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A reader asks "How do I stop myself from making social gaffes?" Good question. I've got three solutions for you.
Being diagnosed as bipolar is a scary thing. It can happen in a number of ways, but if you’re like most of us, you probably didn’t know what was wrong for a long time, then you were misdiagnosed and then sometime later, you got the moniker of “bipolar”. Few of us go right from episode to bipolar diagnosis. But regardless of how you got here, what do you do next?
Family-Based Maudsley Therapy Is Not a Do-It-Yourself Approach There is a mistaken idea out there that Maudsley treatment for eating disorders is something parents can just decide to do without professional support. While I know families who do take on the re-feeding (weight restoration) responsibilities, I think it is important to keep in mind that this is only one part of the approach, and why it works well for so many families.
Recently, someone directed me to this article on parents who give up custody to get help for their mentally ill children. It hits hard now, as I live in a state that is about to vote on its own renunciation of the so-called "Obamacare" plan. We celebrate people living with deadly diseases and chronic conditions, and great strides are being made toward prolonging and improving their lives. But we still vilify people who live with psychiatric illnesses? Am I the only person who thinks this is a problem?
If you struggle with ADHD and insomnia, then you may be able to relate to my pain. I'm a raving night zombie, but I've come up with a plan to help me break the chain. Now, if only I would follow it.
When most of us were young we learned that life isn’t fair. Yes, that boy got a bigger slice of cake than you. Yes, that girl gets better grades than you even though she doesn’t study. Yes, that’s boy’s imaginary friend’s clothes are nicer than yours. Life isn’t fair. But when I was diagnosed with bipolar at 20, my definition of “unfair” had to be reviewed.
Maybe because I was once diagnosed with minimal brain dysfunction, I don’t find the newer label of ADHD so bad. MBD sounds like something the cast of Monty Python and the Flying Circus came up with. ADHD on the other hand sounds somewhat more descriptive and less post lobotomy-ish. This is why I was so surprised to encounter somebody yesterday so embarrassed by the ADHD label, they censored me. Is someone else's ADHD self-stigma something I need to better understand?
It's Summertime, and the livin’s...easy? Maybe not. It used to be, until I became the parent of a school-aged "MI" child.
Recognizing When The Patient - Or the Team - Isn't In Control Because I'm so big on getting parents to get engaged and be empowered to support an eating disorder patient to full recovery, it is hard to talk about the other side of this: letting go. But that is part of the picture, too.
Amanda_HP
Media images can be very powerful. When we see something, especially when it's "based on a true story," our mind removes the words "based on a" and we are left with "true story;" as if what we are seeing on the screen is the absolute truth. In fact, the "based on" means it's an adaptation of a story with a lot of "Hollywood" thrown in to keep you interested.

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B.
This is so validating. Both my brother and I have ADHD, though being a woman I was late diagnosed in my 30s. I'm now in my 40s. We both have a horrid sense of direction to the point where I have been lost and found my way back going against my instincts. I will CONFIDENTLY turn in the wrong direction every time. I have trouble leaving a store in the mall without turning the wrong way once I leave. I have lost my car in the parking lot nearly every time to the point I was convinced someone stole it. My husband thinks it's charming and quirky but I spent half my life lost. Voice and visual GPS has helped immensely but I absolutely hate going somewhere for the first 4-5 times until I am familiar with an area. It's wild to see so many also experience this. Also although my meds have helped a ton it has not helped with this.
Honest
"Charming", "endearing"? When, at what point in the film? This character was neither. She was annoying at best. I had to rewind multiple times before 17 minutes b/c I didn't know what was going on and she was UGH maddening. Egotistical. She was written as stupid, which I do not appreciate in general. Btw, Kristen Wiig TOO OFTEN includes in her performances MOUTHING something. What? What did she say? CC does not pick up mouthing. SHE needs to ALWAYS add into her work on screen or other characters are saying AND for sight challenged people that dialog should be be SPOKEN. Why does she too often do this? I gave up at 25:00 minutes. What is Kristen trying to work out in mer mind playing these types of characters. She certainly is not educating society.
Danni
I can totly relate have been running my own dog grooming business single handled for past 17 years.3 weeks ago a was unwell with a severe flu virus. NOW have extreme anxiety 24/7 have panic attacks at the thought of going back to work ( which I really enjoy). Some days I don't even want to get out of bed,other days I do the bare minimum house hold chores.These last 3 weeks have been awful, can anyone else relate ?
Frank
Hey, I just wanted to reach out and say that many people who are living with Dissociative Identity Disorder can entirely understand and appreciate where you're coming from.

The fact is that there is too much misinformation about fictional introjects online. People will discover the term and find it interesting and exciting. They will disregard the fact that these alters form from severe trauma and will envy the experience of those living with DID because they want to meet their favourite fictional characters, or they want to have a support system that feels like it's magically there for them. It's very common in younger people, especially with the speed at which this kind of misinformation can spread on platforms such as tiktok.

Your scepticism on the existence of introjects is entirely valid. Much of what you described is indeed not reflective of the DID experience and is rather reflective of the internet culture that has fetishised it. Many people with DID, and many fictional introjects elect to not be open about the disorder online because of the very things you mentioned here. These things have also made treatment and mental health support much harder for those with the disorder to access.

I'm sure I'm not alone in saying that the things I've seen online have made me feel deeply ashamed of having DID, and particularly having fictional introjects. I'm truly sorry that you've had to experience situations in which people claiming to be introjects have treated you poorly.

Please be assured that the actions of young, misguided people online is not representative of the DID community as a whole, and it is certainly not representative of living with or as an introject. We're tired of it too.

My biggest recommendation for you is to steer clear of spaces that claim to be geared towards DID, but allow or encourage the above described behaviour. I hope you find yourself in a kinder community soon.

Keep safe - Frank
C
I feel I cannot hold on. For the last few years I have been loosing more and more with no recovery. My breakdowns are costing me my family relationships. They just do know what else to do and they are feeling the pain too. We have no help,hope no one I just kept hoping I do not inhale another breath help