This guy has spent 100 days in Kindergarten! I'm so proud of him. It hasn't been easy and we have had our share of tears and trials, but I couldn't be more proud of this monster. He has learned so much and will likely spend another 100 days, next year in kindergarten, but I have complete confidence in him. He just keeps getting more awesome! Not easier... but he is most definitely worth the effort and patience.
Friday, February 8, 2019
Ian's 15th
I'm just now getting around to posting about my first baby's 15th birthday!!!! That's how it is now... as these people get older I just get busier. I thought it would get easier, but here I am. I will say that it gets super fun the older they get. All these new things I get to do... for instance... teaching Ian to DRIVE!!!????!!!! I used to hold his entire body on my arm! He used to be the size of his current head! I'm teaching him to drive!? So weird and so fun all at the same time. Of all the things that have happened this year with you from girlfriends, soccer again, swim team, maturity, responsibility, black belts, debate tournaments, tech team, breakups, all the way to getting you permit!!!! I love this driving stuff! You are so amazing! I love how we are different and how alike we are. You are and will always be my absolute sweetest.... even with your teenage attitude problem. I love you so much and am so proud of you and the man you are becoming. Your successes are my successes, your tears are my tears, your laughter is my laughter. Now let's slow down going into turns.
Monday, January 21, 2019
6 Years!!!????
Party at Mamaw and Papaw's house! Silas got a new bike that we are still working on riding and a PJ Mask Headquarters from Ian, Lily and Seth. That was the favorite gift this year. M and P got him a helmet and matching game. Sara Lynn brought him all kinds of goodies! I can't believe this guy is 6! Our family is blessed with him all the days and we look forward to all the years of blessings. Thank you God for Silas.
Monday, September 3, 2018
Cover Boy
It was so exciting to have Silas on the cover or our Montgomery Parents magazine this month. September is there annual issue dedicated to Special Needs. When asked to write about what it's like to be Silas's mom....I jumped at that chance! Here is the unedited version of what was published.
I used to be known as Anita McFarland. Now I usually am referred to as Silas’s Mom. Being “Silas’s mom” has changed my life. I used to walk into a room with a quiet anonymity. I’m no longer a mom who can blend in with the surroundings. I enter a room chasing a boy who commands the entire room’s attention. Some days that entrance looks like a train wreck and being Silas’s mom is hard. He wriggles out of my hands or arms and runs wild anywhere we might be… including church, the doctor’s office, or the bathroom at baseball games. He yells things that I can’t understand. He runs up and hugs random men or women on the street or in a waiting room, whether they are creepy looking or not. He flops himself on the floor and uses the full weight of his body to communicate to me that he IS NOT moving another step. He runs a fever for no reason, he sometimes will have a random unexplained bruise, or a cough that lasts for 2 months straight, causing me to wonder and worry and have sleepless nights. These days are the days that WEAR. ME. OUT. These days are magnified by the responsibility of raising a child with a “special ability” (as my daughter describes special needs). I, daily, feel the weight of showing everyone around me that Silas is just like their children. I want everyone that comes in contact with him to know that Down syndrome is not strange, scary or all that different than any other typically developing kid. I want them to know that when he acts “rotten” it’s because he is rotten not because he has Down Syndrome. These train wreck days make that difficult until I remember that I had those same days with my other kids. They had the same “rotten” days. The only difference is that others didn’t excuse their behavior to a disability that they could see.
Then there are days that I enter a room with him and I am reminded of how special it really is to have Silas. These moments and days are filled with kisses, spontaneous “I Love You”s and reaching goals that we have been working on for days, weeks or months, hearing Silas say his brothers and sister’s name as he acts like a typical baby brother. Don’t get me wrong, my other kids and all your kids that were born without uncertainty, without complications, and without special needs (if there are truly children born like that), but having Silas in my life makes this life and my family …. more. He adds a joy that can not be explained or put into 400 words or 4 million words. There is something magical or spiritual, I would say, about loving and being loved by a child with Down Syndrome…. or autism, or cerebral palsy, or any other disability. For all the times that are filled with stress or anxiety, there are 10 more that are filled with excitement, peace, laughter and indescribable love.
Silas has has made me feel scared, unsure, crazy, scared, worn out ….. He has turned me into an advocate, made me feel loved, known, more compassionate, patient, joyful, and has shown me strength and determination. These are only needles in a haystack of what this 5 year old little boy has given me. I would be shirking responsibility if I did not say to the eyes, full of pity and sorrow, who see a burden or a waste of a life or even indifference. I want to be clear. Silas, and all those with differences or disabilities, are important, not only to their moms and their families, but to the culture and the world. These people, these individuals, fill this world with love, beauty, grace, and compassion. These are all things that we will ALWAYS desperately need.
Tuesday, July 31, 2018
Silas stuff to remember....
This is a common scene in our house, Mamaw's house, the car and even the driveway. Seeing Silas draw so intently is one of my favorites. He will sit for over an hour, sometimes, just drawing. He fills pages and pages with his little creations. He once sat for an hour and a half in the driveway and filled 3/4 of the driveway with these little pictures using sidewalk chalk. I love seeing a glimpse into his creative mind. I wish I knew what it all was... I will have to wait a little longer before he can tell me what each line, circle, squiggly represents. When that day comes I promise I will sit for just as long listening to every detail of his explanations. My whole being smiles when I see him like this.
However.... it frowns when it goes from this to the second hour of drawing on his entire body, just as detailed.

However.... it frowns when it goes from this to the second hour of drawing on his entire body, just as detailed.

Saturday, July 21, 2018
Conversation with Seth....
Lying in bed just after singing and praying...
Seth: I think my 3rd nipple popped.
Me: really.
Seth: I think my 3rd nipple popped.
Me: really.
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