Welcome to the March 2012 Carnival of Natural Parenting: Parenting With Special Needs
This post was written for inclusion in the monthly Carnival of Natural Parenting hosted by Hobo Mama and Code Name: Mama. This month our participants have shared how we parent despite and because of challenges thrown our way. Please read to the end to find a list of links to the other carnival participants.
When Moira was very little and just walking on her own, every time we saw a stranger in a wheelchair, or using a cane or a walker, she would run right up to them with an excited look on her face. Usually this was surprising to them, and occasionally startling. I have a feeling that most people with limited mobility are used to small children being scared of them.

But this is my Mom. She uses a cane, walker, and a wheelchair, depending on the length of the excursion. She has MS, and Moira adores her, so she adored everyone who was like her. I managed to find a graceful way through the transaction of extracting my excited toddler from their path, usually with a "Yes honey, they have a walker (wheelchair, cane) just like your Nain does! Let's say hello."
As Moira has gotten older, she's gotten more reserved, and less likely to run full tilt at strangers. She's also gotten more aware that there is something different about Nain. We have talked a lot about why she uses a cane, and why she walks differently. We have talked about what the cuts in sidewalks are for, why there are special parking spots, why we let some people use the elevator before we do if it's a small one, or crowded.

All of this has leaked into her play, as she tries to understand the difference between her and Nain. The first time she picked up a stick in the woods, it immediately became a cane. She even does a pretty convincing mimic of Nain's shuffling gait. She still doesn't think it's weird, but I can see the questions forming in her mind, especially as we meet more of her friends Grandparents. "Why is she different?"

We haven't made it to the whys yet. Why was she diagnosed when I was 16? Why is there a higher rate of MS in the Pacific Northwest then anywhere in the world? What causes MS? Most of these questions we don't know the answers to, and we may never know. I know there will be harder questions though. Like, "When will she get better?", where the answer is "Never." I hope I can meet her questions with the same forthrightness I have the things we've talked about so far. I expect the questions to start coming faster, especially now that we are buying a house to share with my parents.

Books to read with your kids that treat disability like it's part of every day life. (Note to Dad, we only have the first of these.)
The Great Big Book of Families
Zoom!
Just Because
Does your child have a grandparent with a disability? How have you handled these conversations?
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Visit Hobo Mama and Code Name: Mama to find out how you can participate in the next Carnival of Natural Parenting!
Please take time to read the submissions by the other carnival participants:
(This list will be live and updated by afternoon March 13 with all the carnival links.)
- Parenting A Child With Neutropenia — Jennifer at Hybrid Rasta Mama discusses the challenge of parenting a young child who cannot produce enough neutrophils to fight off bacterial infections.
- How I Love My High Need Baby — Shannon at GrowingSlower was shocked to find she is parenting a high-needs baby, but she's surviving thanks to attachment parenting.
- We're a Lot Like You — kaidera at Our Little Acorn talks about how her family is similar to others, even with all their special needs
- The Emotional Components of Bonding with Preemies — Having a premature baby can bring on many unexpected emotions for parents, but working through those emotions can bring about a wonderful bonding experience. Adrienne at Natural Parents Network shares.
- Raising a babe with IUGR: from birth through the toddler years — Rachel at Lautaret Bohemiet shares the story of how her son’s post-birth IUGR diagnosis affected his first days of life and gave her an unexpected tutorial in advocating for their rights as a family.
- When a grandparent has a disability — Shannon at Pineapples & Artichokes shares how she has approached explaining her mother's disability to her young child.
- Taking The Time To Really See Our Children — Sam at Love Parenting writes about her experiences working with children with various disabilities and how it has affected her parenting style.
- Natural Parenting In An Unnatural Environment — Julie at What I Would Tell You gives us a glimpse into how she improvised to be a natural parent against all odds.
- Getting Through the NICU — Laura at Authentic Parenting gives a few pointers on how to deal with your newborn's stay in the NICU.
- Living With Sensory Processing Disorder — Christy at Adventures in Mommyhood talks about the challenges that can come from living with a child who has SPD.
- Our rules for NICU - March Carnival — Hannabert's Mom shares her family's rules for family and friends of a NICU baby.
- Letter from Mineral's Service Dog — Erika at Cinco de Mommy imagines the letter that accompanies her special needs son's Service Dog.
- Blessings in Unexpected Places — That Mama Gretchen welcomes an inspiring guest post from a dear friend who shares about the blessings that come from a child with Down syndrome.
- Tube Feeding with a Blenderized Diet of Whole Foods — Erica at ChildOrganics shares her experiences with using real food when feeding her daughter who was unable to feed herself and needed a feeding tube.
- Abbey and Evan — Amyables at Toddler In Tow writes about watching her preschooler play with her friend who is autistic and deaf, and wonders how she can explain his special needs better.
- How to Minimise the Chance of a {Genetically Prone} Child Being Diagnosed with ADHD — Christine at African Babies Don’t Cry shares her tips on keeping a child who is genetically prone to ADHD from suffering the effects.
- Tough Decisions: Parenting With Special Needs — Brenna at Almost All The Truth shares what has been keeping her up at night worrying, while spending her days discovering just what her options are for her precocious child.
- Life with my son — For Dr. Sarah at Good Enough Mum, life with an autistic child is just another variation on the parenting experience.
- Dear Special Needs Mama — Sylvia at MaMammalia writes a letter of encouragement to herself and other mamas of special needs children.
- His Voice — Laura at WaldenMommy relives the day her son said his first sentence.
- What is 'wrong' with you' The challenge of raising a spirited child — Tara at MUMmedia discusses the challenges of raising a child who is 'more' intense, stubborn, and strong willed than your average child.
- Tips for Parenting a Child With Special Medical Needs — Jorje of Momma Jorje shares her shortlist of tips she's learned in parenting a newborn with special medical needs in a guest post at Becoming Crunchy.
- Parenting the Perfectionist Child — Mandy at Living Peacefully with Children discusses that as parents of gifted children, we are in the unique position to help them develop the positive aspects of their perfectionism.
- Montessori-Inspired Special Needs Support — Deb Chitwood at Living Montessori Now gives a list of websites and blogs with Montessori-inspired special-needs information and activities.
- Accommodating Others' Food Allergies — Ever wonder how to handle another family's food allergies or whether you should just skip the play date altogether? At Code Name: Mama, Dionna's friend Kellie (whose family has a host of allergies) shares how grateful she is when friends welcome them, as well as a list of easy snacks you can consider.
- Only make promises you can keep — Growing up the child of a parent with a chronic illness left a lasting impact on Laura of A Pug in the Kitchen and what she is willing to promise for the future.
- A Mom and Her Son — Jen at Our Muddy Boots was fortunate to work with a wonderful family for several summers, seeing the mother of this autistic son be his advocate, but not in the ways she thought.
- Guest Post from Maya at Musings of A Marfan Mom — Zoie at TouchstoneZ is honored to share a guest post from Maya, who writes about effective tools she has found as a parent of two very special boys.
- You Don't Have to Be a Rock — Rachael at The Variegated Life finds steadiness in allowing herself to cry.
- When Special Needs Looks "Normal" — Amy at Anktangle writes about her experience with mothering a son who has Sensory Processing Disorder. She offers some tips (for strangers, friends, and loved ones) on how to best support a family dealing with this particular neurological challenge.
- Special Needs: Limitation or Liberation? — Melissa of White Noise describes the beauty in children with special needs.
- How I Learned It'll Be Okay — Ashley at Domestic Chaos reflects on what she learned while nannying for a boy with verbal delays.
- Attachment Parenting and Depression — Shannon at The Artful Mama discusses how attachment parenting has helped her get a clearer image of herself as a parent and of her depression.
- On invisible special needs & compassion — Lauren at Hobo Mama points out that even if we can't see a special need, it doesn't mean it's not there.
- Thoughts on Parenting Twins — Kristin at Intrepid Murmurings shares her approach to parenting twins.
- ABCs of Breastfeeding in the NICU — Jona at Breastfeeding Twins offers tips for establishing breastfeeding in the alphabet soup of the NICU.
- Life With Michael - A Mother's Experience of Life With Aspergers Disorder — At Diary of a First Child, Luschka's sister-in-law Nicky shares her experience as mother to a child on the Autism Spectrum. It is filled with a mother's love and devotion to her child as an individual, not a label.
- Raised by a Special Needs Mom — Momma Jorje shares what it was like growing up as the daughter of a mother with a handicap.
- Becoming a Special Needs Mom — Ellen at These Broken Vases shares about becoming the mother of a child with Down syndrome
- She Said It Was "Vital" — Alicia of Lactation Narration (and My Baby Sweets) discusses the conflict she felt when trying to decide whether therapy was necessary for her daughter.
First, those photos are adorable!
ReplyDeleteMy son also has a huge fascination with wheel-chairs. His Gramps (my husband's dad) is in one because of a stroke, and though he can't talk to Bennett, he can interact with him and B loves him. Anytime he sees ANY wheelchair, he runs to it and tries to either push it or climb on it. This has been cool, because like you said, most people with visible disabilities are met with fear from children, not joy. We were at the Children's Hospital once and Bennett saw a tiny little girl in a tiny little wheelchair. He lit up and ran to her! He instantly started pushing her and she was giggling and laughing and havinga hay-day. They played for about 20 minutes and her dad teared up and said NO child has EVER run TOWARDS her.
There is something about innocent little kiddos that is so inspiring.
Beautiful post.
How wonderful that your son was able to share that experience with that little girl.
DeleteMy mother-in-law walks with a cane, having had both knees replaced. I'm not sure how we'll approach it just yet, but Acorn sees a lot of kids with wheelchairs and walkers and other mobility aids every week at therapy, so I hope that it won't be such a big deal for us to discuss...though I suspect that once he starts talking, the question "why" will be a big one.
ReplyDeleteThank you for those book recommendations! I've been hoping to find some books to share with Kieran. And, um . . . what are the cuts in the sidewalk for??
ReplyDeleteThe handicapped ramps in the sidewalks. Funny/sad story: Washington recently started putting a bumpy surface on them so that the blind can find them more easily, but the surface they chose makes it much much harder for human propelled wheelchairs to get up them.
DeleteWhat a beautiful post! We love the book "Zoom" but I will check out the other two for sure. I love that your daughter runs to strangers who remind her of her Grandma. That is awesome!
ReplyDeleteJulie from "What I Would Tell You"
www.whatiwouldtellyou.com
I love "Zoom!" too! I came across it a couple years ago and immediately bought it, even though I didn't have any children at that point. Such a great story!
ReplyDeleteI love the open-hearted exuberance of little ones! It's so cute she just ran up to people. I bet that made their day!
ReplyDeleteWhat an honest post, the questions will come but I'm sure you will handle them beautifully. Thanks for the book list!
ReplyDeleteI think that early conversations and exposures to differently abled individuals helps children retain their open hearts and minds.
ReplyDeleteI've just put the second two books on hold!
ReplyDeleteVery cool to hear your experience, and it might be something we encounter more as my mom's MS progresses. Mikko's fascinated with people using wheelchairs or crutches or who have lost a limb. I try to honor his curiosity while remaining respectful to the person he's talking (loudly) about. It's an interesting balance, for sure.
I love this post! My children are blessed to have four living great grandparents. Two have limited mobility. They love their grandmother's walker. It is quite the "thing" for her toddler great grandchildren to play with! I've noticed that they are less "shy" around grandparents who need assistence because, like your daughter knowns, it is a "sign" of someone they love.
ReplyDeleteThis is a great post for this Carnival! Although my daughter was fortunate to have a great-grandmother for 2.5 years of her life, she never really got to have a relationship with her due to my grandmother's poor health. However, she was able to connect with her and often liked to pretend she was her "busy mima" and get all snuggled up in her chair under a blanket. I love to see that your daughter is also imitating her grandmother. That is a beautiful thing to watch. Great post!
ReplyDeleteI agree with HRM that this is a great post for this carnival! A beautiful side effect of a very debilitating and sad illness, is that your children will automatically grow up to be more inclusive, empathetic, and accepting of those with disabilities. I love that photo of your mom with the baby (not sure which one! =), they look very in love with each other. Babies know no disability or variation, but they sure know love.
ReplyDeleteWonderful post. xo