by yakusoku » Fri May 23, 2014 10:06 pm
First, let me say, I am a mom (of a Kindergartener, and one on the way), diagnosed with DID. I have never been one to have a lot of unpredictable switching. I have to be massively triggered for it to happen without me blocking it. It does sometimes happen, but almost never outside of therapy at this point. So, while I do worry about my DID making me an unpredictable or unstable mother, the hardest thing I think is my occasional crises, which require extra therapy and more help from my H, and make me less able to live up to the high parenting standards I have for myself and I was able to do when more heavily dissociated from childhood parts and their stuff.
Second, I'd like to say, like some others, it sounds like your mother is my mom. Now, my mom has no diagnosis that I know of, of any kind. But, the screaming, throwing, invalidating (both memories of events and the validity of my own sense of self, feelings, etc.), different public representation of herself (not at my school, because she never bothered with that stuff, but at her work, where she is known as some amazing mother). Mostly, I managed to keep myself from the direct line of fire, and my oldest sister was the one who pushed against it and had the brunt of her reactions. I think I learned by watching what to do and not do, and split a lot of my needs off into other parts to avoid being vulnerable to her attacks. I also relate, because somehow I ended up pushing through and getting my B.A. from an Ivy League sort of University.
My mom had a tough upbringing, was abused by a neighbor, had instability in her parents marriage, and kind of crazy mom and a narcissistic dad. I know she loves her kids and probably wants to be the mom that they needed, but was incapable. She just wasn't able to be a safe person. I'm sad for her. Anyway, due to her stuff from at least toddlerhood and her revolving relationships with unsafe men, and inconsistent attachment potential by having so many people in and out of my life, I developed DID. Does my mom have it? I don't know. My T says she sound narcissistic and sociopathic. She probably has at least CPTSD and I have seen her dissociate before. She remembers things differently than they happened, but it's a pattern in my family, and a real mind-f---, for people to do that, and I can't tell if it's plain old denial, manipulation, or dissociation-related.
One thing I will say is that it is probably difficult to not grow up with some real challenges when you're raised by someone who is incapable of being a consistent attachment figure. It's good you had one in your dad, though his lack of availability from working presented some challenges there. We learn the world is a safe place when we are consistently responded to with care, have our basic needs met, etc. When we are responded to by the people we need with erratic or fear-inducing behavior, especially at early ages, it will cause problems. There can be parents who do so, because of DID, and parents without DID who do this. For example, I'm pretty sure, even though I blow it on the regular with my kid, that she is securely attached to me, and I have DID. I think it really depends on the person, their background, their triggers, and what sort of support they have. I was diagnosed when my daughter was 2.5. A lot of the triggers that she has presented in reaching certain ages hadn't come up yet, so I was very lucky to know what was going on when I started getting triggered in my interactions with my child, and have the support of a good therapist, friends at church who I could trust with my diagnosis, etc.
As for telling my child, there is a lot that would go into that decision. As of now, she's too young to understand. If she were actually encountering other "parts" of me, I think it would need to be explained. But, she does not. My system seems to work in a way that prioritizes my role as her Mommy when with her, always. And, for the most part, my alters feel safest just coming fully out in therapy, though have at home around my H and in other situations when massively triggered. She does know that I see a "Dr" whose job is to talk to me and help me work through how I feel about different things. This Dr also sees my H (her dad), because his issue actually triggered the dissociation episode that led to my diagnosis, so I went to see HIS T. She has met him, knows him to be a kind, fun person, who mom and dad both trust.
We also talk a lot about how mom and dad make mistakes and respond badly to things sometimes when we get upset, just like she sometimes does, so that she understands it's not her "fault" when we make bad choices (even if she was misbehaving at the time, it was our mistake), and go out of my way to validate her feelings and experiences. Because a majority of my dissociation and denial seems to have manifested due to my own experience of invalidation, this has always been an important part of parenting for me, though less so for my H.
When she is older, and can understand, and especially if I am still in therapy for it, I will probably tell her about the diagnosis itself, rather than the vagueness of my needing help to work through things. By then, she would be able to understand what it is, and what situations would be appropriate to discuss it (with a close confidante) vs. not (commencement speech, anyone?).
I guess I think, as long as you're giving the message that mom and dad aren't perfect, and they (as children) are not responsible for mom and dad's bad behavior, and not invalidating the bad behavior as if it never happened, or excusing it by blaming the child for it, that would facilitate the point of sharing the diagnosis itself. I mean, sometimes when a kid behaves a certain way, in the real world, people will react and make mistakes, and it's not realistic for a parent to respond perfectly every time, and that will not prepare them for the real world...but that doesn't mean you get to blame the kid for your less-than-optimal response and it's important that a parent be able to deal with their failure, own it, acknowledge it, validate the child. My mom being unable to reconcile her parenting failures with the ideal self she needed to see herself as was the source of my being invalidated repeatedly.
Anyway, off-topic there, sorry. In the case where a parent switches frequently and has no memory, I can see where it would be more important to communicate about the actual diagnosis at an age-appropriate time, though. Otherwise, the contradictions in behavior and memory would be crazy-making for the poor child. Only a parent (maybe along with their therapeutic team) would be able to make the call about what is right for that family, and even each child, when they might be ready to understand...
Sorry for writing so much. As a parent with DID, and as a child who experienced a similar upbringing to yours in some ways, I wanted to reply in depth.