Gabby Update – Medicine Change
During our five day hospital stay the doctor on call who released us to go home had suggested maybe her seizure medicine was causing the confusion. However since she was still having problems with bladder control he wrote a prescription to up her seizure dose by 50mg daily. When he told me ‘there is a chance it will make things better and a chance it will cause the confusion to be worse’ I decided to wait until we were home from our trip before raising the dose. I wasn’t ready to deal with her confusion being worse while on vacation. There are times she gets lost as it is I couldn’t imagine dealing with the ‘unknown‘ while in the Bahamas.
After spending a full week thinking long and hard about what was best for Gab and feeling as if I wasn’t given any true answers I decided to talk it out with her therapist. We looked at a time line and came to the conclusion that the confusion did start around six months ago which was the exact same time that the doctor had increased her seizure medicine. The increase in seizure medicine did not stop the bladder control issue and her EEG showed the same exact results when she was on 100mg as when she was on 200mg so I decided to not raise to the additional 50mg daily. I called and pointed this out to her Neurologist and got the okay to not only NOT increase but to go ahead and decrease back down to 100mg like it was over six months ago. We made this change on Thursday of last week.
I will not say that she is doing better. She has had bladder control loss since then, however that isn’t new, but I have hope. I haven’t noticed any confusion yet but sometimes it doesn’t happen daily. I plan to give it at least another week or two before deciding if I believe it’s helping.
I took a stand today on Gab’s behalf about future procedures. Her Botox injections were done last November which means they have completely worn off. Her Occupational Therapist agrees that on her hand it is best to wait several months before even deciding if we should Botox again and since Gab isn’t complaining about her leg I have decided I am not exploring that outlet again right now. She has been through so much lately that I feel it’s time for a break. Her mood is showing that she can’t handle much more. After the year she has had I believe it’s my job to finally step forward and say that’s enough, especially since I can tell a difference in her. I just want us to focus on getting her medications settled and get her feeling back to normal.


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new #GabUpdate https://lifefamilyjoy.com/gabby-update-medicine-change Medicine change #specialneeds
What a beautiful picture. It is hard to imagine how such a lovely young lady can go through what she has.
I wish and pray that she is stabilized and feeling better soon.
I so hope medicines get back to where they should be for Gabby. This has to be so hard on you, her and everyone in your lives. I am not close enough to give a hug, so I am sending one. I know this is hard, but great things will come, I am sure of it. I am sure with your motherly instincts the doctors will figure out the right meds and get Gabby back to the way she should be!! ((HUGS))
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You are smart to follow your instincts — you are such an advocate for Gabby. I hope you realized how blessed she is to have you for a mom, lady.
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