Hello, Mamas, I hope that summer finds you enjoying lazy days with sandy toes. First, I should assure you that neither Brandy nor I has been abducted by aliens nor fallen into a deep hole from which we cannot escape. We’ve just been busily rushing around like modified chickens with our little heads cut off. I have been struggling over a post for a while and just can’t quite get all that I need it to say into it without tipping over into harpyville. Thus, I have temporarily tossed that post aside to write about something completely different. On “Tell Us Tuesday,” I want to share what pretty much occupies my every waking thought right now and I am begging for any hints those of you who deal with these issues can give me. Continue reading
A few months ago, Michelle Roush from Things I Can’t Say (one of my personal favorite blogs,) said that she was looking for some mommy bloggers for kids with special needs to check out some new products and write reviews. Quick as my little fingers would carry me I hopped on that bandwagon. Then, about 10 minutes later, I panicked because I thought, “What happens if I hate this product? What will I say?” Well, I lucked out because I absolutely LOVE this product and I cannot wait to tell you all about it.
The product I was sent, a card game called “Hidden Rules With Friends,” was from a company called Courage to Change. Courage to Care is attempting to make books, learning and play materials aimed at persons of all ages with learning and/or social and emotional needs. You should definitely check out the link because they have a ton of really interesting products. I think I’ve probably blown about half of my home school budget in my mind just browsing! Continue reading
As most of you know by now, I have 4 kids and three of them have special needs. We see LOTS of doctors in several different locations. We’ve been seeing lots of doctors for lots of years. Add to this that my children have lots of anxiety and lots of sensory issues and, as you might guess, I’ve endured lots of headaches from watching my babies suffer lots of meltdowns. Luckily, through lots and lots of trial and error, I have found some things that really help all of my children get through doctors appointments with far less stress (a lot.) Continue reading
Hey y’all, it’s that time again. Time for us at Modified Mamas to spread a little joy to you modified mamas with the help of my dear friend Beth Wyatt. It’s a pretty great one too. This time around, we’d love to get some information from you guys to help make our site as helpful as possible. To be entered in the give away, we’d love to know either your favorite kinds of posts on Modified Mamas or what you’d like to see. For instance, do you like it when we just dish about our lives, do you prefer the posts about making stuff like modified equipment or recipes or do you like our goofy posts bests? Even better, if there’s something you’d like to see or wish someone was talking about, we’d love to hear that, too! So, if you want to win the awesome bag below, just leave a comment about what you like or what you’d like to see and your name goes right in the pot–easy peasy, right? The name of everyone who comments by 10:00 pm tomorrow, December 18, 2012 will be entered into the drawing for the bag.
Without further ado, here is the awesomeness that Beth is donating to make your modified life a little happier this month. There’s a message just from her in the caption below Good luck, mamas!!!
I have a child that doesn’t sleep. I mean seriously, he doesn’t sleep well at all!!! Newborn, colicky infants have nothing on my sweet boy. His sleep disturbance is part of his disability. His body doesn’t know how to wind down and if he sleeps even a few minutes and wakes up, his brain tells him he’s slept already and it’s time to get up. Yes, he takes medication to help because, otherwise, he’d be suffering physical effects from exhaustion, however, we still needed help. You see, when he wakes up at night, he is prone to getting up and wreaking havoc. Continue reading
My youngest son, Isaac, has a condition called arthrogryposis multiplex congenita. It is a musculoskeletal condition that causes contracture, malfunction and malformation of the joints. As a result, many of his joints do not function quite as well as we’d like, others not at all. Continue reading
I just love Toys R Us. Not just because I’m literally a kid at heart and I love being surrounded by all of those toys; but mostly because they have a special catalog for our kids. Their catalog is called the Toys R Us Differently Abled Guide, and if you haven’t heard of it, it’s a must-read for Christmas shopping ideas for your kiddos. Continue reading