Stella had her follow-up visit with the Neurologist today. We reported that the past 2 weeks have been great. Baby girl is back to her normal self :)
Dr. P drew some blood for routine bloodwork which we all anticipate will be normal. He is also taking her Prednisone down to 5mg. He has asked us to not vaccinate Stella at this time until she is given the "all clear" and he wants another re-check in 2 months.
We told Dr. P that we are trying to give Stella her pills as close to 8 hours as possible but due to our work schedules we have been giving them at 6:30am, 4pm and 9-10pm. Dr. p said this was just fine.
The diagnosis on her discharge instructions reads: recheck for epilepsy secondary to immune-mediated encephalitis.
As I stated before I do not want to go into detail about what transpired with the first neurologist that caused the serious communication breakdown and I am glad that we stuck with our gut instinct and sought the second opinion, however seeing Stella today, 2 weeks later, and the fact that we came so close to doing the unthinkable makes me very emotional. All we want is for Stella to have the best life that she can - the thought that it was almost cut short ......I can't even explain how heavy it makes my heart.
Meanwhile we celebrated Stella's 9th birthday last week!!!
I created this blog to give pet owners like you a chance to follow my Pug's journey with Mast Cell Tumor treatment through a pet owner's perspective - not through the confusing and often-times scary clinical world. I am assuming that readers already have basic knowledge of MCT’S (grading, excision requirements, etc). I do not have any veterinary training and am not an expert on pet health. Please consult with your veterinarian immediately if you suspect your pet has a MCT.
Stella
Thursday, July 25, 2013
Thursday, July 11, 2013
Knee & Neck - I Forgot to mention......
In all the chaos from the past few months I forgot to mention that Stella's partial torn ACL (back left) does not appear to be bothering her anymore. She is walking fine. But because we know it's there we try to give her an "elevator" lift onto the couch and our bed as much as possible so she doesn't have to use the doggy stairs - man alive our pets are spoiled!!
Also, that chicken dance jerking neck thing she did a few months ago while attempting to eat has not happened again. Perhaps whatever issue she was having with her neck was minor and healed itself as the orthopedic surgeon stated it might.
Oh and that issue she had with not correcting her back right foot when it was flipped over seems to have corrected itself.
Let's hope the seizures work themselves out as well.
Also, that chicken dance jerking neck thing she did a few months ago while attempting to eat has not happened again. Perhaps whatever issue she was having with her neck was minor and healed itself as the orthopedic surgeon stated it might.
Oh and that issue she had with not correcting her back right foot when it was flipped over seems to have corrected itself.
Let's hope the seizures work themselves out as well.
2nd Neurologist's Opinion
When we made this second-opinion appointment we were told
not to feed Stella after midnight in case anesthesia was administered if the
neurologist wanted to do an MRI. We were
also told to stop all medications after midnight. Should Stella have a seizure during the night
that we found alarming we were told to go to the emergency room.
Our appointment was in the late morning. Stella skipping a dose of the Phenobarbital
made her less catatonic and a little more steady on her feet. When we met with the second neurologist, Dr.
P, we explained all that that had transpired over the past 6 days. We told him that if he agreed with the
current diagnosis of idiopathic epilepsy and agreed that this current treatment
plan was our only option that we would seriously have to consider doing the
unthinkable. Just typing these words
makes me cry - but we had a long discussion about Stella’s quality of life and we
could not bear to let her live out her life in this current state.
Dr. P, noticing how emotional we were, said “I know you’re
worried, but don’t jump ahead, let’s take this one step at a time”. He then sat back and listened to us intently all
the while watching Stella’s manner and her every move. At one point we noticed
Stella had that same tremoring that she had been doing for days, as if she was really
cold. He watched her and said “those are
seizures”. So even with the powerful
medication she was still having seizures and they were, alarmingly, more
frequent - OMG.
Dr. P said the first thing he would like to do was to flush
her system and rid her of the Phenobarbital as much as possible. He wanted her to stay at the hospital while
they slowly flushed her system through an IV.
Meanwhile he stated he wanted to look at the actual MRI images for
himself. We told him we would go to the
other hospital and pick up a copy of the images on CD and bring them to his office for review – we agree to regroup in
3 hours.
3 hours later we returned and Dr. P came into the room with
a smile and said “you are going to be pleasantly surprised”. He opened the door and in walked Stella –
walking on her own! She was not 100% but
appeared to be at least 90% OUR STELLA!
We asked Dr. P what he did and he said all they did up to that point was
flush her system. He said neither he nor
his staff witnessed and “major” seizures, just the smaller “trembling” kind - which he stated was not necessarily worrisome at this point.
After reviewing the MRI images and having spent the last few
hours with Stella Dr. P said his opinion based on all details of the past week
was that Stella did not have just Idiopathic Epilepsy. He believes she has Idiopathic Encephalitis (inflammation of the brain of unknown origin) which is causing the seizures.
He believes she should be on a low dose anti-seizure medication. He has prescribed Levetiracetam (Keppra) 250mg tablets for the seizures (half a pill 3x a day) and Prednisone 10mg tablets for the inflammation.
Dr. P wants a follow-up visit with Stella in two weeks.
We left the office feeling hopeful - Stella walked herself to the car!
Dr. P wants a follow-up visit with Stella in two weeks.
We left the office feeling hopeful - Stella walked herself to the car!
Wednesday, July 10, 2013
My Opinion on Second Opinions
I just wanted to take a moment and throw in my two cents about seeking a second opinion.
I am a firm believer in educating oneself as much as possible when making decisions. Not only doing as much research as possible but also seeking opinions from experts as well as from family and friends. People will differ with their opinions but I find that helpful because different perspectives will give you insight into things you may not have even thought of and the more information you have the better the choices you can make, the less second guessing you will do and the less regrets you will hopefully have.
Unlike with a home or a car many people seem to be apprehensive in seeking a second opinion when it involves a doctor, whether for themselves or their pet, because they worry about hurt feelings or insulting a professional. They feel an awkwardness will ensue and relationships may be irrevocably broken. My opinion is that true professionals will encourage you to make an informed choice. If someone is insulted or offended by your desire for a second opinion you probably do not want to do business with them anyway. Professionals should always want what is best for you or your pet and that should be the bottom line for everyone involved. In my experience I find that if I seek a second opinion or sometimes multiple opinions, regardless if I agree with all or some or none of them, the more confident I feel about the choices I make.
In Stella's case we would still need to bring her back to the specialty hospital to see the Oncologist so the fact that we may ultimately decide against having their Neurologist treat her may seem, to some, a potentially awkward situation. To us, we are comfortable with the knowledge that we are dealing with professionals and do not anticipate that seeking a second opinion elsewhere would pose any problem.
I guess I'm just trying to say do whatever is necessary for you to feel good about your choices. Educate yourself, write down and ask hard questions, but also know that often times there are no right or wrong answers and sometimes you just have to go with your gut instinct.
I am a firm believer in educating oneself as much as possible when making decisions. Not only doing as much research as possible but also seeking opinions from experts as well as from family and friends. People will differ with their opinions but I find that helpful because different perspectives will give you insight into things you may not have even thought of and the more information you have the better the choices you can make, the less second guessing you will do and the less regrets you will hopefully have.
Unlike with a home or a car many people seem to be apprehensive in seeking a second opinion when it involves a doctor, whether for themselves or their pet, because they worry about hurt feelings or insulting a professional. They feel an awkwardness will ensue and relationships may be irrevocably broken. My opinion is that true professionals will encourage you to make an informed choice. If someone is insulted or offended by your desire for a second opinion you probably do not want to do business with them anyway. Professionals should always want what is best for you or your pet and that should be the bottom line for everyone involved. In my experience I find that if I seek a second opinion or sometimes multiple opinions, regardless if I agree with all or some or none of them, the more confident I feel about the choices I make.
In Stella's case we would still need to bring her back to the specialty hospital to see the Oncologist so the fact that we may ultimately decide against having their Neurologist treat her may seem, to some, a potentially awkward situation. To us, we are comfortable with the knowledge that we are dealing with professionals and do not anticipate that seeking a second opinion elsewhere would pose any problem.
I guess I'm just trying to say do whatever is necessary for you to feel good about your choices. Educate yourself, write down and ask hard questions, but also know that often times there are no right or wrong answers and sometimes you just have to go with your gut instinct.
And one last thing……..if you don’t like that last haircut
you got (and paid for), go to someone else.
Don’t even think twice about hurting someone’s feelings – you’ll look
ridiculous…..literally.
Tuesday, July 9, 2013
Follow-up with Neurologist - Seeking a Second Opinion
We are extremely upset and feel completely lost and
broken. Yesterday, it had been 5 days
since Stella started on the powerful seizure medication (Phenobarbital). We
had waited all this time to finally speak with her Neurologist, which we understand was
unavoidable and just bad timing. Unfortunately we have had a serious communication breakdown
with the Neurologist and the conversation we had with her last night has left
us extremely uncomfortable. We are very
concerned about Stella’s current catatonic state and condition and we are now
left wondering if she is on the right treatment plan. I won’t go into details about our
conversation with the Dr. C. but suffice it to say that we have decided that we
need to seek a second opinion.
We have made an appointment for this Thursday, two days from
now, with another Neurologist.
Incidentally this second Neurologist is one we have gone to before years ago with two of our other dogs. When Stella started having seizures we felt
it was important to keep all of her healthcare under one roof, at the specialty
hospital, and at the beginning we did not know if the seizure activity was
related to her cancer issues and wanted to be close by to her oncologist so we
made the decision to see the Neuro at this same facility. As I stated in a previous post – all the
veterinarians contributing to her current health issue (Oncologist, Neurologist,
our regular vet and the ER vets) all agree that this seizure activity is a
completely unrelated to her cancer history.
For the next two days until we see the second Neurologist we
will abide with the suggestion of the first Neuro that we reduce the Phenobarbital
dosage to half her current dose.
We are hopeful that the second Neurologist can provide more clarity with Stella’s condition and can lead us on the right path….whatever that may be.
Meanwhile Stella's condition remains the same; very worrisome.
Sunday, July 7, 2013
Seizure Treatment Plan - Day 7
Same as yesterday. Same alarming appearance and
behavior. Still catatonic but maybe just a
tiny bit less being off the Gabapentin. Still
having those shivering bouts.
Appetite poor and we're still worried she may drown in the water
bowl. Still unable to walk
properly, still needing to be carried to
the grass to relieve herself.
One more day until we can speak with the Neurologist......so worried......
Saturday, July 6, 2013
Seizure Treatment Plan - Day 6
Stella’s appearance and behavior are still alarming to us. She is catatonic and seems extremely
depressed. We worry that she could possibly
drown in the dog water bowl because her legs are still so unsteady and she continues to fall face-forward so we picked
up the bowl each time we left the room.
She has little interest in eating or drinking but it appears it
is because she is confused and cannot focus.
She has been lying on a kitchen rug for most of the day. At times her eyes are open but she is
completely glazed over.
A few times today I sat on the floor with her and she was
shivering as if she were sitting out in the cold snow – although we have the
air conditioning on it is set at the same temperature as for the past month. Maybe this is just a result of the powerful
drugs?
Still two more days until we can confirm her treatment plan with the Neurologist. We feel so startled by Stella’s current catatonic state that we have made our own decision to stop the Gabapentin and just give her the seizure medication. She is completely non-functional, depressed and we cannot stand to see her quality of life diminished in this way. If stopping the Gabapentin does not help with her catatonic state we have discussed the fact that if the Neuro tells us her current condition is likely permanent we will opt to discontinue the seizure medications altogether even if it means she continues to have seizures and it shortens her life. We cannot and will not allow this to continue.
Still two more days until we can confirm her treatment plan with the Neurologist. We feel so startled by Stella’s current catatonic state that we have made our own decision to stop the Gabapentin and just give her the seizure medication. She is completely non-functional, depressed and we cannot stand to see her quality of life diminished in this way. If stopping the Gabapentin does not help with her catatonic state we have discussed the fact that if the Neuro tells us her current condition is likely permanent we will opt to discontinue the seizure medications altogether even if it means she continues to have seizures and it shortens her life. We cannot and will not allow this to continue.
Friday, July 5, 2013
Seizure Treatment Plan - Day 5
We called the hospital this morning to inquire when we could
pick up our Stella. They stated that she
had just been giving the last of the loading dose of Phenobarbital and was
pretty zonked out so we should not pick her up until late afternoon.
We arrived at the hospital around 4:30pm and were given
Stella’s discharge instructions by an ER technologist. When she could not answer some of our
questions she sent in an ER vet to speak with us. We were told to give Stella ½ tablet of
Phenobarbital (full tablet =64.8mg) twice a day. We were told
this medication schedule is very stringent; we need to stick to a strict
schedule, making every effort to keep it at the exact same times every single day
and to not skip a dose. We were told
this is extremely important for the medication to be effective. We were also told to continue with the
Gabapentin, three times a day. When we
asked why Stella would need to be on both medications the ER vet was unsure and
said that until we spoke with the Neurologist we should continue to give it to
her.
With all the different medications Stella has been on the
last two weeks we asked if it was ok to still give her the monthly
Heartworm medication and Frontline
protection for fleas & ticks. The ER
vet stated she ‘thought” it was ok but since she seems unsure we will hold off
for now. We do not live in a wooded area
and Stella does not come into contact with wild animals and with all she has
been through we haven’t taken her for walks so she is seemingly safe in her own
fenced-in backyard.
When the tech brought Stella out to us in the waiting area we were quite startled at her appearance. She could walk but kept turning her front paws over as if waking on her "wrists" and then would stumble and land on her face. She would stand herself back up but it took several seconds and then she would fall on her face again. Luckily being a Pug she is not far from the ground (and her face is already flat!). Hopefully this is just a reaction to being loaded with powerful drugs and once she is on s steady medication regimen this will wear off.
When we arrived at home, we decided that until Stella could
walk properly, we would line our kitchen with small rugs so she would hopefully
have more balance and not slip on the tile.
We also will carry her to the grass portion of the yard to protect her
from hitting her face on the concrete patio.
*Because we have had
dogs with various issues with walking, whether sick or injured, we have numerous rubber-backed bath rugs that we keep for these such circumstances. I highly recommend that all dog owners have these on hand if you have wood floors or tile – but I hope you never have to use
them. Also the rugs are easily washed in
the washing machine and easy to store on a shelf.
The rest of the night Stella was seriously disoriented, more
like catatonic. Maybe Baby Girl will be
better tomorrow after a good night’s sleep in her own home. We have doggy stairs for the girls to get up
in our bed at night but we are worried Stella may fall so we will have her
sleep in the kitchen to keep her safe - her sister Betty will keep her company.
Incidentally, we have decided her stringent medication
schedule will be at 6am and 6 pm every day.
**HELPFUL SUGGESTION – if your dog is ever
in a situation where they are in the hospital overnight receiving IV fluids be
sure to line your car with WATERPROOF pads.
We have a heavy duty canvas car hammock for the girls in the
backseat. It keeps them confined to the
back seat are and yet they won’t get tangled in seatbelts or leashes. We also keep soft blankets on the hammock for
them (spoiled spoiled spoiled). Even though we let Stella relieve herself prior to getting in the car, once on the road she passed out and as her body relaxed all the fluids from the past 15 hours(!!!!) just seeped
out everywhere; right thru multi layers of blankets and even through the thick “waterproof”
canvas. I have a “Dog Recipe” that I use
to remove pee and vomit and it does work however one of the steps requires
baking soda and although the smell is out of the car I cannot get the baking
soda out of the grooves of the pattern of the fabric on the seat. It looks like a bag of flour exploded!!!!
This “recipe” is the
best method I have ever found and works to get the pee and vomit smell out of
carpeting and upholstery. If you would
like it, leave me a comment.
Thursday, July 4, 2013
Seizure Treatment Plan - Day 4
Stella had 3 full doses of Gabapentin yesterday; it is
making her even more disoriented.
At 12:15pm today she had yet another seizure. Again, lasting about 20 minutes. Less than one hour later she had
another. This last one was the “worst”
one she’s had so far. At one point, as I
held her tightly, her entire body seized into a hard rock; it felt like she had
turned to stone. This lasted for just a few
seconds and I felt her muscles relax and then she just sat there shaking. We made the decision that 5 seizures in less
than 48 hours was too much (I believe it is called a “cluster”) and we decided
to go back to the ER. Although this was
in the middle of the day, the “regular” hospital was closed as this is
Independence Day.
By the time we arrived in the ER it had been one hour since
Stella’s last seizure began and she was just coming down from it; this was the
longest one yet.
ER vet examined Stella and came back to us to explain what
he thought should be done. He stated that
there was no more waiting to put Stella on anti-seizure medication. When we asked about the possible live damage
or failure he explained that we were at a point where we needed to think about
her overall well-being versus just the liver.
He stated that although anti-seizure medication CAN cause liver damage
it doesn’t mean it will happen. If
Stella continues to have seizures, the seizures WILL cause brain damage. So tending to her seizures now takes
precedence over what MAY happen to her liver.
The ER vet told us we should leave Stella in the hospital
overnight so that he can start loading her with Phenobarbital; the anti seizure
medication. We asked why we could not do
this at home and he responded that although we could go home with Phenobarbital
pills they would give her a loading dose thru an IV so that it gets to her system immediately to
hopefully stop the seizures sooner. He
stated they would monitor her closely throughout the night and we could pick
her up tomorrow afternoon. He told us
the Phenobarbital would make her really loopy and he expects that she will sleep
most of the next 24 hours. We proceeded
to ask a gazillion questions about seizures and Epilepsy. The ER vet was very patient and tried to
answer as many questions as possible but pointed out he is just there to
stabilize Stella. All the neurologic and
treatment questions should be posed to the neurologist. We knew this of course but you know how it is
when you’re worried and scared and given so much information to process; your
brain doesn’t stop to pause and your mouth just keeps going. Incidentally, the
neurologist will not be back in the office until Monday 7/8, four days from
now so hopefully Stella will be stabilized until we can speak with her about
future plans.
Later in the evening we called the ER to check on
Stella. The ER vet said that Stella is
responding really well and remains alert.
He said he was surprised as most dogs usually “pass out” from the heavy medication but he also pointed
out that there were a lot of Pug Lovers working on the shift and they were
giving Stella a lot of attention.
There’s nothing Stella loves more than adoring fans!!
Wednesday, July 3, 2013
Seizure Treatment Plan - Day 3
This morning Stella had another seizure; the duration was
about 20 minutes. We called the ER (it was very early in the morning and the
“regular” hospital section was not quite open yet). We spoke with an ER vet and inquired whether
or not giving Stella just two doses of Gabapentin per day as opposed to the
prescribed three might be the cause of this additional seizure. We have
only been giving her two doses per day because our schedules would make two of
the doses just a few hours apart which is not recommended. ER vet stated she was unsure but that we
needed to do whatever we could to try to give Stella the three doses a day as
close to eight hours apart as possible.
She asked if we could have someone come into our house in the middle of
the day or if we could set an alarm clock to give her one in the middle of the
night. Once Stella is on the Gabapentin
three times a day, should she have another seizure, we should bring her back to
the hospital/ER.
We discussed what we needed to do to make this happen. We have decided that we will have to come home from
work during our lunch time each day to assure Stella gets the pill three times a
day. Luckily we only live 15 minutes
from our workplace so it is just a matter of scheduling. If this is what it takes to get her back to
normal, then this is just what we’ll have to do. This regimen started today.
Later this evening, approximately 12 hours from this
morning’s seizure, Stella had another one.
Again, lasting about 20 minutes.
As usual, I sat on the floor with her and held her as she cuddled into
me, shaking and looking scared. As with
the other seizures she was unresponsive to our voices or movement but remained
seemingly conscious – I say “seemingly” because her eyes remain open, whether
or not she is actually “conscious” during the seizures we do not know.
Four hours later I walked into the room and it appeared to me
she may have just finished another bout of seizure activity.
As of this writing, Stella is sleeping quietly on our bed
next to her sister Betty.
By the way, we find it interesting that Betty (nor the cat)
has any reaction whatsoever to Stella’s seizures. I wonder what they think? Do they know just to leave her alone? Are they aware of what’s happening?
Monday, July 1, 2013
Seizure Treatment Plan?
Spoke with the neurologist’s assistant again today (who, in
turn spoke to the neurologist on our behalf). She states that the treatment plan for now is
to keep Stella on the Gabapentin 100mg and wait.
The suspected diagnosis is “Idiopathic Epilepsy”; “Epilepsy with no
known cause”.
We are to continue with the Gabapentin and if another
seizure should occur we are to call. The
neurologist wants to wait as long as possible before putting Stella on
anti-seizure medications because they are very powerful and can be damaging to
the liver We were told it can cause
liver failure. If we are lucky the
Gabapentin will be enough to stop further seizures since Stella’s are
considered relatively “mild”.
Stella remains fairly disoriented. We are hopeful her body will adjust to the
medication and she will return to her silly, joyful, Puggy self.
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