Showing posts with label parenting. Show all posts
Showing posts with label parenting. Show all posts

Saturday, February 9, 2019

Life @ The Dahlhouse: Week 2


Not surprising, I already find myself very behind on weekly updates!  This was a goal I had this year... to consistently update my blog so that I have record of the events.  Are you like me, already struggling with your new year's goals?  The struggle is real!  


Week 2 was CRAZY friends!  Monday came and BAM, 4 appointments that day.  Who does that?  I never plan on that happening, but sometimes, once in awhile, all the stars align.  LOL.  That Monday we had an orthodontist appointment, two doctors appointments in a row and a tutoring appointment.  I was wiped out.  And that little cherub spent a lot of time in waiting rooms that day.
Do you ever go through a season of life and you feel like it is a difficult one?  I am right there with you!  I told Mark the other day that we are in a tough season.  There is something BIG going on with everyone of my kiddos, and I am left feeling like I am just not ENOUGH most days.  How do you spread yourself out?  How do you make sure each one has there needs met?  Regardless, I get myself out of bed each morning and try again.
 #truth
Miss B has been REALLY struggling.  Anxiety has set up shop in her little mind.  I'm telling you, it is like looking at a childhood version of myself.  So many of her struggles I relate to so much!  Separating from me leaves her almost panicky.  I leave her in the classroom each day, and walk home in tears myself.  I never let her see me cry, but I fight everything to not scoop her up and take her home with me.  Does anyone have any suggestions that help kiddos with anxiety?  I am all ears!
 Some days are the perfect storm of organic applesauce and fast food chicken nuggets, while we sit in high school algebra class with the oldest.  I am not great at math.  I don't know much algebra.  But me showing up for him, that is the most important thing.  Even with a toddler in tow, who poops in the middle of class, we want Luke to know we are there for him.

*Luke goes to an AMAZING alternative learning school called River Homelink.  He attends class two full days a week and does classwork at home three days a week.  They are very parent welcoming and encourage parents to participate and even bring our pooping toddlers with us.  Haha!
Do you ever bribe your kiddos? If you do, you are MY people!! Confession, I bribe my kids!  To help Miss B get through the day, I promised her we would make cake pops.  So Friday night we made cake pops.  They are surprisingly easy to make.  They just take time, and make a slightly big mess, but WORTH it!

I ended the week at a VIPKID local meet up.  VIPKID is the online teaching company that I work for. It allows me to make extra income working around my schedule.  And as we know, I need a flexible work schedule (four appointments in one day). I teach English to Chinese students in a 1:1 environment.  I share more about my experience on the VIPKID page tab.

If you have ever wanted to teach online, ESL or work with VIPKID I would love to help you through the interview and hiring process.  Simply click this link VIPKID APPLY  .  Then send me an email misscarissa@hotmail.com, and let me know you applied and I will be in contact with you within 24 hours.
"Life is tough darling, but so are you."  ~Stephanie Bennett Henry~

Thursday, July 13, 2017

Week #26 & 27 @ The Dahlhouse

Summertime is in full swing at the Dahlhouse.  I am enjoying having a more relaxed schedule.  Even within the down time of summer, we continue to have a "schedule".   Monday's find us traveling to and fro from our little community library.  I finally found it!  It is the sweetest little library and perfect for my kiddos to peruse the aisles searching for the perfect book.  Bella calls it "book shopping" and cracks me up each time she says it. 
Water fills many of our hot days. 
Because this little one LOVES water sooo much, we have decided not to set up our big pool this summer.  Instead we have opted for a smaller pool that can be emptied when finished.
However, the size of the pool does not stop the big kiddos from joining in on the activities.  Pool is a pool.  LOL.  Grace is a joy!  She and Matthew have such a special bond and Grace is an excellent helper.  I can always count on her for Matthew help.  She is growing up.  Can't.even.believe.it!

Even though it is summer, the process of fighting and advocating for my kids does not take time off.  Even on a warm Monday, you can find us in the doctor's office with double appointments because this mama has a concern.  Man...I LOVE MY BOYS!  Luke is struggling...he is such a sweet, beautiful soul.  What a privilege to be his mama.  In the midst of Luke's of trials and hard stuff....I am crazy, deeply grateful for my amazing son!  He bring such joy and how I love him and the good God that brought us together.  Pray for him if you think of him.  We've had some very hard days around these parts. 
And oh Matthew...the little person I wished for that I didn't know that I needed!  Matthew is in Infant Toddler Early Intervention.  We have therapy for him for language delays.  He also is tip toe walking. I am concerned and needed the doctor to look at him.  After an exam and four xrays that left us both sweating and crying, he was referred for a pediatric therapy evaluation.  Knowledge is power.  We will be happy if he is fine, and happy to get help if he needs it. 
I finished this book in June.  Wow!  I knew it would be a hard read...and it was.   As a mama that has had both life and death within her...that has said goodbye to three little babies I never knew...my soul needed to read this.  I needed to feel it again.  I needed to grieve a bit more.  I needed to let myself go there.  And I did.  I cried the ugly cry more than once and surprised myself that even after 15, 14 and 12 years ago of losing my babies, the memories, the pain, the dreams and hopes for these little tiny humans were still there.  I allowed myself to feel it and talk about it.  And.it.was.good.  I am glad that I read this book. 
My photobook from Shutterfly arrived.  I designed one about our anniversary trip to Hawaii.  It turned out better than I expected and I highly recommend them.


My scar from my skin cancer is healing very well.  It is better than I could have imagined!  I am very happy. 

 Everyone needs a batman in their life!
 And a baby with a cat on their heads!  Thank you Facebook messenger!!!
 BBQing at Mimi and Papa's.
 Holding on to Hope while parenting on difficult days.
Bella had the opportunity to take a Mandarin lesson through a company called Lingo Bus.  It is a partner company with the one I work for VIPKID.  She loved it!  She is obsessed with Chinese culture.  She loves Panda's, Chinese food and learning people's names in Chinese.  I heart her so!
We've been selling pizza cards as a fundraiser for 4h.  This is our new mini rex rabbit.  She is super soft.
Papa and Mimi took Luke this last weekend for an overnight at their house.  They also took him golfing!  I am hoping that Luke will be able to join the high school golf team in a couple of years.  He really loves it and I think it would be very good for him.
Finally two of my kids promoted grades/classes on Sunday!  Bella moved up to the first grade class.  And Luke graduated out of children's church on Sunday mornings.  He is now going to be a helper for the younger kids classes.  Grace is excited as well because she gets to begin going to youth group.  Tonight is her first night!

Thursday, December 8, 2016

5 Things About Being A Speical Needs Mom Revisited

Out of every 5 households, 1 child will have special needs, which can be a physical, cognitive or medical disability.  That's about 10 million children in the US.

Luke is one of those kids.  Grace is one of those kids.
Luke has several disorders.  Early childhood onset glaucoma, microcephaly, ADHD, Tourette Syndrome, sensory integration difficulties and visual and auditory processing needs.  After many, many doctor's visits they have determined that there is no syndrome that links anything together, but that Luke kind of hit the lottery, so to speak, of congenital issues.

His disorders (or special needs) have caused medical and developmental problems.  He has been in physical, occupational and social therapies.  He has had 3 ear surgeries and heart surgery to close a hole in his heart, CAT scans to look at his small head, eye procedures, music therapies, and behavioral therapies.  He has been through more doctor specialists than I can count or remember.

Grace has obsessive compulsive disorder.  We have been through a lot of testing to rule out certain things.  She struggles with academics but gives her best effort.  At the onset of her diagnosis we went through two and half years of therapy to help her with the anxiety. 
Raising a special needs child, is a blessing and a challenge.  It is rewarding and trying.  It is inspiring and defeating.  It is like you can't have one without the other.  You take the good and the not so good.  I sometimes long to feel "normal" but have accepted that my "normal" is "not normal" and I am ok with that.  Many people will tell me what an excellent job I do with Luke and Grace, and how blessed they are to have parents "like us" but I often feel I am just so blessed to have them in my life.  I don't feel like I am anything special, and most days I feel that I am just "not good enough".  I yelled when I shouldn't have or didn't do enough activities with them.  I fail on so many levels, but I am human.  I am a mom.  A special needs mom.  Mainly though I just like to be known as...Luke's mom and Grace's mom and Bella's mom and Matthew's mom.  As a mom of children with special needs, I often feel a myriad of emotions.  I wrote a post like this one four years ago and I wanted to update where I am at now and share MY "real" honest thoughts about how I feel as a special needs mom.  Maybe you can gain some insight into how it is to be a special needs mom. :)

1.  I am tired...just being a mom is exhausting.  Especially to little ones.  However, parenting special needs children takes things to another level of being tired.  On top of the "normal" parenting things you do with your kiddos, you add therapies into your schedule.  While they may attend formal therapy once a week, there is practice and things to do at home several times a week.  We may visit doctors and specialists several times a month.  Sometimes I feel I live at the orthodontists office, especially now that Luke has braces.  As a kiddo with sensory issues, Luke often has a difficult time with all the weird stuff in his mouth.  Last month, we had a big check up on Luke's eyes at OHSU.  Matthew had a 9 month check up, and there were a slew of other doctor appointments including chest x-ray's for Bella.  If its not the medical needs it is the educational needs.  I have been fighting (what seems like a very long time) to re-instate Luke's IEP (Individual Educational Plan).  I finally have a meeting to begin the evaluation process on Monday.  I keep emailing, I keep advocating, I keep fighting even when there seems to be no fight left in me.  I am ALWAYS advocating for him and Grace and Bella in all realms of life and making sure each child receives what they deserve and need.  The NEW news is that Matthew is about to undergo a full developmental evaluation due to the fact he has some issues that have concerned me (I've only told Mark and my mom).  I took him to a screening and he is being referred on to the Infant Toddler Early Intervention Program.  And while I am thankful we live in a place that has such programs, I am concerned about the thought of added therapies.  The emotional toll of all I carry, causes me to be tired.  I am a worrier by nature and I spend many hours thinking about my kids and trying to come up with possible solutions, new therapies, researching, praying.  Some of my recent thoughts include: what new foods can I give Matthew to help with his sensory issues, what can I do to encourage him to try saying new sounds, how can I help Grace and Luke be more organized...(just to name a couple). 
 2.  I am jealous...I almost didn't put this one down...again.  You can read my post four years ago about what I was struggling with here.  I thought about this again, and sadly it is still SO true.  I don't want to admit that I am jealous, and I thought perhaps in the last four years I have grown and this no longer applies.  But I am being HONEST here.  I feel jealous of moms whose kids can play on typical sports teams, school sports teams or have children that don't always finish last with physical activity.  I feel jealous of moms who don't have sit beside there children and coax them to try their homework, and then don't have to email all their teachers to let them know what they didn't complete.   I feel jealous of moms that can go away for a weekend.  I tried to go away for two nights to an adoption retreat.  Oh how I needed it.  But, I made it one night before one of my children ended up in the ER and I came home.  I was so glad they were ok, but I cried for a couple days because I felt so disappointed that something I looked forward to for so long (the retreat) was over for another year.  I am jealous of moms that have a dozen babysitters on speed dial (or even one).  I get that we have four kids and it is a lot, but having a babysitter that was available would be amazing.  I keep praying about this.  My kids are so wonderful, but they can be difficult.  My mom has been very helpful watching the kids and offering to watch the kids (which I appreciate more than I can express), but she works full time and is tired and sometimes we need someone last minute.  In the last four years, I have also experienced jealousy of moms who still have there fathers.  I miss mine everyday.  Anytime I watch a father hug his daughter, it's there...jealousy.  I just plain miss mine.  He was always full of great insight, help and support.  I grieve still that he isn't here to have a relationship with his grandbabies.  He would have been and amazing grandpa.
3.  I feel alone...  Most days I spend completely alone (with my kids).  I am more comfortable in this role than I was four years ago, but I would still echo as a special needs mom I feel alone.  Mark works a weird schedule these days, so when he goes to work in the morning I don't have much contact with anyone who isn't a therapist, a school teacher, a doctor or specialist.  I try and visit a friend once a week, but it doesn't always happen.  I could use the support of other moms with children who have the same type of issues.  That is why the Called to Love Retreat has been so wonderful for me.  I can physically see that I am NOT the ONLY one who is walking this path.  We recently began attending a new church, and I am happy to report that there is another mama who is walking my same path at church. Which is an amazing blessing! I am hopeful that perhaps we can connect more because I could sure use her friendship.   
4. I am human...I am not a saint, even though well meaning people do try and tell me I am.  I have bad days, off days, days I feel like I am failing and think I am not doing a good job.  Being a special needs mom has really re-shaped my life in many, many good ways.  Luke and Grace have helped me discover who I really am.  I have realized that I am a lot stronger than what I thought.  I have learned to be pushy, confrontational when I need to be, how to fight, speak and advocate for those who cannot.  In the past four years, I have also learned that I have limitations, and it is ok to admit when you need help.  I am in therapy currently for anxiety/depression, and I sought out the help of a doctor and I am on medication.  I am human.  And I am ok with it.  Both therapy and medication have helped me in a huge way.  I no longer spend everyday crying, I don't feel like I am the verge of a breakdown, I am not in a constant state of worry, and I am not over analyzing every weird twinge or symptom in my body.  I still have dreams of things I would like to accomplish, but for now I would settle for reading a book, painting or going to the spa. (A mom can dream right?)
5. I am scared...This one is difficult to admit too...still.  While I don't dwell on this thought too often, it is part of raising children with special needs.  I am scared that I won't do something or find the right therapy for them.  I am scared Luke is going to be blind someday due to his glaucoma.  I am scared I won't know the right things to say when we talk about their adoptions or know how to answers their questions?  I am scared I am not doing enough or that I am doing too much?  I am scared when Luke goes to school that other kids are mean to him, or he doesn't eat his lunch cause he talks too much, or that he isn't following the rules.  I worry Grace isn't turning her work in or she is distracted.   I am scared that time is going by too quickly...moments are passing I won't ever get back.  Have I been enough? done enough? loved enough? advocated enough? taught enough? played enough?
My life is forever changed (for the better) by raising Luke and Grace (and Bella and Matthew too).  They bless me in ways that I can't explain.  When I look into Luke and Grace's eyes, and I see how happy they are, and then I think of the alternative (which I can't describe), I am blessed....a hundred times blessed...to call them all mine.  Every time I break up an argument, model appropriate behavior, remind him "he is not the parent", ask her to "finish the job," tell them "no" or the million other things I do, I remember that God according to His plan choose us for them.  I don't take that lightly.  I was called to this "position"...to take up my weapon and fight for those who cannot.  I know that the mere existence of Luke and Grace is a promise that God has a BIG plan for their lives.  I really believe it.  So even though it may not look so pretty in the trenches, I am there, I am fighting.  I am real.  I am THEIR mom. 

Thursday, December 1, 2016

Parenting Children From Hard Places and Staying Connected

During my time at the Adoption Mom's retreat, I had the opportunity to attend several breakout sessions.  All of the sessions were very beneficial in many ways; however, the session I attended titled, "Parenting the Connected Child" was AMAZING!  I was challenged to look at my parenting in a different way.   The two speakers presented information that inspired me and left me wishing the session was a few more hours.  There was so much information presented that applied to parenting children who have come from trauma, kiddos with special needs, and kiddos that are adopted.

Here are 10 takeaways from the session "Parenting the Connected Child". 

  • As parents, we have to know our stuff. We need to know our baggage. We need to know where we came from, and what our triggers are.  Our kiddos know how to trigger us.  They don't wake up each morning and say, "I think I am going to push everyone of mom or dad's button's today."  However, they have a way of doing that!  We can't go to certain places (hard places) with our children, if we are not willing to go there ourselves.  KNOW OUR STUFF.
  • Flip Your Lid.  I am a visual learner, so any type of picture or visual cue is extremely helpful for me.  Think of your brain (and your child's brain) as your hand.  You have the upstairs brain and the downstairs brain and the part in the middle is the amygdala.  The amygdala is responsible for the our "animal brain" or the "Fight, flight, freeze" instinct.  For the whole brain to funcition optimially the entire brain needs to be connected (think of your hand as a fist).  When your child "Flips their lid" (think of your hand completely opened), your child's brain is not connected and they are operating out of their animal or primal brain.  If our kids brains are flipped, talking and reasoning will do nothing.  Also as parents, our brains need to be connected to parent.  It is impossible to parent out of the "fight, flight, freeze" part of the brain. 
  • We need to connect with our children through our parenting.  Connection disarms fear.  Disarming the fear leads to connection which leads to trust.  
  • Kids from hard places have brains that have been rewired due to trauma.  The brain has memories of trauma and the body has memories as well. 
  • Two Strategies that help you connect to your children are "Mindfulness" and "Engagement".
  • Mindfulness is being aware of you (the parent).  By asking yourself "What do I bring from my past?  Where did I come from? What kind of parenting did I have? We need to know our own "stuff" and then choose what we will and will not bring into our parenting.  What can you let go of?  How does your child perceives you?  What is your voice?  What is your tone?  Human brains are wired to take in 80% tone and 20% words.  Often when children from hard places hear a certain tone they have negative body memories and then they respond irrational.  Body Memory is how a body remembers in certain situations.  The body will remember negative memories but it will also remember positive safe ones too.  When the body has a positive memory it creates new neuro pathways.  When a child is safe it equals connection. 
  • Engagement is to give them a voice.  Much of what has happened in our kids' lives has been things that have been out of their control.  We can help give them a voice by giving them choices.  I find choices can be really difficult sometimes.  I know when I give choices I have to be ok with either choice.  But by giving a choice we give them control and share the power.  Sharing power is compromise and giving them a compromise is huge.  It isn't manipulation but negotiation.  Being present and being connected to our kids is more important than being right. 
  • When teaching or correcting my kids, calmly asking them, "I need you to say that again with respect," is a good strategy.  Even if they just dial it down a little, take it! 
  • Don't ask questions you already know the answer to.  I am so guilty of this one!!!  Instead of saying, "have you brushed your teeth yet?" (when you know they haven't), say, "I need you to go brush your teeth." 
  • Give support until they don't need it.  This was a big "ah-ha" for me.  How many times have I said, "you are _______  years old, you should be doing this on your own."  Mostly said out of frustration.  But if I had reframed and shifted my thinking to this little person needing more support instead of what they should be doing at a certain age I would be less frustrated.  It's my job to support them until they don't need it anymore regardless of their age. 
There is so much more I could share about Parenting kids from hard places, parenting kids that have experienced trauma, adopted kiddos and kiddos with special needs.  Here are a few resources I have found helpful including the book I am referencing from the break out session at the retreat.   
Our children are blessings!  I am so honored to be their mama, and will continue to strive to provide them a safe and connected environment. 

Psalm 127:3~"Children are a blessing and a gift from the Lord."

Tuesday, July 19, 2011

Losing Sight

Sometimes...the routine of the day is exhausting.  There is never a dull moment with the crew I have.  Everything I thought I knew about parenting before we adopted became useless when we welcomed the kids home.  Luke has challenged me in so many ways, and it is because of his challenges that he has caused me to grow up, to be more, to do more, to push myself harder and farther than I would have.

I thought I had already gone through so much with Luke before the beginning of 2011.  There have been the ear tubes and adenoid surgery times 3, heart surgery, more therapies that I can remember at 4 different therapy centers, ADHD, micocephaly and sensory processing disorder.  He was on IEP and I thought I had been doing a pretty good job advocating for him.  Then came the challenge from the Lord.  To really get to the heart of the issues.  To dive into and really explore the issues that Luke was having.  That led to a diagnosis of Tourette's in January, Glaucoma in February, a new IEP in April, and Auditory Processing Disorder in May.  By the time school got out, I was EXHAUSTED.  I felt like I was just bracing myself to keep upright.  "Was this it?"  NOPE...Luke's glaucoma doctor was concerned by the amount of vision loss there was and sent us to another specialist.  A traumatizing test for Luke, and finally we have settled into a routine of therapy on Tuesdays and iLs therapy during the week at home.

Sometimes after a long day of parenting, after I sometimes feel defeated or that maybe I could have handled something different, I reminded about the path that God choose for my kids.  Luke is exactly where God wants him to be.  He placed him with us.  Sometimes I question my ability to parent a child that is losing their SIGHT.  How do you do that?  I know that it is not fun to think about.  But it must be thought about.  This past May I actually called the School for the Blind.  I had to face reality that their services were going to be needed by son at some point.  They have advocates that come into the schools that provided services to kids like Luke.

The TRUTH is I believe that God has the ability to HEAL Luke completely, but also know that sometimes God teaches us things through trials.  As Luke and I were walking hand in hand one night in Disneyland this past June, we talked about making a "mental picture" or "movie" of what we were seeing. I described the lights and people and the smell of waffle cones and popcorn.  I told him that we needed to remember this time at home. I think the more "mental pictures" Luke has the more he will be able to draw from in the future.  Took everything in me not to melt into a puddle right in the middle of the Happiest Place on Earth.  The tears rolled down my cheeks at the thought of him losing is vision and not being able to see things.  How many times do we take for granite that we can see, or hear or taste, etc?  I know I do.  But because of Luke I am able to realize now the gift of SIGHT.

Life At The Dahlhouse: Disneyland Style

In November, we were able to take a family vacation to Disneyland and to visit my brother, David and sister, Katie.  We enjoyed several m...