Awhile back, I had blogged that J started early intervention and I thought I should follow up with that. J had his 6 month IFSP meeting already and is still receiving physical therapy on a weekly basis; I also work with him at home during our play to try. At now 21 months old, J is walking but still waddling because he barely bends his knees (the waddling is lessened with bare feet and exaggerated with shoes), rolls from belly to back and back to belly regularly, starting to push up on hands and knees and does so successfully about 25% of the time, and attempting to pull up. He also kicks items and we are working on bending his knees to squat and pick things up, but again, he does not willingly bend his knees very far at all. J's right side appears to be a little stronger than the left, and he bends that knee a tiny bit more. There are still concerns over the fact that J cannot transition positions 100% on his own yet, which keeps him from being completely independent as he should be.
In shoes, Jeremy falls at least once every time and lands in an odd position that causes him to limp a bit which I informed our PT Jolly (name has been changed for her privacy). As a result, Jolly asked me to have J's feet remeasured at the shoe store, and just tell them we are concerned he may have too much room in his shoe and what the reasoning is as well as to have the pediatrician check J's hips. Today was a gorgeous day so J and I did take a walk to the local children's shoe store, and the shoes absolutely do fit; I was given tips on how to put them on J to ensure they are tight enough to avoid any foot shifting since Stride Rites are made of leather and thus do stretch out over time.
Just this Thursday, J went to the pediatrician so I voiced Jolly's concerns to the good doctor, and she checked J's hips and also had him walk back and forth both with shoes and in bare feet. Dr noticed that J walks with his left foot facing out a little bit but didn't not hear anything strange with his hips; now our priority is going to a physiatrist very soon because there are worries of hip dysplasia even though J had a normal (non-breach) birth.
Ever since birth, J has had various health issues and we have been going to specialist after specialist. Sometimes it feels like there is no end in sight, but I keep telling myself that all of this is going to pay off for him in the near future.
Any other parents have experiences with a child with low tone and gross motor delays, or the early intervention process in general? I'd love to hear your feedback and experiences.