Knightley ate a pill of my migraine medication this evening and hubby and I freaked the hell out. We very very quickly phoned the emergency vet, and I was struggling to hold back tears as I spelled out the medications name. They said a vet would phone me back in 20 minutes as they were dealing with several emergencies.
Both hubby and I instantly got onto google and read up on the med Knightley had eaten in the meantime. We were extremely relieved to find it was one that was actually *given* to dogs, but he had eaten a dose about 4-5 times more than he would have been given. We partly relaxed, but still worried and monitored his behaviour closely as per the emergency clinics instructions.
However, it was nearly an hour later and there was still no phone call, so I called back. I don't know what they had done with me, but I immediately spoke to a vet. He basically said due to the amount of overdose, Knightley needed to be made to throw up, and perhaps there would be other treatments. I wasn't sure whether to take him there or not, as because they had not phoned me back and I had had to phone them eventually, I knew a good part of the medicine would have already been absorbed. But the hubby and I discussed it and we decided since the vet was pretty adamant it was the right thing to do we better do it, just in case. Knightley seemed ok, just maybe a bit quiet - although that could be due to my intermittent tears of guilt (even though I didn't know where the medicine had come from).
So we jumped in the car and drove for half an hour across Canberra to the emergency vet surgery. Virtually as soon as we got there they took Knightley out the back and gave him an IV injection to make him throw up. They couldn't specifically see a green pill in the vomit, but hopefully any lingering stuff came up. Where they injected got bandaged up with this adorable bone bandage. They also fed him a 'slurry' of activated charcoal to absorb any lingering toxins in his stomach and intestines, which he didn't seem to like very much but was well behaved nevertheless. A huge bill later he was emptied of stuff and we were out the door.
He seemed more sprightly on the way home, which was good to see. It is going to take a while for the fur to grow back on his foreleg where they shaved it to get to the vein.
I am going to work harder at keeping my medications away from the front part of the house completely, and will start looking into training a default 'leave it' even if I am not with him. We were lucky that this medication wasn't all that toxic for dogs, but if I am not more careful, I may not be so lucky again.
Oz Working Dogs - Assistance & Working Dog Equipment
For assistance/service dog equipment, as well as guide, therapy, detection, search & rescue, police and dogs in training equipment check out my website http://www.ozworkingdogs.com.au - I make and sell vests, capes, belly bands, harnesses, handles and more... and will post to the world!
Showing posts with label IV. Show all posts
Showing posts with label IV. Show all posts
Sunday, March 4, 2012
Sunday, August 14, 2011
Lupus (SLE), The Spoon Theory and Assistance Dogs
Pre pickup 2 weeks 3 days old
If you're looking for information on whether you can have a service/assistance dog with lupus please read my more recent post here.
So, until this post I haven't actually said what condition I have. Suddenly today I thought it was about time - and past it. I don't know why I have been cagey about mentioning it. I guess I still have issues accepting what has happened to me over the last several years. However, I thought it was kind of silly having a blog all about getting an assistance dog (hopefully, cross your fingers for me) and being unwell and all, and just keeping the manner of unwellness to myself. Especially when I can use this blog to educate, rather than just hide away. Many people don't know what Lupus is, and even when they do, they don't know how amazingly under researched it is, and that only now are we in the first trials of the first new Lupus medication since the 1950s.
So yes, I have lupus, otherwise known a Systemic lupus erythematosus. Or at least, they are like 99% sure. Because it can be a very difficult condition to diagnose - some people can wait 10 years for a confirmation of diagnosis. My diagnosis has firmed up in the last year or so. Systemic lupus is a systemic (in other words, it can effect the entire body) autoimmune condition, where your own immune system can attack anything it jolly well pleases, pretty much. In me it is characterised by joint pain, muscle pain, fever, rash, at times extreme fatigue, sweats and nausea. Well, those are the main symptoms, I could go on all day really :P . In addition I have a couple of bad side effects from medication I take - immune suppression (I get sick easily, eg I got very very sick with swine flu) and dysphasia (I often cannot find the words I want and feel like I have dementia, sometimes misspell obvious words).
An assistance/service dog forum I am a member of linked "The Spoon Theory" (pdf) by Christine Miserandino, someone who has lupus whose article has had a great deal of impact upon many people. I highly recommend you read it, not only is it a great analogy for anyone with a disability, but it gives you a very very accurate idea of what it is like to live a day in my life. A lot of people in disability circles have read the spoon theory these days, and you hear people refer to 'saving my spoons' etc. It hit me quite hard in that it was someone with lupus who had written it, but it also helped me to know that there was someone who day-to-day was going through *exactly* the same balancing act I was. So thank you Christine, wherever you are out there in the world. I am pretty poor with saving and balancing spoons still, I give into people - and myself - too easily, but more importantly, I think having an assistance dog around would give me an extra several spoons per day. As someone with a very limited spoon supply, that is something I very very much need!! So now I have mystified you completely with my talk of spoons - GO BACK AND READ IT! :D
If you're looking for information on whether you can have a service/assistance dog with lupus please read my more recent post here.
So, until this post I haven't actually said what condition I have. Suddenly today I thought it was about time - and past it. I don't know why I have been cagey about mentioning it. I guess I still have issues accepting what has happened to me over the last several years. However, I thought it was kind of silly having a blog all about getting an assistance dog (hopefully, cross your fingers for me) and being unwell and all, and just keeping the manner of unwellness to myself. Especially when I can use this blog to educate, rather than just hide away. Many people don't know what Lupus is, and even when they do, they don't know how amazingly under researched it is, and that only now are we in the first trials of the first new Lupus medication since the 1950s.
So yes, I have lupus, otherwise known a Systemic lupus erythematosus. Or at least, they are like 99% sure. Because it can be a very difficult condition to diagnose - some people can wait 10 years for a confirmation of diagnosis. My diagnosis has firmed up in the last year or so. Systemic lupus is a systemic (in other words, it can effect the entire body) autoimmune condition, where your own immune system can attack anything it jolly well pleases, pretty much. In me it is characterised by joint pain, muscle pain, fever, rash, at times extreme fatigue, sweats and nausea. Well, those are the main symptoms, I could go on all day really :P . In addition I have a couple of bad side effects from medication I take - immune suppression (I get sick easily, eg I got very very sick with swine flu) and dysphasia (I often cannot find the words I want and feel like I have dementia, sometimes misspell obvious words).
An assistance/service dog forum I am a member of linked "The Spoon Theory" (pdf) by Christine Miserandino, someone who has lupus whose article has had a great deal of impact upon many people. I highly recommend you read it, not only is it a great analogy for anyone with a disability, but it gives you a very very accurate idea of what it is like to live a day in my life. A lot of people in disability circles have read the spoon theory these days, and you hear people refer to 'saving my spoons' etc. It hit me quite hard in that it was someone with lupus who had written it, but it also helped me to know that there was someone who day-to-day was going through *exactly* the same balancing act I was. So thank you Christine, wherever you are out there in the world. I am pretty poor with saving and balancing spoons still, I give into people - and myself - too easily, but more importantly, I think having an assistance dog around would give me an extra several spoons per day. As someone with a very limited spoon supply, that is something I very very much need!! So now I have mystified you completely with my talk of spoons - GO BACK AND READ IT! :D
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