Showing posts with label Research. Show all posts
Showing posts with label Research. Show all posts

Sunday, December 30, 2012

90% Improvement in Seizures, My interview with Dr. Ron Thibert!

I recently had the opportunity to catch up with the Angelman communities very own trusted Neurologists Dr. Ron Thibert!

He is the Co-Director of the Angelman Syndrome Clinic at MassGeneral Hospital for Children in Boston. His specialties include Neurology and Epilepsy Service. Many families in our community travel from many other states just to see him.  He really understand how to provide the best treatment for our kids!  Angelman Syndrome is so rare and when it comes to their brain and seizures, our kids need the best! They need someone who has experience to draw from when deciding the best treatments and medications.

Here he is in an interview talking about seizures in individuals with Angelman Syndrome and effective Nutritional therapies like Low Glycemic Index treatment (LGIT) and the Ketogenic diet.


Dr. Thibert has been a long time supporter of dietary therapies in controlling seizures. He has seen the proof in EEG reports for many of his patients.  In fact, in one of my earlier posts entitle Stop Seizures with 3 Nutritional Therapies I shared with you the story of young Jace who has not had a seizure but shares in the typical AS abnormal EEG, showed improvement after beginning the GFCF diet.  His mom told me he is now considered to have a "Normal" EEG!  That's Fantastic!

Dr. Thibert and his team including Dr. Elizabeth Thiele (both are members of the Scientific Advisory Commity for the Angelman Syndrome Foundation) were able to launch a clinical study to determine the efficacy of the Low Glycemic Index Treatment in reducing seizures in individuals with Angelman Syndrome.  In July 2012 the results were in and published in Epilepsia and on the Angelman Syndrome newsletter.

 "The results were better than we had expected" said Dr. Thibert. 80% reduction in seizures and 90% reduction after 1 year and ALL experienced no significant adverse effects! "5 of the 6 individuals remained on the diet" said Thibert.

I asked Dr. Thibert who is the best candidate for this dietary therapy?
   "Anyone with 1 failed antiepileptic medication".

How does one get their child on the program?
   "Patients may come and see me for an initial visit, we can run the necessary tests to monitor medication and a few other things, and they can consult with our dietician Heidi Pfeifer or transfer to a local dietitian closer to them. Food Allergies will be tested. Then see me on a yearly basis. Labs should be monitored every 3 months, which include Electrolytes, Cholesterol, Liver panel, Carnitine, and Vitamin D".

My son is on the Glute Free Dairy Free diet, what are the differences between the two?
  "They are actually quite similar, when you take out the gluten your are removing a large portion of the carbs like pasta's and breads which will lower your glycemic index. The LGIT consists of high fats and meats and cheese are staples of the diet."

Once on the diet, how long before you can see results?
  "It may take a few months to kick in.  The diet must be consistent and limit carbs to 40-60 grams per day."

Who would not be a good candidate for this diet?
  "It is not recommended for those on a G-Tube.  Another option for them would be the Ketogenic diet.  There is a product called KetoCal and it can be used to assist with the ketogenic diet." 

Why don't more doctors suggest dietary therapy as a first and safe option for seizure treatment?
  "My guess is lack of awareness and maybe they do not want to change what they have always done, which is prescribe medication, the evidence is there to support dietary therapy. We are looking into preparing a package of material to help educate other dietitians".

Here is the publication on PubMed.

Dr. Thibert is hopeful that this information will get out into our community and more people will use the Low Glycemic index treatment to reduce seizures.  80-90% reduction is astonishing!  In my humble opinion, if your child with Angelman Syndrome or any seizure condition for that matter is still having seizures, you should try this diet!!  It breaks my heart every time I hear of someone in the hospital with seizures and it's the same thing every time. Doctor's don't know the cause, they check levels or do an eeg and in the end they  just prescribe more meds.  Been there done that too many times with Nathan!  It wasn't until I took his diet into my own hands, armed with good info and a plan and made it happen!!  You can too!  Dr. Thibert is willing to help each and every one of you!
You can contact Dr. Thibert at: Pediatric Epilepsy Program 175 Cambridge Street, Suite 340, Boston, MA 02114-2796 Phone: 617-726-6540

Another person who is willing to help is Angel Mamma Sybille Bellamy.  She has created a facebook page dedicated to what she is calling the Angelman Syndrome Diet.  She shares the recipes she uses for her son Max who has been on the diet for years.  She also shares important dietary info and articles.

For an example, Sybille has given me a meal plan for 1 day for Max

Morning breakfast: 2 tbs steel cut oatmeal cook in coconut cream. 1 table spoon of manna coconut 1tbs of coconut oil 1tbs of mix seeds-hemp, chia, sesame, flax seeds and 1 tbs of walnut butter.
Drink is herbal tea with coconut oil.
At school Max drinks herbal tea with MCT and a lot of water with lemon juice.
Lunch: 3 tbs of sheep yogurt, 2 tbs of grated apple, 1 tsp grated carrot, 1/2 avocado, 1tbs almond butter, 1tsp of MCT.
Nurse give him MCT (medium chain triglyceridearound) 2 pm 5ml at school.
Afternoon snack: home made almond milk, 1tsp coconut flour, cinnamon and 4 strawberries.

Dinner: vegetable soup- kale, spinach, carrots, onions, with one egg, grass fed butter, goat cheese.
He likes to drink before bed- coconut milk with 1/2 tsp of coconut flour.
During the day Max drinks a lot of water.


I hope you find this info helpful in your journey of helping your loved ones achieve the healthiest lives as possible.

~Lizzie

Wednesday, July 11, 2012

Stop Seizures with 3 Nutritional Therapies!

I would like to share some helpful information and get the conversations started about preventing Seizures and tips for the health of our Angels.  I will share with you my experience with my kids and of some other Angel families as well that have used Nutritional Therapies.  While we have great minds working hard in science labs for the CURE, there are things we can do in our very own kitchens that will be helpful for our Angels.

It is so important to know if your child has food allergies and/or sensitivities.  Something as "simple" as food can be causing our kids harm and we may not even know it or see external signs of it until it has become a severe problem.  This is also overlooked most times by our pediatricians.  I know that was the case for both of my children (my Angel Nathan and my typical child Braden) and for countless other parents who have shared their stories with me.  We feed our kids many times a day, but how much thought is put into WHAT they are being fed and how it effects their bodies?

Most of you may know of the famous Dr. Sears, author and pediatrician.  Here is a link to an article that came out recently about this very subject, which I feel applies to many of the same symptoms our Angels have and the possible cause.

7 Signs your child may have food intolerance's
http://m.newhope360.com/allergies-amp-sensitivities/7-signs-your-child-may-have-food-intolerance

1. Spitting up/Reflux - Intolerance to casein (Dairy)
2. Chronic diarrhea - Intolerance to Gluten (a protein found in wheat and other grains) or Lactose (Dairy Sugar)
3. Chronic ear infections - Dairy intolerance or Soy. Research shows 90% of kids with recurring ear infections have food reactions. So why didn't any doctor or ENT specialist ever tell me this when BOTH of my boys suffered with this problem and my Nathan had ear tube surgery??
4. Eczema or itchy skin rash - Gluten, Casein (any dairy), eggs, oranges, grapefruit, tangerines, lemons, strawberries and pineapple.
5. Hyperactivity - Artificial colors and/or sugar, MSG (monosodium glutamate) which is in almost all restaurant food.
Crankiness - Gluten intolerance. Studies linked it to neurological symptoms, which can range from moodiness, chronic headaches, ADHD, and COORDINATION LOSS!!
7. Small stature or Picky palate - Gluten sensitivity or Zinc deficiency.  Gluten intolerance interferes with nutrient absorption, suffering kids often fail to thrive!! Zinc is a mineral that normalizes appetite and through it's relationship with growth hormone, helps the body develop.

The article has more details but I wanted to point these things out because it effects so many Angels and I have seen the proof in my kids.  When I removed the Gluten, Dairy, & processed foods from Nathan's diet, his reflux, ear infections, eczema, crankiness/colic was GONE! Even SEIZURES which were at one time uncontrollable, now under control.  It helped me to identify the only two triggers for seizures which were sleep disturbances and sickness/fever.  And now with further guidance from my Holistic ped and nutritional supplementation, he is not having them.  With our success, I must share some resources with you.

In the battle against Seizures there are things we as parents can do!  We cannot wait for our pediatricians and neurologists to suggest it because it may never happen.

Nutritional Therapy/Dietary Therapy

There are 3 Nutritional Therapies that can help our kids.  Gluten/Casein Free (GFCF diet), The Low Glycemic Index diet, and The Ketogenic diet.

For the GF/CF diet, I will link the document created by our very own Pediatrician Dr. David Berger of www.wholisticpeds.com  This is the protocol for beginning the diet http://www.wholisticpeds.com/uploads/GFCFSF%20Diet.pdf He also lists at the bottom of the doc other online resources and links.

Many of you know Neurologist Dr. Ron Thibert.  He is on the Medical advisory board of the Angelman Syndrome Foundation and treats many of our Angels at Massachusetts General Hospital in Boston.  Here is a good video of him talking about the effectiveness of the Low Glycemic Index diet and the Ketogenic diet.



An AS Family Story: By Angel Mommy Danielle Pinders
"Jace is 22 months old and doing very well. He’s had two EEG’s and both have been clear of any epileptic activity which has contributed to his continued developmental progress. In fact, his most recent EEG which also took place on June 1, 2012 looked better than his first one 6 months prior in December. We believe that this is largely in part of his Gluten/Casein Free diet. His Neurologist in Boston (Dr. Thibert) who is an AS expert also supports a low glycemic diet and its many benefits to children with neurological conditions".




This is amazing proof of the benefits that Nutritional therapies like Gluten Free/ Casein (dairy) Free, Low Glycemic index diet and the Ketogenic Diet can be for our kids!

Dr. Elizabeth Thiele is the Director of the Pediatric Epilepsy Program at Massachusetts General Hospital with clinical interest in the Ketogenic diet.  Dr. Thiele is also on the advisory board of the Angelman Syndrome Foundation and The Charlie Foundation.
Board Certifications: Clinical Neurophysiology, American Board of Psychiatry and Neurology, Neurology with Special Qualifications in Child Neurology, American Board of Psychiatry and Neurology Clinical Interests: Ketogenic diet, Tuberous sclerosis complex, Pediatric epilepsy


I would also like to introduce you to The Charlie Foundation and their dedicated work to raise awareness about the Ketogenic diet to help cure pediatric epilepsy.
Stay tuned for my next blog post when I get the opportunity to have a conversation with famous Hollywood movie producer and founder of the Charlie Foundation, Jim Abrahams! He will share with us the latest news from the foundation and the upcoming Charlie Foundation 2012 Symposium in Chicago this September.

View the clip below and for more info NOW click: http://us2.campaign-archive1.com/?u=eef59c2e88be33ecdcbbb42d0&id=1fb0beeb19


With so many options available, you will just have to see which one will work well for your child.  If your child is on more than one anti-seizure med, I strongly urge you to begin the journey, do your own research and DO NOT be discouraged if your Pediatrician or Neuro downplays their effectiveness.  This does not come in pill form so it is not typically encouraged by the medical community, however, we are seeing more Doctors get on board, who truly want to make a difference in the life of our children.

Monday, November 28, 2011

Florida Angelman Family Fundraiser for FAST



Angelman Families get together for a lunch and social fundraiser for F.A.S.T at BJ's Brewery and Restaurant in Tampa, Florida.



On Saturday November 5th many Florida Angelman families came together for a great cause and to hear from Dr. Weeber.  The adorable Angels ranged in ages from 3-21.  After the Angelman walk last May, I had many parents suggest to me that they would like to spend more time with other families and socialize.  So, I kept that in mind.

Over the summer there was a Vivint voting contest for a charity to receive $250,000.  The Foundation for Angelman Syndrome Therapeutics (F.A.S.T) had entered and as votes came in, the excitement was building.  Our AS community really came together to rally for votes.  We reminded each other for our daily vote and posted on the Facebook "walls" of our friends and family or anyone who would listen.  I know that I told all of Nathan's therapist & Dr's and had them voting.  As I learned that this win would afford FAST the opportunity for the first Human clinical trials, I became excited and determined!  We all did and it felt great. We were all working together to get our kids the cure they need and at the same time, we grew so much closer as a community!  FAST WON! I was laughing and crying with joy as I watched the ceremony online.

It was then that I knew... We had to get together to celebrate as a community and who better to join us than our very own Floridian - Dr. Weeber!   I found BJ's restaurant who supports charities and would donate proceeds to F.A.S.T.
It meant a lot for me to be able to meet Dr. Weeber.  Shortly after my son Nathan's diagnosis my husband found the online article of Dr. Weeber's research of curing AS in a mouse.  It was that article that gave us HOPE.

Just days before our lunch, the highly anticipated F.A.S.T newsletter came out to answer many of our questions about the upcoming clinical trials.
click to view: http://www.cureangelman.org/newsletter/NewsLetter_November2011.pdf

40 people had RSVP'd and told me how excited they were to see all the other families.  We ended up having more people in attendance than expected!  We had so much fun!

*We introduced our Angels to the group

*Shared www.MyAngelman.com (a website created by Angel Dad Troy Davis for our AS online community)

*Gifted Chewy Tubes to all the Angels from www.ChewyTubes.com donated by the company.  You can buy these favorite Angel toys on Amazon.com


Dr. Weeber spoke to the group and answered questions.  Everyone was so grateful to Dr. Weeber and his staff members for taking the time to come out and visit with our Angels and share his research with us.
The families are so excited about the trials that will be here in Tamp and ready to sign up their Angels. They are eagerly awaiting the details of who will be eligible, which we understand will be announced after everything is approved and ready to began.

It was such a great time and my heart fills with so much love when I am in a room with so many Angels and their families.

Thank you to Dr. Weeber, Joe Greico, Justin Rogers Ph.D and all the Angel families who came out to Tampa.

Thank you letting me share with you,
Lizzie

(More pics below)