Tag: doctors


We All Fall Down

28
June

Saturday afternoon at about 4:30, my mother fell.  She’d been having more trouble walking lately, so it wasn’t really that surprising that she fell.  What was surprising was that no matter what we did, we couldn’t get her up off the ground.  Normally, she’s fairly easy to get back up off the floor.  This time, it seemed like everything that we were trying was failing.  We tried for the better part of about 7 hours on Saturday night and debated calling an ambulance.  At about 11:30, my parents decided that they needed to rest and that we would start again in the morning, which we did.

We realized on Sunday that it wasn’t going to be something that we could do on our own this time.  I had to get on my computer and look at the HEMSI website to get the non-emergency line, after my dad called a nurse for the insurance company that handles their Medicare Plus.  (He tried to get through on the insurance company’s line for about an hour, and he kept getting sent around to different people.)  He had tried to call HEMSI before I got the non-emergency line, from a number that was given to him by a local social services agency.  (That number was wrong.)

When HEMSI got here, they asked her if she wanted to go to the hospital or stay here.  My mom made some comments about wanting to stay here.  I told the paramedics that they needed to take her to the hospital.  She had some scrapes and carpet burns on her legs from the various attempts to get her up.  So, they took her to the hospital.  My dad followed behind a little while later.  (The paramedics told him to wait about 30 minutes before he came.)

I stayed home when he went to the ER after her.  Apparently, while he was there, he was treated like he’d viciously beaten and neglected her.  She told me that a social worker counted the bruises that she had on her, especially the ones in the shape of hand prints.  The social worker wanted her to tell her how she’d gotten them.  My mom told her that those were from the attempts to get her off the floor, which is true.  The social worker didn’t believe her.  The doctors and social worker asked my mom if she felt “safe” at home.  I understand why they felt the need to ask this, since my mother was heavily bruised and it had taken us so long to get her medical attention for this fall.  I also understand that they don’t know the full story and are just assuming that my mother is never taken care of or is harmed physically by her family.

The bruises that concerned them ranged from the size of the tips of my fingers to the size of a grapefruit.  They were all very dark purple.  These bruises were on her arms, her legs, her abdomen, and her chest.  (Her back had no bruises.) If the doctors and staff had noticed that my mom continued to bruise every time they assisted her, then I think that they might have been a little less judgmental.  By the time I saw her yesterday, she had additional bruises from where they’d attempted to give her an IV (one huge one at her elbow and one on her thumb, where they’d blown veins and put too much pressure on her) and where they’d put her blood pressure cuff.  Anywhere that she had the slightest bit of pressure applied, she had a new bruise.

The bruises look bad, but they are fairly normal for members of my mom’s side of the family.  Huge purple bruises that pop up for pretty much no reason are something that my great-grandmother (Mama) passed to my grandmother (Nana) and that Nana passed to my mom and that my mom passed to me.  They’re one of the lovely conditions that we all have had to deal with.  (We also have similar psychiatric issues, problems with vertigo/balance/tendency to fall, headaches, heavy periods/early menopause, reactions to most medications, etc.)  Each previous generation has had to explain to doctors that they haven’t been abused.  Hell, I had to deny being abused a few times when I had the old mattress that would cut and/or poke me during the night.

The doctors have run tests on her.  They said that her muscles had atrophied, thus the falling and being unable to get up.  They told her that the breakdown in her muscles had caused certain enzymes to be released that had taken a toll on her kidneys, heart, brain, etc.  (Remember how I was worried because she had gotten so incoherent?  Apparently, there was a reason.)   They’ve started her on physical therapy, which is great.  (I still don’t understand why the orthopedists never suggested physical therapy after she broke her ankles and was forced to stay off her feet for the better part of a year.)  They’re also trying to fix the issues that have occurred because of the breakdown.

I think that the nurses on the floor that she is currently on have figured out that the bruises aren’t from abuse.  I think they’ve also figured out that we do care about my mom very much and never intended to do anything bad/neglectful to her.  My only issue with the nurses on her floor is that they haven’t been taking care of the scrapes and carpet burns.  When my dad and I went yesterday, I wanted to see if they were improving or getting worse.  I was told (and then shown by my mom) that nothing had been done for these marks.  So, my mom had the tech bring her a pan of water with no-rinse soap in it so she could bathe.  (Normally a tech would be the one to help her bathe, but apparently that isn’t one of the tech on that floor’s duties.)  My dad and I helped her, and I helped clean the wounds.  My mom asked the nurse, after we were done, if she could have a bandage placed over any of them.  The nurse said that she might be able to get some Neosporin for them, but she wasn’t sure.  That annoyed me quite a bit.

Oh, the doctor told my mom that she was malnourished.  Apparently, she isn’t getting enough protein.  I think that’s probably true for every member of my family, since we all have various forms of anemia & deficiencies.  We’re going to have to change our diets, which is going to be difficult.  (Higher protein foods always seem to be a lot more expensive, which makes it a lot harder for us to buy them.)

Yesterday, my mom had said that she might get to come home today.  Today, though, the new day for her to come home is tomorrow.  I’m not surprised, since the discharge days always change.

Side note: My back is still hurting from trying to help my mom up this weekend.  (I hurt it about 30-45 minutes into the ordeal.)  I’ve been downing quite a few Tramadol and Flexeril since then.  Hopefully, the pain will lessen soon.  If not, I guess I’ll have to go get it checked out.

Comment » | Confessions, Family, Sickness and Health, So Damn Special

I Promise I Will Be There

24
May

In the past I have had doctors and therapists who don’t do the reminder calls, so I’ve learned not to really expect them.  Sure, I prefer when I get them, since I’ve usually scheduled the appointment weeks (sometimes months) in advance.  But, for the most part, I understand that doctors don’t have to call.

Well, on Friday, The Heart Center called to remind me of my appointment and to do pre-registration.  That’s not really weird, since a call prior to the weekend, is normal for appointments on Mondays and Tuesdays. (Pre-registration is also pretty normal, since the Center is part of the Huntsville Hospital System, so my appointment is sort of like being checked into the hospital for a few hours.)  Well, yesterday morning I got a second call from them.  This time it was their computer system, which required me to confirm the appointment via their automated system.  About four hours later, I got another call from them.  I think that it was a person.  (My dad answered and confirmed vocally, so I’m guessing that it was a person.)  I’ve never had an appointment that required 3 confirmations before.  My mother suggested that it might be that the Center has me scheduled for multiple people or multiple procedures or something.  Who knows?

Of course the idea that I’m going to see more than 1 specialist or that I’m going to be going through procedures is a bit unnerving.  I’m used to the EKG stuff and Holter monitors being a part of my appointment, but they don’t usually do anything other than that when I visit.  There is a chance that this appointment will be different, so I guess I shouldn’t expect it to be just like the others I’ve had there.

I’m no longer certain that it is Serotonin Syndrome, since I’ve continued to have problems with my heart rate going extremely high and my blood pressure getting higher than I’ve ever seen it go before.  The high numbers are especially unexpected when earlier in the day I will have had a fairly low reading or a reading that it close to normal.  A few hours after the high reading, the lower readings will come back.

I’ve also had some massive headaches with and without the increases (and decreases) in pulse and pressure.  Yesterday, I had one of the worst headaches that I’d ever had, which is saying something since I’ve had headaches pretty constantly for 20 years or so.  This headache felt like the front of my skull, mainly in the forehead area, was going to cave in.  It also felt like there was this explosive or maybe implosive feeling in that general area.  It didn’t feel like my standard migraines, tension, and sinus headaches.  It was different, and definitely not good-different.  I know that I probably should have gotten it checked out, but if I had called my family doctor and told them, I knew that they would have suggested that I tell the cardiologist today or that I go to the emergency room.  The ER isn’t really an option.  I know that I can’t rely on them to do anything anymore.  And if I were told to just tell the cardiologist, then I would have basically wasted a phone call.

Sometimes I wish I still had a headache doctor, but I didn’t really appreciate the way that I was treated there and I didn’t like that they kept putting me on medicines that I had already had issues with.  Since there is only one headache specialist in the entire state, I guess I am kind of screwed in terms of looking for others around here.  Insurance might keep me from going to doctors elsewhere, not to mention gas prices and the angst that comes with the idea of really long drives.

Anyway, I hope that the appointment goes well today and that we figure out what the hell is going on.  Otherwise, I worry that I will worry myself to death over it.

2 comments » | Confessions, Sickness and Health

Just Floating

16
April

I have been sick. I’ve had what appears to be the worst sinus infection that I have ever had. My mom and I think it may be the same one that has been dismissed by the ENT as allergies. (The allergist said I had 3 allergies and none were bad enough to make me this sick.) This would be the infection that came along about 2 or 3 months after my sinus surgery last year.

It isn’t really in my sinuses so much anymore. It’s pretty much everywhere else in my body (fever, swollen lymph nodes, chills, etc.), so that would explain the lack of icons, blog entries, etc. It isn’t that I’m purely being lazy. It’s that every time I’m awake and doing anything that requires more than the simplest of brain functions, my body seems to be about ready to fall over. What have I been doing? Reading and listening to music. I’ve posted some on tumblr and I’ve been doing reviews and opinionated stuff–because I’m more tempted to speak my mind when I’m running a real fever.

After two weeks of it being really bad, I finally went to the family doctor. I didn’t see mine, but the doctor that I saw was really nice and really concerned. She had to go see what anti-biotic could be used, because of the Ceclor-Septra-Penicillin-Zithromax allergy + the fluoroquinolone toxicity. I ended up with Doxycycline and I had to promise to go to the ER if I started showing any signs of allergy. So, I’ve been on that for a couple of days and its been less than fun. Hopefully, I will start feeling better soon, though.

Oh, I was watching CNN yesterday and I saw the latest Idol results, which don’t usually concern me. This time I saw a name that looked familiar. Apparently, Paul McDonald, a friend from high school, was on American Idol and got voted off. How did I miss this? Clearly, I haven’t been paying as much attention to Facebook updates as I should have. If I had known, I definitely would have voted for him, even if I’m not a big fan of the show. (Oddly, I always seem to end up getting the latest albums from a lot of the people from the show.)

So, I feel crappy in the whole sick way and I feel like a crappy friend.

Probably doesn’t help that now my mother is sick and seems to want to blame a lot of stuff on me. I really wish that she would stop blaming me for things whenever she feels bad. This week I’ve been the cause of the financial burden, the cause of her sinus infection (I even got called an idiot for not getting it taken care of sooner), the cause of something getting lost (something I’ve never seen), etc. She’s in a bad mood and it apparently is my fault. And before anyone suggests I leave or anything, I want you to remember that 1.) I have no way to leave and 2.) I own the damn house I live in and I get held legally/financially responsible for anything wrong with it, so I shouldn’t have to leave. I would love to go away and never come back, but it won’t happen. I’m stuck here. I’ll always be stuck here.

Comment » | Alabama Weirdness, Confessions, Family, Friends, Janet Goes AWOL, Music Stuff, Pre-College Years, Sickness and Health, Top Artists, Top Songs, Tumblr

Essentially Shook Up

16
March

My mom went to the psychiatrist today. Normally, I don’t discuss her trips to the nutty place, but this one was kind of an interesting/important one. She thought she was reacting to one of her many psych meds, and she wanted to figure out which one the doctor thought it might be.

The psychiatrist, who also happens to be my psychiatrist, asked her if any family member had been diagnosed with an essential tremor.  My mom told her that I had been diagnosed with one at one point.  Well, the psychiatrist told my mom that she was meaning a parent or grandparent.  Basically, she wanted to know if it was something that my mom could have inherited from someone.  She said that there was typically a genetic reason for the tremor, and that it must not be there if no ancestor had been diagnosed with it.

Now, I don’t know if the psychiatrist was having a brain fart or thought that maybe I’m not the biological offspring of my parents, but I’m fairly certain that if I have it, then there still might be a genetic link.  I know my mom couldn’t get it from me, but I could’ve inherited it from her.

Since my mother couldn’t have possibly inherited it from me, and having a child with the condition isn’t a good reason to say that my mom might have it, the doctor settled on my mom’s Risperdal.  She then tried to figure out if she could give my mom a beta blocker.  She couldn’t, since my mom is already on one.  She looked for a calcium channel blocker, but my mom’s on one of those, too.  So, she told my mom that this side effect is to be expected for anyone who has been on Risperdal for over two years (my mom’s taken it for at least 10 years–it was one of the ones she OD’d on in 2001) and that she should come back if it got worse or if she ended up having some kind of seizure-like reaction.

 

2 comments » | Family, Mental Health

Jesus, Wheelchairs, and Radiology

15
March

On Saturday, I fell. No big deal, right? I wouldn’t have thought so, except that when I fell, my left foot slammed down on the ground. My toes started bruising almost immediately, as did many other places that didn’t even hit. My mom tried to get me to go to the ER, but I didn’t want to. Going to the ER generally leads to a 3-4 hour wait, a possible trip to radiology (isn’t always a guarantee for me), and then a rude dismissal from the staff (about an hour and a half after being taken to the back–if I even get that far) because I’ve ended up wasting their time.

‘My foot would get better’ was my initial thought.  I fall quite a bit, and usually I’m okay within a few days.  Instead, by Sunday, the bruises and swelling were worse, as was the pain.  I was also having some stiffness in the joints that connect my toes to my foot.  Still, I didn’t go to the hospital.

On Monday morning, I called the UAB Clinic folks so that I could see my family doctor (or another family doctor in the clinic).  Well, I just so happened to call on the day that at least 2 of the doctors who were scheduled had decided to take a sick day.  (I’m sure they didn’t just decide to take a sick day, and that they were actually sick.)  So, they were too busy for the staff they had and couldn’t see me.  Instead of saying that they would see me another day, they told me that I needed to be seen ASAP.  Well, before they could say where I could go, they had to know what insurance I had.  I told them it was Medicare & Medicaid.  Apparently, none of the walk-in clinic are into the whole Medicare-Medicaid combo, so the only other place to go was (cue dramatic music) the ER.

The ER on a Monday is not the best place in the world to be.  It isn’t necessarily the worst, but it’s pretty damn close to the worst place you could be in town.  I went in and, after filling out a form where I put the symptom as “left foot & ankle”, was immediately triaged, which wasn’t necessarily a good thing.  From the first nurse in triage, everyone ignored the foot part of the symptoms and just focused on the ankle.  I thought it was weird that they would do that, though I don’t know why it would surprise me.

After being triaged, I sat in the waiting room for another 3 hours.  I got to people watch, which was fairly entertaining, but not exactly what I wanted to be doing.  There were some interesting people there.  A guy was sitting across the room, under one of the HD televisions, laughing and talking to himself.  My dad and I tried to figure out what to call the guy.  (Please don’t tell me that it is rude to talk about people in a waiting room.  This can sometimes be the only source of fun when you’re in a waiting room.)  We debated between Charlie (for Charles Manson), Jesus (for, well, Jesus Christ), and some others that were related to the guy’s main look–long, wavy-ish dark brown hair, a dark beard, and a look of being in touch with something “else”. We ended up calling him Jesus. My dad thought the guy was probably just crazy.  I thought that he was probably high, but might also have some craziness.  I regretted referring to him as Jesus later, because though I thought that Jesus might wear acid wash jeans and a matching jean jacket, I didn’t think he’d wear sneakers.  (Jesus would definitely wear sandals.)  There was a group of people that we (and a lot of other folks) paid attention to as we waited.  It was a group of about 10-15 people, who, among other things, were very loud.  The security guards chastised them at one point for being so disruptive.  They tried to bum-rush the back to see their friend, who had apparently been beaten up.  Of the five or six people that were part of that rushing past the door when it unlocked for one or two to go back, only two were allowed to stay back there.  Apparently, the ER rule of two visitors per person was lost on the group.  Though this group of people had gotten there at the same time as me, they left about an hour ahead of me.  The only employee that we ended up watching was one of the security guys who’d rolled me into the ER.  He was confiscating any wheelchairs that had been abandoned, even if the person was in the bathroom.  I made sure to hold on to my wheelchair.  (I’ve learned that the staff doesn’t take hurt feet very seriously if you’re not in a wheelchair.)

By the time I was finally allowed to go back to a room, everyone who’d been there before me was already either seen and discharged, seen and waiting on a diagnosis, or had given up on the process and had gone home.  Several of the people who’d come after me ended up being seen before me.

When I got to the back, they kept talking about my ankle, even when I showed them where on my foot I hurt.  I found out that x-rays had been ordered about 2 hours earlier, but that there was a very long wait for the whole hospital to get seen in the radiology department.  (I didn’t understand why they couldn’t send people to one of the other connected facilities [via the tram] that has a radiology department, but apparently that wasn’t a possibility.)  The doctor, who I saw for a grand total of ten seconds, just told me that it was taking forever to get the radiology department’s attention.  A few minutes later, a radiology tech (or someone from transportation) took me down to the department.  I, then, waited for about 10 minutes for someone to wheel me into the room for the x-ray.

The x-ray was done on my ankle, which I was really perturbed by, but I couldn’t get across to anyone that the brunt of the fall had been “absorbed” by my foot.  (I had, by this time, learned that you never give too much information on those little sign-in forms.)  So, after the x-ray was done, I was taken back to my room.  There had been a shift change in nurses while I was in radiology, so I met my nurse at about the same time that the nurse practitioner came in to tell me that my ankle was fine.  My father and I gave him a weird look that should’ve given him a big clue that my ankle wasn’t the part that was really hurt.  (This is why physical exams, which had never taken place, are important in diagnosis.)  He asked what was wrong.  I said that my foot was the problem.  He said that he would check the x-ray again, but the ankle x-ray usually shows the foot.

That is what a standard ankle x-ray shows.  That little area of where the foot meets the lower leg.  That probably hasn’t changed since I first started getting ankle x-rays over 10 years ago.  That kind of view doesn’t show the part of the foot where the toes (phalanges) meet the foot (metatarsals).  It barely shows any part of the metatarsals at all.  It shows the tarsals, aka the ankle.  If an ankle x-ray was the same as a foot x-ray, then there would be no need for calling them different things on forms and there would be no need for different views.

Well, the nurse practitioner, who was sure that the x-ray showed the right part of my foot, was proven right–though, this happened while he was out of the room and with no input from any other medical professional.  I could’ve complained and refused to leave, because I’ve done that before, but it generally ends with the doctor or a supervisor coming in and defending the position of the staff member who made the shoddy call.  (Generally, it is a call made by a doctor who hasn’t been attentive or this particular nurse practitioner–I think he may have been part of the team that made the decision with my mom’s first ankle break to send her home over the weekend, even though she couldn’t bear weight.)

Now, I know that nurse practitioners can do a lot.  And I know that they are generally really good at their jobs, but this guy didn’t do an exam and acted like there wasn’t really anything wrong.  And his end diagnosis?  My foot is bruised and I have a sprained toe.  I’m not exactly sure which toe is sprained, since 3 of them have been in a lot of pain and 1 has been in a bit less pain than those 3.  Only one hasn’t had any kind of pain, bruising, etc.   On the discharge orders, I was told to take Tylenol for the pain, because I guess it works better for pain than Tramadol.  (That was sarcasm.)  I was also told to follow up with a family doctor.  The discharge orders were signed by the same doctor who’d spent 10 seconds talking to me, and was also the same doctor who (on the day my mom had to come back in with the first broken ankle) had written me a prescription for Ibuprofen (can’t take NSAIDs) and spent 10 seconds with me and all of the other poor end-of-the-spectrum pain cases in the same room.  Of course, that day I didn’t get an x-ray, which I kind of feel like I didn’t get yesterday–except that I know that I did get one, even if it was the wrong one.

The Huntsville Hospital ER has really gone to shit.

Comment » | General, How I Met Your Neighbors (aka An Overactive Imagination), Rants, Sickness and Health

30 Days of Truths: Day 1

8
March

Okay, I saw this on nimil’s blog, which she got from Jennfur, who apparently got it from Angel, who got it from somewhere. I think I might actually be able to do this one.

Day 1: Something you hate about yourself.

This answer really depends on the day. Some days I’ll hate my quick temper. Others I’ll hate how I have let so many people walk all over me. I think that I probably always hate my weight, so can I say that for today? My weight has been something that has pretty much always been an issue.

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That picture is from Easter of 1986, when I was 2 years old. My weight wasn’t really bad then. It started getting worse as the next year or so went by. My mom has always said that my weight sped up around the time I started opening the fridge. She said that I used to eat cheese like crazy as a kid, which I believe since it’s been something I’ve always felt compelled to do.

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That’s me at around 3. I know it’s from when I was 3, but I’m not sure at what point it was taken. And the next is when I was nearing 4.

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Those years were kind of hard ones for my family. At three, my mom and I were in a fairly serious car accident. I had a concussion, but my mom had what was basically a severely dislocated shoulder. She had to have surgery to rebuild her shoulder, and she couldn’t really do much in that time. A few months later, I had to go to the hospital for my asthma, and after that my weight started going higher and higher quite rapidly.

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By the time I was 7, I weighed way too much, but the doctors weren’t acting really concerned at this point. There was more concern over the control of my asthma and no medical professional suggested that I try to lose weight until around the time I was 10. My grandfather, of course, made the suggestions through his cruel comments.

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At 10, I started to a special weight loss program through Huntsville Hospital that was for tweens & teens (along with their parents). Once a week, we had to go to classes with other overweight & obese kids. We’d get weighed. I think that at that point, I was almost five feet tall and 175 pounds. While I was in the class, which lasted about 3 months, I lost less than 10 pounds and I was following the diets really well.

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My weight kept going up as the years passed. By the time I was 13, it was at about 225, with my height being about 5’3″. I was on my third or fourth type of diet through a registered dietitian by this time. My weight would go down 1 pound a week, then go up 2 the next.

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At sixteen, I was about to head into the hardest emotional time period I had ever gone through. I was already feeling severely limited by my weight. I had never dated, kissed anyone, etc. I thought I was horribly ugly and undeserving of any kind of positive attention. I was also at about 275 pounds and 5’5″ here. I would gain 50 pounds over the next 9 months, most of it within weeks of starting on a constantly increasing amount of psychiatric medicines (started with Paxil, then added Xanax and Zyprexa, and finally added Celexa). I was also a high school student when that picture was taken, and within about 6 months of the picture, I was a high school dropout.

At nineteen, I hit my highest weight (to that point), which was 341.3 pounds. I had gastric bypass surgery that year. I began to lose the weight. And by 22, I was at around 195-205 pounds.

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But a year later, I had already regained much of that weight back. And at 27, I hover between 330 and 345 pounds. (It’s different at every appointment.)

On My 27th birthday

Future Topics:
Day 2: Something you love about yourself.
Day 3: Something you have to forgive yourself for.
Day 4: Something you have to forgive someone for.
Day 5: Something you hope to do in your life.
Day 6: Something you hope you never have to do.
Day 7: Someone who has made your life worth living for.
Day 8: Someone who made your life hell, or treated you like shit.
Day 9: Someone you didn’t want to let go, but just drifted.
Day 10: Someone you need to let go, or wish you didn’t know.
Day 11: Something people seem to compliment you the most on.
Day 12: Something you never get compliments on.
Day 13: A band or artist that has gotten you through some tough ass days.
Day 14: A hero that has let you down.
Day 15: Something or someone you couldn’t live without, because you’ve tried living without it.
Day 16: Someone or something you definitely could live without.
Day 17: A book you’ve read that changed your views on something.
Day 18: Your views on gay marriage.
Day 19: What do you think of religion? Or what do you think of politics?
Day 20: Your views on drugs and alcohol.
Day 21: (scenario) Your best friend is in a car accident and you two got into a fight an hour before. What do you do?
Day 22: Something you wish you hadn’t done in your life.
Day 23: Something you wish you had done in your life.
Day 24: Make a playlist to someone, and explain why you chose all the songs.
Day 25: The reason you believe you’re still alive today.
Day 26: Have you ever thought about giving up on life? If so, when and why?
Day 27: What’s the best thing going for you right now?
Day 28: What if you were pregnant or got someone pregnant, what would you do?
Day 29: Something you hope to change about yourself. And why.
Day 30: A letter to yourself, tell yourself EVERYTHING you love about yourself

3 comments » | 10 Years of Madness, 30 Days of Truth, Confessions, General, memes, Mental Health, Sickness and Health, Who I Was - Past

It’s Not All in My Head

23
February

I’m sorry but I must disagree with your assessment of the visit. I took a full history, reviewed available records and did a complete rheumatologic physical exam (which I know is more detailed than most). I ordered appropriate labs and all they are returning normal and negative for rheumatic disease. I am aware that you have musculoskeletal pain and I acknowledged that but I have no treatment for chronic undifferentiated pain syndrome. I have been practicing for > 30yrs and this has allowed me to be more efficient in my evaluations that most. Again , I would recommend that your MD have you evaluated by a pain specialist.

The exam wasn’t complete. Going through the motions isn’t a complete exam. The appropriate labs probably wouldn’t be back by now, since it generally takes more than 36 hours to get lab results back on anything other than simple tests. Pain is not the same as inflammation and it isn’t the same as all of the dryness going on everywhere. The syndrome that he mentioned in the email, which wasn’t mentioned at the appointment, is (from what I can tell) a somatoform diagnosis–meaning that it’s all in my head. So basically, I hurt, feel like crap, etc. because I’m a nutter.

The last time that a doctor diagnosed me with a somatoform illness and stuck with that diagnosis was when I was 13 and I was having problems with my gallbladder. That doctor thought that I was just really anxious and causing the stomach pain. She continued that stance after the surgery to remove the gallbladder. So, I don’t really take stock in doctors who outright say that it is all in my head. And if it were a somatoform issue, then you know what the treatment is? Therapy and anti-depressants. What have I been going through on near-constant basis since I was 16 and off-and-on since I was 13. Yeah, those two things.

Now, it could be that I’m just crazy, but I really don’t think so. (I know that’s supposed to be part of the whole diagnosis with the problem.) I just don’t think it’s possible for me to fake this much stuff. I think it’s more likely that the doctor is just an arrogant ass who didn’t care to look into what might be going on.

4 comments » | Confessions, Rants, Sickness and Health, So Damn Special

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