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.

Depression About Surgery

scarIn August I went to the doctor to get help for an issue I was having with my parotid gland on my right side.  I had a cat scan with contrast and they found several stones and the only way that I can get them out is with surgery to remove the entire gland.  The problem is, it will leave a huge scar on the side of my face that will look like the image to the left.

Most people wouldn’t want to have a huge scar on their face of all places.  I mean, a scar on your arm or your leg or stomach is normal, but your face, that’s like the one place that you want to keep scar free.  Well, without thinking I said that if this is my only option other than living with it, then just do it because I can’t continue living with this horrible pain.

I still feel that I want to get the surgery, but I have also sort of gone into a depression knowing that I’m going to have this on my face soon.  Not only will I have this on November 20th, but I will have a tube sticking out for 7 days which means it will be removed the day before Thanksgiving.  I will have a fresh scar during the holidays.  I know that the holidays are just like any other day to me, but I still don’t understand why I couldn’t have had the surgery by now so it’s all healed up BEFORE the holidays.  I mean, this started in August and we’re in November now.

I’m sorry, I’m scatterbrained.  I’m just going through something right now.  I know it’s all mental, but still, I just don’t want to have to be out in public with this on my face for Thanksgiving, especially since we always go to a restaurant for that holiday.  I know it’s probably silly and you are thinking oh get a grip, get over it, but wouldn’t you be worried about this too?

This is going to go one of two ways, one I will be fine and I won’t think it’s that big of a deal and we will go out and eat and it will be fine.  Or, I will be so depressed that I won’t be able to get out of bed until New Years.

The issue here is this is my face, which is the first thing that people see.  People judge you as a person before they even talk to you.  I know, RuPaul says it’s none of my business what other people think of me and I usually think that too, but it’s my FACE!  Why does this have to happen to me just before Thanksgiving, or at all for that matter?

As if I haven’t been through enough in my life with being diagnosed with HIV at age 21, then upgraded to AIDS at 23, being diagnosed with having Parkinson’s, Scoliosis, being homeless as a teenager just because I was gay and being abused throughout my childhood.  It just seems like I am a target for something messed up.  Why me?  Why do I have such a messed up life?

Well, I guess I should just be thankful that I am still alive despite the fact that I was supposed to die in 2000 and nearly died in 2002 from Steven-Johnson syndrome, which is another messed up thing that happened to me lol.  Eh hem, as I was saying, at least I have a roof over my head and I’m somewhat healthy and not homeless.

I suppose it could be worse.  I could be homeless and not have any medical insurance and would have to just live with the pain for the rest of my life.  So I guess I should be lucky that I can have the surgery.  But I still can’t help but feel depressed about the scar.  UGH!  Life sucks.

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…

Jumping Through Hoops For Surgery

Life isn’t fair, is it?  Murphy’s law says that if something can go wrong, it will.  Well, something is very wrong with how long it is taking to get my surgery.  I have been in pain, no, agony for going on 2 months now and I was told I could get surgery to help, yet I don’t see it coming.

I was diagnosed with Sialolithiasis which means my right Parotid gland (saliva gland) has stones in it.  You know how you get kidney stones?  Well, the saliva gland can get stones too.  The problem is that the stones are preventing the saliva from being released into my mouth and that causes it to swell up.  I can push on it and I can feel the saliva squirt into my mouth, and that relieves the pressure which is very painful.  I have been doing that for years, yes this has been happening to me for many years.  I would guess up to 10 years that I can recall.  I know it’s more, but I can’t be sure when it began.

So first thing that happened was it started and I waited a few days to call the doctor.  I figured that it has happened so many times in my adulthood and that I was almost positive it would go away from pushing on it, but it wasn’t going away, it was just getting worse and worse and there was a blockage preventing the saliva from releasing.  I made an appointment which meant I had to wait for a weekend.  I went to the doctor and he gave me an antibiotic and saw me again in 7 days.  I came back in 7 days and he gave me another antibiotic and told me that I might need surgery.  If this antibiotic doesn’t help in another week then I could get surgery if I chose to.

Naturally, it didn’t go away after that 2nd week.  In the past it has always gone away after taking the antibiotics, but this one has stayed with me.  He sent me to have an ultrasound which showed that I had a stone that was 1cm.  Look at your ruler, that’s nearly half an inch.  He then referred me to an Ear, Nose, Throat specialist who sent me for an CT scan with contrast which showed that I have multiple stones, not just on the right side, but also on the left.  The left side swells up as well, but not as bad as the right side.  The doctor said that the left side were much smaller, so it’s not as big of an emergency as the right side is.

The ENT doctor referred me to a surgeon at Kern Medical Center aka KMC which I always joke and call it KFC.  He gave me my options and I chose to go to LA, but then changed my mind and wanted to have him do the surgery.  Before he can do anything, he needs my original doctor to sign off on it because I have some other health concerns that had to be tested before he would do surgery.  My doctor had blood drawn and did an EKG which showed heart trouble.  UGH!

heart monitor I finally went to the heart doctor today and they gave me another EKG and put a heart monitor on me that I have to wear for 24 hours.  It has been recording since around 2pm or so.  I had to change my physical therapy for my scoliosis issue tomorrow from 10:45am to 2:30pm.  I hope that gives them a full 24 hours, but the nurse told me that I could take it off before 24 hours was up if I had to.  They also made 2  more appointments for me, one in 2 weeks and then another in October.

October?  What?  I needed my surgery like a month ago!  I’m so sick of this pain.  I mean, the pain isn’t as bad as it was for 2 months, but it’s still bad.  The pain from my saliva gland makes me think my teeth need to be pulled.  I know having my teeth pulled isn’t the answer because that’s not where the pain is coming from, the pain is just travelling to those places.  When I don’t have pain in my saliva gland then my teeth are fine.  If the problem was my teeth then I would feel the pain in my teeth when I didn’t feel pain in my saliva gland.

So I am hoping that I can get my surgery in October because I don’t think I can wait very much longer after that.  I just can’t take it anymore.  Nobody should have to live in constant pain every day like this.  There really isn’t anything I can do, so I guess I have no choice but to deal with it.  I really hope that it gets taken care of soon.

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.

Week 35

week 35 collage

I am absolutely freaking out that I can’t seem to lose weight anymore, and instead of maintaining my weight, I am actually gaining.  I have no excuses so I’m not going to say that it’s because of my back pain, which turns out to be scoliosis, because I got my bike back and haven’t been riding it.  I have no excuse for not riding it.

So why haven’t I been riding my bicycle and why have I been gaining weight you ask?  Well, I’m not going to blame anyone because I am in control of what I eat and what I do, or don’t do.  I would like to say that because I haven’t been able to afford the Smart Ones meals every week that that is why I haven’t been able to lose weight, but that’s no excuse.  Although I have been eating, or trying to eat healthy fruits and vegetables, I have also been eating the Banquet dinners which are a lot cheaper than the Michelina’s.  One of the Banquet meals was green in the Noom app, but all the rest have been either yellow or red.  But you can’t say I haven’t tried eating healthy because I have been eating 1 1/2 to 2 cups of broccoli or mixed veggies with broccoli, cauliflower and carrots before eating the Banquet or Michelina’s frozen dinners.  I have also been eating Malt-O-Meal for breakfast, which shows up as green in the Noom app.

I have been doing everything right, well, except for every time my partner buys cookies, I end up eating half of the package.  I have also been extra hungry and been snacking on more wheat thins than I’m supposed to be snacking on.  I’ve also been snacking on other things because the mad hunger seems to be back like it was before I went on my weight loss journey.  It’s hard to calm down my food cravings when I have deprived myself for so long.  Even though I know something is bad for me, I’ll want it that much more.  I could be eating much worse, trust me, but I’m doing my best to stay away from much worse.

So yeah, I am very disappointed in myself, but I got my check and printed out some coupons for the Weight Watchers Smart Ones frozen dinners and we’re going to go to Food Maxx today to buy some and more Malt-O-Meal.  I love those.  I am also going to ask my partner if he will please stop buying cookies and any other snacks, and if he does, be sure to hide them from me so I don’t see them and eat them.  I am also going to ask that he not ask me if I want to go to the Mexican restaurant or McDonald’s anymore because those are too tempting for me.  I don’t mind Subway, but even that is bad because of the bread, despite the fact that I always get the 9-grain wheat.

I have been doing exercises at Physical Therapy 3 days a week for approximately 30 minutes each day, which averages out to 177 calories burned each time, but I need to step it up with riding my bicycle.  I haven’t been riding it, and again this is no excuse, because my back and front tires keep going flat on me and I don’t know why.  I don’t understand why this keeps happening to me.  It’s frustrating to me.  I can’t pump the tires with my hand pump because it irritates my carpal tunnel syndrome, and I can’t keep wasting the Co2 cartridges to keep air in them daily.  1 tire uses more than 1 cartridge of air.  That’s why I haven’t been riding, because I hate having to pull over every time my tires go flat, and I can’t find what is causing them to go flat.  It’s frustrating as hell.

I wanted to save the money from the Etsy shop to buy a new bicycle, but nobody is buying anything and the Etsy shop is costing me more money every month than I am making in profits.  If people don’t start buying keychains and earrings, I’m going to have to close my Etsy store because I just can’t afford to keep paying the fees.  Of course, I will keep what items I have listed because I had to pay to list them, so I will keep them until they expire, but if nobody buys them before then, then I won’t relist them.  Whatever doesn’t sell will end up being Christmas presents because I don’t know what else to do with them.  Boy that sure showed me how unpopular my ideas are.

Wow I have totally gone off topic, haven’t I?  Anyway, I will try to do better with my diet.  If I can’t lose weight, then at least I’d like to maintain a healthy weight.  I’d love to maintain 190 if I can, which means I need to lose 6lbs again.  I’m hoping the Smart Ones will bring me back down.  I need to start saying no more too.  Those are my 2 goals for the next month.  Hopefully I can get back down to 190.  Hopefully…

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.

Health Update

Health_Update_rainbow

In my previous health update on my back I mentioned that my recent x-rays showed that my spine was curving like a parenthesis (.  Today I had my appointment with the physical therapist who told me that it was like that on the top, but the other way on the bottom, so basically it’s in an S shape.  ( on the top and ) on the bottom.  I like to think that I am such a huge Superman fan that my back is turning into the Superman S, which means hope on his planet, of course.

The physical therapist office wants me to come in 3 days a week for my therapy.  They gave me some homework exercises to do in the morning or at night, but at least do them daily.  She also suggested that if I could go swimming, I should.  I told her I didn’t have a pool and because I have a weak immune system already, that it’s probably not a good idea to use a public pool.  I get bronchitis if someone coughs 30 feet away, I can’t imagine how sick I will be if I’m in a pool with children lol.  She suggested that my bicycle is a better alternative since it doesn’t cause pain.

Today I also went to have a cat scan with contrast, which by the way… ick!  All I taste and smell is Iodine lol.  They will hopefully find out what the problem is with my swollen parotid gland so they can fix the problem.  My regular doctor suggested surgery, but the ear, nose and throat doctor doesn’t know my doctor’s diagnosis and isn’t exactly sure why he should care.  At least that’s how it seemed to me by the way he spoke to me.  He didn’t seem to have any of my doctor’s notes or even know why I was there.  I basically have to start from scratch with him as if I have never come to any doctor with my problem.  It would be nice if when a doctor refers you somewhere that they tell that doctor why they are being referred.

I will see my regular doctor this Friday and the ENT doctor on Monday.  The place I went to today for the cat scan said it would be released to both doctor’s offices in 2 business days.

I woke up in the middle of the night with THE worst headache and pain from my saliva gland.  I was also sick to my stomach so I had a PB&J.  Right now I have nausea and all I smell is Iodine still.  I hope that goes away soon lol.

More updates as they happen. 🙂