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Autism

Autism Speaks ~ AutismCares Ipad 2 Grant Open till Friday

Ipads can have a huge impact on an autistic child and his/her family.  I have witnessed it first hand with my own children.  However IPads are expensive, too expensive for most families who are also taking on the financial impact of having a special needs child.
When I saw in the Autism Speaks newsletter today that Autism Cares is accepting applications this week for their Ipad 2 Grant, I wanted to make sure I shared it with everyone!
There are some eligibility requirements as listed on the AutismCares website,  so if your interested I highly recommend you link over and read about this program.
http://www.autismcares.org/site/c.mqLOIYOBKlF/b.4745901/k.BD21/Home.htmhttp://www.autismcares.org/site/c.mqLOIYOBKlF/b.4745901/k.BD21/Home.htm

 

One IEP Done ~ Success!

Puma
We had another IEP meeting for Anthony, and I am relieved we came out with a plan I am excited about.
Last spring, I had rejected Anthony’s IEP plan and took him into Children’s Hospital for their full learning disabilities program testing.  After two and a half years with the same type of services (language and reading pull outs 2-3 times a week) on his IEP and no visible improvement, I was tired of the black and white meetings.
Once I entered the world of autism with Aidan, it really opened my eyes to what it takes to advocate for your special needs children.  Prior to last years IEP meeting I always blindly trusted the school system.  Big Mistake!  Don’t get me wrong, Anthony’s teachers have all been remarkable, especially his SPED teachers.  However they don’t get to make all the decisions on what services your child gets, there’s a bunch of people behind the scenes who may in fact care about what your child needs as a student but its also there responsibility to care about the schools budget.
Last year when I brought his education up to some teacher friends I was told “the squeaky wheel gets the goods” another words, if you don’t push for what you think your child needs, there’s a good chance you’ll get jumped over to the parent who’s making a fuss.  Well it definitely feels like I’ve become the squeakiest wheel in the city with the 3 kids.
The testing revealed that Anthony has a severe language disorder that will not improve with the education plan that the school had continued to lay out.  Anthony needed a smaller, language based program, comparable with an ESL classroom but in a sped setting.
When we reconvened last week, I was pleasantly surprised that the school already had their language class room’s teacher in the meeting and a plan to put Anthony into the program for a majority of the day.  I also instantly fell in love with how well his new language teacher advocated for him.  By the end of the meeting she had gotten him more services than I had even planned for.
All in all I am excited for this year because understanding fully what the issue is and having the right service plan in place gives me great hope that he will be able to catch up to his peers.

At what point did ignorance become OK?

My cousin posted this photo on my Facebook wall the other day, because she knew I would love it! 
 
Aidan, like about 1 in 50 children, has Autism, he is not a spoiled brat, he is not an undisciplined, loud mouth, pain in the A**!  He has a disability and he has to cope with it everyday as a toddler/preschooler!  My heart breaks for my child when I see him wonder aimlessly around flapping his arms, my heart breaks when he falls into a complete and total meltdown that leaves him screaming and inconsolable.  Imagine walking through life not knowing where your body was in space, imagine the rubbing of clothes against your body feeling like needles all over you, imagine not being able to listen to a sentence because a bird chirped outside and you cant block it out.  Now imagine dealing with all this as a toddler, not being able to vocalize how your feeling.
 
Yet we as a family still have to function, I have to go grocery shopping and run errands.  My children still deserve a sense of childhood so we still go to the playground and museums.  I refuse to let my son become a caged animal because others are ignorant.  I get the looks, the stares, I hear the comments under peoples breaths when Aidan begins to scream at the wrong moment.  I’ve heard stories from other Autism parents of being asked to leave shopping malls by security because of melt downs and children being kicked out of daycare facilities.  This makes me SICK!
 
Autism is an invisible disability, you cant look at a child and understand for a second what that child and their family goes through, yet for some reason it seems ok in our society for a person to be blatantly rude based on their own ignorance.  SO to everyone my child annoys in public, to everyone who snickers, who stares, who doesn’t understand why I am comforting a screaming child instead of disciplining him…. TOUGH, I will continue to live everyday, bringing him everywhere any normal child should be able to go…. Because my motto is, There is no cure for Autism, Ignorance on the other hand has one… Education!  So stop judging everyone else around you and go educate yourself!
 
 

RSV, Asthma, Phnumonia? who knows!

Lilly started her normal cough she gets 2-3 times a month, that congested type cough that she gets that keeps her up all night coughing to the point of gagging and throwing up if she’s eaten anything within the hour.  At first I thought, oh great here we go again! Cause we’ve been battling this cough for months with no resolution.  Have gone to the pediatrician frequently, had an inhaler but  the pedi had never heard wheezing so “asthma” was never truly diagnosed, there’s no cough medications for 3 year olds, so we had sort of learned to live with the cough remedying it with honey and warm baths hoping she would grow out of it. 
 
However this episode quickly turned from bad to worse.  She developed a fever, and needed to have tylenol and mortin alternated almost every 4 hours through out the night.  In the morning when I was expecting things to calm down like past episodes of this cough, things got even worse.  I couldnt break her fever, motrin…. didnt come down! tylenol…. didnt come down!  Ice packs…. came down for a few moments then spiked back up! Cool bath…. only kept it down for just under an hour! 
 
So off to the Pedi we went, they checked her and her oxygen levels were low so they sent us over to the ER.  This is where a week long battle began!  I learned alot in this week and came to realize…. when a mothers instinct is telling you something, LISTEN! No matter who your going up against, doctors, specialists, nurses, other mothers… doesnt matter! you know your baby better than anyone else could possibly understand, so always trust that feeling in your gut.
 
We went to the local ER, that was about 15 minutes away.  Its one of those town/city hospitals, ya know not a major hospital, just the average community type hospital, but it had been where I had alway gone before so thought nothing of it brushing thoughts of taking the extra 15 minutes and heading into the city to Children’s Hospital.  We where in the ER for about 6 hours, with continuouse oxygen, labs, and chest xrays.  according to the ER doctor who seemed to understand Lilly, there was a good propability of phnumonia.  It was on the line whether it was viral or phnumonia but with the fever and the oxygen not helping they started the antibiotics thinking better safe then sorry.  Also starting steroids and nebulizer treatments.  It was getting late, the fever was low and staying low but they couldnt stabilize her oxygen levels which were in turn causing her heart rate to raise so they decided to admitt her to be safe, but the ER doctor asumed we’d be “discharged in 24 hours, 48 hours max.  It was just a matter of getting the antibiotics and steroids in her system”.  This all made sense, I have a medical assisting background and was one of my grandmothers primary care givers in her final days so I figured out alot about oxygen levels and such with her constant cycles of phnumonia and sever asthma along with COPD.  We were moved up to the pedi floor and tried to get some rest through the night.
The next morning she was off the oxygen and I was excited at the apect of her getting better of course but of going home also, because i never imagined being admitted and was beyond unprepared.  The boys are ALOT of work and while they have a wonderful dad, he’s working from home so the boys arnt monitored the way they need to be concidering the autism factor.  So the on call doctor came in that morning, which happened to be one I knew because he worked in the kids pedi office, he decided to keep us another night just to let her get off the oxygen over night, ok still making sense.  Then struck me with a wammy, “the xray doesnt really show phnumonia, so we dont need the antibiotic, its viral”  I was confused but figured well he’s the doctor right? well by the end of the day she was back on the oxygen, and had gone from out of bed jumping around to not wanting to move from the bed falling in and out of a nap.
My gut was telling me “its the antibiotics, she should never have been taken off of them” but the doctor, the nurse, the respitory therapist all seemed in agreement.  We spent two more sleepless nights on oxygen in the hospital, some nurses would get her up and moving, blowing bubbles and what not but once rotations happened the next nurse would put her back in bed and on oxygen so she wasnt getting anything coughed out of her lungs.  I was exhausted and I didnt know what to do but the following night scared the adrnealin right back into me!  around 4:00 in the morning her levels dropped again, but didnt go up with the oxygen, nor did they go up following the nebulizer treatment.  They called the on call house doctor in, who was out of Children’s hospital Boston, which is where the kids see all there other specialists.  He came in sent us down for a new xray, which showed no change, he started us on antibiotics again immediatly and ordered some blood work.  I was astonished and felt like what? we just waisted 4 days for nothing!  The levels raised within a few hours and I tried to get Lilly hushed back to sleep.  That morning as the daily rounds started the nurses knew I was furiose and sent the pedi into our room first.  He ran an RSV test which came back positive, ok she does have a virus, but he seemed adiment on getting her home that day.  He insisted that getting her up and out of bed would get her oxygen up and with RSV theres no true reason for the kids to be in the hospital while it clears, sounded awesome right? A light at the end of the tunnel is what it sounded like!  Two boys at home, a house surely destroyed, a autsitic daughter going on 6 nights no sleep and having melt downs about wanting her bed, and a Mamma who hasnt slept in over a week and had been eating out of a vending machine all week!  Well the doctor went on his way, and I sat waiting for the nurse to come let us off the machines, but they seemed to conserned that her oxygen levels wouldnt stay up when they took her off the oxygen machine for only moments at a time.  Looking back at that day I realize I knew there was way to many people calling the shots, one doctor does something another changes it, one nurse starts a routine another changes it.  I realize my gut was saying she should be on antibiotics from day 1 and I should get her out of here this place is a circus but I had faith in the “professionals”, I was exhausted, and I was doubting my intuition.  Later that day Daddy came in and let me go home, shower, rest, cuddle my boys, and refresh myself.  I got back into the hospital with real food in my belly, some sleep, and a sense of peace that the kids were ok at home.  That next morning after not seeing the prior days pediatrician sense the morning before, actually not seeing any one of the doctors more than once over the past week, I was ready to lay into whoever came into the hospital room next.  To my delight it was her pediatrician, finally!  I looked at him dead in the eye and said “we are  leaving today! one way or another, we are out of here!”  he seemed a bit caught off gaurd, but I wasnt backing down.  He continued on saying she wasnt ready to get off the oxygen and lets continue trying through out the day, hmmm the same thing I’d heard all week from all 7 prior doctors, nope no way was I taking this, and from her own pediatrician! Really? your supposed to be the one who knows her, fixes her, understands I have 3 kids with disabilities, knows my overnight back is full of all my prescriptions, and this is what your offering me? More of the same B*llsh*t!
I began packing our stuff, insisting I would discharge her myself without medical advise if they didnt decide on another course of action, and infuriatingly telling them if she’s so sick that we need to spend another night in the hospital it needs to be spent in Boston at Children’s Hospital.  At first they wouldnt agree to a transfer saying her case wasnt severe enough and didnt warrent a transfer, but when they realized I was fully prepared to walk out with MY daughter and simply drive the extra 15 minutes into the city and walk into that emergency room, there mood changed and an ambulance was there within the hour transporting us.
I think the following 24 hours were extremely enlightening.  I have always favored Childrens Hospital, there the best, the specialists are top notch, I am always comfortable with my kids care through that hospital.  However for some reason I left my daughters care and choice of her needs in someone else’s hands besides my own, and that will never EVER happen again.
Within an hour of being at Children’s my daughter was in a new bed, had xrays, met her new nurse, and her pediatric staff on the floor.  The same doctors were always rotating on her floor and they had a list along with photos on the room walls so parent knew who was taking care of their kids.  Nurses carried cell phones and within seconds of a machine beeping they were in the room, I could press the call button and my nurse willingly came in (smiling!)  I was in awe at the difference.  I had just spent a week dealing with nurses who spent more time gossping at the station then caring for my daughter, and having far more respect for the wonderful women who would come in to clean up and change the sheets then I did for the licensed medical staff. 
That day I saw a asthma specialist, had a diagnosis of RSV, Phnumonia, and Asthma.  Also had a treatment plan for home, along with a well mapped out course of action and what goals to look for.  I was simply amazed.  Lilly was off the oxygen within a few hours and stayed off for the remainder of the day.  That night Lilly’s oxygen dropped twice once the nurse came in repositioned her, patted her back, and helped her get it back up with out putting her back on the oxygen.  The second time she only needed it for two hours and the nurse came back in shut it off to check her and it stay up so the oxygen was turned off.  When you spend a week seeing nurses take an hour to come in leaving you with a buzzing machine peircing your brain only to throw a mask on the patient and leave not to come in again till the morning, the change makes you have a deep respect for the way these new nurses cared for a floor full of kids.  The following day Lilly stayed off the oxygen even through a 4 hour nap so we were sent home, only a little more than 24 hours after being transferred.  There is not a doubt in my mind that had I listened to my gut and gone straight into childrens, Lilly would have been home within the initial 24-48 hours. 
 
I have spent years advocating for my kids against school systems, educators, insurance companies, exc.  but it never dawned on me that I know my kids health better than a doctor, till now!  I will never again let anyone tell me what my children need without feeling a sense of peace with the course of action again.  A mother’s bond is more powerful than anything, even a PHD!

How to Make your Own Weighted Blanket DIY

Make your own affordable weighted blanket easy DIY instructions.

Make Your Own Weighted Blanket DIY Tutorial

 

Why I made a weighted blanket DIY

When Early Intervention told me I should get Aidan a weighted blanket for his Sensory Processing Disorder, I had no idea what SPD was, never mind a weighted blanket!

Make your own affordable weighted blanket easy DIY instructions.

So what did I do….. Google!
 
BUT these lovely blankets that were supposed to make my dear little boy able to relax and stay still for a few moments cost over $200! Yes, I would save every nickel and penny if need be to help this little cutie feel better, but really $200 for a few pieces of cloth and some stuffing? Heck no!
I could feel the Martha in me coming out!  Time for a Weighted Blanket DIY!

 

So I went over to Walmart to get the essentials:
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions.
The fabric was on sale for 75% off because they were discontinuing the fabric section of the store… Yippy!
1 Yard Dinosaur Cotton Fabric: $.93
1 Yard Red Flannel: $1.04
2 Bags of Polyfil Pellets: $7.90
And to add some fleece fringe that Aidan loves to rub against his face
1/4 Yard Coordinating Fleece: $.67 the $200 blankets don’t have this!
I got home and got to work as soon as the munchkins were in bed, all together it took me about 3 hours, but I have to say I am not an expert sewer and this machine has probably only sewn a hand full of times in the last year…. but I love that it embroiders 😉
Make your own affordable weighted blanket easy DIY instructions.
So this is how to make one:
 
Cut off all the ends and lay out the fabric right sides together and smooth it out, then cut any extra that you may have.
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions. 
Pin along three sides of the blanket, you will use A LOT of pins!
and sew up the three sides.
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions.
Trim the corners so that they won’t bulk up, and turn the blanket right side out. flatten it out or iron it so that its easier to work with.
Make your own affordable weighted blanket easy DIY instructions.
Now comes the fun part, Start by deciding how heavy you want it, how many squares you want. I used 10% of my son’s weight but you should always check with your child’s doctor to see what the best weight would be for them.
I had 15 squares. So I sewed 4 vertical lines from the open end of the blanket down as equally spaced apart as possible.
Next I got out the pellets, knowing I wanted 15 squares I divided the 4 pounds of pellets up equally into 4.3 ounces. try not to spill the pellets they are not the easiest to clean up! I know.. I poured the 4.3 ounces into each collum of the blanket, then smooshed them all the way down to the bottom of the blanket and sewed a horizontal line accross the blanket to keep the pellets in, creating squares. Becareful to get all the pellets down so that you dont sew over them and break your needle. Continue doing these steps all the way to the top of the blanket and close it up.
Make your own affordable weighted blanket easy DIY instructions.
At this point the blanket could be done, but my little guy likes to rub soft things against the top of his lip to help him fall asleep, so I decided to add some soft fringe to the top. I took a fat strip of fleece and sewed it to the hem of the blanket and cut the fringe. That’s it, an easy peasy weighted blanket DIY!
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions.
Make your own affordable weighted blanket easy DIY instructions.
and the best part… Aidan loves it!
Make your own affordable weighted blanket easy DIY instructions.
Great project and great blanket for cuddling:)
Enjoy!
 
Are you making your own weighted blanket?

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