Detroit transplants living in Dallas

Tag: Monty (Page 6 of 6)

Trying to Stay Positive

I caught Bailey comforting Monty today (in his own way), and have to admit it’s probably just as hard on him with emotions so frayed in the apartment right now.

There are small things that seem positive today though: there is more activity to his left side, his activity level in the last 24 hours has been the highest I’ve seen since coming home, he’s responding to noises from out in the hall again, and he’s eating and drinking. Unfortunately he still seems very ungainly on his feet, continues to have bouts of heavy shallow breathing/panting, restlessness, and lethargy. These are all listed as side effects of the prednisone, so I have a call in to the Neurologist to talk further about that.

Side Effects

Little man seems a bit more aware and functional today. On the morning walk he actually made a left turn (though it may have been completely accidental or unintentional) and was able to navigate the sidewalks without too much issue. He seemed a bit more spry and some of the real Monty came out as he recognized all of the places we would usually stop for him to mark. Ate breakfast, but about an hour after his morning meds he sank back into the antsy yet lethargic pacing and shifting from place to place. Hoping this means it’s just the prednisone side effects and not his overall condition worsening.

He’s Home

Monty came home today at 11:00am, but the celebration has been short lived. He has explosive diarrhea (which we were warned to contact the doctor if we see) so I’m picking up another prescription that is supposed to help (125mg metronidazole twice daily). He seems to be stiff and have some mobility issues, and has pretty much only moped around from one spot to the next as if he is uncomfortable. He is not himself and seems just as bad or worse as he was on Sunday.

I spent $57 on materials to build him a patio potty using a washing machine drip pan, he’s not sure what to do with it yet but when I put him on it at 4am this morning he used it so that’s a good sign.

At the Neurologist for 2 Days to Begin Treatment

7/16/12:
MRI shows multifocal or disseminated Granulomatous Meningoencephalomyelitis (GME), the worst kind. They tried to confirm with the spinal tap but respiratory distress caused them to back away and wake him up. Spoke with the doctor around 4pm and he is awake and started on 15mg prednisone and 50mg cyclosporine twice daily for initial treatment of inflammation in the brain. Also getting prylosec to protect the GI (20mg twice daily). The doctor recommends addition of cytosar (cytarabine – chemo drug) for an aggressive treatment; 4x 150mg injections 12 hours apart over 2 days, which unfortunately means more time away from us.

7/17/12:
Vet tech from the office called with morning report. She says he seems more active and aware, but reading between the lines I hear no real improvement. Spent the entire night researching GME but now I have more questions than answers. Different treatments, drug names and doses are racing through my head and wish I could make more sense of it, wish I was a vet. Dr Wolfe to call this afternoon with an update, I want to discuss aggressiveness of current regimen.

Just got back from visiting Monty this evening. He seems slightly better in that he is more aware of his surroundings, has partial vision back in his right eye but still blind in left. Also still having trouble with turning left but is not just doing circles. We were there for an hour to keep him company, watched him eat, comforted him and talked to him, but he seemed to grow very tired very quickly. Had a long question and answer with Dr Wolfe and can confirm she definitely feels we are doing all we can for him, but after lots of internet research in the last 24 hours still nagging questions remain as to whether another treatment protocol could do him better. After his last chemo treatment we will be able to bring him home tomorrow, but I’m not liking the whole “wait and see what happens” approach.

Monty and GME – The Story So Far

7/7/12:
We had good friends over with Monty’s friend Gunner. For a dog that does not become friends with just any other dog easily, Monty and Gunner have been fast friends since being introduced. Several hours of fun ensued for both human and canine, and there were no behavioral or physical abnormalities observed.

7/12/12:
Time for the monthly Frontline application for both Monty & Bailey – this was the second of three doses in the package I had purchased for summer. Applied around lunch time, and my daily 4pm walk with Monty would be the first clue that something is wrong. We took a much different route around downtown than normal, and Monty had some real difficulty in spacial awareness bumping into several parking meters only feet apart, trees in the sidewalk median, and trouble figuring out the right way to enter doors. Back in the apartment he started bumping into objects in the apartment that had been there for some time, so something was up. I called to schedule an appointment with our Vet Dr Naugler for the following day. After reading some internet posts I gave Monty a light test for pupil dilation which revealed one eye completely non-responsive. I called the vet back to move the appointment up to noon the following day.

7/13/12:
What I first thought was disorientation and/or panic with loss of vision has developed into difficulty turning left during the morning walk and the hours to the noon vet appointment drag on to no end. Dr Naugler confirms blindness in one eye and recommends opthamologist for emergency appointment at 2pm. Opthamologist Dr Beaumont sees Monty and immediately suspects neurological condition, most likely due to a brain tumor. She recommends we have an MRI and a spinal tap done to assist diagnosis, but because the prescription (steroids) she recommends would cause complications if this is a bacterial infection and false results for a spinal tap, we opt to monitor for 24hrs. Schedule an emergency appointment with the neurologist for Monday morning the 16th with instructions to call if conditions worsen.

7/14/12:
Walks have deteriorated to meandering circles in the park. Monty seems completely unable to turn left.

7/15/12:
We have spent the entire weekend with Monty and are now very concerned, he has become very lethargic and developing difficulty drinking water. We call Dr Beaumont back and get the prescription for prednisone (steroids) to begin treating the symptoms regardless due to the acute onset. 20mg dose at 7:30pm and within a few hours of being administered he seems to have perked up, but the other symptoms remain.

7/16/12:
Side effects of the steroids are immediate, he has peed on the floor 3 times already overnight. Our morning walk goes fairly well as long as we only make right turns, but out in the open area of the park we only end up wandering in circles. We head up to Carrollton and drop him off with the neurologist Dr Wolfe for the MRI and spinal tap. These procedures require full sedation however so he has to stay overnight for observation.

Monty diagnosed with Granulomatous Meningoencephalomyelitis (GME)


For those of you who don’t know him already, this is Monty, our 7 year old French Bulldog diagnosed today with multifocal or disseminated Granulomatous Meningoencephalomyelitis (GME). We have no illusions for the seriousness of the disease, but being the feisty, stubborn boy full of attitude that he is we hope that we can fight to keep him with us as long as we can, as long as he is willing. I hope to use this space for updates on his condition in the coming weeks as well as provide some type of resource for anyone else out there who may be struggling with a similar diagnosis.

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