A very dear friend of our family's, my Dad's oldest and closest friend, was diagnosed 4 months ago with glioblastoma, a very aggressive form of brain cancer.  The prognosis is very grim.  These last months, I have felt helpless - desperate to do SOMETHING. 

Then, several weeks ago, in my daily researches, I came across a reference to the use of the ketogenic diet in brain cancers and immediately did a search on PubMed.  Sure enough, up popped a whole bunch of references, and what I discovered is that cancer cells cannot use ketones for fuel.  Starving them of their one source of fuel - glucose - may definitely help keep tumors from regrowing.   (...)


 
 
  1. Firstly, welcome to my new and improved website.   I intend to start blogging on a more regular basis, so please, check back frequently.
  2. It now been 3 ½ months since I started Alex on our ketogenic experiment.  I am now starting several clients on the diet as well.  Is it helping?  I am not sure, but since I committed to it for 6 months, I intend to stick with it that long.  Alex’s response to it is muddled by another situation that has arisen.  (Isn’t it always that way?!)  That is, I (correctly, as it turns out) diagnosed him with cluster headaches.  The diagnosis was subsequently confirmed by a neurologist, and Alex’s response to the serotonin-agonist pain-killing migraine medication, sumatriptin, provided the final confirmation.  Cluster headaches, as I found out when I looked it up (seeing as Alex’s episodes of screaming occurred in bunches), are considered the worst possibly headache.  In fact, they are also called “the suicide headache” for self-evident reason.  Alex also has what are called “intractable” cluster headaches, meaning that – while most people have months off in between clusters – his never go away.  Alex has these headaches one to five times per day, nearly every day…and has had them for years.
Why did it take so long for anyone (me and his many doctors) to figure it out?  Mainly it is due to Alex’s inability to express himself.  However, with is new IPad, communication has become markedly better and he’s hitting that “I have a headache” button for all its worth. Secondly, cluster headaches are rare.  Thirdly, I believe his doctors fell into that all-too-common mistake of crediting his “tantrums” to his autism.  It was the old, “He’s screaming because he’s autistic” error.  I remember that one only too well from Alex’s earliest days: “He has profound diarrhea and vomiting because he has autism.”  Not, “He has colitis.”  Or better still, “He has autism because he has vomiting and diarrhea and colitis.”  (...)

 
 
Alex has now been ketotic for more than 2 1/2 months, and there is not doubt about it – it is helping him enormously.  Granted, I am also doing  GcMAF at the moment.  However, last spring when I first tried GcMAF – and Alex was off SCD – he was doing nothing but regressing.  The change in diet is the only thing new that I am doing.  I do believe the GcMAF is helping…but I think that without the diet, he’d be too sick for me to see that.

A quick summary of the changes so far:

a.  Most importantly, Alex’s mood has stabilized.  He has very few tantrums now, and when he has one, they are very short and not nearly as severe.  There has been a very big improvement in the last two weeks on this front.  That alone would make all the effort worth it!

b.  He has lost 10 pounds (which was needed) and looks great.

c.  His acne is clearing up.  His skin is 100 times better than it was just 2 months ago.

d.  His nails are starting to grow more normally.  The perpetual peeling (below the nail line) has dramatically improved.

e.  Almost the most exciting…he is sleeping!  8 hours a night, with no help (supplements or medication).

 
 
On September 16, 2 1/2 months ago, an article was published entitled, “Impaired Carbohydrate Digestion and Transport and Mucosal Dysbiosis in the Intestines of Children with Autism and Gastrointestinal Disturbances.”  Its authors include, among others, Dr. Tim Buie (GI at Harvard), Mady Hornig (well-known researcher at Columbia), and Margaret Bauman (one of the foremost researchers in the world on the autistic brain).

The paper rocked my world.

To sum up very briefly, the paper confirms Dr. Horvath’s findings of a decade ago – that children with autism and GI issues have low levels of disaccharidases (enzymes from the brush border of the small intestine that complete carbohydrate digestion), hampering their abililty to properly break down carbs.  But it went much further: these researchers also found that these children have low levels of mono-saccharide transporters in the enterocytes.  What does that mean?  Glucose is a single molecule of sugar that feeds every cell in our bodies.  To get it from the intestines (from food) into the blood stream, the cells on the villi of the small intestine have proteins on their surface known as transporters, that bring the glucose into the cell, and then out the back side into the blood.  The children tested had low levels of these transport proteins meaning that even if they manage to break the carbs down into absorbable glucose, they can’t move the glucose out of the intestines properly.  And as Elaine Gottschall would say, this leaves all kinds of sugars in the intestine which feeds all sorts of bacteria, leading to a monster dysbiosis issue…exactly what these researchers found.