Yes we'll walk with a walk that is measured and slow, And we'll go where the chalk-white arrows go. For the children, they mark, and the children they know the place where the sidewalk ends.

-Shel Silverstein

Sunday, February 1, 2009

OUR LITTLE MAN

I thought I would update those of you who have written kind words about our Cameron. Boy has it been a rough couple of weeks!
I want to preface this by saying that I had a conversation with someone at church right about the time we decided to take Cameron off of his meds. There is a family at church who recently did the same thing with their son who has severe ADHD. I was talking to the dad in the hallway at church and he said that the first month off meds was "hell," and then after about a month, he emerged a new boy. In that moment I knew that I was supposed to hear those words...really HEAR them.
Cameron went from bad to worse to unbearable in the days that fallowed. His days at school were complete mayhem. He was so out of control, he was often removed from the classroom for safety reasons. He spent most of this past week in the Principal's office screaming for hours at a time and trying to turn over desks. He had a couple of days where he was so paranoid, he screamed and cried that everything was "scary" including his starwars action figures that he believed were going to kill him. If you don't think that I was tempted to give that boy some pills...good gracious it was scary for all of us. Thank Heaven for the kind Teacher and staff at his school who were in daily communication with me and gave him constant support and reassurance. They started him on a program where he repeats "self soother" phrases to himself througout the day, like "I will be OK if I make a mistake."
Cameron began seeing a new Occupational Therapist this past week. He was in a frenzy for their entire session. She said she "sees this all the time..." meaning kids who originally did well on meds, suffered extreme side efects, were taken off and went crazy for a period of time afterword while the stuff was getting out of their systems. This was so reassuring to me that we were on the right track.
During all of this, I was researching alternatives. I kept having the distinct feeling like we needed to take a more "natural" approach to treating Cameron. We've taken him swimming as often as we could, as swimming has always been a very calming activity for him. Off the meds, he has finally been able to play in his "quiet room" again for a couple of hours a day, which he hasn't done in a long time (another calming activity for him). He was so wound up, he hadn't hardly touched a toy in months. We found a pediatrician close to our home who uses the biomedical approach to treating Autism. Amazingly, he is covered by our new insurance and we were able to get right in to see him. We saw him yesterday and he was just wonderful. He drew a bunch of blood to run a bunch of tests and we started yesterday on an intensive program of supplement's and vitamins etc. The next step is starting to incorporate a wheat free, dairy free diet.
We are finally starting to see dramatic changes as this past week came to end. He is starting to be more of his old quirky, emotional, inflexible self...but not the scary stuff we were seeing last week. He even said this morning "This is the happiest I've ever been!"
I have thought a great deal in the past few months about when we brought Cameron home from the hospital. We had wanted a baby for so long. We had worked so hard to get him here and I had been so sick during my pregnancy...first with extreme nausea and then pre-eclampsia. When he was just a couple of days old, I remember holding him on my lap and just weeping with joy, and fear...fear that he would ever hurt, that anything bad would ever happen to him. I loved him with a love that felt almost suffocating, if that makes any sense. Like all first time parents, we hung on his every achievement and beamed with pride at the early signs of his brilliance. He astounded us with his passion and amazing memory. I tell him all the time, he is so special because he made me a mom, and being a mom is the best part of my life. Many of you have heard the story of when Cameron was four. I was putting him to bed and he came to give me hug. He started talking about how much he loved his family and how he was so glad "Jesus gave (him) this family." He then put his fat little hands on my cheeks and told me "Mom, my family is my only chance." Those words have rung in my heart every day these past few weeks. I know that God will direct us. I know that our Father in Heaven is the only person who loves Cameron more than we do and wants the best for this extraordinary little boy. I am proud to be his mom and I know Evan is proud to be his dad. I am so grateful for the knowledge that God can guide us in parenting him. Please continue to keep us in your prayers.

11 comments:

vicki said...

Bless you! And hang in there! I am here for support if you ever need it.

what kind of a name is abra said...

We really missed you today. I was all ready to kick people off 'our' bench. Are you all sick? Do you need dinner tomorrow? Call me.....

Lane & Janka Cameron said...

It was a wonderful birthday gift yesterday when Cameron told me he was happy. What else can a grandmother ask for than grandchildren who are happy, and loved by their parents. We love you all. Mom

Sara and Spencer said...

We Love You Cameron! We are especially happy that you are happy. Please call us if and when you need help. We love you all!

Sara and Spencer said...
This comment has been removed by the author.
thesearlesociety said...

You guys are amazing parents. I don't think I'm strong enough to go through what you guys have to go through. I can barely take it when Isaac throws tantrums! Cameron truly was sent to a special family who will help him be the best he can be. Love you guys!

Meilani said...

You are a good mother Rebecca. I appreciate your influence through all of your comments on my blog and emails. Parenting is hard enough without such serious difficulties. I will pray for you. But it sounds like you are already getting inspiration and heaven sent help. Lots of love! Meilani

Kam said...

Hi Rebecca,
I just logged onto your blog through Randi's. I loved seeing the pictures of you and Randi together, and of gorgeous Baby Anne. I'm sorry for what you must be going through with Cameron, and will certainly pray for your family, and for him. I loved reading your thoughts about when he was born. What a special boy he must be. We have a nephew who has been struggling to get the proper meds, as well. It's such a blessing we live in this time with so many people trained, and medicines specifically designed, for whatever ails us. But still so hard to know exactly what's best for everyone in every situation. We'll pray that you'll be directed the right way for Cameron, and all your family.
--Kamber
ps. I'm glad we're now friends on facebook. I don't use it too often, but I do like getting to know people better that way.

Anonymous said...

Hey Rebecca - I have been "blog hopping" and just found your blog. Congratulations on little Anne - she looks so precious. Wow, it seems like you have your hands full with every thing going on. Our blog is www.mojosmemos.blogspot.com. But, it is blocked because we are in the process of adopting a sibling set of 4 through fost/adopt. And I can not post their pictures on a "public" website yet. So if it is blocked I am allowed to. But, email me so I can tell you how to view it and so we can "catch up". Noelle Philpott

Anonymous said...

This just shows you how fried my brain is with 5 kids. I forgot to give you my email address: ncphilpott@yahoo.com sorry.

Sherry said...

This is a wonderful and revealing entry. I didn't know you were going through the switch of meds and dealing with the scary challenges of living through it. I don't think I could have stuck it out.

I melted into tears at Cameron's grateful phrasing about your family being his "only chance". It is so true, the expression..."Out of the mouth of babes".. truths are revealed.