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Wednesday, 31 March 2010

Unity Among the Autism Community

Posted on 17:21 by tripal h




On the eve of April - Autism Awareness month, I feel compelled to get this off my chest. See I have been holding my tongue for some time and I absolutely cannot stand it anymore. The ‘infighting’ among the autism community grates at my inner core and I find myself needing to come forth in order to release the charged feelings I am experiencing ... I understand it may not do any good, but at least I will have said my peace.

At a time when autism numbers are soaring, we need the mainstream folk to become involved. And yet, our own community cannot support one another despite our differences … How, I ask, can we possibly expect others to take a stand and advocate for us, when we can’t do so for each other? It is time to set aside our differences and unite for the greater good of the autism community as a whole.

Our children (and adults) diagnosed with autism need support, protection, advocacy, and empowerment as well as other necessities.

Personally, dare I say, that I actually relate to both sides in my own unique way; the neuro-diveristy and the pro-cure. I don’t think that makes me hypocritical. I am just a concerned mindful mother wanting the best for her child.

The nuero-diversity camp promotes that we accept our differences and honor each person in their unique sense of self. Truthfully, that really is the foundation of my personal advocacy group, Exceptional Beyond Labels. I, also, believe that despite any label (autism, aspergers, pdd-nos, ect) that each person behind the label is just that… A PERSON! They are a person not defined by this label, but rather a person defined by their unique individualization... And that person is phenomenal and capable of anything given the proper tools. Autism is not something to be ashamed of, in fact, I believe it is those on the autism spectrum that will make profound changes in the systems that are no longer working in our world(but, that is a whole different blog entry). I believe that all research and programming and legislation should include parents and adults on the spectrum ... I agree that we cannot determine their future without their input!!

On the flip-side, I find myself praying for a cure and requesting unbiased 3rd party research. I long for a day that the ‘infantile autism’ label that limits my child is shed like the skin on a snake. I am motivated to prove the diagnosing psychologist wrong when she said to us without a blink of an eye that our young daughter would never have a productive career, meaningful friendships, marriage, a college education or independent living. I have read countless books and surf the net to wee hours of the night to discover what others are doing to help their child diagnosed with autism to 'recover', so that I might be able to pull her further into our world closer to a functional life. I have tried diets, alternative therapies, holistic medicine, traditional therapies, and anything else that was within my arm’s reach. I want, like every parent, to have my child have a bright future full of possibilities.

I don’t do these things to change her core essence, but to remove barriers so that she can have a productive future; to improve her quality of life; to reduce her fundamental frustrations that are demonstrated through a profound expressive and receptive speech delay, an heightened autonomic nervous system response, the sensory and auditory processing complications, a curious eating disorder, awkward socialization skills.... let's not forget that I do this to end the never ending fear of her risk of elopement ending in a catastrophe or to end the nightmares about what will happen to her if her parents were to tragically die or to end the fear that resides in the knowing that if someone were to violate her she would not have the functional words to tell me (and the list goes on) …

I have come to understand that some cases of autism (possibly more aspergers than infantile autism) is genetically based and hereditary while other cases are more environmental. Our geneticist concluded there was no biological foundation for the autism, yet denied environmental possibilities. That doesn't make sense to me. How can biological and environmental factors both be ruled out? This is a hot topic and has caused some to even proclaim hatred towards a certain celebrity. However, I cannot rationalize for one second how the toxins in the vaccines could possibly be safe in the amounts given to the tiny bodies our child inhabit. Yes, I know that the CDC and FDA have cleared them to be safe but common sense tells me otherwise. (I am not going to elaborate on this as there are many resources out there stating the facts… go check them out). I, also, am concerned that no one is talking about maternal vaccine history and its effects on the offspring she bears or the Rho-Gam (Anti-D) vaccine given to pregnant women with negative blood. If the toxins cross the blood brain barrier during critical fetal nuero-development could that not affect the brain and cause autistic-like symptoms?

Now, I do believe that the camp that takes this stance should be less cynical and sarcastic in their presentation … tastefulness goes along way. I wonder if a certain publication ever considers that their point of view would be better accepted by mainstream, the autism community, government, and big-pharm if they added a little more class to their presentation. But, their opponents create face book pages like I Hate Jenny McCarthy. So, what do you do?

This has to stop. We have to have a truce!! We have to say we can understand both perspectives and respect the needs of both parties. We have to stop organizations getting rich off of the challenges our children and adult friends diagnosed with autism face. We have to unit for the common good for all involved regardless of etiology beliefs! We have to unite to promote advocacy, education, safety, insurance inclusion, 3rd party research, affordable early intervention, awareness of alternative and holistic health modalities, resources on self-esteem building, education advocacy and inclusion, elimination of seclusion and restraint, as well as promote things like education for mainstream professionals like the police, firemen, teachers, store clerks, life guards, and public transit authorities.

We have to put aside our differences for the greater good of our community; a community desperate for answers and desperate for acceptance.


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Posted in autism, Autism awareness month, Children's health, Jenny McCarthy, Mercury, mercury and gestation, national health crisis, Reiki, RhoGam, self empowerment, Toxins, Unity, Vaccination | No comments

Monday, 29 March 2010

The Coffee Klatch presents Temple Grandin

Posted on 14:30 by tripal h


The Coffee Klatch (TCK) is a real time twitter chat room founded and moderated by Moms of special needs children. TCK brings knowledge and empowerment into front rooms across the globe. I have found other mothers (and fathers) to be my best resource in advocacy, education and support; and TCK ranks up there with the best! Visit their web site for more information and transcripts from former shows.

Last night TCK had TEMPLE GRANDIN as their guest! I have posted some of my favorite tweet-quotes from the interview below. I do not intend to take away from the whole interview process nor do I mean to take anything out of context, but wanted to pull out some of the concepts that seemed to me to be important to emphasize. Please note, I still encourage you to view the Full Transcript from the Temple Grandin Show here.

My Favorite Temple Grandin tweet-quotes from TCK interview:

ABOUT SPECIAL DIETS

"yes it cleared up my yeast infections - I hav ecut huge amounts of suger out of my diet - with success and I talk about it in "the way"

"Im doing wheat free myself"

ABOUT INCLUSION IN SCHOOL

"You have to look at your particular situatin in your school - you might want to look at "unwritten rules of social relationships"

"there are some aspergers kids that get tortured in high school and may need to be taken out but - I am much more of an advocate for inclusion for elementary school kids - I want to emphasis that decision about this depend upon many unique variables with particular"

ABOUT MEDICATIONS

"the big mistake with antidepressants in the autism spectrum is too high a dose. some need only 1/4 to 1/2 the starter does - they are microresponders and you need to read the book very very carefully"

ABOUT SIBLINGS

"Find shared interests that they can enjoy together like painting pictures playing games sports any activity they both enjoy"

ABOUT DSM IV & DIAGNOSIS

"Aspergers according to dms IV is minor autism with no speech delay - it is not a seperate disorder - autism is a continuum to veryfrom mild and a little nerdy to no language and severe problems - Einstein in todays school system would prob be labeled autistic"

"According to DSM IV guidlines I would be HFA because I had speech delay"

ABOUT SPEECH DELAY

"I recommend that they read the book "How can I talk if my lips dont move. It is written by a person that is non verbal with autism - written Tito anybody working with non verbals should read that book"

ABOUT THE DIFFERENT WAYS WE LEARN

"You need to build on the childs area of strength."

"photo realistic visual thinkers like me are very good at art design drawing and graphics but I am really bad at algebra -some visual"

"the second type is the pattern thinker - or music and math mind - it is a more abstract form of visual thinking - these children may. thinkers can do geometry and trig"

"the third is the word mind - these children know huge amounts of verbal facts about their favorite subject "

ABOUT TEACHING

"Never taught in the abstract it has to be taught with specific examples"

"Mother told me to take my turn - turn taking was taught using board games -to understand the concept of turn taking I had to learn it"

"He took my interests and channeled them into motivating me to study - good teachers build on a child interests if a child likes trainsteach reading with trains math with trains - you want to use the motiviation of the fixation to motivate academics and career work"

ABOUT SOUND SENSITIVITY

"sometimes the sound sensitivity can be reduced if the child can get used to the sound on recording and the child can turn it up gradual"

"sound sensitivity - ear plug or head phones can be worn but - they must be off for half of the day to prevent the ears fromgetting more sensitive"

ABOUT TACTILE SENSITIVITY

"tactile - soft clothes that are well washed several times will be less scratchy"

ABOUT VISUAL SENSITIVITY

"two other things that help is using a laptop computer which does not flicker and try printing reading materials on pastel color papers"

"interventions- if visual some ppl find colored lenses are helpful - pale pink blue ligt brown and purple sunglasses"

ABOUT AUDITORY PROCESSING

"sensory probs are very variable - some have aud processing probs where difficulty hearing hard consentant sounds like D AND G"

ABOUT EARLY INTERVENTION

"keep the mind engaged"

"most imp is 20 or more hours a week of 1 to to teaching with an effective teacher. this is for very young children from 2 to 5 yrs old - not to stop at 5."

Full Transcript from the 3/28/10 Temple Grandin Show here.

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Posted in autism, Children's health, emotional health, language, nutrition, self empowerment, sensory processing, Temple Grandin, The Coffee Klatch, twitter | No comments

Sunday, 14 March 2010

Kidney Stone Update...

Posted on 15:58 by tripal h

The CAT scan revealed I had a total of 18 kidney stones.

5 on the right side, ranging 2-4 millimeters.

13 on the left ranging side, 2-8 millimeters.


They blasted the 6 & 8 millimeter ones on the left with sound waves... I have been passing gravel since Ground Hog’s Day.

The remaining ones have to be passed ‘naturally’. Tonight I am in severe pain and am pretty sure that I am passing one of the larger ones on the right. All I can do is drink water since the remaining stones are all 4 millimeters or less. But, do not let that size mislead you... it hurts.

I am perplexed as to how I got so many, and am darn annoyed with how much water I have to drink. All I can do is drink, send Reiki, and try to stay active... activity helps move them. However, tonight I choose to park it on the couch.


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Posted in Home Remedies, kidney stones, physical health, Water | No comments

Saturday, 13 March 2010

Back in the Saddle at Riverwind Equine

Posted on 16:11 by tripal h

It had been four long months since we had gone to the horse barn… you could feel a calm excitement in the jeep on ride there. As we pulled up Sahara yelled, “There it is!!” Emily clicked off her seatbelt and eagerly reached for her helmet and bag of apples then disappeared.

As we walked down the broken concrete path, we were met by a wet, cold, muddy day. Nevertheless, there was complete life emerging before our eyes. New horses stuck out there heads and nodded at the new people that they had yet to meet. The old ones looked up with a certain relief to see that part of their herd had finally returned.

It did not go unnoticed that many things had been tended to throughout the winter; there was a certain sense of aliveness brewing on the land and within the structures. I immediately feel enamored by the beauty of the barn, the peace it emitted and the mindfulness of all the people that congregated on this land. Each of them have uniquely become a part of our family.

The head of the Arabian herd, Silk, was so pleased to see the children. He seemed to take extra care in his footing and movements today. Emily confidently started with a walk which quickly turned into a trot and moved Silk over the 3 poles with grace. Her cantor and post was shaky a first, but the concentration and determination paid off. As she dismounted Silk, I realized that I hadn't had to walk or look away once. This meant that I either found peace within myself about my child riding this one ton creature or they worked so well together as a team that fear did not beckon me... I suppose it was both.

Silk looked at Sahara with intensity when it was her turn. She mounted him and said, "Yee Haw." They walked a few laps and surprisingly I did not have an urge to nudge my husband to walk beside them. She melted into the saddle and had such poise; her body moved with grace with each step and bump. We all laughed as they rounded the gate and heard her say, "Run, run!!" As the horse came to a stop, she spoke fluently again, "More..... Walk On." Last year at this time, Sahara's expressive and receptive language was limited at a 12 month old's ability. To hear her request that she continue her turn and to give oral commands to this beautiful Arabian Horse was music to my motherly ears.

I whole heartedly feel blessed to have this horse in our lives and treasure the moments like this one that will be forever be embedded in my children’s childhood memories. I am sure that the girls will vividly look back to their horse barn days at Riverwind Equine Boarding like I do fishing on Lake Erie aboard the Sea Breeze with my father at the helm in his faded jeans, white t-shirt and red baseball cap while my mother sat in her chair at the stern with her oversized hat and sunglasses.


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Posted in adventures, animal, autism, Children's health, Energy, fathers, gratitude, Hippotherapy, language, mothers, Siblings | No comments

Thursday, 25 February 2010

The Cleavers We Are Not

Posted on 15:05 by tripal h
Since I was cooped up for the last few weeks (and I really didn't feel like cooking), we decided to venture into the world of eating out tonight. I called ahead to check out what they had on the buffet to be sure each child would have adequate choices. Problem? We choose a restaurant that was foreign to Sahara.

As she entered the building, she scoped out all of her surroundings and off she went. She had to walk (a.k.a. run) the entire perimeter of the restaurant before even glancing at the life-less food presentation. I tried to persuade her to entertain food options that she would have some interest in (pizza, plain noodles, plain lettuce, broccoli), but I knew the vast amount of odors were overwhelming her as was all the noise and people. She was over stimulated and on overload... and so was I.

However, it was the gazing and whispers of the bystanders that raised my anxiety the most.... I just wanted to yell, "she has autism... quit staring!". But, I bit my tongue and withheld my tears. I felt them burning in my eyes... but, I forced myself to not let my weakness conquer me. I felt a quiver in my throat as I told my husband to eat fast. Emily asked, "Why?". I scanned the room for just one understanding smile, but am left feeling disappointed, "I don't feel good."

Partly that was true. I was having high anxiety and I was sick to my stomach to see my child out of control. It is moments like this that we see how far we have to go. It is moments like this we realize that we do not have a typical life. It is moments like this that I look at all the other families with envy as they quietly sit and eat their meals. But...

The Cleavers we are not! And now that I am back in the comfort my home and the children are calm in the familiarity of smells, sights and sounds... I find peace. Yeah, the Cleavers we are not, but we are the Richardsons. We have diversity, unconditional love, courage and a unique view of the world and for that I am grateful!

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Posted in autism, decision making, emotional health, Food Sensitivity, sensory issues, sensory processing, Siblings | No comments

Tuesday, 23 February 2010

Bedtime Stemming and Emotions

Posted on 16:23 by tripal h
The clock flashed 1:11 am....

My ears had been listening to the non-stop vocal stemming for 4 hours now. My eyes could barely stay open. I had tried every trick I had up my sleeve; brushing, reiki, floor-time... This was just something we had to ride out.

1:24 am...

I was tired, I knew we had a busy day ahead of us; Music therapy, occupational therapy, physical therapy, and speech therapy. Mondays are our busy days... coming off of a 3 week bout of the kidney stones my mind and body was tired and weak. So tired! Patience has been drained from my essence... I snapped in a voice that must have seemed ferocious to her, "SAHARA, PLEASE GO TO SLEEP!!"

She started to cry. Not a tired cry, but a pissed off 'you hurt my feelings kind of cry!'. She was screaming on top of her lungs this dramatic forced angry cry!! Then she yelled, "I HATE YOU!" (pause) "I HATE YOU!"

I was stunned!!

I laid there in disbelief, not sure if I should cry or laugh. I rewound to the moment my older daughter, Emily, uttered those painful 3 words. I remembered the devastation in my heart and felt a twinge of motherly pain.

1:28 am...

I wasn't sure how to respond, so I laid there listening to the screams and cries of her processing the foreign emotion of being pissed off at her mother. I felt bad I raised my voice. I felt guilty knowing she couldn't control the stemming. And I felt helpless in the knowledge that if I interrupted her, she would have to start all over resulting in a long sleepless night.

1:30 am...

Part of me was quietly relieved as I reached over to rub her warm back. She uttered those hateful words! This had huge significance! It meant that she understood she was pissed off and she understood she was pissed off at me... not the stemming, not the autism, but at her mother for losing her patience. She had come out of her stemming and appropriately experienced her emotions.

1:34 am...

She rolled over into my motherly arms and rest her head upon my breast. She whimpered as she fiddled with my fingers. "Sahara, I love you," I gently whisper as I stroked her tears away. "I love you more than the infinite universe."

1:36 am...

All was quiet. I heard the rise and fall of her exhausted sleep. I brushed away my tears and sighed, "I am so sorry."



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Posted in brushing, co-sleeping, Floortime, language, occupational therapy, self empowerment, sensory issues, sensory processing, speech therapy | No comments

Sunday, 21 February 2010

Recipe of the Week: GFCF Sunday Morning Muffins

Posted on 09:14 by tripal h
Mommy is back!!

This morning Emily asked for Blueberry Muffins for breakfast. After spending 3 weeks confined to the couch with kidney stones, I decided to put on the apron and jump back in. Of course, I wasn't lucky enough to have a pre-packaged mix in the pantry. So, I decided to wing it. I found all the ingredients for a coffee cake, surely if I tweaked it a bit I could come up with something... I have to say this was so yummy on a quiet Sunday Morning!!

GFCF Sunday Morning Muffins

1 Egg
1 Egg White
1 Cup Almond Milk - Original
1/2 Oil of choice
1 Container of Diced Pears, drained
6 ounces Fresh Blueberries
1/2 Teaspoon Allspice
2 Cups White Rice Flour
2 Teaspoons Xanthan Gum
1/2 Cup Brown Sugar
1 1/2 Tablespoons Baking Power
1/2 Teaspoon Sea Salt

Topping:
1/2 cup Brown Sugar
1/2 cup Pecans, chopped
1/2 teaspoon Allspice

Preheat oven to 350 degrees.

Whisk egg, milk, and allspice. Stir in oil and fruit.

In separate bowl combline the rest of the ingrediants. Mix wet and dry together. Fill muffin tins 3/4 and top with 1 teaspoon of topping.

Bake 20 minutes... enjoy!!
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Posted in GFCF recipe | No comments
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tripal h
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