I forgot to mention something about PJs visit. More of a rant probably.
I asked Dr when my next kitty was due in. We've been off schedule this past year. So he says Olive hasn't been in lately. I reminded him it's because she sees another so we could get cabergoline.
He says it doesn't work. I replied it does help, Ollie's symptoms are mostly gone, her insulin dose is half what it was, she is comfortable, even plays occasionally, she is maintaining weight. Labs are for most part normal. HCM has not progressed. Her walk is confident and sure now.
So here is my rant. I'm so tired of hearing how caber doesn't work. I get they need the studies. Yet IMO, they were not long enough. Change in dose was not tried in any of the ones I read. Some parents pulled theirs out of study after a few month, some did develop other issues and removed. Yet don't they need to know how caber works with other issues?
Penicillin was unknown, polio vaccine unknown, cardiac stents and bypasses were unknown. All until someone did it anyway. And yes those early ones didn't make it but paved the way for what are now very common treatments. I just don't get it.
I jokingly mentioned to Ollie's Dr when we started the caber, maybe she could write a paper or do a case study. Yes, we don't know the outcome, but so many doctors in the U.S. don't even know about it and automatically say no without even thinking about it. I just don't get how some can be be so closed minded.
Rant over.