll be speaking on one of the panels.  The organizers were in love with the pic’s that Dodi took of Jonah while in OR, their blowing one up as a poster.  There will be hundreds of who’s who is the rare disease community there all looking at my adorable boy.

I was also nominated  for an award for the Leadership in Advocacy presented by the Association of University Centers On Disabilities.  They’re a network of interdisciplinary centers advancing policy and practice for and with individuals with developmental and other disabilities, their families and communities.  Not sure what happens if I win it, funding would be nice.  However the nomination itself is an honor.

I submitted a poster to be presented at the NORD/DIA conference.  I hope it’s accepted.  Since my first conference I wanted to have a poster for one of the poster sessions flanked by scientific posters presented by PhD’s.  We also applied to speak about Phoenix Nest-JJB-ODDT and the Partnering for Cures conference.  I’m pretty sure we’ll be accepted for that conference.

Lots of exciting stuff going on.  Most importantly, Jonah is happy and healthy.  Back to work.  I’m absolutely obsessed with winning a huge grant from CHASE.  SO pretty please vote for Jonahs Just Begun and Sanfilippo Research Foundation.  You only have to vote once and you only vote for 2 charities.... Unless you have a CHASE account then you can vote 2 more times!

Just follow the links:
Jonahs Just Begun
Sanfilippo Research Foundation
p.s. VERY IMPORTANT.  Remember to promote.  Once you cast your vote hit like and send to all of your friends!

Thanks in advance,
JJB/Jill