Tag Archives: Living Autism

Dad of Divas (www. dadofdivas.com)

While I do not live with autism daily, this was an interesting read. I appreciated how in-depth the author was in regards to what parents have to deal with in an honest, upfront and truthful manner. The book was easy to understand and the author talks to you as if you are a trusted friend. That being said I was very impressed with the amount of information that was shared and I can honestly say that I learned SO much from reading this that I was not aware of previous to reading. The book is definitely a resource that will offer hope and resources for anyone touched by autism. The daily reflections really make you think differently about autism and what this means to you and the people around you!

*I received this for review – all opinions are my own*

Kelly

When I received Pamela Bryson-Weaver’s Living Autism day-by-day, I knew that it would be of interest to several moms that I know.

It begins with an informational intro, then transitions into a journal of sorts. Each day has a story, quote, and /or info, and has a space for notes or reflections. It’s a great hybrid of clinical information and lovely thoughts and quotes. I thought it would be a great resource and personal notebook for the parent of an ASD child.

I gave the book to a friend and asked for her review, as someone who is very knowledgeable on the subject and truly is living autism day-by-day. Below are her thoughts:

“I appreciate Mrs Bryson-Weaver’s positive breath of fresh air on a variety of topics that are very difficult for most parents of an ASD child. Daily she provides a famous inspirational quote, a topic to revel over, and a small daily objective to strive for. She covers advocating for the ASD child as well as advocating for yourself to find the answers you seek, the support you need, and acceptance of your child for who they are.

Her knowledge and suggestions are current in terms of biomedical and dietary treatment approaches. I’m not so sure that all of her ideas are reasonable though. As a mother myself of a child with an ASD, I was quite surprised to find her “home schooling” suggestion.

On a whole, the book is a must read for parents of a newly diagnosed child!!”

CACI: A Circle of Love and Support

One of the hardest struggles of autism is finding a community that supports its intricacies. Life with autism can be a tough one, often leaving many families on their toes. We all know that amidst the rising numbers of autism cases across the globe, there are still communities out there who chose to turn a cold cheek on families who needed their support and understanding the most.

I am, however, lucky to have found a compassionate and supportive community of like-minded people whose core values revolved around uplifting families, parents, and siblings battling not just autism but a plethora of neurological disorders. The Community Autism Centre Inc. or CACI is a community-based non-profit centre offering support for families, parents, and siblings such as resource information, music programs, educational programs, social skills group, training and advocacy, workshops and mini-workshops, and (yes!) consultation for adult support.

I was hosted by CACI one night and had tremendously enjoyed the time spent with them talking about my family’s journey and my own journey with autism. I presented my book (Living Autism Day.by.Day) to them, too, and the overwhelming support from these people truly tugged at my heartstrings. Like me, they also undergo the same rollercoaster ride with autism and hearing them share their experiences was enlightening and inspiring. It made me feel like having an extended family to reach out to, to hold on to when the going gets tough, and to laugh with on certain encounters that bring tears of joy to the eyes.

Feel free to check out their Facebook Page – https://www.facebook.com/groups/cacisaintjohn/ – for more information, and on November 29th at 7pm at the Buccaneers Pub on 24 Main St. West, CACI will be holding its Steak N Stein dinner and live auction extravaganza. Tickets are at $25 with the proceeds going directly to the CACI community of support. Mark your calendar, folks!

Lisa

My kids were so excited seeing their faces in the book and truly, the book is a beautiful honoring of those with autism as well as parents on that journey to support their little ones…. 

I’ve gotten my son to show it to his Autism school, Pathlight School, the only dedicated-autism school in Singapore and they are interested to get copies of this to either sell or have in their library – am waiting for them to tell me what they intend to do – but so many teachers and the vice-principal has already seen the book and everyone’s so taken in by the book! So honouring you and the gift of your book to the world! Thank you once again for the heart you have for autism and for the little ones you hold dearly. 

Will reconnect soon once I hear back from the school on what they would like to do… cheers and divine blessings for you always! 

Kimberly Arsenault

Thank you so much for the advance copy of your book! The book is fabulous, and I highly recommend it! The website is also fabulous, and will continue to be a wonderful resource, I look forward to seeing it continue to grow and evolve! 

You are such a wonderful mother and such an inspiration! Keep up the amazing work and know that you are making such a difference in this world! God Bless!

Rita

I had such a crazy thing happen to me this morning that I just had to share it with you.

I went into work today, which was not required, to participate in a new student orientation program.  I was unsure where I was suppose to go, so I walked into a classroom where 2 of my co-workers were talking.  I had several rooms that I could chose from, but randomly picked the one I did.  As I walked in they were in a deep conversation so I just stood back for awhile to let them finish.  To my amazement the conversation was about the son of one of them who is currently in the process of being diagnosed as autistic.  I couldn’t believe it.  Her son is 4 years old and they are in the run around stage of trying to diagnose her son.  I immediately shared your information with her.  She was very excited to have another resource and I am sure she will be checking out your website.  I sensed she was feeling the frustration of trying to find out what is happening with her son.  It sounded like some intense testing is coming up soon.

It was so crazy that I just had to share this.  I had no idea she was dealing with this with her son.  Again, I think the stars must be in line.  It felt so good to me to be able to share your information with her.