Showing posts with label Advocacy. Show all posts
Showing posts with label Advocacy. Show all posts

Thursday, August 27, 2015

So, what in the world has been happening for the past eight months?

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It has been a long while since I have posted here.  I figured I'd give a little update on things going on in our world.

1)  We transitioned Ayden from his school and teacher he had been with since Kindergarten (and some of his classmates since he was 3!) at the end of the year.  Change is scary.  Really scary.  We also moved from a traditional calendar to a balanced calendar (basically year round) and moved from special education busing to general busing.  It was a BIG change - and all because Ayden was just doing so well in school he no longer qualified for the program he was in.  So, it was all very bittersweet.  We are now a few weeks into school and it is going better than I could have imagined.  Sure, there are kinks to work out.  Adjustments to be made.  We (as usual) have an amazing team though who continues to work us to give Ayden everything he needs to succeed and continue to push him to meet his full potential.

2) I was invited late last year to take a seat on the Board of Directors for the Fragile X Association of Michigan.  It has been interesting learning the ins and outs of how things run versus my idea of how I thought they ran.  The other Board members are great to work with though and I have been extremely happy to sit on the planning committee for our first conference hosted by our group since the International Conference for the NFXF was here.  We are about six weeks away and in the final planning stages.  Dr Marcia Braden is our guest speaker, one of the Fragile X experts for behavior (many would argue she is the best). You can check it out and purchase tickets at http://fxam2015conference.eventzilla.net/  They are only $25 / person and include lunch - super affordable!

3) (Not Fragile X related) I became completely hooked on a product last year, and ended up signing up to sell it.  On top of my many other roles, I now sell Jamberry nail wraps.  I do it mostly for fun, partly for the product/discount, definitely nice to meet more women.  Bonus:  My nails look amazing.  For real.  Check out my Instagram linked to the right to see some examples.   If you are interested in learning more about them or tying a sample, shoot me an email or check out my business page.  You can also request a sample here:  https://goo.gl/calDPf

4)  My most current addition to our life.  I am not our district representative to the county's Parent Advisory Committee for Special Education.  I am extremely excited about this and the potential to change and make the special education process easier for parents.  I remember just feeling alone and lost when we started navigating the whole process of IFSP, IEP, therapies, and services.  It is a lot and often topped with just learning to deal with and manage a diagnosis.  I think a parent last evening said it best "Sometimes parents are just struggling to get dinner on the table each day, giving them an ear to listen and a hand to help guide is more often than not essential for the whole family."  Helping other families has always been my passion when I talk about this 'world'.  It is why I started this blog in the first place, it has guided me every step with new things I take on (right behind doing everything I can for my own kids).

As you can see, my plate is awfully full.  It is all good and necessary things, but it leaves little time for blogging and sharing.  I will try to update more than every six months though.  And for anyone reading this who needs support or resrouces, please email me or comment here or even look me up on Facebook, Twitter, or Instagram.  All the links are on my page and I would be more than happy to help!



 
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Thursday, May 23, 2013

The Saga Continues

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We are currently in limbo phase with the STX 209 trial.  We know it has ended, but haven't yet received either a kit to wean or a call from the clinic on how to do so.   Not that I'm worried about either of these things.   We have heard and were told when we were notified the trial has been terminated that May 31 would be the last day we could begin to wean from the medication, although we have enough to last through August.   We have a few big things happening in the next few weeks which is when we are supposed to wean, the biggest of these being my sister-in-law's wedding.  The one Ayden is in.  I don't know if it will be allowed but I am going to BEG for us to be given eight more days.   That would give us enough time to get through the wedding, but not school.  School for us ends on June 12.

I have no allusions about how the weaning is going to go.  It was difficult in the blind portion.  (Though, technically we still don't know if he was on it - all evidence supports that he was).  I really would like to avoid any situations that are triggers during that time until we get a little more settled.  We will be in need of many thoughts and prayers during this time, not just for Ayden but for those around him.  I'm hoping that the baclofen will at least help with weaning, not make it so difficult. The best thing we could hope for is that it works about the same as the arbaclofen does.

Through all this, I've been reading a lot about clinical trials and the FDA approval process.  Another FX mom piqued my interest with a few comments so I decided to look more into it.  It's all very interesting.  There is a very unique challenge being faced by the pharmaceutical companies pushing forward with Autism and Fragile X medications.  Both are spectrum disorders with each individual displaying a range of symptoms.  I think we will find then that different therapeutic interventions tend to work differently as well.  I also believe this is the same reason we are seeing the varying results in the studies for STX 209.   This medication is treating the underlying cause and thus the reaction and measurable changes will differ from person to person - a more personalized therapy treatment as opposed to this drug does this one thing.  Essentially, the FDA approval is not setup to handle this type of medication.  They require a primary endpoint set and to be met for a trial to succeed.  Even if all the sub points succeed (as in the autism trial for 209) the study itself will fail as it did not meet the primary endpoint.  So while we are seeing results in individuals taking the medication being backed up by tried and true tests like Vineland Adaptive Behavior and we know this is working - the FDA approval process essentially doesn't accommodate treatments that have specific benefits for certain patients. 

I do know that this whole experience has been eye opening.  I'm glad I took the time to learn more about the FDA approval process.  I'm definitely glad we took part in this trial, it truly is groundbreaking - even if arbaclofen never sees approval, we will have been part of a huge learning process working towards getting treatments for Fragile X Syndrome.   With everything we did to try to keep this trial alive (which I won't go into now), it was also good to see our fragile x champions in congress also stepping up and doing what they could to help.  Congressman Greg Harper, Congressman Eliot Engel, Senator Stabenow, and Senator Isakson.  I think the past few months have opened my eyes from saying one voice can make a difference in Washington to SEEING my voice make a difference.  Seeing our politicians use their constituents voices as their own.  It's completely refreshing.

I'll keep updating as we continue on this journey....







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Thursday, May 16, 2013

BE The Change

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So much love and support has been pouring in all day from family, friends, even people I don't know.  While this is circulating on Facebook, I want to get a copy here as well.  I don't know what the future holds for Arbaclofen (STX 209), but I know that when this community, my X-Family, comes together we are a force to be reckoned with.  I know we have done all we can for the many that are currently benefiting from this drug, and hopefully the many more that will.

So...what can you do?

1)  Make some NOISE!  Now is not the time to sit by quietly.  NOW is the time for action.

FACEBOOK users:  SHARE SHARE SHARE.  Repost the following blogs:

Holly: http://itswhoiam-fx.blogspot.com/2013/05/3-12-years-when-drug-trial-ends.html
Melissa: http://www.basicallyfx.com/fragile-x-news/today-we-start-again/
Bonnie:  http://www.fragilexfiles.com/2013/05/the-shocking-end-of-drug-trial.html
Kristin:  http://kristin-thecarvers.blogspot.com/2013/05/the-end-of-stx209-for-usand-now.html?spref=fb
Cortney:  http://fxsadayatatime.blogspot.com/2013/05/stx-209-almost-final-update.html

TWITTER users:  Tweet, tweet, and re-tweet.  Use this message and/or the blog links above.

#WishfulVoting wish Congress was funding #fragileX research so effective meds are available and funding doesn't run out before the FDA approval

2)  Contact your local media.  Call your TV, newspaper, and radio.  Have contacts in other media?  Utilize them.  Call in favors. Pull strings.  Make it happen.  Big or small - each piece matters.

3)  SIGN and SHARE the petition:  https://www.change.org/petitions/pharmaceutical-companies-sponsor-arbaclofen-stx-209-for-chidren-with-autism-and-fragile-x

4)  Contact your congressmen.

You can find your representative here:  http://www.house.gov/representatives/find/
You can find your senator(s) here:  http://www.senate.gov/general/contact_information/senators_cfm.cfm

You can click HERE to find the sample letter I used. (many thanks to Melissa for the template!)

5)  DONATE.  Yes, I'm going to shamelessly plug our fundraiser here because let's be honest - every single penny counts.  The National Fragile X Foundation and Fragile X Association of Michigan were key in getting me to Washington DC this year to advocate for this EXACT thing..funding for research.  They will be key in other families returning or attending next year as well and we want to give back.    Mr Awesome and I are hosting an awareness day event/fundraiser in July - and have put the donation site active.  You'll see a link on the side of this blog, but can also donate by going here:  http://www.firstgiving.com/fundraiser/adatp/abouelseoud

6) Please just keep being amazing.  Your support means so much more than you could imagine.  We few, we family of FX parents are always strong together..but we are even stronger with our extended family, friends and AWESOME network of support.  THANK YOU.  From the very bottom of our hearts.  The outpouring of love today has been nothing short of inspiring.


Finally... Thank you to Holly for putting this list together and Melissa for the letter template she posted earlier today as well.  Your hearts are breaking with the rest of ours and still you both find time to be advocates.  We are one voice, but of you are so often are the megaphone for this community.



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Tuesday, March 12, 2013

How Can YOU Help?

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I hope you read my post on Advocacy Day.  If not, please take a minute to read this before continuing on with this post as it is directly related.

I decided to do another post regarding Advocacy Day because I want to not just touch on what I did, but what our group was actually asking for.  I'm not going to cover everything, but want to touch on the Acts and give places to find more information about each of them. These things aren't just important and relevant to Fragile X, but also to autism and countless other families living with special needs.   I would like to share this information and then challenge each and every person that reads this blog to submit their own letter to their members of Congress.

Achieving A Better Life Experience Act (ABLE Act)
The purpose of the ABLE Act is very simply to allow for those persons with disabilities to have an account that they can set aside money to help with expenses for living but where they will not lose benefits provided to them such as SSI or Medicaid.  Currently, to receive those benefits there are restrictions on income and a total allowable assets of no more than $2000.  Simply put, the current laws actually discourage anyone with any type of disability from having a job, home, or really being productive, independent members of society if their income would exceed that amount.

If passed, the ABLE Act would become a subsection of Section 529 of the Internal Revenue Code.  It would follow all the requirements of a traditional 529 qualified tuition program.

You can read more about the ABLE Act with these links:

A brief overview of the ABLE Act in 113th Congress
Read about H.R. 647 in its' entirety and see who has co-sponsored it.
Read about S. 313 in its' entirety and see who has co-sponsored it
Current news article about the ABLE Act

Transition toward Excellence, Achievement & Mobility Acts (A Three Bill Package) also known as TEAM Acts.
This is a really big act, and I'm going to make it as simple as possible.  This set of bills would help those with disabilities with the transition from school age to adulthood by re-aligning current federal programs to focus on helping youth become gainfully employed, pursue a post-secondary education, and engage in typical community settings/activities upon leaving high school.

Each parent works hard for their child to be as independent as possible upon leaving high school, a parent of a special needs child is no different except our children often need more help to achieve those goals.  These acts are really just updating older laws in place to encourage those with disabilities to become productive members of society. The original laws it is trying to change were put in place when it was a normal thing to institutionalize those with disabilities, it really is very archaic and not at all helpful to society as a whole.

TEAM Act Overview from NDSS
TEAM Act Summary from Autism Society of Ohio

So now that you know a little bit about these bills...I need your help.  Your voice.  I'm going to make it SO SIMPLE for you.

1)  Find your local Senator(s) and Representative HERE.
2)  Open THIS document and either download it or copy it to a blank email.  Fill in your Senator(s) and/or Representatives name at the top, then your personal information at the bottom - these sections are in italics.  You may also update the first paragraph to personalize it more if you wish.
3)  Print off and mail to your representative OR email them - their contact information will be on that first link you went to.

If this STILL isn't simple enough for you... email me.  cmasters (AT) gmail.com  [you'll have to type that one out].  Include your zip code and personal information and I will prepare the letter for you, then email it back to you so you can submit it.   It doesn't get easier, folks.  Five or ten minutes is all it should take.  Stop only thinking about politics during election years or financial crisis - take action NOW.  When it matters.

These adorable little faces (and the faces of many others affected by a developmental disability) will thank you.

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Friday, March 8, 2013

Advocacy Day 2013

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Wow.  I'm still in awe of how amazing the past couple days were.  I was excited for this, I knew what an amazing experience it would be - but I was not prepared for how much more it would be than what I expected.

I arrived in DC on Tuesday and met up with my roommate at the airport.  A small thing that I am so thankful for!  I had a small knot in the pit of my stomach from the second I left the kids and Mr Awesome at the airport.  Having a buddy to travel to the airport with and eat lunch before training really helped.  I was feeling much better by the time I walked into training - but began to fall apart [inside] shortly after.  Shortly after training started we were asked to introduce ourselves five different times in five different ways to someone else in the room that we had not met before.  Each way was specific - but it also put me entirely out of my comfort zone.  (as if I wasn't already).  By the time the five introductions were complete, I sat back down in my chair ready to vomit from anxiety.  Thank goodness I had time to recover and focus on training for a while before I had to speak or move again.  I had just about recovered when break time happened, and then forced myself to do a couple more things that kick started my anxiety yet again.

First, I hunted down the amazing Tracy and Mouse from Developmental FX.  These two women are amazing.    I've used their articles so many times to help with problems with Ayden and even to hand out to his teachers/school.  I introduced myself, told them a little about Ayden and asked if I could pick their brain later on a couple things.  They most graciously offered me their card and told me to call them if we didn't run into each other again over the next day or two.  This moment right here alone made my entire trip worth it.  If everything else had gone poorly and I had a terrible time (which was NOT the case at all) it all would have been okay because of this.

Second.  Well, I don't need to say anything about this other than I still cannot believe I agreed.  Yeah, that's me with the big green X.  (Thanks, Melissa  :P)


Training finished, and we broke into groups for dinner.  I had met the lovely Kathleen of My Son's a 'retard'! whom I had been following her blog since advocacy day last year during those five introductions I talked about above. She had invited me out to dinner with the group she was with.  Thankfully, there was a cash bar after training so I was able to enjoy a nice glass of wine to help with my anxiety before dinner.

Dinner itself that night was...let's go with "undesirable".   The company was outstanding, the food and restaurant not so much.  Let me just put a small sample of the menu - and make sure to pay close attention to the highlighted dishes in this picture:



The next day was the reason I was there.  As the evening before progressed, essentially every single flight out of DC was cancelled for Wednesday because of the impending snow storm.  Some channels were predicting 12-14 inches of snow.  By 4 am, the federal government was officially closed.  At 7 am - we received a call from Congressman Harper who had graciously scheduled a tour of the house floor for us.  Congressman Harper also has a son with Fragile X Syndrome - he takes especially good care of our Advocacy groups while in DC each year.  We were advised by him to head to the Capitol and that our tour was still on - so off we went!

Our first stop was a tour of the House Floor - a place not open to the public.  We were not allowed to take any pictures or anything really into the room itself.  The amount of history in that one room is just utterly phenomenal to sit and think about.  Congressman Harper talked about the 1954 House Chamber Shooting and showed us the actual table that was damaged during the incident.  (Which I was sitting one desk over from - the bullet hole still in the drawer and repair marks on the surface of the table quite visible).  He also talked about how President's Roosevelt's speech on December 8, 1941 was made in that very room.  There were other things talked about, but those were some of the highlights.  On our way to our first meeting, I was able to visit Statuary Hall and see the newly unveiled Rosa Parks statue as well.

At some point during the morning, it was decided to run a condensed version of our scheduled appointments.  This meant that we were to head to each Senate and House office that we were assigned to and request an early appointment.  I personally met with staff members from the offices of Bill Huizenga, Daniel Kildee, Mike Rogers, John Conyers, and Sander Levin.  Our group also met with staff members from Dan Benishek, Fred Upton, and Gary Peters offices.  For the other six representatives we left a packet of information about Fragile X and the different things we were requesting their help with.  On the senate side, we were able to personally meet with Senator Levin for almost an hour.  Turns out the "snow storm" was a blessing in disguise for us because so many offices had meetings cancelled and time to meet with us.


The meetings them-self were so incredibly amazing.  I've never felt like my voice has really been heard in the government even though I do my part and vote.  This though, was not like that at all.  It was such an amazing, empowering feeling to leave those offices knowing that we actually were making a difference.  Seeing the person we were meeting with become interested and start asking questions..well, it was awesome.

Our day at the Capitol ended as the House was voting to extend their pay freeze and uphold the current sequester until September 30 (end of the fiscal year).  It was quite something to be sitting in Dan Kildee's office with his Chief of Staff watching the house members vote in the room I had just been sitting in earlier that day.

I ended the actual day at a dinner with a whole lot of other Fragile X families - something not in short supply while I was in DC!



Following dinner, I headed to the National Mall to visit many of the memorials and monuments with some of my new friends - a must for my first time in DC.  You'd think visiting these places at night wouldn't be as awesome, but I'm fairly certain it was the best possible time to go (in spite of the cold).  It's humbling and breath-taking to see and I was very thankful the weather had cleared enough for me to go.


There was just so much that happened while I was there, and I wanted to make sure I really covered the reason I was there.  I would be leaving out a huge part of my time there though to not talk about all the amazing people that made up this day who also took time to do the same thing I was doing.  There were around ~180 other parents, family, friends, and self-advocates for people with Fragile X with us and they are the MOST AMAZING group of people I have ever been a part of.  We are very alone in the aspect that until recently I have not even met another family living with a child with Fragile X (since knowing about it) and in two days I met more than I can count.  People that are eager to share ideas about their kids and happy to hear about yours - especially the bad!  Mom's who share this carrier status - and make you feel normal when you're around them (instead of like the crazy one).  Even though I was more than ready to return home to my family, my X-Family as I'm going to call them have been missed every second since I walked out of breakfast yesterday morning.   I am counting down the days until I am able to see them again.




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Friday, February 15, 2013

Advocacy Day 2013

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In one of my last posts I talked about how much I really wanted to attend Fragile X Advocacy Day.  Just as I had resigned myself to being unable to attend, a couple things fell into place that have allowed me to go.  I'm so completely excited for this opportunity, I've been struggling to put all this excitement into words since I found out and still can't, but wanted to put an update on here anyhow!

Since we received Ayden's diagnosis, I have been actively sending letters to representatives and senators about Fragile X (with the help of the NFXF).  To be honest, I've never taken part in anything like writing letters or contacting representatives until then.  I've voted, I stay informed...but never more than that.  It's a shame that I haven't been more involved, really.   This past election, I found my voting decisions strongly swayed by the way elected officials dealt voting on all subjects related to Fragile X.  For the first time, I spoke out for someone running for office - one in particular, Debbie Stabenow (who I am very much hoping one of my meetings is with during Advocacy Day!)  This, is my next step and to be honest I am terrified.  I'm not good at meeting or speaking to other people, and I'm not just talking about the people I'll be meeting with on Capitol Hill  There are around 175 other people attending Advocacy Day, many of whom I follow online via Facebook, the Fragile X group, or blogs - but meeting them in person is quite different.  I had a dream the other night that I was laughed at and told I shouldn't have come and to stick to doing things online because people liked me better there.  There was more to the dream, but it certainly did not help my anxiety!

I don't really think that would happen...mostly at least.  There are quite a few people who I look up to an awful lot that are going, and I am going to be honored to meet them.  That's the other part of this really, the part that is for me.  Where I get to finally meet other Fragile X parents.  The ones that have been there for both of our diagnosis and helped with IEPs and behavior issues, cheered me on when I have been down, and have SO MANY ideas to make things better.  The ones who don't make me feel like I'm alone in this, not ever.

I can't wait to fill everyone in on my first Advocacy Day experience...so look forward to that sometime after March 7!
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Thursday, January 31, 2013

Brief Updates

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An update on the kids, STX 209, Fragile X Advocacy Day, and Fragile X Awareness Day.  Lots of short blurbs to close out the first month of 2013!

We have quite a crazy month approaching as we head into February.  I'm not sure how much time I'll have to update here - but certainly feel free to follow along on Facebook, Twitter, and Instagram.  I wanted to post a few small updates about a few things before we got into the craziness....

Ayden:  We are now in the STX 209 open label extension.  We have another trip to Chicago in February, then one in April, and then we will be on every three month visits.  We've upped his dosage one time since we started so he is currently on 10mg (5mg two times per day).  We are seeing many good changes on this dosage and opted to stick this dosage out for now to see how Ayden is doing.  The change happened very quickly when we upped his dosage (within a couple days) and we are still seeing improvements after a week on this dose.  We will have to decide whether to try to up his dosage and try to get a little better result, but want to leave him on this current dose until we stop seeing improvements.   We are still assuming (even moreso now) that he was on a high dosage in the blind portion of the trial, the top dose he could have had was 10mg three times per day.  If we go up from where we are at, the next step is 10mg twice per day.  Lots to consider, but for now we're just watching.   In related news, Ayden made his very first two-word [spoken] sentence yesterday.  I'm just amazed at the difference this is making for him.

Issac:  The one who normally gets left off the blog...is really turning into a boy rather quickly.  He's developed quite an attitude recently doing the full body sigh when we tell him something he doesn't want to hear and bursting into full-fledged tears when he doesn't get his own way.  He's also picked up asking "why" to everything in addition to "what".  Of course those are the things that make me want to pull my hair out, but he also has the best sense of humor and a giggle that can't help but make you smile.  His favorite thing to do lately is play video games - Mario, Sonic, and Skylanders.

Emma:  Baby girl's first birthday is about a week.  I'm not quite sure how it came so quickly...but wow!  We'll have her birthday, then her party, and near the end of the month head to South Carolina for a research study then to North Carolina for the second part of another research study.  I'm very excited to work with both teams at USC and UNC again, not so much looking forward to traveling/flying/driving by myself but it will work out. In case you're tallying at this point, all these trips also mean I'll be physically in five different states in over the course of a week period and more if you count flying over them.  YIKES.

The other thing I want to touch on briefly is Fragile X Advocacy Day.  Advocacy Day is sponsored by the National Fragile X Foundation.  It is basically a really big group of parents, grandparents, siblings, and self-advocates that go to Washington DC to advocate for Fragile X funding and other things related to Fragile X.  This is the first time I have really wanted and felt I needed to do something even close to this, but probably will not be able to attend.  Financially, the cheapest we could do it would run between $600-$800.  That number includes flight, hotel, food, and something to wear (stay at home mom clothes just don't cut it when you're meeting senators!).  I've been watching flights since October of last year and trying to decrease that cost but it just isn't happening.   There are a few scholarships available that I'm waiting to hear back on, but I expect at this point it isn't going to work.  I don't talk about money on this blog a lot, I feel it's very personal to each family.. I'm going to make a small exception now though.  We are very thrifty with how we live to make it possible for me to stay home with our kids.  We cut corners, make sacrifices, do whatever we can and it is totally worth it.  It also means that we cannot pull an amount that high out of our pocket.  Especially after cutting into our budget for all the trips to Chicago we've been making for Ayden.  I'm very grateful that we are able to make it work, at times like this though it is so hard!   Whatever the case, I will be doing what I can from home and I hope when I post again closer to the date that each and every reader will take a few minutes to write their legislators with me.  If I can't be there, my voice and hopefully each and every voice of my readers will be heard.  So, stay tuned.  :)

Fragile X Awareness Day is less than 6 months away, and I have PLANS this year.  Plans..fun, secret plans.  I can't WAIT to share them.  Hopefully I'll have something I can share in the next month or two so others can make plans with me.  

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Wednesday, December 19, 2012

2012 WEGO Health Activist Award Nomination

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I was nominated for a 2012 Wego Health Activist Award in the Advocating for Another category.  If you would please take a few minutes to "endorse" me I would greatly appreciate it.  I would love to see Fragile X get more recognition, and these seems like an awesome way to do it!  Anything that brings more awareness to our community is great news for all of us living with Fragile X and especially for those that are not yet diagnosed and struggling for answers.  You can click on the green "Endorse Me" button below or on the main page.  Thank you SO MUCH for your support.

Learn more about the Activist Awards here:  Wego Health Activist Awards


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