Update on Writing Projects

I wanted to post a little update on my writing projects.

Freethought House, the publisher of my poetry book, was also going to publish my memoir about mental illness, recovery, and atheism. However, they recently had two people resign and they are no longer able to move forward with my project. I haven’t decided what I’m going to do with it yet. Maybe break it up and post it here or maybe find another publisher.

I recently submitted two entries to a short story contest. I rarely write fiction but I really enjoyed working on my entries. I am now convinced that I should spend a little more time working on fiction. Winners will be announced on October 31st and I’m currently looking for more contests to enter.

Also, I will be submitting my erotic poetry book to a poetry collection competition later this month. I have been working on this book for a really long time and this is the kick in the butt I need to wrap it up. 

I have been struggling with depression for the past few months and recently had a med change because of it. While I’m waiting for the meds to kick in, these writing contests seem to be the distraction that I need. I love to write and this is giving me something to work towards. I’m having a lot of fun with it.

As always, I am so grateful for your support. I will keep you all posted on my projects from time to time. Wish me luck with the contests!

The Downside to Being Open About My Mental Illness

In my early twenties, I was diagnosed with schizoaffective disorder and an eating disorder – both of which I struggled with in childhood. I’ve had my ups and downs over the years but recovery remains an important part of my life. I’ve always been open about my struggles thinking I have nothing to hide, but it doesn’t always go as planned. Here are the downsides to being open about my mental illness:

When conflict arises, people assume I’m the problem because I’m the one with the mental illness, but it’s usually not true. They think I’m too sensitive or too crazy so they place all blame squarely on my shoulders instead of taking responsibility for their part.

I always feel I need to prove myself. I may have a schizophrenic disorder but I’m far from fragile. I have a full life and I can take on a lot. I assume people think I’m not capable. I feel the need to show the world what I can do – even though it’s probably not necessary.

People can be overly concerned and it makes me uncomfortable. I get annoyed when people ask me how I’m doing over and over again. I told you the first time, I’m fine. Don’t ask me about my therapy appointments because it’s none of your goddamn business. If I need help I’ll ask for it.

People see my illness – not me – and assume my feelings are symptoms. What I feel is valid – just as valid as the feelings of someone without a mental illness.

Being open about my mental illness has shown me I can’t depend on everyone – even loved ones. Not everyone has the capacity to be supportive and that really hurts sometimes. I’m learning to be more selective in who I trust.

It’s hard to be around other people who have unresolved issues and are unwilling to get help. I remember what that felt like and I’m not going back to that place. Of course, with everything I’ve been through I have an urge to help but I can’t save everyone. I have to focus on saving myself.

Despite these negative effects, I choose to continue to be open about my mental illness. My mental illness is a part of me and I feel I have a lot to offer the world. Dealing with people in my own life can be painful, but I hope one day my story will help others and that alone is worth it.

An Atheist in Recovery: What Matters and What Doesn’t

Living with a mental illness can be an absolute shit show. I’ve had some serious ups and downs over the years, but I’m going to tell you a few things I’ve learned. Cherish what matters and forget everything else.

What Matters: Having a Voice

From speaking up at appointments to sharing your story with the world, it’s important to make your voice heard.

When it comes to dealing with my treatment team, there have been so many times I wished I would have asked for help sooner. I’d put it off. I’d think maybe it’s not that bad yet. I wouldn’t reach out until it was absolutely unbearable. Once I finally asked for help and started feeling better (such as a med adjustment), I’d kick myself for suffering longer than I needed to. That’s happened more times than I care to admit.

Also, sharing my story is therapeutic. It keeps me grounded, validates my experiences, and sometimes I even have the chance to help someone else. My story and mental health journey are important parts of me. My illness doesn’t define me but it often explains the challenges – and sometimes triumphs – in my life.

What Doesn’t: Other’s Expectations

Trying to live up to others’ expectations has given me a lot of heartache. My mental illness started early in childhood and I always felt misunderstood. My life swings pretty wildly between painfully normal and completely unique. Despite the doubts and anxiety, I have learned to follow my own path. Maybe people think I’m weird but I’ve learned that when you find someone who gets it you hang on to them. If only I could have told myself all this when I was younger…

What Matters: Purpose

Purpose is not just having a reason to get up in the morning but also having something to look forward to.

I look forward to writing. Even when I’m not well – sometimes especially when I’m not well – I always have something to write about. Sometimes it’s healing and other times it stirs the pot. Either way, I have something to say and look forward to putting it down on paper.

What Doesn’t: God

Maybe some people find peace in a little faith in recovery but having worked in mental health for the past fifteen years I’ve seen firsthand the damage religion can do to someone with a mental illness. It’s pouring gasoline on an already raging fire.

 

That’s my list. Now it’s your turn! Let me know what matters and what doesn’t.

Painful Lessons: Setting Boundaries and Toxic People

A common rule for people recovering from an eating disorder is to avoid conversations about dieting, so when I came home from treatment, I politely asked my loved ones to not talk about counting calories or losing weight in front of me. After all, if I was a recovering alcoholic, I doubt they would talk about drinking around me. It was a simple request really…

and they can’t do it. Every time I’m around my family there’s food shaming, body shaming, and general negativity around eating. After everything I’ve been through…and they just can’t keep their mouths shut.

What’s worse is my six-year-old daughter is hearing all of it. Eating disorders are very much a family problem and I am busting my ass to break the cycle.

One of the most difficult things I learned about in treatment was setting boundaries. I’m a bit of a pushover and people pleaser so stating my needs with confidence can be terrifying. It seems like every time I stand up for myself, I piss people off.

When my family makes comments about dieting, it’s not even the comments that bother me anymore but rather the fact that they won’t respect a boundary I set.

I actually think this can be a common problem for people when they come home from treatment. I’ve grown and I’m healthier but I came home to a family that hasn’t changed. How do I stay healthy among people with unhealthy habits?

After the trauma and pain of going through treatment, I am well aware that others are fighting their own battles, but I can’t let that derail my own recovery.

I hate thinking about how confronting family members might affect my daughter, but at the same time, I want to teach her to stand up for herself. We teach others how to treat ourselves so if someone disrespects you it must be addressed — don’t allow it to continue. This is something I was never taught growing up and I’ve paid dearly for it.

I’m in a fragile state so right now I am choosing to surround myself with supportive people and distance myself from those who are not – even with my family.

So, as always I am looking for your input. Do you have any advice on setting clear boundaries? And what do you do when someone disrespects them? How do you deal with unsupportive people – especially family members?

Toxic People

How do you know when a person is toxic enough to remove them from your life?
I have a toxic person in my life who I’ve endured for a few years and the time has come to weigh my options. Do I tolerate this person to keep the peace in my close-knit family? Or do I sacrifice the relationship to keep my recovery intact?

I really want to think about the benefits and consequences because if I choose to cut this person out of my life, it will have a ripple effect on my relationships with several other people.

How will this affect my daughter? What am I teaching her?

This will make family functions difficult. Is it worth it?

How do I find more supportive people?

I keep coming back to the thought that life is too short to be miserable.

Right now it feels selfish to take a stand because I’ve never done it before. It’s painful now but in the long run, I know it’s best for my well-being.

I know you don’t have to forgive and forget. Sometimes it’s best to just move on. I just want peace.

I would love to hear your input on this as well. Have you ever cut a toxic person out of your life? How did it feel? Was it worth it?

 

I want you to know that through it all my husband has been absolutely amazing. I am so grateful for his unwavering love and support. My battles have been relentless since coming home from treatment and he has stayed by my side. While I may struggle with the rest of my family, he has always had my back.

I also want to say thank you. I have written about some difficult topics since coming home from treatment earlier this year and you all have been wonderful.

Eating Disorder Recovery — 12/26/21 Wedding Anniversary in Treatment

I want to share another journal entry with you from my time in treatment in Chicago. It’s the day after Christmas — my wedding anniversary. This was written while doing a virtual partial hospitalization program just a few days before being moved to a residential program which is a higher level of care. Our program was virtual due to a Covid outbreak at the treatment center. I was being treated for symptoms of anorexia, avoidant/restrictive food intake disorder (ARFID), and rumination disorder. I kept detailed journals of the whole experience. I was discharged last February.

This entry includes thoughts on meals, body image, values, goals, and even a little poetry.

12/26/21 Day Eleven

I had a dream last night that I did a bike tour again like when I was younger but this time I didn’t finish. I felt defeated and embarrassed.

Every morning I look in the mirror and touch the underside of my belly – especially on the sides closer to my hips. I did this back home, too. Is that body-checking? Because I told them I don’t do that.

I wish I could just be at peace with my body. How do you do that?

I don’t want to be really thin – I like being curvy. Just take some off my belly. That would be enough for me. That’s what bothers me the most.

I’m about to give up (again). I just attempted breakfast. I opened the container and there were two hard-boiled eggs. I started gagging pretty hard just at the sight of them. There was no way I was going to put those things in my mouth. They’ve been sitting in the fridge for two days. I could smell them.

Then there was a bagel with cream cheese which normally I would like, but it was a plain bagel and there was very little cream cheese. It was like eating a plain piece of white bread only thicker and harder. As I chewed it got bigger in my mouth. With my first bite, I chewed and chewed and chewed. Then I gagged so I decided my second bite would be smaller but I still chewed and chewed. Then the bagel ended up in the trash.

The only good thing about breakfast was that I had orange juice to wash that crap down with.

Will I ever get better? Will I always be picky and that’s just how it is? It’s like I’m not even trying but I can’t help it. I have a very physical reaction to food.

The treatment center gave us little gifts for Christmas – a coloring book and a sensory toy. It might seem childish but everyone loves the sensory toy – myself included. It’s a squishy, stretchy centipede with little legs and a bumpy texture. Mine is the color of my favorite Sharpie, “sky”, so it feels kind of special to me.

AM snack was white cheddar popcorn. I tried my best but didn’t get very far.

Lunch was a turkey and cheese sandwich and a cookie. It was okay. Happy to have mayo.

I named my centipede Fred.

Cheez-Its are disgusting. I only ate one cracker and I don’t think I’ll ever get the taste out of my mouth. Unfortunately, they smell how they taste. Now I can’t stand to be around them. They’re like rotting vegetables.

Now I’m smelling something my roommate made. I feel like my olfactory sense is really sensitive right now.

I’m organizing my pills like my psychiatrist suggested. Going to CVS to buy the pill minders was the first time I left the apartment in five days.

I don’t like going outside. The city kind of scares me.

I was finally able to see the results of my Covid test from the 21st – negative. However, since then I’ve developed a cough, runny nose, and dull headache. Hopefully, it is just a cold. It’s just quite a coincidence that it happened right when so many people I was around have covid. I mean, within just a couple of days. I have to do a test tomorrow, and then another one later in the week. Hopefully, we can get back to in-person programming on the 3rd, but I kind of doubt it.

Just Door Dashed Jimmy John’s and got a turkey sandwich. I gagged and spit it out twice. Most of it ended up in the trash. It’s so stupid. I could have made a turkey sandwich here. Why didn’t I get something different? I didn’t think it was possible, but I think I’m actually sick of turkey sandwiches. That’s one less safe food. I don’t have much left.

I am really struggling with meals and snacks. I’m clearly not equipped to handle virtual PHP. I mean, this all went down on my fifth day here. I still hope they move me to residential.

I’m a little scared because during process group today many people said they would never go back to residential or they will do everything they can to stay out of residential. I really didn’t think they should be allowed to talk like that during group. I think residential is the best move for my recovery but now I’m pretty nervous.

I hope I hear from my case manager tomorrow.

I really haven’t eaten much today. This is getting really difficult and I’m struggling. I want to eat but I can’t. I need some serious help. It’s too easy to have behaviors sitting in this apartment all day. At this time, it’s too much freedom.

One of my favorite motivational phrases is, “move forward from here”. It’s hard to say that when I’m slipping backward every day.

I thought it was really interesting during ACT group when our pro-T said values can change – like when we get older or meet new people.

 

Values important to me when I was young –

Freedom

Loyalty

Creativity

Values important to me now –

Loyalty 

Family

Security

Humanity

I think becoming a mom is what changed my values the most.

I haven’t learned too much about values yet at the treatment center, so I referred to a list of values I Googled. I’m really looking forward to doing the value sort activity in the next week or two. I think it will be interesting.

My Goals as a Mom –

Color more with my daughter

Help her with homework/popcorn words

Make a strong recovery, be a good role model

Be honest with her

Make sure she bathes every day

Teach her to be kind and to respect others – even if they are different than you

Teach her to love, respect, and take care of her body and mind

Make sure she gets enough sleep

Make sure she has clothes that fit

Make a safe, nonjudgmental space for her to talk and express herself

Let her be her own person

Support and encourage her passions and interests

Let her decide her own post-high school plans

Teach her about money and be realistic

Teach her you don’t have to smile

I’ve been here a week and a half and I have yet to shave anything. Today I finally plucked my eyebrows but that was only because I noticed a few hairs in the middle and growing down my nose. I don’t do much to my hair but I still wear a little makeup every day. I don’t dress up. I don’t go out. This is about as casual as I’ll ever be. I think it’s the same for many others here.

My husband seems to have this fantasy that this place is filled with cute, high-maintenance skinny bitches and that I’ll have my first lesbian experience here.

Well, I’m sorry to burst his bubble.

There’s a little bit of everybody here – fat, skinny, all genders, LGBT, straight, etc. And I’m not thinking a lot about sex right now.

I have yet to meet one “high-maintenance” person here. Honestly, I might be the most high-maintenance person here.

 

Tripping over my feet
while trying to reach
for the stars.
The floor is only
six inches beneath me
but I bruise
just the same.

It’s the middle of the night and I’m up worrying about how I’m going to get my stuff to residential. I have two suitcases. Do I make two trips? Do I ask for help? What about getting an Uber? I’ve never done that before.

My anxiety is killing me.

Also, the apartment still smells like whatever my roommate made for lunch yesterday and it’s making me gag.

Now I’m up crying because my family is having another holiday gathering when I get home because I was sick on Thanksgiving and in treatment on Christmas. My family is amazing. I already miss them so much. I’m so lucky. 

Does being a skeptic make you more resilient?

When you are in recovery, you are bound to encounter the topic of “resilience”. It’s a certain toughness – an ability to bounce back from adversity. 

Not only am I in recovery myself, but I also spend a lot of time working as a peer supporter to help others. “Resilience” is the topic for a support group I’m going to facilitate. Obviously, I’m not going to bring up atheism or religion in the support group, but I thought it might be interesting to discuss here.

One of the ways I have overcome a lot of difficulty in my own recovery is by finding ways to stay grounded. As a person who has experienced psychosis, this can be especially difficult. Being an atheist grounds me. I know everything has an earthly explanation – even my psychotic symptoms. I am very aware of my illness which keeps me in treatment. I have seen my medications work so I choose to stay on them. The evidence presented in my wellness is key. 

Skepticism when it comes to my mental illness symptoms is crucial. I need the ability to question what I see, hear, and think. This also keeps me grounded and strengthens my resilience. It also lets me know when to ask for help.

Sometimes being resilient means keeping the bigger picture in mind. Knowing that a better life doesn’t exist after death reminds me to pursue the things I love and live with passion – right here and now. 

Are you resilient? Can the ability to question the world around you make you a little tougher in the face of adversity? I’d love to hear about your experiences.

Does being an atheist affect your values?

What do you value? Do you think about your values consciously? Unconsciously? Does being an atheist affect what you value?

I recently received treatment for an eating disorder and the center I was admitted to emphasized a “value-based” recovery. We did this activity called “value sort” where we were given 100 cards. Each card named and described a value. After several rounds of narrowing down the values that were important to us, we made a list of our top ten. Here’s mine:

  1. Passion
  2. Family
  3. Purpose
  4. Acceptance
  5. Loving
  6. Loved
  7. Creativity
  8. Achievement
  9. Sexuality
  10. Contribution

Once you had your list, we often used our values in groups and activities. 

This was unlike any other mental health treatment I had ever received before. It was tailored to what was important to me and my life. Treatment was very intense but also meaningful. 

The values I chose feel like what I would have chosen ten or twenty years ago. I don’t change much. Many of the values were ingrained in me as a child and fit my personality.

There were values such as “faith” and “spirituality” in the deck of 100 cards – obviously, I didn’t pick those. But other than that, I don’t feel being an atheist affected my other choices. Maybe it affects the way I view and live my values but not necessarily why I chose them. I am really curious if any of you feel atheism affects your values.

Also, do you ever spend time thinking about your values, or is it more of a natural undercurrent in what you do in life?

The worst stigma is my own. (Mental Illness Recovery)

This is a tough post to write. Stigma is a sensitive topic; when it comes from yourself, it is associated with embarrassment and shame. Living with a mental illness is not easy and I don’t know any different. Medication is a game-changer but not a cure-all. Even when your symptoms go away you are left with a label. 

Stress exacerbates symptoms. So what do you do? Do you stay home and take it easy or do you see what the world has to offer? Either option is going to cost you. 

I have taken lithium for years.

In my early twenties, I tried several mood stabilizers with little success. I was still pretty new to the game having only been in recovery for a couple of years. My psychiatrist suggested lithium and it was definitely a drug I had heard of before – something I associated with “crazy” people. The routine bloodwork sounded scary as well. This was serious. As much as I was scared of being labeled “crazy” I also really wanted relief, so I reluctantly tried the medication.

Starting lithium came with some mental anguish, but now I’ve been on the med for many years and I take it every day without thinking twice about it. It really works for me. The stress I felt trying lithium was meaningless and counterproductive. 

I was treated for anorexia at 200 pounds.

This was more recent. I’ve struggled with eating disorders since the sixth grade. Last fall I felt myself slipping fast. I was very sick and I hit a point of no return around Thanksgiving. I knew I needed treatment. It was so difficult to reach out to treatment centers because I didn’t think anyone would take me seriously. I was overweight but also starving myself. I thought I would never get the treatment I needed, but thankfully when I called for help, people listened. 

It’s embarrassing to talk about having symptoms of anorexia when you look like me, but when I was admitted to the treatment center I saw people of all sizes. I thought I wouldn’t get the help I needed, but I was wrong. 

I was also treated for avoidant/restrictive food intake disorder (ARFID) and rumination disorder which I find much easier to talk about. 

I’m still very embarrassed about struggling with anorexia. The truth is eating disorders affect people of all sizes. I’m still coming to terms with that.

I still believe that no one will take me seriously.

Worrying about being taken seriously is a common theme in my life. I’m sure people see me as “crazy”. I’m open about my experiences which probably makes it worse, right?

I know my mental illness doesn’t define me, but it does explain a lot about why I do the things I do. I’m always trying to prove myself, mostly by taking on more and more projects. I want to tell the world, “look what I can do!” I feel that with having a mental illness that’s necessary.

But what if it’s not? What if no one actually cares if I have a mental illness?

My Pledge to Myself

My recovery will be a lifelong process. There are so many outside forces at play when you have a mental illness but the important conversations happen between you and your doctor. I let the world get to me and internalize negativity. My pledge to myself is to keep an open mind when it comes to treatment and mental health in general. This is my life and no matter how “crazy” I think I look my health is important. 

Can anyone relate? What stigma holds you back?

Does anxiety get worse with age?

I’ve always been an anxious person – even in childhood. I write about it a lot. Sometimes that’s all I can do with this nervous energy.

When I think back on certain events in my life it has become pretty clear that my anxiety has gotten worse with age. This is most apparent when it comes to my fear of driving. In the past, I was willing to drive greater distances. I even took a road trip by myself in my late twenties. Now as I inch closer to my 40th birthday, I stay within a few miles of my house. It even makes me nervous to take my daughter to school which is only a four-minute drive.

I’ve also noticed that since I had my daughter my anxiety has exploded. Can any other parents relate? I have a lot of sleepless nights and she’s not even a baby anymore.

I have a lot of mental health issues, and I see a therapist every week, but I think I need to do more work on my own to prevent my anxiety from getting any worse. I need to gently push myself to do the things that make me nervous. Any suggestions?

I have a hard time with the grocery store. People and food make me nervous and I never go shopping alone. Maybe I should start there.

Obviously, I will address this more with my therapist, but I always love getting your input. Are there any other anxious people out there? Did your anxiety get worse with age? How do you cope?

Atheism and Recovery – What if I didn’t have a mental illness?

I became an atheist early in my recovery and it remains an important part of my life to this day. I was diagnosed with schizoaffective disorder in my twenties. Dealing with psychosis was confusing and frightening but when I tried medication everything changed. I had always been skeptical but when I experienced hallucinations that were spiritual in nature I was left with a lot of questions. A moment of clarity came when the anti-psychotics kicked in. My hallucinations aren’t real – and neither is god. I was always looking for an explanation. I just never considered the explanation to be a mental illness. My diagnosis came with some relief – this is treatable.

That moment of clarity flipped a switch and I declared myself an atheist. Years of suffering came to an end with a simple solution – medication. 

But what if that moment never came? What if I never had a mental illness? Would I still be an atheist?

First of all, my husband asked me this question and it is so hard to picture. My mental health symptoms started in early childhood so I really don’t know any different. I am not my illness but it is still an important part of me. It often explains why I do the things I do.

My journey to becoming an atheist may be a little unique, but I still believe even if none of the mental health issues happened, I would still be an atheist.

I’m a curious person – it’s always been in my nature to question. I questioned the existence of god in childhood and the judgmental people in the town where I grew up definitely made me question the goodness of Christianity. Mental illness or not, I always knew I didn’t want to be like them. Questioning at that time came with a lot of guilt and fear but I feel no matter what I would have ended up with the same conclusion – I am an atheist.

Were there any specific events that led to your atheism? If those events hadn’t happened, do you still think you would be an atheist?