Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Sunday, October 28, 2018

Siblings: The Unsung Hero's


Down Syndrome Awareness month (DSAM) is October and for the entire month  I usually bombard my social media feeds with facts, blogs, and images in an effort to raise awareness about my son Blake and his community of people with Down Syndrome. I actually do this all year round, so it is always "awareness" and education month for us. This year for DSAM I want to focus on the not so talked about topics like siblings during this awareness month.

In the past Blake's siblings have written a blog that was feature on The Mighty (Read here) and expressed how they felt having a brother with Down Syndrome. Today it's my turn. I also will include the thoughts and perspective of another mom, Nicole in our community who is a few years behind us on this adventure.

Just like everything else in life there are both positive and negative aspects to being a sibling and I feel both sides are more enhanced when that sibling has a disability. In my home the highs are really high and the lows are devastatingly low. My daughter is along for this roller coaster ride. As mother's we do our best to divide our time if we have multiple children but to be honest my son gets more than his "fair" share of my time and energy, because the nature of his disability requires more. I know this leaves my daughter feeling frustrated and hurt as she approaches her tween years. She has expressed it to both my husband and I. As she is aging, I know she also has fears and concerns for his future, much like I do. She asked me, "what happens to Blake when you and dad are gone?" not to long ago. I explained that we are working for Blake to be independent and live alone but reminded her that he will likely always have a need for support. I don't want her to feel pressured to have to be his sole caregiver in the event of our deaths. It may seem premature to be discussing with a 10 year old but anything can happen in life at any time. I want her to know that she can care for Blake if she chooses but it is not her responsibility.


Fears and frustrations aside she is  his biggest fan, my greatest helper and an amazing big sister! I know that his presence in her life is making her a better, more patient, compassionate and understanding young lady. Blake has opened a whole new world for everyone. We have met so many people we would have not otherwise, attended special events, and participated in activities in a way we wouldn't have been able to otherwise. The benefits are not lost on her, neither is the joy he brings or the love they share.

She is and always will be my SHEro .. and his.


Nicole shares her perspective ...

With Down Syndrome awareness month coming to a close, I  feel it necessary to pay homage to the unsung hero in my house. This would be my 6 year old (typical) daughter, Olivia. Olivia is less than 2 years older than my daughter with Down Syndrome, Amelia. Like most parents with two or more children, we struggle to divide our attention equally. The fact is that Amelia needs us more, plain and simple. That is hard for a six year old to understand, but Olivia does. Amelia has odd behaviors that make even the simplest tasks, like walking one block to school, difficult and time consuming. For the most part, Olivia seems to have unlimited patience with her sister. Olivia and Amelia’s relationship, like Amelia, is more typical than different. They fight, they play, they fight some more, they love each other.  They are siblings. 


Overall, I think having a sister with Down Syndrome has made Olivia more patient, kind and selfless. This year Olivia and Amelia are attending the same school. I asked Olivia what the best part of going to the same school as Amelia; her answer? “Getting to hug her everyday day at lunch”. Olivia makes my heart full. When I asked her what the worst part was; she responded “ Sometimes Amelia hugs me too tight”. 

I guess for Olivia, she only knows what it’s like to have a sister with Down Syndrome. I’m sure that Olivia notices her friends with typical siblings play together and I often wonder if she’s jealous, if she wishes that Amelia didn’t have Down Syndrome. If she does, she never lets it show. Olivia just accepts Amelia how she is...her sister.


Cheers to raising strong girls, supportive siblings and SHEro's!

Wednesday, March 4, 2015

Take The Pledge



Today we bring awareness of the R word.Yes people still say it. Stop. It is offensive, hurtful and reflects only your lack of intelligence. I will happily distribute thesauruses to those who need assistance in choosing another word to express dislike over something. To those who say it to hurt another person or to insult them I will happily dispense my disgust. The R word is as unacceptable as the N word and other rude words. Keep your BS excuse about your First Amendment rights to free speech to yourself also. I have my rights too as a mother, advocate and human being, hence this post. Show compassion, respect and love to others. Show yourself respect by expanding your vocabulary and eliminating this word. People first language in ANY situation is always a more appropriate alternative. Many people say "It's only a word" as if it is no big deal. If that is the case it should not be a big deal to stop or refrain from using it either.

Blake and I Thank You.

Will you take the pledge to put an end to the R word?





Friday, October 14, 2011

Blake's Story: DOWN but not OUT

In honor of National Down Syndrome Awareness Month I teamed up with my friend and loving mother of 3 Tori Spelling and contributed my story to the Raise section of her eMAG EdiTORIal yesterday.

Read My Story: DOWN but not OUT HERE


Blake 2 days old - Special Care

This was my reality in the first week of Blake's life. He fought to be here and it was his courage that inspired mine.

As I look back on the last 5 months of Blakes growth I am forced to think of my own. Never has my character been so tested, my constitution so tried or my values and belief system so rocked. What I have realized is that our energy, collectively is best spent celebrating our differences and not judging them. We are ALL guilty of it (Myself included). What a boring, generic world we would live in if we were all the "same" or "similar". Where applicable apply the label of LOVE only.





The comments I have received from my family, friends and most of all virtual strangers in the last 24 hours have been overwhelming to say the least. I cried a lot yesterday while reading the public comments as I realized how many amazing, genuine, good hearted people in there are in this world, more than enough to drown out the negative, ignorant ones.



I look forward to what the future will hold with Blake and the rest of my family. A future that is unknown for all of us. We will enjoy our moments together confident in the fact that the world may knock us DOWN but they will never take us OUT! This is just the first you are hearing from me but I fully intend on becoming a LOUD voice of advocacy and information as I strive to give children with DS a voice. Sharing facts, and feelings in an intelligent and empowering way! I am PROUD of my son's extra chromosome ... Turns out thankfully MORE is MORE xo


"Every human being is intended to have a character of his own; to be what no others are, and to do what no other can do." - William Henry Channing


For more information about Down Syndrome visit the NDSS website.

Want to read more personal stories from the DS community? Many mothers reached out to me yesterday and shared their virtual spaces of LOVE!

Kellie: Enjoying the Small Things
Christine: Brody's Buddy Ride
Amy: GiGi's Playhouse
Kayla: Loving Austin
C. Smith: Results Not Typical
Amy: Mayson
R-WORD: Pledge to choose your words wisely and kindly!


Julie: Nina's Story