Getting Out Isn’t Always the Answer

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Many, many times, when I have been severely depressed or anxious, I have heard the repeated suggestion that I just “get out and do something”. I think this is a common misunderstanding that people have about depression and anxiety, that the cure is always just going out and finding something to do.

Personally, I can say that if I am mildly or moderately depressed or anxious, getting out can indeed be a huge help. It is a good way to distract myself and can make my life feel less empty and more meaningful.

However, if I am severely depressed or anxious, “getting out” is absolutely NOT the answer, and I know this from experience. Whenever I have been severely depressed and I somehow managed to make myself leave the house, I have just been a teary, numb mess who ends up feeling worse for being unable to stop the tears in public. During these times, I am unable to join in with anything going on around me and will just sit there and cry and feel embarrassed, wishing desperately I had never left home.

As for times of severe anxiety, I often also deal with severe irritability and a tendency to snap at others, even when I don’t mean to do so. “Going out” when in this state can actually damage relationships because people wonder why you are taking it out on them, even if you absolutely don’t intend to do so. Not to mention the fact that severe anxiety often comes with intense panic attacks, which are something that is horrible to experience in public. Panic attacks suck no matter where you are when you have them, but given the choice I would always choose to be in the comfort of my own home dealing with one rather than out in an unpredictable public environment.

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Family Issues and Ex-Pastor’s Wife Resentment

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So I am going through a couple things right now. For one, my already strained relationship with my mother seems to be going farther downhill. To get a bit of the backstory on our relationship, you can check out this post. Anyhow, ever since I confronted my mother about the past, I could feel her slowly backing away. She now lives in another state and at first she would call me once or twice a week and would call back within a day if I called her. Now she doesn’t return my calls for a week at a time and it has been three weeks since she last called me, even though she said she would call me in a few days the last time we talked.

I can’t help but feel a little snubbed and like I am slowly being phased out of her life, which doesn’t surprise me now that she has remarried and doesn’t need me so much anymore. This has always pretty much been the pattern when she gets a man in her life. I stop mattering as much. Honestly, there have been times I’ve considered going “no contact” because the little bit of contact we have now only tends to make me sadder, and the more I feel put aside and ignored, the more I hurt.

I’ve also been dealing with some pent up resentment I didn’t even realize I had about the years I spent as a pastor’s wife. For the first 11 years or so of our 15 year marriage, my husband was a pastor. In the past few years we have kind of drifted from the faith and become agnostic, which is a huge change from what our lives used to be. However, I just realized when having a conversation with my husband the other night, how much being a pastor’s wife for so many years deeply bothered me.

For one thing, I constantly felt judged by the congregation and compared to previous or other pastors’ wives that the congregation knew. I was not old-fashioned. I was not meek and submissive. I did not want to teach, play piano, or lead anything. It just isn’t my personality. My social anxiety makes leading anything a horrifying thought for me, but yet, I found myself almost forced to sometimes be in these roles I hated. I was pretty much forced to teach at times, and while I loved the kids, I felt panic at the responsibility. No one helped or trained me, I was just thrown right in. At one point, I had a panic attack and burst into tears about my fear of teaching in front of the head pastor, his wife, and my husband and yet none of them seemed to take it seriously and pretty much just patted me on the shoulder and said I would be all right. But I wasn’t. Even when I found out I had autism and tried to explain to the head pastor why that made social things so hard for me, his response was that everyone has those problems. But no – everyone does not!!!

My husband now realizes how many mistakes he made by pushing me. He is sorry and has genuinely apologized for putting pressure on me and making me feel like I had to do things that made me anxious to the point of sickness. He realizes now that he learned that behavior from his own parents who pressured him constantly about being involved in church and often tended to ignore his feelings if he didn’t want to do something. Like most people, he was acting out the unhealthy patterns of his family as an adult and unfortunately, I got the brunt of it.

I’m Super Grumpy and Annoyed Today

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I am in a mood today. Seriously grumpy and feeling like crap both mentally and physically. I was supposed to go to a support group meeting today, but the absolute last thing I want to do when I feel like this is socialize or go anywhere. Instead, I just want to cocoon on the recliner or in bed, watching tv or YouTube and letting my grumpy butt get over this particular mood swing.

I could feel this irritability building and creeping up on me the last few days. Even when my husband and I took a walk in the park and I posted those pictures of snakes, turtles and frogs in my last blog post, I was starting to feel more and more off kilter. Every time a couple or family crept up behind us on the trail and made noise, I just wanted to throttle them, which isn’t like me. I normally love kids and adore having them around, but that day I just wanted to ship them all off to Siberia. I felt somehow personally offended that other people were simply sharing my space…and even though I knew how irrational that was, I still felt that way.

Last night I noticed that I was falling into one of those moods where I wanted to spit and hiss like a cat at anyone who dared touch me or even looked at me wrong. I’m still feeling that way today, so it is probably a good thing that I’m home alone right now lol. Hopefully this feeling will pass soon and I will get back to my more humane self.

Anger, Mania, and Standing Up for Myself

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Last night I had a definite episode of mania. Wanting to stay up all night again, feeling like doing a million things at once, wanting to jump out of my skin, tempted to spend way more money than I should, barely able to sleep. If you read my rant yesterday, then you know that I was already dealing with a lot of anger, so I can’t help but wonder if anger can bring on a manic episode? I honestly don’t know whether that is possible or not, I should probably ask my psychiatrist, but it does seem interesting that after being upset and angry I became so manic.

Something else happened last night that made me even angrier than I had been when I wrote the rant post yesterday. Someone else in that Facebook group commented on the post I had written that only 1 or 2 of my mental or physical conditions could be disabling. They said that the Asperger’s and Bipolar might be disabling, but the PTSD, Social Anxiety Disorder, Fibromyalgia, CFS, Plantar Fasciitis, IBS, chronic infections, Degenerative Disc Disease, and bulging discs are NOT disabling. That really set me off.

At first I just told the girl that she should research the conditions and learn more about them if she thought that. However, she went on to say that I was the one who was ignorant and that I would probably “argue with a brick wall”. That really made me mad. I even asked her why she was being such a bitch because I hadn’t done anything to her. For me, saying something like that is EXTREMELY CONFRONTATIVE, but I also felt so proud of myself for standing up for myself for once in my life. Standing up for myself has always been a real challenge for me, so much so, that many people have told me over the course of my life that I needed to stop being a doormat and quit letting people walk all over me.

In person, I would still likely have a really hard time standing up for myself, mostly because when things become confrontative or stressful, I tend to struggle with selective mutism, which is a common thing for people with autism to deal with. Throughout my life, whenever I was bullied or abused, I almost always found myself temporarily struck dumb, unable to formulate a response or rebuttal. It generally only happens when I feel threatened in some way, but it is very frustrating. I figure standing up for myself online is at least a start though!

Social Security Disability Rant

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Ok, so I had another subject planned for today’s post, but I need to rant a bit, so I’ll save that topic for later. I hope you won’t mind listening to my frustration today.

So, I’m part of a group on Facebook for people with certain mental issues, and I have noticed many of the people in the group getting social security disability solely for those mental issues, which I happen to share. I am not upset that they got disability for their problems, but I can’t help but compare it to my own situation and feel angry at how I have been treated by the system.

I’ve been fighting for several years to try and get disability benefits, my worst conditions that affect my ability to work are: Bipolar Depression, Asperger’s, PTSD, social anxiety disorder, fibromyalgia, chronic fatigue syndrome, IBS, degenerative disc disease and bulging discs, chronic bronchitis/ear infections, and severe plantar fasciitis. ALL THAT and yet I am still fighting! It pisses me off because I know people who got it much quicker for SO MUCH LESS or just ONE of my conditions. And none of these conditions are light, even the last rejection letter from social security said the conditions are indeed severe…and yet I got turned down AGAIN? I have a plethora of medical evidence and have tried to follow medical advice to the letter. What more can I do???

I DO have an attorney (my 2nd actually), and I am now waiting for a court date, the 2nd time I will have to go to a hearing for this. The last judge I got had a record for barely approving anyone, which seems unfair in itself. How can it be a fair system when some judges approve a majority of people and other judges approve hardly anyone? Were it not for my husband, I would likely be homeless by now.

To make matters worse, one person in the Facebook group insinuated that plantar fasciitis and chronic ear infections/bronchitis aren’t severe enough to affect your ability to work long term. Well, I’ve had the plantar fasciitis for 15 YEARS. I’ve seen specialists, done meds, physical therapy, long-term steroid therapy, custom orthotics, cortisone shots, nothing helped. Doesn’t seem like it will magically get better at this point. It is so severe I have a noticeable limp and have almost passed out from the pain at times when I was forced to be on my feet for long periods of time.

As for the recurring infections, I’ve had chronic ear infections and bronchitis for many years, often getting up to six within a six month period. I’m now on my 3rd course of antibiotics this year (2018) for the chronic ear infections and bronchitis. Again, I’ve seen specialists, tried a host of medications and other treatments (both medical and alternative) and nothing has worked so far. The amount of antibiotics I have had to take has led to issues with antibiotics not working as well anymore, worsening IBS symptoms, and even episodes of MRSA, C Diff, and colitis which I had to be hospitalized for. These are not minor, fleeting problems.

To make matters worse, I have TRIED to work while fighting for disability. The last job I had (working only two days a week) I was let go from for missing work too much due to medical issues, most of which I was in the hospital or ER for, so they know I wasn’t just “faking”. I also tried being a greeter at Walmart, since it is about one of the only places that actually hires really disabled people and I couldn’t even do that due to my social anxiety, depression, and other health issues. I am not even fighting for welfare here, only the benefits I worked for over the years!

Going No Contact with Abusers?

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Lately I have been really struggling with the temptation to go “no contact” with someone who has been abusive to me throughout my life in different ways. If you follow my blog closely, you can probably guess who I might be talking about. I did manage about a year ago to get some physical distance from this person, which helped a lot, but I still have such feelings of dread, sadness, anger, hurt, and despair whenever I hear from them (or more consistently lately, when I am ignored by them).

I know my therapist would probably do a happy dance if I decided to go “no contact” with this person. They won’t say so outright, but it is clear to me that they see that the relationship is not conducive to my healing. The last time I saw my therapist, she asked me what I was getting out of hanging onto the relationship…and I couldn’t really say. Other than hurt and frustration, I’m not sure I’m getting much at all.

However, I can’t help but feel that if I totally disengage with this person, it will cause me to feel guilty and fearful. Guilty because I was groomed from a young age to feel responsible for this person and to be their caretaker. Additionally, I feel guilt about what my other family members might think. The fear would mostly be due to the fear of confrontation, whether in person or through more passive-aggressive avenues. The thought of letting go also plays on my fear of being all alone and unloved.

Psychiatrist Visit Anxiety

Today I see my psychiatrist again. These appointments make me nervous because there is always worry that my meds might get changed and I might have a bad reaction to another one, like I did the Cymbalta. I also often wonder what to share with him. I want to be as honest and open as possible, so I get the best treatment, but I also sometimes have a tendency to overshare or over-explain things that might not be pertinent.

I figure the things that I should share with him most this visit are my “episodes” of rage and paranoia the past couple months, even though they only lasted a few days to a week each. I have actually had a couple “episodes” of feeling almost hopeful and optimistic recently, so that is good I think. It was really odd that during one of these times of having at least a few days in a row of feeling pretty good, I had one of the worst days I have had in a while, where I was so horribly depressed and so full of despair that I sat on the couch holding a bottle of pills and wishing I could take them all and maybe not have to wake up again, but of course, I know that wouldn’t be the right thing to do. Especially to my husband. Oddly enough, the very next day I was back to feeling fairly decent overall.

I also always wonder how much to address my physical problems with the psychiatrist. After all, he isn’t a doctor who treats those conditions, but those conditions greatly affect my depression and anxiety levels. When the physical pain is extremely bad for a few days in a row, that tends to bring on a kind of despair that is hard to cope with. It blackens my view of my entire future and makes me honestly feel sometimes that life isn’t worth living if you have to be in this kind of pain. I probably should take my Tramadol (opioid pain killers) more during those times, but I am afraid of becoming dependent on it if I take it too often.

Well, thank you for listening to me overthink things as I always do lol.