Loneliness

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Dissociation / fractured mind

Hi 👋 I don’t have DID, but BPD and PTSD with dissociation symptoms. It’s less than a year ago since I was told by my therapist that I have this. I had never heard about it before.

I’ve tried to understand and learn about it, but it’s hard when my fractured mind/memory even makes me forget some days that I have this symptom. There has also been a lot of grieving. Understanding and seeing that my mind has erased, and is still erasing memories - as a part of a survival technique that I have no control of. It all happens automatically.

My BPD splitting happens so fast. My whole perception of the world and people changes. Some times I don’t even remember what this version of me says or does. It’a painful to find a bag of clothes and my passport, knowing that this version of me packed my bag in despair - probably over a minor argument.

It’s hard to write down childhood trauma, only to forget about this days later. Having to re-read my own trauma, and re-remember over and over, and learn that these things happened. Having to re-remember, in order to remember why I should stay away from family members to protect myself - to this day.

I am tired of not feeling like a whole person. Even good memories feels like another person - or that it actually didn’t happen to me - just another version of me.

Days waking up wondering if I’m really here. That I’m still alive, and not the zombie I see in the mirror.

I’m grieving over the little girl in me who used to hide in the woods. All alone and nobody to talk to. Not even knowing how to talk about feelings. So lonely that a tree could feel like a needed friend.

It’s hard to not be able to see the whole picture - my own timeline - most of the time. And the constant erasing of memories makes me feel like living in a fog. I want to be whole. I want to be here.

#dissociativeamnesia #PTSD #BorderlinePersonalityDisorder

(edited)
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Dissociation / fractured mind

Hi 👋 I don’t have DID, but BPD and PTSD with dissociation symptoms. It’s less than a year ago since I was told by my therapist that I have this. I had never heard about it before.

I’ve tried to understand and learn about it, but it’s hard when my fractured mind/memory even makes me forget some days that I have this symptom. There has also been a lot of grieving. Understanding and seeing that my mind has erased, and is still erasing memories - as a part of a survival technique that I have no control of. It all happens automatically.

My BPD splitting happens so fast. My whole perception of the world and people changes. Some times I don’t even remember what this version of me says or does. It’a painful to find a bag of clothes and my passport, knowing that this version of me packed my bag in despair - probably over a minor argument.

It’s hard to write down childhood trauma, only to forget about this days later. Having to re-read my own trauma, and re-remember over and over, and learn that these things happened. Having to re-remember, in order to remember why I should stay away from family members to protect myself - to this day.

I am tired of not feeling like a whole person. Even good memories feels like another person - or that it actually didn’t happen to me - just another version of me.

Days waking up wondering if I’m really here. That I’m still alive, and not the zombie I see in the mirror.

I’m grieving over the little girl in me who used to hide in the woods. All alone and nobody to talk to. Not even knowing how to talk about feelings. So lonely that a tree could feel like a needed friend.

It’s hard to not be able to see the whole picture - my own timeline - most of the time. And the constant erasing of memories makes me feel like living in a fog. I want to be whole. I want to be here.

#dissociativeamnesia #PTSD #BorderlinePersonalityDisorder

(edited)
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Dissociation / fractured mind

Hi 👋 I don’t have DID, but BPD and PTSD with dissociation symptoms. It’s less than a year ago since I was told by my therapist that I have this. I had never heard about it before.

I’ve tried to understand and learn about it, but it’s hard when my fractured mind/memory even makes me forget some days that I have this symptom. There has also been a lot of grieving. Understanding and seeing that my mind has erased, and is still erasing memories - as a part of a survival technique that I have no control of. It all happens automatically.

My BPD splitting happens so fast. My whole perception of the world and people changes. Some times I don’t even remember what this version of me says or does. It’a painful to find a bag of clothes and my passpart, knowing that this version of me packed my bag in despair - probably over a minor argument.

It’s hard to write down childhood trauma, only to forget about this days later. Having to re-read my own trauma, and re-remember over and over, and learn that these things happened. Having to re-remember, in order to remember why I should stay away from family members to protect myself - to this day.

I am tired of not feeling like a whole person. Even good memories feels like another person - or that it actually didn’t happen to me - just another version of me.

Days waking up wondering if I’m really here. That I’m still alive, and not the zombie I see in the mirror.

I’m grieving over the little girl in me who used to hide in the woods. All alone and nobody to talk to. Not even knowing how to talk about feelings. So lonely that a tree could feel like a needed friend.

It’s hard to not be able to see the whole picture - my own timeline - most of the time. And the constant erasing of memories makes me feel like living in a fog. I want to be whole. I want to be here.

(edited)
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I can choose

I have multiple health issues. The main three are #POTS #EhlersDanlosSyndrome hypermobile type and #Fibromyalgia I have #Osteoarthritis , early disc degeneration and other spine and neck issues related to my hEDS.
I say "mine" because it is mine. The pain is mine. The experience of living with chronic illness is mine. The discouragement is mine as well. And, yes, I will claim the loneliness as mine, also.
None of us asked for this and I'm pretty sure most would want our health issues to be taken away, especially the pain.
But, do you know what is also mine? My choices. I can choose to praise God, even through the pain, or I can complain. I can choose to love my family, or let my pain overshadow the enjoyment of being a mom of many! I can choose to be compassionate to someone else's struggle or belittle their issues in comparison to my pain.
I can also choose to push myself or just accept my limitations and rest. I can choose to do my PT, eat right, take my supplements, ask for help and do things I enjoy.
Sometimes, the only thing I can do, is to lie on my back, in my bed or in the recliner and watch a movie with my children.
I did not choose my Trifecta of Misery, as I refer to my POTS, hEDS and fibromyalgia. But, I alone get to choose my experience with #ChronicIllness .

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Ineffective Collision

The loneliness is robbing every part of me
I have nothing left to give, no breath left, no energy
I am always waiting on you, praying that you will one day realize that time is not on our side
I think back on our early days, how in love we were; was it all just part of the honeymoon ride?
In science they talk of an ineffective collision - something that has a big impact yet without putting in energy and it never changes
I feel so lost, without words (is this us), a mistake as I flip through our wedding day photo pages
I reach out every chance I get yet you are miles away
You say you are tired too, are you too tired to stay?
I wish I had the answers to get our boat afloat again and I could reconnect with you
I am told the effort must come from my side to fight for what I want and then do
Yet I just feel like no priority to you at all
Thus this is my fear, that we are closer than we think to our downfall

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Ineffective Collision

The loneliness is robbing every part of me
I have nothing left to give, no breath left, no energy
I am always waiting on you, praying that you will one day realize that time is not on our side
I think back on our early days, how in love we were; was it all just part of the honeymoon ride?
In science they talk of an ineffective collision - something that has a big impact yet without putting in energy and it never changes
I feel so lost, without words (is this us), a mistake as I flip through our wedding day photo pages
I reach out every chance I get yet you are miles away
You say you are tired too, are you too tired to stay?
I wish I had the answers to get our boat afloat again and I could reconnect with you
I am told the effort must come from my side to fight for what I want and then do
Yet I just feel like no priority to you at all
Thus this is my fear, that we are closer than we think to our downfall

Post

5 Reasons Why ADHD People Have a Shorter Life Span than Neurotypicals

I saw a video recently where two people were talking about this topic and they blamed it solely on drugs, alcohol, smoking and bad choices, this is wrong, and a misunderstanding, It is mainly driven by our struggles with executive dysfunctions that permeate every area of life in a world designed for neurotypicals that have high executive functioning.

I want to talk about a topic that is very close to me. My aunt died in her sixties, aside from other health problems, the circumstance I believe were due to undiagnosed ADHD and lack of support, a lot of misunderstanding and a lot of judgements around her leading to critical isolation and preventable early death.

I made a good friend in the pandemic that I believe also was an undiagnosed ADHD woman in her late forties who died in similar circumstances that could have been prevented and mitigated due to the following 5 issues that ADHD people struggle with.

5 Reasons Why ADHD People Have a Shorter Life Span than Neurotypicals

Studies suggest that individuals with ADHD may have a shorter life expectancy compared to neurotypical individuals, primarily due to increased risks related to accidents, impulsivity, substance abuse, and health complications. Research indicates that:

On average, people with ADHD may live 8 to 13 years less than neurotypical individuals.

A 2019 study by Dr. Russell Barkley found that severe ADHD cases might reduce lifespan by up to 25 years in extreme cases due to poor self-regulation, increased stress, and unhealthy lifestyle choices.

The biggest contributing factors are higher rates of accidental injuries, risk-taking behaviors, obesity, and untreated mental health conditions.

However, proper diagnosis, treatment, and lifestyle changes (such as therapy, medication, exercise, and structured routines) can help mitigate these risks and improve longevity.

Would you like strategies to help improve life expectancy and health outcomes for ADHD?

Why Do ADHD Adults Have a Shorter Lifespan?

1. Executive Dysfunction & Life Management Struggles

Difficulty maintaining a livable environment (clutter, unsafe conditions).

Forgetting to eat properly or drink enough water.

Inconsistent hygiene and self-care routines.

Poor financial management leading to stress and instability.

Forgetting or mismanaging medication, missing doctor appointments.

2. Higher Risk of Accidents & Injuries

Impulsivity increases risk-taking behavior (reckless driving, not wearing seatbelts, unsafe sex, etc.).

Forgetfulness and inattention can lead to accidents, fires, injuries.

Difficulty following through on preventive health care (checkups, screenings,).

3. Chronic Stress, Burnout, & Mental Health Issues

ADHD is often accompanied by anxiety, depression, and emotional dysregulation.

Difficulty managing stress leads to higher cortisol levels, which contribute to heart disease and other health issues.

Overwhelm and burnout reduce motivation to take care of oneself.

4. Social Isolation & Support Gaps

Struggles with maintaining friendships and relationships.

Lack of a strong support system, which affects mental health.

Social rejection leads to loneliness, which increases mortality risk.

5. Unhealthy Coping Mechanisms

Higher likelihood of using alcohol, smoking, drugs, or food to self-soothe.

Irregular sleep patterns and chronic sleep deprivation (which increases risk of cardiovascular disease, obesity, and diabetes).

Is It Just Poor Choices? No—It’s a Systemic Issue.

It’s not just about making "bad choices"; it’s about living in a world that isn’t designed for ADHD brains. Neurotypical life requires strong executive functioning, which ADHD people struggle with. This leads to constant small failures (missed bills, health neglect, disorganization), which add up over time and take a toll on both physical and mental health.

What Can Help?

Externalized systems: Reminders, alarms, habit trackers, accountability partners.

Simplified self-care: Small, sustainable habits instead of all-or-nothing thinking.

ADHD-friendly financial management: Automated payments, budgeting apps, financial therapy.

Preventative healthcare: Setting appointments in advance, pairing medication with daily habits.

Community & support: Finding ADHD-friendly groups like The Mighty, find an ADHD check in buddy, coaching, therapy, and social connections.

Would you say your struggles fall mostly in one category, or is it a mix of everything?

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Just one list of journal prompts I did this week

Emotional Processing

1. What's been the most challenging part of this transition/change for me?

Nox: Having to keep track of everything and make calls and coordinate appointments. The meds change has been pretty taxing. But the hardest part of all is having to put so much energy in without getting anything in return, such as going out and having fun.

2. How have I been feeling lately? Try to describe it in as much detail as possible.

Nox: Completely drained, feeling like I’m chasing my tail. The depression from the negative medical news is draining and I still have to put all my energy into going to appointments and talking to doctors so I can answer their questions. I feel like I’m trapped in my body. I feel like I have no exit from this roller coaster. I’m also extremely lonely.

3. What are some emotions that I've been avoiding or trying to suppress?

Nox: Panic and paranoia. Dread.

Coping Mechanisms

1. What coping strategies have I used in the past to deal with difficult situations?

Nox: Talking to friends and my therapist. Listening to music, cooking and baking, meditating, arts and crafts.

2. Are there any new coping mechanisms I'd like to try?

Nox: I’m curious about crocheting.

3. What self-care activities can I incorporate into my daily routine?

Nox: I can do more mindful tea rituals.

Reframing Perspective

1. What's one positive aspect of this transition/change that I can focus on?

Nox: Now that I know what’s happening, I can focus on treating the underlying problems.

2. How can I reframe my negative thoughts about this situation?

Nox: I have good doctors that are taking good care of me.

3. What would I say to a friend who's going through a similar experience?

Nox: I would ask them what I can do to best support them through this trying time.

Goal Setting

1. What's one small goal I can achieve today to help me feel more in control?

Nox: I can schedule transportation to Binson’s for Monday so I can get the compression stockings.

2. What's something I've been putting off that I need to tackle?

Nox: The only thing I’ve been putting off is getting the compression stockings.

3. What's one step I can take today to move forward?

Nox: Delete number three.

Self-Compassion

1. What would I say to myself if I were a compassionate friend?

Nox: Let’s go out for coffee.

2. What's one thing I can do today to practice self-care?

Nox: I’m gonna make a really special coffee drink today.

3. What's something I'm proud of accomplishing, no matter how small it may seem?

Nox: I did really well in the Draw Me school when I was younger

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