Today we hit the ground running as Fridays are special needs clinic day. I asked in advanced what that means and what to expect. I was told mothers travel for up to 6 hours and line up to to see the Physiotherapist. On most Fridays only one PT, Solomon, sees up to 30 kids in 3 hours which is maddening. Today we had one OT, one PT, one peds PT,one aide, and Solomon on stand by. At 9 am we thought, this isn't so bad and then we saw them. Mothers walking up to the clinic in African style which is to say these mothers carry their special needs children on their backs in long wraps tied tight to hold the child in. I am talking teenagers with cerebral palsy, on their mother's backs, for hours upon hours. Wow, wow, wow. It was like nothing I have ever seen before. These mothers are dedicated with a triple !!!! So, we spent time listening to them, talking to them, and doing what we can to help. Again, thank you to the vendors who sent supplies. The Faith Fund that supports this clin
Dear families, friends, and most importantly my babies and kiddos I take care of... I am off in a few hours to Kenya with a full heart and full suitcase. This trip has been a year in the making and I could not have gotten here without the help of many people to include: My life support and business partner Jennifer, it is a huge sacrifice for me to leave for this long. In addition Abilitations has provided a great many resources for this trip to happen. Robert Walters, BioTech orthotics, has provided a lot of supplies for the Faith Clinic there. Tom Powell and Rich Brewer, Powell Medical, have donated seat cushions for children in need of pressure relief. Brent Wright, East Point Orthotics, for his assistance and guidance on what is needed for my journey. Thank you to the generous donations from families and friends that I have worked with to make this journey possible. I also thank you for your patience in my absence and my running around like a made woman for the past 6 months t
Monday is neuro clinic today which means we saw children with spina bifida ranging from 2 weeks old to 4 months old. One of the nice things about working in this clinic is that we are right beside either the neurosurgeon or the orthopedic surgeon. We all talk as a team and they explain what procedures they are going to do. More importantly they learn what we actually do as therapists. Back home I feel some compartmentalized from the doctors and vice versa. They have learned from us as much as we have learned from them. Recycling is important in all forms. We have been cleaning the clinic, getting shelves built, organizing the materials. In the midst of this we found a post card from a teenager from TN who sent 50 pairs of orthotics, all of which she had worn as a child due to herself having cerebral palsy. Today, the cutest thing I have ever seen came into spina bifida clinic, Ruse, to see the neurosurgeon. This family traveled from Uganda which if you refer back to your maps you w
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