As a result we had the cast cut off locally. It was a very hard decision, as we really wanted this one to last longer. The ordeal of travel, general anaesthetics and xrays mean that the longer a cast can last, the better. However the change in her mood was demonstrating that something was wrong. We found that again there was a pressure sore on the point of her kyphosis. In the same spot as the last one. This sore was slightly wider, but thankfully not as deep as the previous sore.
It is disappointing, but I am glad that we made the right decision. Leaving it longer would have meant a deeper sore, and a longer time for it to heal without any sort of support. On the positive side, Evelyne is enjoying her 'freedom' and she can now put on her shoes and socks by herself. The sore is healing well and we may even be able to put her brace back on her this week. Plus the first bath in 5 weeks was exciting!
P.S. Milly had her 'cast' cut off too. Evie talked her through the procedure and she was very brave.
Glad to hear the sore wasn't as bad as last time. Evie looks very brave in the photo of the cast getting cut off. She is looking pretty happy to be having a bath. Does she need to get another cast done when the sore heals? Love Linda
ReplyDeleteSo glad that both Evelyne and Millie are doing well. Perhaps a photo of Millie next time? Love Dad xx
ReplyDeleteNo photo unfortunately. But I can say Millie was very brave :)
DeleteHello!
ReplyDeleteThank you for your "Life With Beals" blog! It is truly interesting and inspiring!
My name is Rukaiyah and I am part of a team currently participating in an internship with the Rare Genomics Institute. The Rare Genomics Institute is a not-for-profit organization that supports families who are affected by rare diseases. As the majority of rare diseases are genetic in nature, the Rare Genomics Institute uses donations and grants to give patients access to cutting-edge technologies and leading medical experts by funding full genome sequencing for patients. By analyzing the results, experts hope to find the cause of the disorder. From there, treatments and therapies are developed in an attempt to cure the disease. To learn more about the Rare Genomics Institute and read some of their patients’ stories, please visit: http://www.raregenomics.org/.
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Thank you very much for your support!
Have a great day!