Skip to main content

The Limbic System



Since Ryan was born in 2001, I have read hoards of information on Autism, child development, healthy eating, and alternative therapies to name but a few and as I have said previously I am in no doubt that foods play an important role in explaining some of Ryan’s difficulties.

I try very hard (but am not perfect) to maintain a healthy Limbic System as I believe it has a strong role in our health, wellbeing and development.

The Limbic system supports a variety of functions, including emotion, behaviour, motivation, long-term memory, and olfaction. It appears to be primarily responsible for emotional life and it has a great deal to do with the formations of memories.
Susanna Heinze

Obviously all of these are very prevalent characteristic ‘symptoms’ of autism, so by trying to maintain a healthy balance and approach I hope to better support Ryan on a day to day basis.

As warm-blooded mammals, we are dependent on the development of emotional attachment to the parents. We feel good when we are safe, well fed and we know where our parents are. In that state of well being, we learn and develop language and social skills. Conversely, when we are lost, hungry and in danger, we experience panic. That panic involves the immune system and begins with an adrenalin release. The immune system takes over from the emotional system, and we revert to a more primitive state of fight-or-flight, survival instinct. In that state, learning, language development and social skills are not important to survival.

It is believed by some that in autism, the immune system is reacting to lutein as if it were a life-threatening pathogen. The immune system takes charge of the body's vital functions - digestion, metabolism, breathing, heart rate, temperature - and all superfluous activity, including social activity, stops until the reaction ceases. But for the autist, the reaction doesn't cease because lutein is coming into the body too often. In the infant, there are generally few exposures to lutein, but during the second and third years lutein-containing foods begin to enter the diet frequently. The response to the first exposures might be fever, and many parents report fevers during early childhood. (I have already commented on Ryan’s illnesses and ridiculous fevers). The child often begins to refuse some foods (can can become a very fussy eater). The altered immune system often over-reacts to immune challenges as is seen in the frequent reports of adverse reactions to vaccinations. Then, as the lutein exposure becomes continual, the immune system has to adapt, as continual high fever is dangerous to the brain. With an ongoing immune system activity, the limbic system switches over to a state of defensiveness and survival. Development of social behaviour is arrested in favour of survival, defensive and coping strategies to minimise arousal and social expectations. Depending on the innate strength of the individual, mental and intellectual functioning may develop, despite the social handicap, in idiosyncratic ways. For some high functioning autists, the strategy of avoidance takes the form of developing unique skills, or intensive reading and studying, or focus on a particular branch of math or science or music.

Secondly The hippocampus is linked to learning and memory. When the hippocampus is removed from an animal, it will express a series of behaviours classified as self-stimulatory. These behaviours are repetitive body movements or movements of objects . For example, tapping ears, sniffing people, hand flapping, scratching, or rocking back and forth. Two hypotheses of this behaviour have been drawn. Either the actions are to stimulate (hyposensitive) or to calm (hypersensitive). In the case of the autistic person, the second hypothesis makes sense. To the autistic the environment is too stimulating and by doing a repetitive motion the environment can be blocked out. The environment is too stimulating because the brain can not process the sensory inputs as fast as they are being received. New information can not be entered into the memory quick enough.

From my own research I have complied the following information on e-numbers that particularly affect Ryan. Now I am not for one minute suggesting these are all inherently bad or that anybody should take my word as absolute fact and eliminate these as of right now. I am simply sharing my findings with anyone interested enough to know more about our journey with Ryan’s autism.

E 102 Tartrazine                         
E 110 sunset yellow FCF
E 120 cochineal                                  
E 124 ponceau 4R
E161 Lutein
E 211sodium benzoate
E 621 Monosodium glutamate (MSG)

For a full list of my e-number research see my separate page.

Go to the following website for tips on maintaining a healthy Limbic system.


Comments

Popular Posts

Missing Education due to Illness

The Importance of Attendance If you read any news articles on education, correspondence from your child’s school, or are simply clued up on parenting then you will know the importance of school attendance. Schools place a great deal of focus on targets and will often offer incentives and competitions to encourage and increase attendance figures, but what if your child has a serious illness. What happens if they really are not well enough to attend school. What happens then? Attendance targets at Ryan's school are currently set at 95% attendance for the school year. Therefore realistically your child can only miss 10 school days due to illness. Medical appointments such as GP or Dentist do not count, but you are encouraged to make these appointments outside of the school day where feasibly possible. If your child consistently misses school, even if it is only one day a week, that equates to 39 days over the school year. Even missing one day in a week results in pressure on the ...

Questions to ask after Cancer diagnosis

Cancer Sucks I have shared with you Ryan's lymphoma journey where we have talked about the ups, the downs, the protocols for drugs, the side effects, but I realised recently I have never shared the questions. This post is all about what to ask when you receive a diagnosis of cancer. Receiving a cancer diagnosis is never ever going to be seen as good news. It can never be dressed up or made pretty. It is devastating, it is gut-wrenching, it is life-changing. There is so much information to process you will not think of the questions you need to ask or you will have hundreds of questions you want to ask all at once. These are just some of the questions you can ask once you have processed the news, in order to gain a better understanding of your fight ahead. General Information What type of cancer do I have? Where is it located? What are the risk factors for this disease? Is this type of cancer caused by genetic factors? Are other members of my family at risk? What lifestyle c...

Chemotherapy Cycle 5

What is Normal? With this being our penultimate cycle of chemotherapy I have had several family and friends comment to me “oh I bet you can't wait to get back to normal”. This has really thrown and upset me because it seems to come across that they have failed to comprehend the fact that we have 2-3 years of maintenance ahead and at least two more general anaesthetic surgeries. Not to mention physiotherapy as it is expected Ryan will take 12+ months to heal from the effects of being poisoned from the inside out. Normal is long way off yet. While everyone else appears to all be getting excited that Ryan is coming to an end of his chemotherapy protocol treatment, Ryan himself is becoming more and more tired with the cumulative effect of the onslaught of the chemotherapy drugs and is spending long periods of time in hospital after each cycle with infections due to his impaired immune system now as a result. Ryan is far from excited. Ryan is exhausted. We still have one more cycle t...

Peritonitis

Emergency Surgery On the morning of 25 October 2016 Ryan was complaining that his PEG feeding tube was unbearably painful. He was due for a review anyway that day at Velindre Cancer Centre and a PEG specialist nurse came for to look at Ryan. She said the site was a bit weepy and raw, she thinks he possibly caught or pulled it in the night. She is confident that it is fine and she also gave it another good clean.  A week on and we are back to square one. The district nurse came out on Monday 31 October 2016 to advance (turn) the PEG tube as is needed each week after the first month. The nurse was unable to move the disc and caused Ryan an incredible amount of pain. We ended up having to go to the Teenage Cancer Trust ward in Cardiff, where two gastro nurses met us and spent the best part of an hour, torturing Ryan while they 'forced' the PEG to move, which they eventually did. Or so they thought.  The following week, 7 November 2016, the district Nurse came again to the ...

Cancer Survivor Story

Cancer Doesn’t End When Chemo Does Ryan finished his chemotherapy treatment on his brother's 18th birthday in May 2017. The last two years and eight months were a blur of stress. Yet coming to the end of treatment coincided perfectly with Cancer Survivors Day on the first Sunday in June, each year, so what better way to mark this day than with our own survivor story. Ryan's weight at diagnosis was a staggeringly poor 42kg. He had lost so much weight not being physically able to eat due to the tumour in his throat, but with thanks to his own determination and the feeding tube that he had. Ryan's weight as we start his final chemo cycle....drum roll....prepare yourselves.... was an amazing 57kg. A year on in 2018 and despite going through treatment for the second time after relapse. Ryan weighs an impressive 65kg. Chemotherapy Cycle six Started on Monday, 1 May 2017 for hydration and the week went well without any drama. His final chemo took place on Friday, 5 May wh...