Tag: sick


A Pain In The Head

20
January

On Wednesday, I went back to the neurologist, after the office called me Tuesday afternoon and told me to show up at 3:45 the next afternoon. I got there at about 3, since my dad had a physical therapy appointment an hour earlier at the building right across the street. Being there forty-five minutes early wouldn’t have been a problem if I had been called back to a room sometime before 4:15. Of course, since it was a doctor’s office, it wasn’t humanly possible to be seen on-time. No, I didn’t go back until about 4:45 or, maybe even, 5:00.

After going to the exam room, I waited…and waited…and waited. Finally, the doctor came in. First, he apologized for having been too sick to see me before then. (I didn’t know he’d been sick.) Then, he went over the results.

He said that the MRI had revealed 5 white spots (aka: white matter lesions) on my brain. He said the radiologist report said there were 10, but that he’d only seen 5 legitimate ones. (The other five were apparently blood vessels and other anatomical parts.) He said that these were normal, especially for people with migraines. He told me, after that, that my EEG had some abnormal electrical activity, which seemed to be related to migraines. I asked him about my myoclonic jerks being worse lately–again, I was told it was the migraines. The dystonia is apparently due to the migraines as well. So, he basically told me that migraines are all powerful, evil problems that cause a hell of a lot of pain and torment for people.

While he was telling me about the results, he told me that he would’ve had the MRI results sooner except that, according to him, his computer just suddenly started writing other files over the disc the hospital sent him. This resulted in him having to get another disc. I’m not exactly convinced, but…who knows?

Anyway, I am now scheduled for a “BOTOX evaluation” because he said that he didn’t think that just treating me with pain medicine was going to cut it anymore. Apparently, I need something more permanent or long-lasting. (From what I’ve read, there is no conclusive data about the level of permanency of BOTOX injections when used to control neurological conditions.) I don’t know if my insurance will cover BOTOX. (I’m now on a Medicare Part C program.) So, I don’t know if I’ll be able to have it done or not. If I do have it done, then I can tell people I’ve had a nose job and BOTOX. Fun, fun, fun.

3 comments » | Confessions, Sickness and Health

The Battle Has Begun

3
January

I am in an epic battle with my sinuses.  (10 points to Gryffindor for the proper use of epic, please?)  They’re not only filled with gross mucus crap (sorry for the visual), but when I get that stuff out I start getting not only the dried blood, but lots of not-so-dried blood, too.  (Again, sorry.) I don’t know why they have suddenly decided to intensify the crappy feeling, but they have.  It may be that I’ve been without my Flonase for around a month now, which I could probably remedy by calling my family doctor (or my allergist or my ENT doctor), but I haven’t done that and I’m not sure if I want to do that.  Well, I would like to have my sinuses not feel like crap, but I’m not sure if fixing that feeling is worth the anxiety of calling any of the doctors.

I still do not know the results from EEG and MRI.  I do need to make that call today.  I was going to call yesterday, but I am pretty sure that the neurologist wasn’t there yesterday and I was asleep for most of the last twenty-four hours.  (I took 2 Flexerils at 4 AM yesterday, then took 2 more at about noon yesterday, and doing that kept me asleep most of the day and night.)  I would probably be asleep right now, but my iPod had reached the red section of the charged bar, so I needed to recharge it so I could listen to music instead of having bad dreams.

It’s pretty damn cold today, which shouldn’t be surprising since it is winter, but it is kind of shocking to the system since I was running around in shorts and short-sleeved shirts last week.  Right now it is 21°F (or -6.1°C) outside (unless you’re in some parts of Madison County where it is 9°F or -12.8°C), so I had to change from my warm weather clothes to my cold weather stuff. I wish that I wore socks right about now because that would keep my feet a bit warmer, but I don’t, so no socks for me.

Oh, I had a weird dream yesterday. It was one of the few bad dreams that I think that I’ve gotten while doing the listening-to-music-the-whole-time-I’m-sleeping thing. I’m not exactly sure how it started, but apparently, different parts of my family actually had money in the dream. My parents and I were living in this huge house in an affluent neighborhood, and the house was right across the street from Deb, Nana’s first cousin who was raised by Mama and Papa (Nana’s parents) after her mom died. Apparently, in the dream, Deb’s husband was involved with an organized crime organization, which would never happen because he is way too nice and too good of a person to be involved in a crime enterprise. Deb had apparently found out and gotten him to turn someone in, and when the group found out, they made him choose between his life and hers, so he basically ordered a hit on her. She was killed in the house my family lived in, which I apparently witnessed, but couldn’t remember because I had some weird form of amnesia. Anytime anyone would bring up her name or what happened, I would start crying or saying that it didn’t happen. It was very, very, very strange.

I had planned on making icons everyday during 2012 for my icon/graphic community, but I haven’t made any so far.  So, I need to make some today.  I was planning on doing some Colin Morgan on the 1st, Kate Bosworth on the 2nd, but I don’t remember who I planned on featuring today.  I guess I could make the first two and do some others today, as well.

Ugh, I need to not pay attention to Rand Paul making his dad sound like this über-cool guy.  I don’t like or trust either of them, don’t get the appeal of either of them, and don’t want either of them involved in decisions of the government.

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I’m Not Doing That Again

24
September

First, I guess I should update the suspicion of a UTI situation that I mentioned the other day. According to the family doctor, she’s pretty sure that I don’t have a urinary tract infection. She did an abdominal exam on me, and found out that I had pain all along the right side of my abdomen, as well as above my hip bones and at my belly button area. (I managed to make enough noise to get her attention, which has always been my problem when doctors have been examining me.) She told me that she thought that I was having the UTI symptoms because of a combination of gynecological issues and my chronic diarrhea issue. She ordered an ultrasound and a urine culture. (I don’t get why she’s ordering the urine culture if the in-office test came back negative.) Oh, and, like always, the nurse had trouble getting my blood pressure. Instead of trying 3 times and deciding to do it manually, she tried it six times and gave up when the machine couldn’t get it any of the times.

Anyway, I did the ultrasound yesterday. I still haven’t done the urine culture. I was going to do it after the ultrasound, but I felt really bad. (I had had too much water plus I had had some [bad] cranberry juice [because the juice normally helps as a diuretic], which made me feel like utter crap.) So, instead of doing that test, my dad and I came home. I had a headache and was nauseated the rest of the day. The headache kept getting worse and, eventually, spread in to my neck.

So, at about 3:30 in the morning, I decided that I was going to try to go to sleep. Usually, I can sleep better if I can find the iPod and listen to some music that relaxes me. I couldn’t find it, and the pain was worsening, so I decided to take my pain medicines and muscle relaxers. I got 4 Flexeril, 4 Zanaflex, 2 Tramadol, and 1 extra-strength Tylenol. (The Flexeril, Zanaflex, and Tramadol doses were the maximum of each that I can take at one time. I added the Tylenol in because it sometimes helps the others boost the pain control.) Maxing out the doses was not a smart idea, though.

Sometime later in the night, I needed something from the kitchen. My mom offered to get me some water and whatever else it was that I needed. I told her that I could do it on my own. That was not a smart idea, though. I think she knew that I was too out of it to do anything, especially when I asked her if she had something on her face and arms. (It looked like she had lots of blue and some yellow & orange lines on her face.) When I realized it was just hallucinations, I was fairly amused. Anyway, I proceeded to go into the kitchen, where I managed to have my legs feel like Jello. That was the last thing that I really remember before I realized that I was on my back on the floor. I considered just staying in the floor the rest of the night, but I wasn’t exactly sure that would be a good idea, especially since I knew that I would be out until sometime this afternoon. I figured out how to get back up. I got my water and I think I got something salty. I came back in the living room, where I may have had my blood pressure checked or not. I think I did and that it was 90-something over 60-something, but I’m not sure because I was just completely gone mentally at that point. I wasn’t even sure that I had actually fallen or fainted until after I woke up and asked my mom an hour or so ago. She told me not to take so much medicine again, and I think that sounds like a fairly sound idea.

The only good that came out of last night is that my headache went away for a while. Oh, and I slept about 8 and a half hours, which is pretty good. (It’s less than what I normally sleep when I take half of the Zanaflex and Flexeril doses, which is odd.)

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Once Upon My Life

22
September

I get to go to the doctor tomorrow. I think I have a UTI, which probably embarrasses me more to mention than it would embarrass anyone else to read. (I have this whole shameful feeling issue when it comes to bodily functions.) I tried to ignore it for the first half of the week, but around the time my back and side started hurting, I decided that I needed to see a doctor. So, even though I ignored my need to go because of the continuing sinus/lung crap, I am not going to ignore this particular issue.

Since I really don’t have much else to mention, I guess I could share my new Google+ profile. When my old Google/Gmail account became disabled after the massive spam issue., I also lost my Google+ account. So, now I have a new one. Feel free to add me. If I don’t add you back soon, please let me know in the comments. Sometimes I have this very ditzy tendency that can manifest in scatterbrained behavior. It can range from simply seeming dumb to being completely clueless about various things.

Oh, last night, while writing that massively moody post, I realized that I must be going into my severe depressive season. Actually, I think I’ve probably been in it for a while now. I don’t know that I ever really stopped being depressed after I started going into the sad/tired/worthless moods last Fall. Around the time that I decided that I didn’t have any real friends, I guess I just started tuning out of my life in general. I’ve ignored a lot that people have been saying about their private lives. I’ve not been as talkative on Twitter or Facebook. When I am talkative on any site, I seem to be picking more fights, which is something I do when I start feeling more depressed. (I also do it when I’m in a mixed episode.) I guess it just became easier to not function at all in the world. And I don’t know if I’ll be able to start functioning anytime soon, but I want to and that’s gotta count for something, right?

Comment » | Google+, Mental Health, Sickness and Health

You Don’t Know a Thing About Me

21
September

In a little over a week, I will be back in court. Even though I know that the city was lying in court back in July about the grass, I am still very, very nervous. Since, according to one of my cousins, Municipal Courts are basically set up to be revenue sources for the city, it is unlikely that I will be found not guilty. So, I will be told that I have to pay between $200 and $500, plus court costs, and I could go to jail for “not more than 30 days” for the violations.

I don’t have that money. I will not have that money anytime in the near future, but it will still be expected of me. And when I tell the judge that I’m on a fixed income, he’ll suggest two months. If I tell him that two months won’t do a damn bit of good (in a nicer tone, of course), he will say that that doesn’t really matter. I guess once you’ve been a lawyer long enough to be a judge that you don’t really understand the idea of having less than $500 a month in income coming in.

And while I’m dealing with all of this court crap, I’m also dealing with all the stupid family drama. My mom and I got into a really big argument the other night. She threatened to call DHR on me, which I told her that she could go ahead and do. She started saying how they would move her out and suggesting I would go to jail.

I love how my mom’s memory is so great that she remembers that DHR said that she could be moved out of the house if conditions weren’t good enough for her care, but she didn’t remember that the social worker told her in the same breath that I could also be removed from this house if conditions were not good enough for my care. Of course, my mom’s always been good with the revisionist memory when it could suit her.

My mom and I got into the massive argument, which had basically been brewing for weeks now, because she wanted me to take garbage out. She was demanding that it out right that moment. It was about one o’clock in the morning. I don’t live in a really bad part of town, but I didn’t want to go outside by myself in the middle of the night. I told her that I would do it later, which wasn’t good enough for her. So, I took it out. She and started bitching back and forth at one another, which led to me telling her that I some point she needs to learn to get up off her couch and start getting her water and her food for herself from time to time. This fight occurred after two straight nights of being awakened twice to bring her water and food and being ordered to get my father up because she couldn’t walk five more feet from the bathroom to the door to the bedroom. (She can walk to the bathroom most of the time, and that day was no exception to that ability.)

During the fight, she went from claiming that she had fallen the night before to basically admitting that she’d just stumbled. (Bouts of stumbling are regularly classified as falls from her.) I tried to get her to understand that she isn’t the only person prone to falling, and that when I fall, I generally hit the ground. She was then trying to explain how she just can’t walk and she just can’t go back to physical therapy and she just can’t get the doctors to understand that she has problems with things like her memory or her ability to get around. I have a feeling that if they aren’t understanding that she “can’t” do these things or that she’s having trouble with things that it is probably because she is not telling them things properly. She is probably telling them something that she thinks that they expect her to say. She does this on the phone with people and I’ve seen her sit back and let doctors think that nothing is wrong with her. Regardless of what she says, I think she does enjoy having things done for her. And I don’t mind doing things for her if she absolutely cannot do them, but I have a feeling that she can do more than she lets on. I also have a feeling that she doesn’t completely grasp just how difficult she has been, as of late.

I know that she thinks that I whine too much or that I’m lazy. I know that both of my parents think that. I know that friends that I know both online and offline think that, too. And I guess that maybe I am lazy. Maybe two years of being on what seems like an endless shift of care-taking (i.e. fetching things for my mom, sleeping in the living room so that if she needs me I will hear her, sacrificing sleep so that I can make sure that I do actually hear her if she needs me, standing around fixing food and water in the way that she likes, hearing how I’m doing something wrong, hearing how I don’t get things to her quickly enough, and taking care of almost anything she asks me to do, and some things that she doesn’t) has worn me out. Half the time, I feel so damn exhausted that I think that if I died it might actually be a good thing. I have given up on ever having a life. I have done a lot of that for my mom. I could still be hanging out with my church “friends” and doing things that they liked doing (not that I really enjoyed them that much) but every time I try to get away, it seems like I get to go through a guilt trip. Hell, I get guilt trips even when I’m here all the time. I am tired. I am really tired. And I was so tired the other night that I told my mother, among other things, that maybe she should move in with my aunt–her sister, aka the one who won’t talk to me. (This is also the aunt that my mother has recently begun waxing poetically about how perfect she is and how wonderful she is, even though the total contact that her sister has truly initiated in the last 2 years was a Get Well Soon card.)

I guess I have to accept that this is my life. Misery is apparently my destiny, so I guess I should just get accustomed to it. And in case you’re wondering what the fight with mom and the court stuff have to do with one another: I am often reminded that this house, though it is in my name legally and though I can be fined and imprisoned for things related to it, doesn’t belong to me. I am a guest here. And sometimes I really feel like I am definitely unwanted.

I could probably bring it up in therapy, and the therapist would probably suggest I move into low-income housing. This would lead to another fight, my self-esteem tumbling even more, and absolutely no good coming out of it. I can’t go back to school. Even if I could focus, there is no way that I could ever pay for it. So, I’ve got to figure out how to get out of this damn house and out of all of this unhealthy shit before I go off the deep end.

Comment » | 10 Years of Madness, Confessions, Family, Friends, General, Mental Health, Sickness and Health, So Damn Special

The Elephant In The Room

14
July

Yesterday, I was finally able to go get my ears checked out.  The doctor determined that I have a sinus infection, which I already knew.  (It never got better from the last time I had one in April.)  He declared it was my sinuses causing the problem he had examined my ears, sinuses, glands, throat, heartbeat, and lungs.  He also asked if I had had pressure when I would try to blow my nose.  I told him that I had never really been able to blow my nose.  (I tried to learn how after the sinus surgery last year, but I never really caught on about how you do it without encountering the whole ear-bubble feeling.)

Before he went to ask his attending what antibiotic he could give me (because my reactions are so super-fun), he asked me if I realized that I am overweight.  It was one of those comments that is supposed to represent a question, but is not really fully stated because the asking party is a bit embarrassed.  I told him that I knew that I am obese and that everything that I have ever tried for weight loss has resulted in me staying at a fairly high weight.  I mentioned the gastric bypass surgery, which led to him asking how long it had been and if I still saw my surgeon.  He also asked if anyone had checked my blood for the post-surgery standard work-up.  I told him that my blood gets checked fairly often.  Oh, and he asked if I had ever had my thyroid checked.

I’m wondering how many people who are significantly overweight to morbidly obese don’t realize that their weight is high or haven’t had their thyroid checked.  I’ve had mine tested so many times by so many doctors that I can’t imagine any doctor thinking that by the age of 27 that it wouldn’t have been tested.  I also would think that if this particular doctor had looked at the lab report section of my chart that he might have seen that yes, I’ve had it tested.  (Since it is on the computer and is fairly easy/quick to find anything that is available, I don’t see why he couldn’t do that.)

Oh well.  When he came back from his attending, he wanted to put me on Keflex.  I immediately asked him if this was a wise idea.  I thought that may it wouldn’t be very smart to give someone who has both a penicillin allergy and a Ceclor allergy a drug that has warnings against dispensing to people with either type of allergy.  When I started my question, all I got out before he interrupted me was the penicillin allergy.  He told me that it would be okay since it was a cephalosporin and not a drug from the penicillin family.  (They are related, though.)  When I finally got out the Ceclor allergy, he realized that he couldn’t give Keflex to me.  His next try was Cipro, since it had been given to me by the clinic before.  I threw up a red flag at that one, too.  I’m not technically allergic to it, but once you have a reaction in the toxicity group, you can no longer take any from that group of drugs.  So, he settled for Doxycycline.  He wanted to know what I’d had it for in the past, and I told him that it was prescribed for this same infection.  I don’t think he believed it could be the same infection.  He clearly doesn’t know my immune system, then.

So, maybe this round of antibiotics will work.  Hopefully it will.

2 comments » | Confessions, Sickness and Health

Intervention: Janet-style

29
June

About thirty hours ago, my mom called me.  Only hours after telling me to tell my dad that we should stay home and stay out of the (very) rainy weather, she was calling me.  At the first phone call, my mom sounded confident (almost happy–for her) and was sure that she was going to spend the day sleeping.  By the time she made the second call, she was having a panic attack.  She was crying and worried that Willow wasn’t getting enough attention while she was at the hospital.  She tried, at first, to conceal the crying.  It didn’t take long, though, for her to break down.  I could tell, by the shift, that she was depressed.  She sounded extremely depressed.  Extremely depressed doesn’t go well with my mom.  She told me that she wasn’t getting her pain medicine.  (She was still getting morphine instead of Talwin NX.)  She also said she was getting half of her psychiatric medicines.  (I found out when I got there that she wasn’t even getting some of it.)

When she started crying, I knew one thing above anything else.  I knew that I had to get there.  I knew that if my mother was sitting there depressed and no one was checking on her or giving her the proper care that she was going to get worse.  I was afraid that if we waited too long to get there that she would harm herself.  I thought about trying to see if any of my friends who work in the medical district (or at the hospital) could get a few minutes to stay with her so she wouldn’t be waiting alone for the half hour or so that it would take us to get there.

I didn’t ask.  I knew we could get there quickly.  I hoped that she would be okay.    All I had was hope for her and anger at the hospital.  When we finally got there, though, my mom was about ready to break down more.  She then told me that her nurse was also being rude to her.  The nurse told her that she couldn’t help her get up and get around.  She also told her that she needed to give them at least 30-45 minutes notice of anytime that she needed to go to the bathroom.  This was the day after they had had my mom on a catheter, so she wasn’t fully aware that she needed to go until she went.  (This is normal, according to the nurse that took last night’s shift.)  She had been hostile towards my mother and was not concerned about helping her get her doctor to order the proper medicine.

When the nurse (Tabatha) finally came in, she was half-assing around the room.  When she looked at the bottles of pills that we brought in to show that my mother was definitely prescribed certain pills, she just said, “Oh, I gave her that.”  She didn’t pay attention to the doses, and (for some) she said that my mom had been given pills that were never ordered.  She was quite snippy prior to my saying anything.  I could tell that the only way to get her attention was to get loud and assertive.

I never really yell at people.  My yelling is generally ineffective, but there have been instances where it has worked.  I called on the temper that used to get me some level of respect and awe from my social work program days.  I started by telling her that my mother was depressed and that she was not being given the proper medicine and that which was being given was not at an adequate level.  Tabatha denied it, getting a bit more hostile with my increased temper.  I asked her if there was a way that she could possibly contact the pain clinic or the Mental Health Center to get proper orders for her pain and psychiatric medicine.  She refused.  She said that the only doctor who could consult was my mom’s family doctor.  That is bullshit. She also said, in a snippy manner, that she had 6 other patients who were on pain medicine so she really couldn’t keep up with the medication.  This is also bullshit.

If you’ve read this blog anytime since November of 2008, then you might know that my mom has been in the hospital a few times.  I understand the hospital system from that.  I’ve previously dealt with this hospital system when my grandfathers were patients.  There is no time when a doctor who isn’t the primary care giver is considered irrelevant to a person’s case.  The family doctors don’t always know what is going on at other clinics.  They don’t always understand the specialties.  (When I finally talked to someone from the UAB Clinic, they said that they had never heard of Talwin before my mom’s case.)  The whole reason that specialties exist is to make sure that people get proper care for their specific issues.

Apparently, Tabatha was not aware of this.  I tried to change her perspective.  When it didn’t work, I asked to speak to her supervisor.  (If you can’t get the proper treatment  from one level, you go up the chain of command until you do.)  She (eventually) brought her in.  The charge nurse was nice, and she tried to defend her nurse.  (I understand why she did this.)  I expressed, quietly and calmly, the concerns that we had over my mom’s care.  Tabatha, when she started giving her opinion, got very defensive and was being quite offensive.  The bad thing (for her) was that she was still being rude with her boss standing right there.

After explaining what was wrong, what we needed to be done, and what behavior I thought was inappropriate, I brought up that Tabatha said that she couldn’t keep up with the pain medicine for more than six patients at a time.  This brought out the fire in Tabatha’s personality.  All of a sudden, she was saying, “I never said that.  I wouldn’t say that.  I’ve been a nurse for a long time and I can be a good one.”  She did say it, though.  I repeated, verbatim, her excuse.  I then requested that the charge nurse take my mom off of her caseload, so that my mom could get proper care and so that Tabatha could better devote herself to the other six patients.  The charge nurse agreed and, for the next few hours, my mom was cared for by not one registered nurse but three.  She also had her (very sweet and thoughtful) tech Mea helping her out whenever she needed it.

Later, the charge nurse came in and told me that my mom couldn’t be given her Effexor at the full 300 milligrams because her doctor said it was too high for her kidneys to handle.  I didn’t dispute this, even though my mom’s nephrologist had told her before that Effexor is mainly broken down in the liver and doesn’t really hurt the kidneys much.  (Some people do get kidney damage from it, though.)  She did, finally, get her on the proper pain medicine.

After my mom’s pain medicine was fixed, my mom’s blood pressure went from 174/80 (yesterday afternoon) to 153/82 (last night) to 135/66 (this morning).  The whole time she was on the morphine, her blood pressure was sky high.  She also was having more trouble sleeping prior to getting the Talwin.  Afterward, she finally relaxed.

She also relaxed after my little outburst with the nurse.  She wasn’t feeling up to taking them on, and she was afraid of reprisals.  I knew that reprisals were still possible, even with a different set of nurses.  I also wasn’t feeling very trusting towards the staff at this point and I was still worried that she might get extremely depressed/self-destructive if left alone, so I asked my mom if it would be okay with her if I stayed overnight.  She was okay with it.  I also okayed it with my father.  He let me go grab some food from the cafeteria before he left, because we didn’t want to leave her alone.  I brought the food up and ate my meal while she was having hers.  I didn’t leave her at any time until the morning, when I went down and got my breakfast from the cafeteria.  I also brought that meal up and ate while she was eating.

While I was there, we brought up the Effexor thing with the UAB doctors.  They said that that was ridiculous.  Apparently, her Effexor dose had never been changed.  They had no intent to change it.

My mom got discharged today.  Of course, before she was discharged, she had to talk to an actual Madison County DHR social worker before they’d send her home.  (My dad also had to talk to the social worker.)  The social worker had my dad and I leave the room, and she asked my mom (in various ways) how many times my dad had hit her or beaten her or what forms of physical abuse or torture did she go through on a regular basis.  I could hear what was being said through the door, so it wasn’t a 100% confidential environment.  (By my ability to hear discussed, the social worker was breaking certain rules set up by the NASW.)  She spent around an hour trying to get my mom to say that she was assaulted.  She also told my mom that the bruises that occurred from the fall and from being on the floor were different ages, which was not true.  My mom kept telling her it wasn’t true.  She didn’t take into account that my mom had been having bleeding/clotting issues the whole time, including a blood test that had to be redone because it separated between it being taken and it getting to the lab.  (It did this within minutes.)

The social worker then took my dad down the hall and interrogated him.  She tried to get him to say that he had physically assaulted my mother.  She also, apparently, used a very accusatory tone toward him in many ways.   She told him that in her fifteen years as a social worker she had never seen something like this, which has got to be crap.  In social work classes, we got to hear about much worse cases of familial neglect and abuse.  So, if she hasn’t seen people who’ve gone through worse, then she clearly hasn’t been dealing with many cases.

At about 3:30, my mom was finally discharged. Then, of course, they had to find a wheelchair to take her downstairs in, which took a little while. But now my mom is definitely home.  And we will definitely take care of her, even if the hospital and DHR thinks that my dad is a major domestic violence case and that I’m not competent (or too afraid) enough to stand up to anyone who is wrong.  (After the nurse thing, I don’t understand how they thought this, but whatever.)

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