- Elon Basketball fell a little short the last two games but we had fun traveling around to watch them. #caasports… twitter.com/i/web/status/1… 1 month ago
- I thought Greg Roman liked to run the ball? Just not in the 4th quarter apparently. #RavensFlock 1 month ago
- Nothing like getting run out of your own gym on the “white out” night. #terps 1 month ago
- On the way to work yesterday, the car in front of me threw a banana peel out of the window at a traffic circle like… twitter.com/i/web/status/1… 1 month ago
- RT @NCAA_FCS: Welcome to the FCS Playoffs! #FCSPlayoffs x 📸 @ElonFootball https://t.co/skXnMp8ZzA 2 months ago
a collection of random thoughts and ideas from me, her, and sometimes us
it’s been a while . . .
October 19, 2017Posted by on
updates since march, including the biggest news that came yesterday.
march: thanks to amazing people, zack and i were able to get out of town kiddo-free for five days. we strive for fun anniversary plans (seven years!) each year, and were able to get to charleston, sc this year to spend time with elon friends, explore, and sleep! we also received a clean-ish bill of health from orthopedics. the orthotics we had since october were doing their job and we have ruled out surgery for the time being. BBA is planting his feet better and continuing to use the muscles in his heels to strengthen himself! we did our first neurodevelopment screening at KKI – we were underwhelmed at the time, but have made huge strides since then, much of which came in the form of acceptance of information received.
april: bi-annual endrocrine visit that resulted in continued stability and increased conversation that when BBA turns 3 (eek – as i type that is now only eight and a half months away!) we can try to ween him off of his current medication and see if his thyroid problems were a result of post-birth stress, less so an actual permanent thyroid condition. we will report back next summer on that process.
may: we were referred to a new daycare option for BBA and got the chance to tour it. that singular day reassured us that with intensive work, we could see more progress with BBA. may 5 was the day we became obsessive stalkers – calling this daycare weekly to try to get him a spot. we started BBA on a new medication to assist with muscle relaxation. it was titred up over time and has helped him to loosen his legs and open his hands – two of the most challenging aspects of him prior to being on the medication was his stiffness. in preparation for summer birthdays, we were gifted with a swingset – that was delivered in 10,072 pieces (or something of that varietal). we spent memorial day weekend building and were able to get our kiddos into the swings by the end of the weekend. in nearly two years, swinging was the first moment that all three kiddos were able to do the exact same activity at the exact same time without any accommodation. it was magical.
june: i had been traveling a TON and our lives are clearly not without stress. @littlepund had been complaining about stomach pain for at least a week and we finally decided it was not attention seeking and took her to the doctor. we got our first x-ray back, inflicted horrible at-home treatments on her, had approximately 24 hours of being free of pain, and it all started again. more about this in june. BBA went for his quarterly ophthalmology visit. the recommendation was not glasses (i was disappointed – kiddos with glasses are the cutest!) but, instead, to patch his left eye (the stronger) to give his right eye (the weaker) the chance to strengthen itself.
july: we did another x-ray on @littlepund followed by allergy testing and the first round of disease-specific testing. results came back flagging celiac disease. this led to an immediate gluten free diet for her, and our home. our house is now completely gluten free (except for ice cream – i love my kiddos but there are some things i cannot give up, including cookies and cream ice cream).
august: BBA was admitted to the hospital at the beginning of the month in respiratory distress. less than 48 hours from when the constricted breathing started to when we were discharged, but not the best moments of our lives. we started on a nebulized steroid that he will be on for at least three months. directly following discharge and very fortunately, we were able to spend close to three weeks at the beach. all the kiddos loved the time away. just back from vacation, we were able to get into the hopkins pediatric gi clinic for @littlepund. they, too, felt strongly about the celiac diagnosis and recommended a confirmatory endoscopy and biopsy, which was scheduled for october.
september: one-year repeat MRI was scheduled for september 11. the intention is to review the images to determine if they are unchanged or show degeneration. BBA was the third (and final, thankfully) to get the stomach bug that was going around our house the night before the MRI. it was rescheduled for october and we ended up with a little more “sit and wait” time. we did our quarterly ophthalmology visit and they were quite optimistic. while we will most likely receive a strabismus diagnosis, for the time being we are continuing to patch his left eye to strengthen his right. no surgery proposed at this point.
october: october 2 – MRI day. BBA did great and seemed unphased by the process. it’s funny, but zack and i sometimes feel more at home at hopkins – the halls and people seem so familiar and comforting to us. october 13 – BBA finally started at that amazing daycare we were previously unable to get him into. two days a week and we are figuring out the other three days. the hope is that he will get a full-time placement in january 2018. october 16 – endoscopy and biopsy day. @littlepund was nervous but calm. she impressed people with her attentiveness, listening, calm, and ability to finish other people’s jokes (knock knock, who’s there, cows, cows who, NO! cows moo!). endoscopy showed no apparent tissue damage (which is ideal) and we are still awaiting biopsy results (they may come back as early as today). october 18 – neurology follow-up . . . and the big update i teased when i started typing.
the MRI showed no additional degeneration from the image taken in september 2016. of the options that were available to us at this point, this was the ideal result. officially, we are at the following place:
non-progressive neurological disorder with a diagnosis of spastic quadriplegic cerebral palsey.
remember that acceptance note from march. we have spent two years seeking an answer. this one is good, generally. no additional degeneration expected moving forward. BBA will continue to develop skills, just at a slower rate. he continues to make progress – reaching for toys/people/our ice cream spoon, holding a spoon himself, reaching for/grabbing his bowl of food, lifting his arms up on command, looking over his shoulder when he hears your voice/noise/knows someone is there and is trying to find him/her, army crawling, tucking his knees under himself either to get comfy in his crib or to make forward movement, biting and mashing solid-ish foods, moving backwards in his gait trainer, babbling and trying to get words out (i swear he can say “whoa”), making definitive choices by eye gaze, engaging on his ipad, and giving high fives. the answer was never going to be that everything would be what people would consider normal. of the options that we were presented with, this diagnosis is the best. BBA does not have a genetic syndrome that causes large-scale, whole system problems. we will continue to adapt. we have a path forward. now, we just need to buckle down and do some more work.
of the things that have happened in the last two years, the one i am most thankful for is that our kiddos are kind, (generally) healthy, empathetic, energetic, and, most specifically, happy. we have no shortage of laughter and smiles. we all need to get ourselves stronger – physically and mentally – to keep going. but i suppose that is a task for everyone.