Showing posts with label girl power 2 cure. Show all posts
Showing posts with label girl power 2 cure. Show all posts

Monday, September 16, 2013

Intro to Blended Food for Rett Girls

Are you relying on formula to feed your daughter through her G-Tube? Have you heard about a healthy alternative called a "blended" or "blenderized" diet? Here's the scoop:

A blended diet is simply taking everyday foods and blending them so they can be given through a feeding tube.  A blended diet can be very intimidating at first (it's much easier to open a can and have peace of mind that "everything is in there") but don't over think this one.  Think about how you eat, how your other children eat and how your Rett Girl ate before getting a g-tube.  A blended diet is as easy as preparing a meal - then blending it into a soup-like texture! (note: you will need a blender with a soup setting to get it to the best consistency - see below for recommendations).

We're here to give you a starting point and the resources you need to make an informed decision about blending.

The Benefits:


A blended diet is perfect for those who have food allergies or intolerances and those who are looking to add more fat, calories or proteins.  Your Rett Girl will essentially be able to eat the same nutritious foods you serve your whole family.

Bonus: Since you are in control of the ingredients you will be able to stay gluten-free, dairy-free, soy-free, etc.  You can add more fats if your Rett Girl needs to increase her weight, you can blend raw foods or cooked foods.  You will also have control over whether the ingredients are organic, the proteins are free-range, the dairy's are grass fed and the grains are GMO free. 

Many families have switched from formula to blended foods and have experienced wonderful health benefits. It's hard to say exactly if or how exactly your Rett Girl might benefit from a blended diet since each child is different and each family will blend different food and in a different way.  But what is clear is that fresh, whole foods are always everyone's best source of vitamins, minerals and nutrients.

Fresh whole foods are far superior in nutrients to anything that is processed and put in a can.  One of the most noted benefits of starting a blended diet is that the tube-fed person digests food better.  Of course! That's because food was designed for our bodies to break it down and use its nutrients. We weren't designed to break down chemicals.  With better digestion comes a list of positive outcomes to include: healthier looking hair, nails and skin; improved weight gain or weight loss as the case may be; less gas/bloating, constipation, reflux, and vomiting after feeds; and more energy - to name a few.

The nutrients that come from foods are just not the same as the nutrients that come in a can.  Science cannot replicate fresh whole foods.  Fruits and veggies are packed with antioxidant phytochemicals, which are basically just the natural compounds of the plant. There is also a natural combination and interaction of phytochemicals and macro nutrients (proteins, fats and carbohydrates) that occurs with whole foods that can't be duplicated by mixing different vitamins together. 

Where to Start:



This is the hardest part, starting.  Don't feel as though you have to jump right in, don't get overwhelmed.  Starting a blended diet is a process -- a very slow, gradual process. You will learn as you go.  

The very first thing you need to think about is what exactly your Rett Girl needs.  Make a list of any intolerances or allergies.  Next, decide whether your Rett Girl needs to maintain or increase her weight.

Finally do a little research into a simple, balanced diet and an approximate calorie amount.  This is the step that scares a lot of people, but think of it this way: it's not so scary to prepare a balanced meal for an oral eater and you typically don't spend too much time counting the calories on the plates of your other family members, so relax and don't overthink this part, either.  Ask your daughter's GI specialist or pediatrician for a referral to a registered dietitian or a nutritionist who may be able to start you out on the right foot if you want some support.

Transitioning:  


This is the part where you need to go slow.  A few things that will determine how slow your transition will be: how long your Rett Girl has been on formula and if she is still able to tolerate some oral feeds or not, and her overall tolerance.  

If your Rett Girl has not had oral foods in a number of years and you are not yet sure if she has any intolerance to certain foods you may want to start with introducing one ingredient at a time just as you did when she was a baby first starting out on solids.  You can either introduce them on their own in between feeds, or blend them in with her formula.  As you add foods you can start to combine them to give her more of a complete meal, decreasing the formula as you go.  

Some families start with baby foods.  Stage 1 baby food can be given straight through the tube and can sometimes be an easy and much less intimidating start when moving to a blended diet.  Stage 2 and up foods need to be blended and put through a strainer to make sure they will go through the tube.  Many families will start this way and just replace one meal or feeding for a certain amount of time and then replace another feeding and gradually work up that way.  
Other families jump right into blending and will choose to blend whatever the entire family is eating at a certain meal or create a "staple" meal that includes all the nutrients needed but can be customized by changing the fruit, veggie, or protein to give some variety.

You can find information on how to create your own recipe here or check here for some sample recipes.  Here is an example of one of the recipes:

1 C. dark chicken meat
1 C. amaranth
1 C. brown rice
2 C. sweet potatoes
1/2 C. walnut oil
handful of fennel seeds
4 C. water to blend

If you're not sure exactly how to move forward you can see how one Rett family moved through the stages of starting out here.


There are many different ideas of a "balanced" diet out there but a place to start is just by starting with the basic food groups and using appropriate portion sizes for your Rett Girl's age.  Or, you can get a little more technical and start with the "macro nutrients" or the proteins, fat and carbohydrates (carbs) in foods.

Every person has different needs but a starting point is to go for 40% of the total calories from carbs, 30% from protein and 30% from fat.  Carbs and protein have 4 calories per gram and fats have 9 calories per gram.  So, if you have a food that has 5 grams of fat then 45 calories of that food are from fat.  You can do this simple equation for each macro nutrient in each food that will be blended and get a total of what your Rett Girl will take in through her diet.  

Tips 


1.  Always check with your Rett Girl's doctor before changing her diet, but don't be intimidated.  You are your child's best advocate and if you see a benefit to transitioning her to a blended diet make sure you voice your position.

2.  Seek the advice of a registered dietitian or nutritionist.  If nothing else then for peace of mind that you are including all of the nutrients that your Rett Girl needs.

3.  Remember water!  You can find general guidelines of hydration needs here and can add the amount of water you need to each feed.  Some parents, however, find a huge benefit to giving water 30 minutes before each feed.  Even just an ounce or two can help "prep" her stomach for food and maybe help with gastric emptying.   

4.  Invest in a good quality blender like the blendtec or the vitamix.  These blenders have the ability to liquefy food so you don't need to strain your blend before you put it through the tube.  They can be pricey, but contact the company and they should give you a refurbished one that is discounted with a doctor's note.

5.  If you are planning on overnight pump feeds you will want to be very cautious about the food spoiling.  Try the Koala by Feeding Essentials to keep food cool throughout the night.  

Resources:







By Bridget MacDonald, RettGirl.org Coordinator
Bridget graduated from Western Michigan University in 1999 with a B.A. in Nutrition.  She worked as a clinical, registered dietitian at William Beaumont Hospital and was a program director at the American Diabetes Association prior to having her daughter, Annie, who is diagnosed with Rett Syndrome.

Wednesday, August 8, 2012

IEP HELP!

Our second blog post for back-to-school is all about the IEP (Individual Service Plan).  Ugg, we even hate writing those dreaded three letters, but, fear not, we're here to equip you with lots of tools to get your Rett Girl all that she deserves from school.

Before even getting to the IEP planning stage, however, take time to educate your daughter's team about Rett Syndrome. Use this easy link to our Q&A for Therapists on the PediaStaff website to send out to teachers, aides, therapists, counselors, and even the school principal. The sooner they understand your daughter's complex issues along with her strengths, the sooner you will be able to develop a good plan for her.



IEP BANK:
The first thing you need to know about an IEP is what one looks like: what are some goals, what do other Rett Girls have written into theirs and what is really important to include?  We have a "bank" of IEPs that are organized by grade level.  Check out our IEP Bank HERE and get some great ideas.  Then, stop by our Example IEP goals and Objectives page HERE for even more ideas!


RESOURCES:
COMMUNICATION:
Communication is always one of the biggest issues with our Rett Girls.  Our girls need to have a way to communicate, they have so much to say and need a way to express themselves.  We encourage you to push your school to allow your Rett Girl to utilize an AAC (Augmentative and Alternative Communication) device or system.  Apraxia makes it very difficult for our girls to be consistent which can some times be mistaken as them not understanding.  A couple great resource to use and pass on are Linda Burkharts Multi-Modal Communication Strategies for Children who have Rett Syndrome and this letter from RJ Cooper about Girls with Rett Syndrome.  These may help your team understand your Rett Girl a little better and may be helpful with setting up communication goals.  
SOCIAL GOALS:
Lastly, we all know how social our Rett Girls are so don't forget to include social goals in her IEP.  A great way to help her classmates learn about her abilities and understand her a little better is to send a letter home to the parents in your child's class.  This can help answer lots of questions and make your Rett Girl a little less intimidating to their peers.  We have a sample letter drafted HERE.  


Remember to take a deep breath, try to relax and know that as nervous as you are for a new school year to start your Rett Girl is equally as nervous.  Help her to ease into a new year by being confident about her goals and where she's placed.  If you need any assistance Rett Girl is always here to help!  

Monday, May 7, 2012

Poor Circulation in Rett Girls


Many of our Rett Girls have very cold hands and feet due to poor circulation.  Sometimes they can also look blue or purple.  The easy remedy for poor circulation is typically to get up and move around to get the blood flowing.  This can be difficult for our non-ambulatory and non-weight bearing girls but even if our girls are able to get up and move around many times it doesn't help because their poor circulation is usually due to a vasomotor disturbance that is difficult to treat.  

Google dictionary explains vasomotor this way:  "Denoting a region in the medulla of the brain (the vasomotor center) that regulates blood pressure by controlling reflex alterations in the heart rate and the diameter of the blood vessels, in response to stimuli from receptors in the circulatory system or from other parts of the brain".  


So what can we do as parents and caregivers to help our Rett Girls circulation and the pain that can sometimes come with it?

Keep them warm:  Poor circulation means cold feet, even in hotter weather, so keep them warm with socks and loose fitting shoes, boots (like UGG's) or slippers.  A heated blanket works well too but be sure to check her often so the blanket doesn't get too hot.


Circulation socks:  There are lots of circulation socks on the market for adults so if you have an older Rett Girl you can easily pick up circulation socks at your medical supply store.  As for our younger, smaller girls we have found these Nike compression socks typically used for sports.


Keep her feet elevated:  When your Rett Girl's feet are elevated it's much easier for the blood to get down to her feet and circulate back up.  In the car you can keep feet up with this great foot rest.  We have also heard that it works great when used with a booster seat attached to a chair.

Don't let her feet dangle:  When feet are dangling not only is it harder for the body to pump blood but typically the back of the leg is stressed and can further hinder circulation.  One of the places where feet dangle a lot is the bathroom.  If you don't have a potty seat with a foot rest check out this one (for very young girls - this one is small).  Or you can find a foot stool at a height that would keep your Rett Girl's knees at a 90 degree angle. 



Massage:  Massage works to speed circulation, you can even try this cream by Burts Bee's to stimulate the circulation even more.

We hope that these suggestions help in your Rett Girl's circulation.  If you have found any additional resources please share them with us.

Tuesday, March 27, 2012

Finding Funding for Our Girls

A few posts ago we talked about The National Organization of Rare Diseases (NORD) and discussed how this organization has some resources to help financially with the cost of living with a rare disease.

That got us thinking.

We thought, there must be more help out there. Help for not only rare disease but children with special needs in general so parents don't have to feel like they need to figure out how to grow a money tree!

We did some digging and we're glad we did because we found some amazing organizations and resources that are out there and are willing to help girls and families like ours. We hope that if you are in a tight position and wondering weather you can afford to give your Rett Girl the equipment that you know she needs or pay for the therapy that you know she will benefit from that you will check out these links.


AMS Vans : Provides a list of available grants and other funding available to help pay for a handicap van.


Ability Found: A wonderful non-profit organization whose goal is to empower all individuals with disabilities. Ability found helps to find medical and rehabilitation equipment free of charge to people with disabilities who can't afford it. They use a team approach to accomplish this, working with the client, the provider and the vendor.


The Prayer Child Foundation: The mission of the Prayer Child Foundation is to have a hand in answering the prayers of parents with special needs children and helping these children to have the joys of a normal childhood. This foundation may help fund the request of children ages 18 and under.


The Wheel to Walk Foundation: The Wheel to Walk Foundation is a non-profit organization dedicated to making a difference in the lives of children age 21 and younger with special needs. They help children who experience difficulty obtaining funding from their insurance companies.


United Health Care Children's Foundation Inc.: The UnitedHealthcare Children's Foundation is a 501(c)(3) non-profit charity dedicated to facilitating access to medical-related services that have the potential to significantly enhance either the clinical condition or the quality of life of the child and that are not fully covered by the available commercial health benefit plan. This “support” is in the form of a medical grant to be used for medical services not covered or not completely covered by commercial health benefit plans


The United Cerebral Palsy Organization: Click on this link to find your local chapter who may be able to direct you to local organizations that aid in funding the needs of special children.


Easter Seals: Much like the United Cerebral Palsy Organization, Easter Seals has local chapters that may be able to direct you to local organizations that may aid in funding the needs of special children.


The Home School Foundation's Special Needs Children's Fund: Enables financially struggling homeschooling families to provide a quality education for their children with special learning needs.


In addition to these resources you may want to contact your Rett Girl's local Children's Hospital. Many of them offer a list of local resources that may help you with the financial challenges we face. Here is a great link to Cincinnati Children's Hospital.




Or you may want to contact your local Kiwanis Club or Lions Club who have been known to rally around their local special needs kiddos helping them with everything from funding equipment or medical bills to assisting with funding their parents travel expenses to conferences regarding their child's medical condition.


If your Rett Girl is on a Children's Health Waiver or a type of Children's Medicaid you may also want to contact them or check out your state's website to see if there are any special needs funds or resources that you can take advantage of. Here is a link to Michigan's Children With Special Needs Fund.


We hope that you find these resources helpful! If you do find the assistance that your looking for all we ask is that you give us an update - we thrive on seeing our Rett Girls shine!

Tuesday, November 29, 2011

Some "Tips" for the Holidays




With December upon us, and holiday decorations sprouting up all over, we are all gearing up for a special season. Yet, the biggest thing to overcome during the holidays is just pure stress. Everyone out there feels it, but when you have a disabled child thrown into the mix, stress can rise to a whole new level. Stress of disappointment over your daughter’s condition, stress of your daughter’s anxiety as the routine and activity level changes, stress of how family and friends act towards her, stress of travel, stress of food choices. Mix this in with some certain lack of sleep and it is a recipe for disaster.

So, think about changing things around, being more open to doing things differently, and being more open with those around you about what they can do to help make this holiday a more positive experience. Do not try to fit your daughter into your traditional routine. It is time to make some new traditions, keeping her needs in mind.

Handling anxiety and sensory overload – two key issues for Rett girls.

Anxiety often comes from not knowing what to expect. Talk to your daughter about events coming up several times before they happen. Explain to her where you are going, who will be there, what will happen, and what is expected of her.

TIP: Consider bringing along a portable DVD player with her favorite videos as a fallback. Although it is heartbreaking to feel she is not included, sometimes it is just better for her to be engaged with something familiar.

Sensory overload can strike us all. If your daughter can’t tolerate being amidst all the festivities – gift opening, big dinner, singing, etc – be sure to have a plan for her and talk with her about it.

TIP: Tell your daughter, “Today is a very special day. We have people coming to visit. If you are feeling anxious, you can stay in your room with your music or television. And then this afternoon we will have a special time where each person will come to you and spend a little time with you and give you a gift. I will help you give them their gift, too. Maybe we can even have pictures of each person and you can pick you who would like to see and give your gift to next!”

Creating a more relaxing environment:

Rett girls usually love twinkly lights. Consider having them in more places than around the tree and outside. How about in her room?

Opening presents: Traditional paper gift wrap can be a nightmare. Rett girls will get paper cuts and even try to stuff the paper in their mouths, so maybe someone else handles opening for them. But imagine the combination of loud ripping paper and someone else opening your gift? I think I would cry too.

TIP: Wrap her gifts in fabric. Even if it is just one of your colorful T-Shirts with a big bow! It will look pretty, feel soft, and it will be quiet – and she can actively help open her own present!

Help from visiting family members and friends:

This is a great opportunity to be a really big help! Even just 5 or 10 minutes here and there with your special Rett girl will be very welcomed. Consider these things:

Read her a book.
Brush her hair and put pretty bows in for her.
Help feed her.
Take her for a walk.
Give her a foot massage.
Listen to some music together.
Sing her a song.
Tell her a story from your past holidays.


Make this holiday a real team effort. Start talking with you family now about ways to help.

And be sure to check out our Holiday Gift Idea List! Happy Holidays everyone!!! I hope you each find that magical moment that makes your heart skip a beat and brings a smile to your face.

- Ingrid

Monday, November 21, 2011

RettGirl. We've Got that!



Good Day RettGirls!

Over the last week or so while viewing other Rett Syndrome Support Boards or while on Facebook I kept noticing a trend. Is it possible people really don't know about RettGirl?

Over and over I watched as people asked advice on what to get their daughter for the holiday. We've got that! Find a wonderful list and links to lists past by clicking on our Holiday Gift Ideas button on our Homepage.

Just moved to a major metropolitan area and are at a loss about where to find a Doctor or Clinic near you? Chances are we have that. Just click on Doctors/Therapists at the top of our Homepage.

It doesn't stop there - we have one click access to EVERYTHING Rett. Don't see what you need? Send us your question or info you would like to see! We want to keep everything organized and searchable so more families can learn from our Rett community.

We have tips from parents just like you.

We have product reviews on:

Feeding

Communication

Clothing/Shoes

Sensory

Positioning

Mobility

Media

Sleep

Toys

Travel/Camps

The list goes on and on.

Do you need ideas for apps for an iPAD? We have a button just for that where you will find
Link apps, accessories and more.

Would you like to see videos of our girls thriving and achieving? We have that!

What about a place just for school stuff where everything you need is all in one place?

Websites

Care Notes

Example IEP's?

From Constipation to Communication, we have all that and then some at RettGirl.org!

Come visit us today and share with your friends, coworkers, and staff!

Have a great week everyone!

Terri V~For RettGirl

Monday, October 3, 2011

Rett Syndrome Awareness Month - Mom on a Mission

It's Rett Syndrome Awareness Month - let's make some noise!

It's me, Terri. I am Mom, Rett Mom, Advocate, wife and all around Autism awareness terrorist. I run RettGirl.org and a YouTube channel called Rett We Can for Girl Power2 Cure.

Why? Well thank you, I’m so glad you asked. I hope you can pass on this blog and help us spread the word about the hundreds of thousands of girls fighting Rett Syndrome.


My 7-year-old daughter Abby has Rett Syndrome - an X Chromosome Linked form of Autism and the only form of Autism with a known genetic cause. Because the gene mutation is on the X Chromosome, it mainly affects girls, but there are a handful of boys that have it too and they are just as deeply affected.

The gene of which we speak is called MECP2. It is known as the regulatory gene between your brain and your body. It is the gene that tells every other gene when to turn on and off. Strangely, this gene doesn’t play much of a role until your child is between 18 months and 2 years of age. Up to that point you have a seemingly normal, typical child doing all the things they are supposed to do.

Once this gene kicks on, if it is faulty like in Rett Syndrome, everything start s to shut down. There is a rapid period of regression where most every acquired skill is lost. Most purposeful hand use disappears almost immediately and is replaced with a constant wringing, tapping or hand mouthing. All speech goes during this regression stage, and your child turns physically back into an infant where she will stay…trapped in her own body until a cure is found.

Good news! Rett Syndrome is poised to be the first curable neurological disorder. It was announced in 2007 that Rett Syndrome had been reversed in laboratory mouse models. It’s there and until we can get it funded in a way that gets it right for humans, our babies remain locked in a world they can only observe.

One major debilitating factor in Rett Syndrome is called Apraxia. Apraxia is like this: the will to carry out intent is there, but the physical ability is severely delayed or not there at all. Some describe it as having Autism, Cerebral Palsy and Parkinson’s all rolled up in one little girl.

Need to Knows:




  • Debilitating neurological (movement) disorder that predominantly affects females.


  • Baby girls are born "normal" but begin to lose acquired skills between the ages of 1-3 years old.


  • Caused by a single gene mutation that leads to underproduction of an important brain protein.


  • The most severe form of autism.


  • The leading genetic cause of severe impairment in girls - most cannot speak, walk or use their hands.


  • Despite their physical disabilities, girls with Rett Syndrome are believed to be functioning mentally at a much higher level than previously thought.


  • As prevalent as Cystic Fibrosis, ALS and Huntington's.


  • Another little girl is born with Rett Syndrome every 90 minutes.


  • Rett Syndrome is a potentially REVERSIBLE disorder. Research has proven once protein levels are back to normal levels, symptoms subside.

Why have I never heard of this you may ask? That’s why we are here today. To inform, educate and raise awareness so little girls like my Abby will no longer be held in the unknown.

Want to learn more about Abby and contribute to research? Follow this link to her personal story at Girl Power 2 Cure: http://girls.girlpower2cure.org/abby

Thank you - PASS IT ON!

Terri

Wednesday, September 21, 2011

Nuk Brush

Good Day RettGirls.

This week's feature at RettGirl.Org is the Nuk Brush. You can find this neat little item in our Product Reviews under Sensory.


I have had a Nuk Brush in the bathroom for Abby since her teeth started coming in. Recently, I have had several parents tell me that it is a great tool for oral stimulation. One even commented that it really helped their tube fed child learn to eat again.


Last week at Hippotherapy the Speech Pathologist that runs the place had me bring Abby in early so she could do some oral motor exercise with her. Abby has become quite the drooler lately.


The first thing she got out was this Nuk Brush set. She ran the round brush in a C pattern in her cheeks. She used the flat brush to go over her gums. When she put it on her tongue she immediately wrapped her mouth around it and sucked on it like a straw. I haven't been able to get her to use a straw for almost a year. In one session!


We took the set home and have been using it every day. In the last week we have gotten Abby to at least sip from a straw and eat whole jars of food instead of one bite. I didn't expect results that fast but I'm going with it.


======================================================

from the company website:


This brush is recommended by Speech Pathologists as well as feeding clinics to wake up the mouth before feeding.The Nuk™ brush massager is used for oral massage, oral stimulation and exploration. It stimulates lateral molar ridges, reduces oral hypersensitivity, and helps develop a tongue groove. The flexible, nubby texture offers valuable sensory input for the child’s mouth. Though this brush was designed initially for teething infants, it has made its way into therapeutic settings as an invaluable tool for sensory exploration. The nubby surface can hold tastes of liquid, purees or crumbs while it is used with supervision as a “spoon” for initial feedings. The NUK brush is approx. 5″ long. Use only under adult supervision.


=======================================================

Good luck everyone!



http://rettgirl.org/2010/08/nuk-brush/




Terri V~For RettGirl

Wednesday, January 5, 2011

RETT WE CAN!

She can't do this. She can't do that... It can be a real downer for Rett Girls every day. But... only if we let it be that way.

To kick off the New Year with an empowering attitude, Girl Power 2 Cure and RettGirl are launching a new YouTube channel called RETT WE CAN!



Here is why we created this channel (inspired my Rett mom Terri Vejrosta!)

* to share the "Rett" experience by showing the things Rett Girls CAN DO
* to put an empowering, positive, human face to Rett Girls
* to have a place to send therapists, family members, volunteers, and donors to see Rett Girls staying strong
* to have all the great YouTube videos ORGANIZED by category*
* to get inspired
* to explore different things to work towards with Rett Girls
* to educate others about Rett Syndrome

If you have a video you would like us to include, please send us the link! (post a link on Rett Girl's facebook page or email us at rettwecan@girlpowe2cure.org)

Please know that there will be a wide spectrum of girls featured on the site. Not all girls will be able to everything here. For instance, I know my Sarah probably will never water ski like Jade, but others just might!

The point is to always reach FORWARD. Always explore and challenge and keep Rett Girls active. All of us have a role to help bring these girls to their full potential. Each girl's potential will be different, but we want to make sure everyone stays inspired to believe...and have the tools to inspire everyone who lives or works with a Rett Girl.

Check it out now at www.youtube.com/rettwecan!


========================

* Our current categories are Walking, Hand Function, Eye Gaze, Communication and Expression, Sports and Adventure, Therapies.

NOTE: When you visit the site and see the category listings, click on one...then you will see all the videos under that category. Remember to send us suggestions and even category recommendations! We want you all to be a part of making RETT WE CAN a great resource!


2011 is a NEW YEAR! Best wishes and strength to all!
- Ingrid

Wednesday, September 15, 2010

The Power Of The Purple Card!


October is Rett Syndrome Awareness month and it is fast approaching! We want everyone out there to know about GP2C's Purple Card!


If you are like me, and I'm sure you are..You hate having to tell the who, what, when, where and why's of Rett Syndrome everyday. Especially if you have your daughter with you. Mine gets particularly upset and looks at me with those eyes as if to say "I am so sick of hearing this and I am sitting right here! Stop talking about me!"

We have a Store category at RettGirl and have added GP2C's Purple Cards.

It's basically a handy little card to keep in your wallet to hand out to people who need info.

Just one mother's opinion:

"I don't know what we would do without our purple card. We have used it everywhere. In the store when strangers are staring. When those uncomfortable moments come where people are asking too many questions and it is neither the time nor the place. When people are arguing that your child has that "Aspirin disorder." Or when they keep telling you that it is not Rett it is Tourette.

I love being able to hand them a card with facts and a place to learn more.

When our daughter was in the hospital we handed it to residents, nurses, surgeons. We had to send someone home to get more after doctors and social workers kept coming in and asking for them.

We have been told that they are they best idea ever for a special needs kid with a uncommon disorder. I could go on and on. Every member of our family has a handful in their wallet!"

You'll never know the power of the purple card until you try! It is a great way to share your Rett
Syndrome story anywhere! Imagine, you won't have to explain all about it in front of your
daughter ever again!

Highly recommended!

http://rettgirl.org/2010/09/the-purple-card/

Terri V- For RettGirl

Monday, September 13, 2010

Teaching Learners With Multiple Special Needs


Hello RettGirls!
We are so excited about all they new things we have up at RettGirl.org. We have been all about education lately and PROVING to everyone that are girls are in there and more than capable of learning. They just need a little more help than the Neurotypical Child.
With this in mind we have found a wonderful website we are very excited about. It is called, "Teaching Learners With Multiple Special Needs."
We didn't stumble on this site by accident. The person who runs it is very good about keeping up with special children and have offered advice to some of us when we were having education, communicative and many other issues related to schooling our daughters.
I have spent hours on their site taking notes and sending links to others. Just some of what you will find at this one website:
60 Things to Do with a Switch
AAC Dynamic Display Devices
AAC Funding
AAC Increases Verbal Language
AAC Programming and Tech Support
AAC Resources and Products
AAC Static Display Boards for Purchase
AAC Text-to-Speech
Activity Sharing
Alternate Format Books and Stories
Calculator Options
Email for Everyone
Fabulous Freebies
Free and Low Cost Head and Eye Tracking
Free Boardmaker Boards, Activities and Tutorials
Free Online Activities
Free Software
iPod App Round Up
Online Switch Activities
Paraprofessional Resources
Photo and Picture Symbols
Reading Websites
Seizures in the Special Needs Classroom
Signs and Symbols
Software for Special Needs
Special Education
Special Needs Scissors
What an incredible resource. You can find this and much much more at your fingertips at http://www.rettgirl.org/