This is a chronicle our everyday life as we live, laugh and love raising our teenager, our toddler and our special needs baby. Normal isn't always what it seems...
Tuesday, January 8, 2013
A call from GI
Today, I got the final word back from our GI doc. We are going to do our best to treat these new symptoms that we are seeing. For now, we've decided to increase the dose of one of Lydons GI meds and add a new medication. This new med is used for neuropathic pain and suppose to have very little side effects. So we are hoping that is exactly what we get. Decreased GI pain, and no side effects! We are staying in close contact with our GI doctor and his nurse. For now, we play our favorite game ( insert sarcasm), watch, wait and see... We will check in with them again on Friday and see how things look then.
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