Minecraft Handbooks

image

It is one thing to be a nerd and play a video game and enjoy it, but when you go out of your way to spend money on actual hard cover books, you know you are addicted and a hard core gamer.

I’ve only been playing Minecraft on my PlayStation 4 since the week before Christmas and I think I’ve made some headway, but there are still a few things I think I need to know before I continue. I can look them up on the Minecraft Wiki page or just Google whatever I am looking for, but somehow I think reading these official handbooks might help give me a better understanding of the game I am playing. Or it could be that they are only like 60 to 80 pages each and won’t help me at all. It’s okay because they were only $5 each.

lego marvels super heroesWhile I was on Amazon today I decided to buy another game. I absolutely love the Lego games. I have all of the PSP Lego games, and now that I have a PS4 I would love to own all of the PS4 Lego games. I already have Lego The Hobbit that I bought as a digital download, but I bought Lego Marvel Super Heroes on disc because it was cheaper to buy the disc than the download. It’s $40 on the PlayStation store and I only paid $23.89. Last week it was on sale on the PlayStation store for only $25, but I didn’t have the money for it. I could have used my credit card, but I would much rather have the disc to run the game because it installs less on the PS4 hard drive. It’s a matter of between 500mb from the disc or 3GB as a download. The more games I download, the less games I can buy, so I would just rather buy the discs if I can.

I would love to buy the Lego Movie Videogame and Lego Batman, but I can buy those in the future when I am ready for a new game. I haven’t even made a dent in Lego The Hobbit, so I don’t want to overwhelm myself with all these games lol.

I am having fun with my PlayStation 4, but my right forearm is in a lot of pain from using the R3 stick with my thumb and pressing the buttons. My left arm isn’t having any issues for some reason, but perhaps it’s because I’m not doing as much work with my left thumb lol. Who knew that something as simple as pushing buttons with my thumb would cause so much pain. I need to limit myself to only an hour or 2 a day rather than 4 to 8 lol. Perhaps that’s the problem. But I’m just having fun since it’s a new thing. I’m sure the novelty will wear off and I won’t play the game as often. Maybe when my shows come back on I will pay more attention to watching TV.

The nerve of some people

nerves-facial-morris

The subject of this blog is not a complaint about someone’s character, rather a discussion on nerves, more particularly the nerves in my face since my Parotidectomy surgery in November.

You can read the details of my surgery in the link in the previous paragraph, or I can give you the cliff notes version.  I had a stone growing in my saliva gland and it had to be removed because it was causing a massive amount of pain.  It was removed by a surgeon at the Kern Medical Center on November 20th 2013.  It left me with a huge scar and a golf ball sized chunk taken out of my face.  It has been numb ever since, but the feeling is coming back, more importantly pain is coming back.

You see all those nerves in the diagram above?  Everything is connected.  Even though most of my face is numb, I can feel electrical impulses when I touch certain parts of my face.  If I touch my jaw line near my chin, I can feel electrical impulses in my earlobe.  If I touch anywhere near the incision area, I can also feel it all the way up my ear.  If I touch my earlobe, I can feel it in the spot on my jaw line near my chin from before.  There are certain areas that even the slightest touch can cause pain from the electrical impulses.  Even blowing on my skin can cause the feeling and possibly pain.

I’m not bothered by it as much as I probably should be because I know that my face is still healing.  The numbness is still there, but it is going away.  It’s like that pins and needles feeling you get when you sit on your foot for too long and your foot goes numb and then you get the pins and needles, although the pins and needles only shows up when I touch my face, and it doesn’t show up in the exact spot that I touch.  It’s a very strange feeling, but I am getting used to it.

The other day my partner touched my face and I recoiled in pain and he was a bit shocked at my overreaction, but he didn’t understand what I am feeling.  Heck, I didn’t quite understand it until now.

My last appointment with the surgeon at KMC was yesterday and he told me that there are more stones growing in the saliva gland on the left side of my face so eventually that will need to be taken care of like the right side, but that may take years to happen.  I am not going to worry about that until the pain comes from that.

Speaking of pain from nerves, am I having massive tooth pain and need to visit the dentist in May when my dental insurance kicks in again.  Right now all they will cover is emergency extractions and right now I am having an emergency in 3 or 4 teeth and I would much rather have fillings than more extractions.  I am using a sensitive toothpaste, but it doesn’t seem to be helping me very much.  I’ve flossed and flossed and that only makes it worse and my teeth are so jagged that they cut the floss in half and I can never get the floss out of between my teeth.  The Listerine helps numb the pain when I finish brushing, and sometimes I just swish with it just to numb the pain 3 or 4 times per day.

It seems I am always in pain.  I feel like I was the worst person in the history of humanity in a previous lifetime and I am paying for the bad karma in this lifetime.  I sometimes feel like I am earning some of my karma back by being a good person, but it doesn’t help at all.  I wonder who I was and what I did to deserve this.  Oh well, it doesn’t do any good dwelling on the past, especially a past I don’t have any memory of.

Anyway, I am looking forward for my next round of pain to end at least before my birthday lol.

Until next time…

New problem seems to be no problem

I mentioned in a previous post that I was having complications from my recent surgery to remove my parotid gland. The problem was that I am still generating new saliva which is causing some pain when it fills up too much and because it doesn’t drain into my mouth, but instead my neck.

I have an update on the issue. It doesn’t seem to be getting too big and I can feel it drain on its own without me having to push on it to milk it, for the lack of a better word. How it does it is very strange, it feels like sweat is running down my face along the scar along my ear. Although I am not positive that that is what it is, that could just be my scar tingling as it has been doing. I am feeling it right now as I type this because I just ate a bowl of cereal which generated some saliva in the gland.

I actually don’t know where the saliva would drain from that gland.  When I have pushed on it before, I feel a vein bulge inside of my mouth which is near where the parotid gland used to be in front of my earlobe, so it is possible that there is a vein, or tube or whatever you want to call it that allows the saliva to travel to reach its destination to release somewhere.  Perhaps that was releasing into my parotid gland which would release into my mouth, or perhaps it had a tube in common with the parotid gland, which is now gone since the parotid gland is gone.

So I don’t think that I have much to worry about. It seems to be correcting itself, despite how freaking strange it feels lol.

december 18 2013 When I look into a mirror I don’t even notice it much anymore. I mean, I see a little lump, but it looks normal considering there is still a hole beside it. The hole isn’t even that noticeable anymore. I mean, when I look at it in the mirror with a shadow on it, it’s very noticeable, but I just took a picture using the flash and you can barely see it. All you can really see is the scar, which seems to stand out along my neck. When I touch it with my fingers I can still feel a hole, but it does seem to be filling in.  When you look at the image to the left you can definitely see where the saliva is filling up in the saliva gland which has no exit into my mouth, but instead in my neck.  It’s that little marble sized ball.

I will definitely be speaking to my doctor about what is happening because he told me that there was a collection of “spit” (his words) that has collected and it will be absorbed into my body, but it’s nothing to worry about.  The very fact that it is still collecting, or generating new “spit” that is draining into my neck seems like it should be something that I should worry about, but I am sure it is hardly a problem considering if it were draining into my mouth, I would end up swallowing it, so it ends up being absorbed into my body regardless of how or where it drains, so again, I don’t see that much of a problem.

So that seems to be it for now.  My appointment with the surgeon isn’t until March, but my next appointment with my regular doctor is in January. I will mention it to both doctors and if it is an issue then I will post another update, otherwise I don’t see much of a reason to add another update on this because it doesn’t seem to be causing as much of a problem.

Parotidectomy Surgery Complications

glands

It has been 3 weeks since I had my surgery and everything seems to be healing well.  My scar isn’t red and it isn’t too noticeable, except for the scar from the hole from where the tube was draining the fluid for 2 weeks which is quite visible, but disappears with a Band-Aid.

My face and ear are still numb, although the feeling is coming back slowly, but it is coming back.  But it still feels very strange.

The only thing that seems to have gone wrong is that I still have a saliva gland that seems to still be producing saliva with nowhere to go.  According to the image, there are three glands.  Parotid, which was removed, Submandibular and Sublingual.  The Sublingual gland is under the tongue, no problem.  The gland that is still producing saliva is my Submandibular gland which is below where the Parotid gland used to be.  It is still producing saliva, but it is not releasing into my mouth.  Instead of releasing into my mouth, it stores the saliva.

This is a really big issue because that is what my Parotid gland was doing.  It wasn’t releasing the saliva, so I was having to push (or milk) it out of the gland and into my mouth.  I have been trying to do that with this gland, but it is not releasing into my mouth, instead, I can feel it releasing under my skin.  I can tell because it tingles.  I don’t want it to release saliva inside of my body, but if it doesn’t get milked, it just gets bigger and bigger and next thing you know I will be rushed to the emergency room because of how painful it is.

The surgeon told me when I came back last week to have the tube removed that it was just some saliva that will be absorbed by my body, but I had no idea it was still producing more saliva.  I only know it is producing more saliva because I could feel it getting bigger and under more pressure when I ate some chocolate the other day.  Sweet and tangy are what seem to generate a lot of saliva for me, which over the years has been a major issue for me because when I start generating a lot of saliva after drinking orange juice, my saliva gland would get backed up and it wouldn’t release the saliva into my mouth.  That’s what I was trying to get surgery for, forget the stone, I want my saliva to be able to release into my mouth as it normally would without me having to milk it.

I can live without orange juice, which I have lived without for years because I know that sour causes this issue.  The one thing I don’t think I can live without is sweet, because I have a sweet tooth.  I love sweet flavors, such as sweet tea, or sweet coffee, or sweet oatmeal.  I can live without chocolate and cookies and so on, but I can’t avoid other sweet flavors because there is almost always something sweet.

My next appointment with the surgeon isn’t until March, but my next appointment with my regular doctor is next month and he will advise me on what to do.  I just hope by then it isn’t too painful.

I was hoping that my last post on this issue was my very last post.  I guess I jinxed myself by saying it was my last post.  This seems to be a pattern with me though.  I say I will never have to worry about something again, but then it comes back and I have to worry about it some more.  It’s a “if it can go wrong, it will” type of thing.  Murphy’s Law.  Why does Murphy seem to always be hiding in the shadows cursing me?  Darn you Murphy!

I will certainly update this issue if it becomes too unbearable and I end up in the ER or when I see my doctor in January, whichever comes first.

No More Tube!

tube removed december 6th

We went to the surgery clinic at Kern Medical Center today to have the tube removed from my neck.  It would have been removed last week if it weren’t for the fact that my surgeon is only there on Fridays, and that was the day after Thanksgiving.  I honestly did not mind having the tube for that extra week because there was still more fluids draining, so I feel the extra week was warranted.

I don’t have very much swelling anymore, thank goodness.  When I did have swelling, it felt like my stitches were going to pop so I used ice to help bring the swelling down.  I think the swelling was what hurt the most, besides of course having a tube inside my neck, which hurt like hell every time I accidentally yanked on it.

Without me even having to ask, my surgeon Dr. Trang told me that they tested the stone that was in my parotid gland and they did not find any traces of cancer.  I didn’t think there would be, but it’s good to know that there isn’t cancer anyway.  I do have more stones growing in my left parotid gland, so there is a good chance that I will have to go through this all over again in a few years.  Hopefully not, but if it happens then it happens.

You can’t even see the stitches along my ear, but you can see it behind my ear and along my neck.  You can’t see my neck in the picture above, but it’s there.  I’m not too worried about scarring.  If I have a bad scar then I will buy some scar cream, if I don’t have a scar then yea for me lol.  It really doesn’t phase me one way or the other.  I’m just glad I don’t have a stone in my parotid gland, well, I don’t have a parotid gland anymore either.

There is a mushy lump on my face down near my jaw near my ear, but Dr. Trang told me that it is just saliva that has collected in that spot and it should absorb into my body.  It will go away on its own.

The thing that I am most happy about is that it is all finished and I can move on with my life pain-free, well, until my back starts hurting again, or some other thing causes issues lol.  I know it’s going to happen, it always does.  You know the saying, if it isn’t one thing, it’s another.  That’s how life is for me.  It sucks, but I think it is why I am such a patient person.  That has too meanings lol.  Get it?  I’m patient as in not impatient and I am a patient as in going to the doctor’s office lol.  I thought it was funny.

If you have no clue what I am talking about, please read this post: Parotidectomy Surgery

Anyway, this is hopefully the last thing I have to say about this issue.  It’s all good!

Parotidectomy Surgery

parotidectomy surgery

Yesterday was my parotidectomy surgery to remove the entire parotid gland on the right side of my face.  It’s also known as the saliva gland.  There were several stones that were blocking the path which caused the saliva to stay in my gland causing it to stretch, which hurt like a mother trucker.

When I woke up in the recovery room I was totally confused.  I had no idea where I was or how I got there.  I felt like I had been in a car accident, like a Mack truck crashed into my face lol.  That’s a bit severe, but you know what I mean.  I had trouble waking up too.  You know how when you didn’t get enough sleep the night before and people are forcing you to wake up and your body is fighting you and you can barely open your eyes?  That’s how it was waking up in recovery.  I wanted to wake up, but I was having a hard time.

The nurse came over to me to talk to me.  I asked her what happened, why I was here because I was still confused, but then the memory of what happened started coming back to me.  I said oh wait I remember.  She asked me why I was there and I said to remove my parotid gland.

The doctor came to me and was telling me what he found.  The cat scan with contrast told them that the stone was 1cm which is pretty big, but it wasn’t just 1 stone, there were 3.  After the surgery, he told me that it was the size of his pinky finger tip, you know the part of the tip that has the nail and he held his fingers up to where the finger bends.  That was how big it was.  Plus he said there was a lot of infection in the gland.  He sent it to the lab.

He wanted me to come back in 7 days to remove the tubing that is sticking out of my neck into a ball which collects the drainage, and I just called them to make that appointment, but this doctor is only in the surgery clinic on Friday’s and he won’t be there next week due to Thanksgiving.  She wanted to make the appointment for December 6th and I was like whoa, I thought I only had to have this for 7 days.  I asked her to ask the doctor to call me to tell me what to do.  Since he is only in the clinic on Friday, I hope he calls me this Friday to tell me what he suggests I do.  If I can just come in as a walk in and have them remove the tube then that would be fantastic, otherwise I will have to wait until December 6th to have it removed.

During surgery, they intubated me to help me breathe.  When I speak now, it’s with a lower volume and a softer tone.  I’m sure it’s temporary, but I kind of like it lol.

Dr. Trang at Kern Medical Center did a wonderful job with the surgery.  He made sure that my nerves weren’t damaged and the stitches are beautiful and I know it will heal nicely so you barely even notice them.  Scar cream is a bit on the expensive side, but I will use some of that to make the scar go away.

2013-11-21_13-07-57Anyway, he prescribed 2 medications for me.  Keflex which is an antibiotic and Percocet for pain.  I have never taken Percocet before so I don’t know if it’s addictive or not.  I hope not because I don’t like to have any vices.  It says it’s Oxycodone/Acetaminophen which is generic for Percocet.

I told my aunt that I was taking Keflex which by the way I’ve taken before.  She told me that it will cause a yeast infection (YIKES!) so I need to eat at least 1 yogurt a day.  My yogurt of choice is Yoplait.

I fortunately don’t have any pain and I am not as exhausted as I thought I would be.  I mean I’m not laying in bed feeling sorry for myself.  I actually have my normal amount of energy if you can believe that.  My partner said that it looks like the hole in my face is already starting to fill up.  I don’t know how, and I certainly can’t see it filling up or what it would be filling up with.  I’m positive that everything will go back into place and the scar won’t be too bad and everything will be fine.  I don’t have any worries.

Here are a few more pictures.

Parotid Surgery

A couple of months ago I mentioned that I had pain in my saliva gland aka my Parotid gland.  I went to the doctor who gave me an anti-biotic medicine and said I may need surgery and even asked me if that was what I wanted.  He sent me to Kern Medical Center and that surgeon told me that I had Sialolithiasis which is apparently a very common thing.  I’ve never heard of it.

The surgeon at KMC gave me some options, have it removed with a scope in L.A. or have surgery to remove the entire gland.  My partner didn’t want me to have it removed because it would leave a huge unsightly scar.  He said we could go to L.A. to have that procedure, but then we discussed how many trips we would probably end up making, so he changed his mind.  See, I told the surgeon that I wanted to have him perform the surgery because I knew it would cost money to drive to L.A., and you know that I would have to come 2 or 3 times.  But the surgeon today told me that the stones are too big to be removed with a scope anyway.  The scope would fit in the, I’m just going to call it a vein, but the stones were way too big to be pulled out of said vein.  So surgery is my only option.

My surgery will be in late November, which just happens to be 1 week before Thanksgiving, and I will have a port in the back that will drain into a container which I will have to be mindful of.  I will have to keep that on me for 1 week and then he will remove it.

On one hand I’m very excited to finally have this removed to fix my problem, but on the other hand I’m not looking forward to having a huge scar on my face lol.  I mean, if that’s what it takes to end this constant agony then so be it, but why did it have to be my face?  Why couldn’t the gland be inside my mouth?  Or why couldn’t the stone be somewhere in my stomach where I never have to worry about people seeing my scar?  Why of all places did it have to be on my face?  I mean, I’m not a model so it doesn’t matter, it’s not like I’m going to lose any modeling gigs, but still.  You never want to do something that will put a scar on the first thing people look at when they see you, or bring too much attention to yourself when you are trying to stay invisible.

Well, it’s inevitable, so there is nothing I can do but learn to live with it.  I’m sure the scar won’t be too bad and I can use scar creams that will make it disappear, so there is something to look forward to.  I’m just glad the pain will finally be gone soon.

So until November…

Weight Gain

WeightGain

We went to the doctor’s office today so I could get my clearance note for surgery to remove my parotid gland.  They had me step on the scale and I was shocked to see that I was 205lbs.  So yeah, I’m a bit verklempt lol.

One of my issues with exercising is that when I walk or ride my bike or do anything that burns calories, the Noom app tells me that I can eat more calories, so I end up eating those extra calories, but then I might even go over those extra calories because I think to myself that I did such a good job that it’s okay.  Well, that’s not how it works.  I should still stick with 1400 calories, 1500 at the most.  Even if it says I can eat 1700, I should draw the line in the sand at 1500.

I’ve been using the Noom app for my cardio, but I decided to download the Noom Cardio Trainer.  I’m sure that it will still show the extra calories in the Noom app, but I just want to see how it goes with the Noom Cardio Trainer.

I’ve been eating those Quinoa and Tofu burgers every day with hamburger buns which is not a good idea; I should be eating them without any bread.  Here is my typical day:

Every morning I will either have a bowl of Malt-O-Meal or a banana for breakfast, which by the way the Malt-O-Meal is a green food (which means healthy) and the banana is obviously a green food.  For my morning snack (second breakfast?) I usually have a banana.  For lunch I normally eat a Weight Watchers Smart Ones frozen dinner, although I’ve been eating the Quinoa and Tofu burgers, both by the way are green, except for the bun of course.  Afternoon snack (linner?) is typically a banana or crackers or sometimes I will have a bowl of broccoli.  That has been consistent.  Dinner is typically a Weight Watchers Smart Ones, but I’ve been eating the Quinoa and Tofu Burgers.  For evening snack I’ve been eating a lot of crackers.  I need to stop doing that, but I get so hungry that it feels like I’m famished.

I’m assuming that my issue here is the bread and the crackers.  I also have to admit that I’ve been eating candy corn, but not daily.  I’m guessing that the amount that I’ve eaten so far is finally catching up to me, so I will stop eating them for the rest of the season.  If I am having this much difficulty from the candy corn, just imagine how it’s going to be when Eggnog is available in stores.  I’m going to go crazy because I just LOVE eggnog lol.

So getting back to the Noom cardio trainer, I have set up 5 days a week to go riding on Mondays, Tuesdays, Thursdays, Fridays and Saturdays.  I’m going to go out 5 days a week to do at least 11 miles per day, if I can do more, then great, but I’m not going to push myself that hard.  The app suggests 5 days a week, so I’m giving myself 2 days off, but not 2 consecutive days which is why I chose Sundays and Wednesdays as my days off.

balance ballI am also going to buy that Gaiam Total Body Balance Ball Kit which is sold on Amazon for $20.  It has an exercise DVD with it which I can watch while doing the exercises in my bedroom.  The doctor at Physical Therapy told me I should buy one so I can do exercises for my back since I only have 3 more sessions left.  My insurance only pays for so many sessions, then I’m on my own.  My back isn’t in as much pain as it was, but anyone who has, or anyone who knows anyone with scoliosis knows that the pain is really bad.  The only thing that really helps my pain is the exercises.  Pain meds don’t do anything for my back pain, they help my parotid gland pain, but not my back pain.  $20 is a small price to pay for pain relief.  I wanted to buy one at Target, but they were the same price, but without the DVD.

I really hope I can get back down to my comfortable weight of 192lbs and possibly get back on track with my weight loss so I can get down to my ultimate goal of 170lbs.  Considering I lost 70lbs this year, 35lbs shouldn’t be that difficult to lose, although it’s harder than I thought.

So to recap, my goal is to stay away from Halloween Candy and any other holiday sweets, bread and to exercise more and to try not to eat more than 1500 calories per day, even when the app says I can eat more.

Ready… set…  GO!

I am finally not in any pain

pain

I have been going to Jacobo Physical Therapy 3 days a week for a few weeks and I can’t believe it but, I am not in any pain.  I can’t say that this is a permanent thing, because I do occasionally feel pain, but it’s not a constant nagging in my spine like it normally is 24 hours a day.

A few years ago I was diagnosed with degenerative disc disease, but recently in the last month I found out from x-rays that I also have scoliosis.  I was wondering why I was in constant agony, now I know why.  My doctor sent me to physical therapy and I go there three days a week.  They give me certain exercises I can do for 30 minutes, then someone comes in and gives me a soft tissue massage.

Dr. Jacobo told me that my insurance will only cover so many visits per year, so once I’m done with physical therapy, I’m on my own.  She said they will see me three days next week, but after that I can come once a week.  I am not sure if my insurance will pay for once a week, but I hope they do.

weider total body works 5000She told me that they can give me a printout of all of my exercises in case I forget what they are so that I can do them at home.  I have a Weider Total Body Works 5000 which I can use to help me.  Some of the exercises I do use weights, so that’s where my home gym will come in.  Not all of the exercises will require using the gym, so I will have to remember them and try to make it a daily ritual to keep my back pain down to an absolute minimum, if that is possible.

I’m wondering if I should set up my video camera so I can do all of the exercises so if I ever forget how to do them, I can always refer to the tape, or well, DVD since it’s a DVD Camcorder.  I think that would be a good idea because I know I will forget if I don’t make it a habit.

I bought that Weider Total Body Works 5000 in 2005 from Wal-mart’s website for $99.  Now they are $149 at Wal-Mart and $159 at Target.  It’s $400 and $1000 on Amazon, which is amazing that they would sell it for that much money since you can buy it much cheaper at Wally World and Target.

My gym is outside in our patio which makes it a miserable experience because it’s way too hot out there to use it, but there isn’t any room for it inside the house.  I’m pretty sure I can deal with using it out there for half an hour per day if it will help me with my pain levels.  Although I can’t say that I will get my massages, but I guess I will just have to deal without those lol.

The good thing about these exercises is that they taught me how to stretch my legs while laying down when I start and when I finish, so I can use that knowledge for when I ride my bike.  It’s always a good idea to stretch before and after a bike ride.

I really hope my pain levels aren’t as high as they used to be without going to physical therapy 3 days a week.  If you have ever suffered from back pain, then you know what that constant nagging pain feels like, so you understand.  Most people who don’t have any back pain never understand.  In fact, some people feel that because they don’t have that same or any pain that they don’t think we are in any pain at all.  It’s a “if I’m not in pain, then you aren’t in any pain either” type of thing I guess.

Pain meds don’t always help me.  I’ve taken Ibuprofen, Vicodin, muscle relaxers, Tylenol, Advil etc.  Nothing works.  Although when I broke my arm I was constantly medicating myself with Vicodin which took ALL my pain away.  I think that was the best vacation from pain I’ve been on in a long time.  When my arm healed and I stopped taking the Vicodin, the back pain returned.  I have taken more Vicodin since then, but it doesn’t do any good.

I think I spoke too soon because I’m getting shooting pain in the middle of my spine.  YIKES!  Well, let’s hope that it doesn’t get worse.  I think I will take something for it now.  I bought some generic “Pain Relief PM” from Dollar General for $1 to help with the pain and to help me sleep.  I really hope that doing those exercises at home will help because I don’t think I can take being in as much pain as I was before going to Jacobo Physical Therapy.  That really is no way to live.

Today I found out that I have Sialolithiasis

Sialolithiasis

I have been dealing with a problem in my right saliva gland, called the parotid gland, for at least the last 10 years.  It comes and goes at the least 2 times and at the most 5 times per year.  The doctors have always given me antibiotics, or by the time I get to the doctor it has gone down so I don’t mention it.  This time around I had the issue and I made a special appointment for it because it was too painful to ignore.

inches and centimetersThe doctor put me on antibiotics which lasted 1 week.  I saw him a week later and was still in pain and it was still swollen and he gave me more antibiotics.  Because it wasn’t going away, he sent me to get an ultrasound and when he found out that it was 1cm, he suggested surgery, but asked me if that was what I wanted.  Not everyone wants to have surgery which would scar you, so he wanted to know what I wanted to have done.  For scale, see image (left).

He referred me to an Ear Nose Throat doctor who sent me for a cat scan with contrast and when I saw him on Wednesday, he told me that I needed to go to yet another doctor.  Are all these doctors getting a kick back for these referrals?  I mean honestly, why do I need to have so many referrals?  Anyway, he was trying to send me to Los Angeles and I told him that I’d rather go to a doctor here in Bakersfield because I don’t want to have to drive (well, I don’t drive, I’d have to be driven) all the way to Los Angeles just for a consultation to be told that I have to come back for the surgery and then after surgery.

So I went to a doctor at Kern Medical Center today for the consultation and he told me that I have 4 options

  1. Live with it.
  2. Ultrasound which they don’t do there and my insurance doesn’t cover.
  3. Surgery where they use a scope to go in there with a camera and grab the stone and pull it out, which is also not available there, I would have to go to LA and most likely make several trips, which we can’t afford and my insurance might not pay for it.
  4. Have him do surgery to remove the entire gland and give me a huge scar.

I decided on option 4, but when I told my partner out in the lobby he said “Oh no tell him you want to go to LA.”  Without thinking I went back to the counter and said I need to tell the doctor that I want to go to LA.  Then we got to talking, my insurance company probably won’t want to pay for that because I bet you that will cost more than having it removed.  Plus, we’d still have to go all the way to LA and probably make several trips.  I can’t afford that dammit!  If I could have afforded that, then I would have just done that in the beginning.  Sheesh!

Well, the doctor at KMC told me that before he can do the surgery (when I had told him I was up for option 4) he needs my doctor to sign off on it.  So I made an appointment for Tuesday of next week so I could talk to him and tell him that I need him to call that doctor’s office and give them his okay.

This is what I have.  It’s called Sialolithiasis.

parotid gland “Sialolithiasis (also termed salivary calculi,[1] or salivary stones),[1] is a condition where a calcified mass forms within a salivary gland, usually in the duct of the submandibular gland (2) (also termed “Wharton’s duct“). Less commonly the parotid gland (1) or rarely the sublingual gland (3) or a minor salivary gland may develop salivary stones.”

This is what he said will happen.  They will have to start cutting right at the edge of my sideburn just at or near the top of my ear which is where my glasses are, go all the way down below my earlobe and turn towards my neck and go down my neck.  It’s a big gland as you can see in the image above, so naturally they have to cut a lot.  He said there will be a pretty big scar, but I’m okay with that.  Neosporin has a cream for scars to help them disappear.

I have no issue with scars.  In fact, I feel scars give you character.  Perhaps the doctor will let me keep the stone so I can have something to show when I tell the story of how I got that scar on my face.

As always, I will keep updating this blog on the progress.