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Showing posts with label Changing Minds Foundation. Show all posts
Showing posts with label Changing Minds Foundation. Show all posts

Tuesday, July 2, 2013

Mission Possible Videos From The Cruise




If you missed the Mission Possible cruise last February on the "Liberty of the Seas" to Jamaica and Haiti.....we have good news!  All the videos from the speakers were videotaped!  You will be able to hear Dr. Teresa Cody speak about GABA, Prozac and the Changing Minds protocol, as well as ALL the other speakers from the event.  They are all recorded and you can listen to them ALL for the low registration fee of $29.95 per year.  They are available on the Mission Possible website: http://www.missionpossiblecruise.com/.   While you are there, you  might want to check out the details of their next cruise to Alaska from Seattle, Washington in July of 2014.

We wanted to show you some of the previews of Teresa too.  Just click on the links below to watch the short previews of each talk.  If you like what you see....just go to the site and watch them all!

The Nitty Gritty of GABA:   http://youtu.be/iSjYER1V1E0

Prozac: Pride or Prejudice:  http://youtu.be/En-Zs4RszgU

Changing Minds About Down Syndrome:  http://youtu.be/qh6OdX4xF2I




Tuesday, March 5, 2013

Freezin' For a Good Reason

Check out this video of Jordan Blevins and many others plunging into icy cold water to support Special Olympics. 

http://www.indianasnewscenter.com/news/local/Freezin-for-a-Good-Reason-191552001.html

The 6th Annual Polar Plunge in Ft. Wayne, Indiana, is a fun & crazy event where people jump into 8 feet of icy cold water to raise money to buy uniforms and equipment and pay for facility rentals for the Special Olympic team. 

Jordan Blevins, in the bright green shirt, is one of our own.  He has taken the CMF protocol for several years and he is doing very well! 

Friday, February 8, 2013

Mission Possible Cruise -- this month!!!

Hey.......how many of you are coming on the DS cruise from Ft. Lauderdale, FL to Haiti and Jamaica at the end of this month???  We are really looking forward to it!  Put a comment at the end of this post if you are coming and let us know what you are most looking forward to.  Dr. Teresa Cody is going to be speaking on the CMF protocol, as well as details about GABA and Prozac.  Hope you have plans to come with us.  If not......it might be recorded.  We will let you know if it is going to be made available for purchase later. 

Tuesday, December 11, 2012

The Pure Joy of Independence!!

This is a video of Mac Austin playing the game of Trouble with his little brother, Griff.  His mother sent this to me and she wrote the quote below:

"Hey ladies.... A little brag here. This is a video of Mac and Griff playing the game Trouble totally independently!! Taking turns. Moving his own pieces. This is a huge step for Mac! And I just loved watching them play a game by themselves!!!"



Mac is 8 years old and he has been taking the CMF protocol, along with some additional supplements,  for almost two and a half years.  He is doing amazingly well.... wouldn't you agree? 

Thursday, August 2, 2012

CMF Success Story -- Robin 14 yrs.

Robin is now 14 years old. We started him on the CMF protocol 4 years ago, when I read about it on the awesome site by Miriam Kauk  "EINSTEIN SYNDROME".


Although we had been following a neurodevelopmental program since birth, as well as a nutritional protocol from International Nutrition which included Piracetam and Nutrivene D, once Rob got to be of school age, I felt that he could do even better academically. So I decided to give CMF a try!


Both my husband and myself were/are very pleased at Rob's gains in the last 4 years.


Physically:

-biking without training wheels
-batting and catching a ball
-riding a horse with voice and leg commands on his own
-balancing and using the monkey bars (brachiation ladder) unaided
-taking a more active part in contact sports (soccer, volleyball, softball)...but he would rather watch a      movie or play on his Xbox...ha!

Academically:
Rob has a full day of academics at our local school. Although he is not mainlined, I teach him myself but he is in daily contact with the rest of the student body. He participates in drama/music/art/sports with the rest of the school.

Reading:
Completed the second level of the Edmark reading program. Currently on the Reading Horizons protocol and doing well with minimal assistance.

(Read the rest of the story on our website at   http://www.changingmindsfoundation.org/success_stories.html)

Tuesday, July 10, 2012

Thank You Note From Pocatello!!!

Hello Teresa,

I want to thank you for taking the time to travel to Pocatello for your presentation.  Since my 2 year old was born (with Down syndrome), I have been searching for 'something more' than practically nothing... When I saw your website, I became truly hopeful that there actually was something biological to accompany a treatment plan.  This makes sense to me. I am a fix it girl...I don't settle ' because that's how it's always been',  and I see my personality in you.  I am so grateful that your medical background allowed you the path to take necessary steps to begin physiological questioning, and your mom experience allowed you to take a risk because mamas do what they have to do to protect their kids and anything to help them be successful.  We have already begun our journey toward a brighter future!

Thank you and your sweet team for your time, dedication and effort!
Parent from Pocatello, ID

Monday, June 18, 2012

More Is Better.....especially when it's Ginkgo Biloba!

I have shared with all of you on my blog that the dose for ginkgo biloba on the Changing Minds Foundation website is a minimum dose to see results.  I have suggested to all I meet that dose is important and the more you give the more results you will see.  My son, Neal, takes 4 to 5 times his weight in ginkgo.  See below what happens when you do increase the amount of ginkgo your child takes.

Below is an email I got from a parent who recently increased her daughter's ginkgo:

My daughter, Whitney, is 7 and has been on NutriChem’s customized vitamin therapy since July, 2010 where we saw major improvements globally with her.  She was diagnosed with PDD-NOS in October, 2009.  I’ve written about her vitamins under the blog section of our website www.bcdsc.org  As noted she went from no expressive language to finally developing expressive language.  Even though she was on 100 mg per day of gingko biloba her processing seemed to have stuck at 3.  A few weeks ago I attended the AutismOne Conference in Chicago and finally got to meet Dr. Teresa Cody.  After our talks, and her suggestion that I increase the gingko significantly, on May 28th we began increasing Whitney’s Gingko to 220 mg per day (50 mg in morning with custom vitamins, 120 mg at lunch with AOR , and another 50 mg before dinner with custom vitamins).  She weighs 42 lbs.  Within a week her teachers at school were noticing increases in ability and more talking (not always clear but more).  One teacher she has on Friday’s was really amazed at the change she has seen week to week.  In addition, I have noticed that Whitney is sleeping longer in the mornings.  So far no 6 am (or earlier) wake ups. 
On June 7th we increased the dose to  110 mg with breakfast, 120 mg with lunch and 110 mg with dinner (340 mg per day).  On June 10th here is what happened:

I’ve been really puzzled this last year as to why Whitney has still only been able to scribble and draw a few circles (roughly) and nothing else.  At lunch today Whitney was drawing on one of those erasable pads and did this:

Drew two parallel lines with a line across the top and said “house”, then put a line in the middle and said “door”, then drew a line with some curly things on the top to the left of the house and said “tree”, then on the other side drew another tree and said “another tree”, then scribbled the bottom and said “grass”.

This for my darling 7 year old daughter is really significant.   All of it, we believe from ramping up the gingko biloba.  Thank you to all the parents who have been saying how important the gingko can be for our children and to Teresa Cody for suggesting that we should try and significantly increase the dosage for Whitney.

Whitney’s teachers, the school aids and other students are all noticing that she is functioning better, not just cognitively but also better co-ordination on the playground and the gym.
We are really impressed and so thankful for Teresa Cody.  It’s unfortunate that Teresa did not get an opportunity to speak at the AutismOne Conference, however, we are very much looking forward to having her on our Cruise and I look forward to hearing more about Gingko and Prozac.  Hopefully she will be speaking in a city close to where I live before the Cruise as I’d like to hear all of her talk.
Best regards,
Rosalie Newell-Wagner
2013 Down Syndrome Cruise Conference
http://www.rosalienewellwagner.cruiseshipcenters.com/Promotions.aspx

Friday, June 1, 2012

Pocatello Welcomes Changing Minds!!!

Our Next One-Day Seminar for the Changing Minds Foundation will be on June 23, 2012 from 9:30am to 3:30pm in Pocatello, Idaho.  Our hosts will be Maria Neumann, Jodi Williamson, and the South East Idaho DS Support Group.  We will be meeting at the Marshall Public Library, 113 South Garfield, Pocatello, Idaho 83204.  There is no charge for the seminar --Donations only!  Lunch will be available to attendees for $10 per person.  It will be catered by Dutch Oven Delights.  You can register for this seminar and get all the details at the link below.  We hope to see you all there!!  Please let us know if you have questions 281-341-0101.   (Photo is MaKenna age 4yrs.)

                  Register Here





Tuesday, May 1, 2012

This is a note that was sent to us from a parent who attended the Butterfly Flutter By.  Her son is on the CMF protocol and doing very well!  Below is a conversation she had with him one night before bed:

Son: I love you to the moon and back.
Me: I love you to Jupiter and back.
Son: I love you to Pluto and back. Mommy, is Pluto cold?
Me: yes, very cold.
Son: why is Pluto cold?
Me: because it is so far from the sun it never gets warm, like when the sun warms us here on Earth.
Son: And is Jupiter cold, too?
Me: Yes – it is a big cold ball of gas – not solid like the Earth.
Son: So Jupiter is a cold planet and is made of gas, not solid (he pauses to think) but does Jupiter rotate around the Sun?
Me: (smiling) Yes, it actually ‘revolves’ around the sun, but yes.
Son: what does revolve mean?
Me: (still smiling) it’s the word we use to say it goes around the sun.

Why was I smiling – this was a conversation I was having with Warren, my 8yr old child who happens to have been born with Down syndrome.

Tuesday, January 24, 2012

The Reviews Are In..........

 Changing Minds had one of our One-Day Seminars in Tucson, Arizona, this past weekend, and we wanted to share one of the comments we received in our email box upon our return home.   We think it might be the best review we have ever gotten!!!!  The photo is of Raquel's son, Noah, all dressed up for Halloween.  Isn't he cute?




Hi there, 

Regarding the seminar in Tucson... It was fabulous!!!  Great information, loved the delivery from all the speakers... Also, have spent this morning trying to schedule appt's to get my son Noah, age 5, on the entire protocol, Prozac included :)
Was very hesitant about having my son take a medication, but the delivery and explanations from Dr Teresa made my decision a very simple one.  She truly used both visual explanations as well as personal testimonies to convince me to try this.  I believe that this may be the Holy Grail that I have been searching for since my little man was born in 06'.  This may truly be the "One Small Step for Mankind" that is needed in today's world!

Thank you!

Raquel mom to Noah Bryce



Thursday, August 4, 2011

Make Plans to Attend the 2nd Annual Golf Classic......or at least Buy a Ball!!

Changing Minds Foundation's biggest annual fundraiser is coming up on October 28th.  It is the Golf Classic, and it will be held at Wildcat Golf Club in Houston, TX.  Last year was our first year and it was so successful, thanks to David Moehlman, a CMF parent and the sole organizer of the tournament, that we are doing it again!  We hope you will plan to participate in some way.  If you golf, you can sign up a team of 4 to play.  If you don't, your company can be a corporate sponsor, or you and your family and friends can buy golf balls for the Ball Drop Contest.  At the beginning of the tournament, we will have a helicopter hover over one of the holes and drop 2000 golf balls at once.  The ball that goes in the hole or is closest to the pin wins!  The winner gets a trip for two to the Four Seasons Resort in Costa Rica!  For more information about this fundraiser, or to register, go to the link below:

 http://www.changingmindsfoundation.org/golf_tournament.html

Below is a photo of Teresa Cody and David Moehlman from last year's Golf Classic

Wednesday, July 20, 2011

Evansville Is Warm and Wonderful!

The Changing Minds seminar in Evansville, Indiana, was a big success!  We had many parents, teachers and medical professionals there to hear all about the science behind the protocol.  Teresa did a great job delivering the information and answering everyone's questions.  We sold several DVD's, which is always a strong indicator of interest.  We hope that everyone reading this is doing their part to spread the word about available treatment for DS.

Pictured are: (front row) Tess & Mary; (back row) Mercy, Miriam, Stacy, Teresa, Nina & Andy

Thursday, July 7, 2011

Would You Like To Write a Review of Changing Minds Foundation?

We found a website called Great Non-Profits and it is a place where people can write reviews about any non-profit they  have personal experience with.  We would LOVE it if anyone out there that has any personal experience with Changing Minds Foundation would write a review.  I have given you the link below so you can find it easily.  Thanks for your help in spreading the word about available treatment for many of the problems and symptoms of Down syndrome.

http://greatnonprofits.org/reviews/changing-minds-inc-1/91605/

Friday, June 24, 2011

Saturday....June 25.....Evansville, IN

Miriam does a great job on TV. Watch her now. Come join us at the Wired Coffee House Auditorium, 111 NW 4th Street, Evansville, Indiana at 9 am - noon.

Wednesday, June 22, 2011

Changing Minds Workshop

Watch this short tv segment from Evansville, Indiana. Miriam Kauk, the parent of a child with Down syndrome, is promoting an upcoming seminar for the Changing Minds Foundation. Dr. Teresa Cody will be speaking about the Changing Minds protocol and the amazing results that parents, teachers and doctors are seeing in people with DS. The event is sponsored by SMILE On Down Syndrome, a parent organization in Evansville, IN, for parents with loved ones that have Down syndrome.

Changing Minds Workshop

Thursday, May 19, 2011

Neal is really learning math!!!

My 13 year old son, Neal, has a tutor that works with him 2 days per week after school.  This week they were working on some double digit math addition.  She always writes me a note to say how Neal did that day, and here is her note:

"We had a Mexican stand off today in math.  We did about 3 problems together -- then he shut down on me.  So I just sat there.... and he started working by himself and got ALL of them right !"

So....I started wondering if maybe he is just capable now of doing it by himself and he gets frustrated and maybe even insulted that his tutor works each problem with him.  He is changing and learning in leaps and bounds these days, thanks to the protocol!  It is really exciting!  Below is his work:

*Notice how he adds the first two numbers and then writes their sum off to the right, then carries the one over and adds the next column.



Tuesday, May 3, 2011

Neal's 2nd Piano Recital -- He does great!!

This is a video of Neal, my 13 year old son.  He is playing in his second piano recital.  He is much less nervous this time.  He is playing a song called "Sledding Fun".  Neal has his music and he is reading it.  He knows all the notes and it sounds like he doesn't miss a single one!  I am so proud of him!

Tuesday, April 19, 2011

Watch Warren read a level 4-5 book !!!

Warren is a first grader who was born with Down syndrome.  He is taking the CMF protocol and has been taking it for almost 2.5 years.  He is doing amazing things!  Watch the video below to see for yourself. 

Thursday, April 14, 2011

Check Out Jordan's Spelling Skills !!

This is a 16 year old boy with Down syndrome.  He has been on the CMF protocol for 5 years.  He was one of the first kids to take the protocol.  His mom works with him on spelling words each week and she decided to film their session this week.  Isn't Jordan amazing???  I think he is!

 

Saturday, April 2, 2011

Fox 19 in Cincinnati Free Seminar April 9th

Spread the word .... we have a spots left for One Day Free Seminar in Cincinnati, Saturday,  April 9! Breakfast, drinks and lunch included. Donations welcome.
Come learn how to help your child with Down Syndrome.
Details of the event
News Coverage Fox 19: Click here