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Jasper MRI update ❤️ Yesterday was a very long, very emotional day but we finally have some answers. Jasper’s MRI and anesthesia both went well. The neurologist sat down with me afterward, showed me the actual MRI images and walked me through what they were seeing. We’re still waiting on the full written radiology report, so I’ll share the exact medical wording once I have that in front of me. Unfortunately, the results are serious. They found multiple significant problems in Jasper’s spine. There is a disc issue causing compression on his spinal cord, and there is also serious disease lower down in his spine around the lumbosacral area where nerves are being compressed. On top of that, they saw what appears to be a mild spinal infection. The infection has to be dealt with first, so Jasper has started antibiotics and will be on them for six weeks or so before we can move forward with the next steps. After that, the plan is to bring him back for an injection and have a meeting with the senior neurologist about surgery. We’ll also have blood drawn and do a formal DM test. Surgery is a strong possibility, but the really hard part is that surgery would not “fix” Jasper. The neurologist explained that this is progressive. The goal of the injections and potentially surgery would be to improve his symptoms and slow the deterioration, not cure it or completely stop it. That’s probably the hardest thing for me to process right now. There isn’t a magic fix here. This is going to be about managing him, slowing things down as much as we can, keeping him comfortable and watching his quality of life as things progress. His mobility will likely continue to decline over time. We were told that some of the continence issues may not come back and there is a possibility that his mobility could become significantly worse in the future. How soon, we don’t know. The one thing I desperately needed to hear was that the neurologist told me this itself is not expected to shorten Jasper’s life. The concern is his comfort, mobility and quality of life over time. So no, this wasn’t the news we wanted. I’m really sad, scared and still trying to wrap my head around what Jasper’s future may look like BUT we do finally know what we’re dealing with and we have a plan for the next step. For now, we treat the infection. Then we try the injections, speak with the senior neurologist and decide whether surgery is the right choice for Jasper. It comes with very serious risks and I was told I can’t take them lightly. I also want to say that the neurology team at Alta Vista was fabulous and I’m genuinely so grateful for the care Jasper received. The discharge/front desk experience, however, really upset me. I had already been waiting almost an hour and a half when Jasper was finally brought out, still heavily sedated, barely able to walk on his own and pooping/peeling all over the lobby in front of everyone and my bill still wasn’t ready. I was there alone trying to physically hold up an 85 lb dog, bawling and was essentially told to “wait my turn.”… I assumed the 1.5 hours I waited WAS waiting my turn 🫪 I genuinely don’t understand why a heavily sedated dog would be brought out before the discharge and payment were ready, leaving one person trying to manage him in a busy lobby while waiting even longer. This is in no way meant to bash Alta Vista. Their neurology team was wonderful with Jasper, and they’re one of the only specialty neurology options available to us. I just genuinely hope someone there sees this and that the next person standing in that lobby scared, overwhelmed and trying to manage a heavily sedated animal is met with a little more empathy and practical help than I was. Joe is home now and we’re going to do everything we can to keep him comfortable and give him the best quality of life possible for as long as we possibly can. ❤️ THANKKK YOU, truly from the bottom of my heart, to every single person who helped make this MRI possible, and all the next steps too. Knowing that we can focus on Jasper and make decisions based on what he needs instead of what we can afford means more than I can ever properly say. We are eternally grateful. ❤️

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