Sign the Guest Book and share your Blogs!
WELCOME!
Many great people have visited and commented on this blog. But this good stuff gets buried in the volume. So, I’d love to capture something about you here – whatever you’d like to share, even if just your first name. (Or nothing – just thanks for coming!)
Here’s some stuff to consider sharing -
- Your first name or username/handle
- Your diagnosis or challenge
- If you are here as a supportive friend or family member (thank you!)
This can also be a way to share your OWN webpage or blog! (NONE OF THIS IS REQUIRED!)
- Address of your webpage, blog or forum
- A way to contact you (e.g. email)
- YOUR favorite places on the Internet
- Anything you find help for FUN
(The comments form may ask for your email and webpage. I do not publish these, and I believe you can comments without providing anything but a name/handle.)
Thank you for coming! My best,
Emily et al.
49 Comments»
Dear Emily,
Thank you for leaving your comment under the article of my story in Newsweek Magazine, “Inside Karen’s Crowded Mind”. I recently started my own blog “Ask Karen” on our http://www.switchingtime.wordpress.com. website. Please visit. Dr. Baer and I are looking forward to our paperback coming out on September 9th., 2008. I am now answering questions and would love to hear from you! Also, I am glad to hear you are interested in writing your own story. There is so much yet to learn about MPD/DID. I wish you all the best!
Karen Overhill
“Switching Time”
Hi Emily,
Thes things you know, but hey, who can resist a guest book huh?
My name is Anna. I used to go by many names, most often Leonie and Imoh and Anne, as I has a number of personalities created in response to severe childhood trauma. (More than those three, but they were the three main “fronters”)
After many years of therapy I have integrated and love it very much. I still miss my personalities, but less so the more I remember that I/Anna am really them, after all, just with one thread of beingness now, not many.
My journal can be found here,
http://tigerweave.livejournal.com/
and I write about whatever takes my fancy. Often it can be about DID/Multiplicity, and often it can be about my writing. I am writing a fantasy book I am aiming to get published soon.
With love,
Anna.
emily,
i miss you.
i hope you are ok.
i see you having trouble with people stealing your stuff. that is not right. good for you for standing up for yourself.
you are one smart lady.
Dear Emily,
I am glad I found your blog. I am newly diagnosed DID ( one month) and just getting to know my internal system. My system first presented in emotions, all separated with different jobs– as I continued to write…..the parts came out in colors and names that are related to the part’s function.
Its actually pretty intense and draining….just wondering if anyone could share tips on how to handle getting to know more about one’s parts and if any one experienced their parts coming out in stages like this.
Thanks for sharing through your blog!
Kathyscolors
Dear Emily,
Thank you for the encouragement and support. Funny, for years I have been feeling that writing would be the thing that saved me–I’m just now beginning to grasp how.
This morning I read a post here about continuing with a therapist that does not have the neccessary experience with DID. This was so helpful . I am transitioning from a therapist who is/was accepting, supportive, warm, etc….but who simply doesn’t know what to do with me at this stage to one who trained and has worked with DID clients for 20 years. I can already see more markers on the path. Not that we know exactly what will happen next–its more that I feel that she knows what to do with what comes up as it unfolds. Your post confirmed for me to trust my often hard to find gut about this.
I look forward to reading more! Thank you, thank you.
Kathy
It is a very thought provoking site. You are supportive and encouraging but you are not afraid to ask the hard questions. I am glad because the questions I ask myself are hard too. This is not an intellectual excercise with me. It is intrinsic to my system. Doubting was what kept me from being assimilated. I was Dx’d nine years ago with DDNOS because I have few alters and because I am co-conscious. Well, not competely. When I had a crisis last year and switched I could not remember the event for a week. The demeanor and emotions I exhibited – child crying, mature adult speaking logically switched back and forth in a way that inspired my doc to order a psych eval. As far as I was concerned though I was not afraid at all. My child alter was terrified. My wife is very supportive of me. She is more supportive of him than I am. She has said many times “if I could take a video of you, you would never doubt again.” She want the whole me. I feel empty sometimes. My child told her I was a shell. The others had to be taken down because I could not be hurt as much. That was a paraphrase. His way of talking and thinking is rather idiosyncratic and concrete. At any rate I am glad I found your site.
cami, In the beginning my wife sat in on some therapy sessions. She and the therapist said that if they could take a video of me then I would not be able to deny the child’s existence. I said “whatever” but they never got around to doing it. One night when I was half asleep she was talking to the little one. That is when he talked about them “going down” I suppose that in more abstract terms what he was saying was that went underneath my conscious awareness. He, the little one apparently was down there too. He called the place where he lived a tree because it was like being in the hollow of a tree. It was a very small dark place and there was no way to get out. He could not touch anyone and no one could hear him. No one neven knew he was there. He was alone. That is what he talks about as he cries “alone alone alone” I cannot understand i those feelings. All I can think is that it must be how a person would feel after many years of isolation. It doesnt make sense though because I never was isolated like that. In fact, I do not care about being with others. I never get lonely. When he came out I was able to see things through his eyes (you know what I mean by that). It was strange. The world looked like an entirely new place. I had never imagined what that would be like but there it was.. What mattered to him about it was sensory things like colors. Then there were all those objects for which he had no name and explanation. What he liked the most was the sky because unlike his tree which was very small there seemed to be no ceiling. He would talk endlessly about blue and how it goes up and up. And the sun too because he world had been dark. I have been to therapy off and on for a long time. I have observed that he apparenly is unable to construct images in his head, that is, he cannot imagine things. Except for his peculiar ideas which have meaning only to him, a thing is just a thing. Therapists never got that and when they said something like “lets build a house” He would say he could not and when they insisted he could he would get angry at them. He knew he could not build a house. One thing I found that seemed to validate my impressions of him was when I studied how eye movements reflect inner cognitive processes. Having watched him for a long time (from the outside, as it were) I realized one day that his eye movements indicated that when he thought all he ever did was recall and at NO time did he ever make anything up. That supported what I had already seen and it went against my idea that this whole thing was something that was made up. He never makes things up. That is the way he presented himself in the very beginning and in all this time his personality has remained constant That is who he is. My wife says he has the extremes of my emotions. both sadness and happiness. I am deficient in both. Maybe in some ways he is more real than I am. Now that is a weird thought! Ok I think my posts are too long. Ty for replying
NOt sure where to start really…for years I have struggled with depression and anorexia/bulima, then had a major episode 9 years ago, and diagnosed with ptsd. Before this I really thought I was crazy, worked in health care, was convinced I was schziophrenic, just kept trying to push things away. Once I was diagnosed with ptsd, researching it I came across information on dissociation..wow I thought that is so me, I was so afraid to tell anyone for years about voices in my head, lost time, forgetting how to drive etc, even then though I found some way to rational all of these things as normal. Two years ago started seeing a new therapist for ptsd mainly because she did EMDR, she has been great, but even after two years we have not been able to get to the point of doing EMDR. As time went on and I trusted her more I guess I told her things.Just recently she recommended I see a doc for medication review and she told me this doc specialises in dissociation issues. Anyway they had me do the MID test, I do not have the results yet, but the whole test freaked me out big time. I found it very hard to do, and struggled with telling the true, questioning if I even was telling the truth, that I was just imagining it all and was looking for attention etc. I have spent the last week researching and I have great access to university liberary and reputable journals etc, I was desperately looking for anything to debunk DID on one hand and on the other looking for validation of my symptoms. I also was very angry, and scared. I dont have alter with names at least I dont think so
, but do hear voices, get images in my head with these voices. I have a child that can fly, jump to high places, a bit of a superhero, and I am freaked as I am wondering now what if she is an alter /part and it how I have fracture a vertabrae, cracked ribs, sprain ankle and have no idea how I did that. I know I for sure dissociate and I accept that… but could I really have DID, i just feel right now that everything is coming to a head, my head is full of noise, and emotions are on and off constantly. I did tell my therapist the other day something that I did unaware of the time that is vastly out of charachter for me, kinda embarssing, intially I told her it in a half truth I think checking her reactions to it, and then felt it was ok to tell her the real truth which given everything I have read about DID does truly point to that. Sometimes I am very aware of voices telling me what to do, or commenting, but they dont have a name , so maybe I am not. I too am very weary of the implications of this diagnosis, I have two kids that I adore and live for, they keep me sane, and while |Im not a perfect mom, I do a pretty good job, actually between work and them, I structure my life pretty good and feel safe most of the time. Any any input or advice would be great, I know there are other test out there other than the MID, Multidimensional inventory of dissociation. Although all the studies done using the MID were bang on, with confidence intervals over 95%, proper P values etc..my rational side and educational background can t argue with it, but man I still try. oH ya that the other think i never say We or us, although my ex husband still teases me as I always used to say I had a talk with myself, but again its all me and I…so maybe im not DID. Thanks for the great website and info it has really helped I thinki
Thanks for replying it means alot to me. What gave me the courage to post was the fact you like to research like me..Im obsessive about it. Also I read you bring in articles info to doc to discuss, I do too. Your advice re diagnosis hit home, yes I need hard science but DiD research is what I consider soft science as its subjective, how did you get your head around that. The evidence is there within me and my actions, but I just cant seem to accept it. It doesnt help that a voice is belittling me for even thinking that I might be, telling me im nuts etc, I think this is also the voice that prevents my T from getting anywhere with me, its stubborn and feisty, but \i think at heart its very afraid. Does that make sense. Anyway sorry if this is an inappropriate place to ask this questions etc, but I am just so relief someone actually anwered me.
Thanks again and sorry for bugging you for info, if my slang seems weird or anything its because I am irish and it comes out sometimes even though I have lived in N America for a long time.
Thanks again for your time
Hi,
We found your blog through SecretShadows just recently – although I’m being told by another part that she found it ages ago when you did a post about needing to change therapists. Ok that sentence probably gives an indication that this body carries the diagnosis DID.
Similarly to what anita has mentioned earlier, we experience cycles of denial about the diagnosis. We recently changed therapists in the hopes that the previous therapist was causing all the symptoms and encouraging the dissociation. As librarians we’ve read many peer reviewed articles which describe DID in a very negative light. In many ways it was easier to believe that we were making it all up – why would anyone want to own the history of this body?
We’re incredibly detached from this body and everything at the moment. We have a blog, but there is a tension about what it should do and be. We’re not good advocates or examples of what it’s like to be living with DID. We’re not sure how to balance sending a positive concept of the functioning level of someone with DID and being honest with the craziness that goes on in this head at times. We also just don’t have a gift with words. We have a background in the Sciences as this didn’t need emotion or creativity – concepts we’re not particularly good with.
We’d just like to say Thank you for the great blog you have created here. Anything positive about DID is always good to see.
Take care
castorgirl
Hi Castorgirl
It doesn’t matter to me how you get here, or how many times it takes you to find me! Welcome welcome welcome to all of you!!!!!
I am SORRY that you have the idea that your therapist brought this about. I can understand that – you find this out in therapy…and just wonder. Especially about the stuff with the False Memory Syndrome.
Castorgirl…Anita…each of you…right now, it doesn’t matter why you are here, or what is going on inside you….you are YOU! No matter what is inside. SCREW WHAT OTHER PEOPLE THINK!!! You are learning about you…that is what is most important…you will be like me…and research all the time. That is fine. But like me, you have to start giving some credence to the voice inside that tell you, yes, Gastorgirl, this is who you are. And just hearing those parts of you… will help with the denial.
I will admit…I am in the very beginning of my own journey, and I realize that after talking with people here, especially David. I also have made progress…there is such a range. I know it is hard, but try not to give yourself a hard time. Just learn about YOURSELF. If your first therapist somehow planted this in you… that will come out. Don’t push it. Just work on who you are.
(hugs)
Emily (and some Camigwen)
Hi Emily and Camigwen,
Thank you… Instinctively we know that we’re not making this all up. Aimee and some of the others remember vividly the father telling them to stop talking in all those silly voices when the body was about 9… which was each of the younger ones talking in their own voices. Our solution to this was to create a spokeswoman
The mother is a nurse and now realises behaviours that she saw during the teens were dissociative.
But in order to keep going we had to have parts that kept this perfect childhood happening. So it’s like there are these parallel truths and its trying to get them to mesh or be worked out that’s the hard bit. I was born to keep being a happy teenager… I know this and I know the facts about why I needed to be born. Doesn’t make it any easier to cope with though. So some of us look at the images of the perfect childhood and hope that it is the truth.
We’re three years into therapy, but only had the DID diagnosis for a year or so. As the others said, most of us aren’t good at emotions so the whole therapy thing can be a bit of a struggle… We’ve got a couple who openly told the last therapist to shut up with the “b****y therapy c**p”… Ohhh yes we must be the ideal client for any therapist… lol
Again, thanks and take care…
Sophie
Emily,
This is the first DID site I’ve come across that I feel like I can relate to. I was diagnosed DID almost 20 years ago. Now back in therapy for work on integration. Thank you for your intelligence, humor, and creativity. I very much appreciate the honesty of your writing and the variety of opinions that I find here.
Thank you, thank you,
Cerulean 468
greetings Emily, I’m Bob & I would like to let you know that I emphathize with you . I helped Nomad with her journey by being a support person, I am a person in her book, titled Snow Angels, that you can see reviews and excerpts on http://www.nomadrose.com. Please feel free to email me if you have any questions. I hope your path is going well, sincerely Bob…
Greetings Emily&all, Hope all is peaceful with your system, I remember as NomadRose was learning about herself &the rest of her, there were some pretty rough times. It has been very peaceful for quite some time. If you get a chance peek at her web page. I would be glad to try to answer any questions you might have. There are many therapists out there,some open and some not, many different techniques to therapy, some will be progressive and some may even cause set backs. Never give up,there is always some stream of hope. I hope you have a good support system. Please take care of yourself. Bob…
Greetings Cami/Emily, I hope you got my email, I have not been blogging long,infact your site is the first I wrote on. Should I have responded to your email on this page?? I wrote on the forward of the email you sent me. Please let me know if I am goofing up,as I know I am technologically challenged. But, a very quick learner. Please take care of you and yours. Later Bob…
greetings from Bob, I know now my tech/error, sorry but that one went to cyberspace. I answered your question concerning Nomad’s story. I am the character referred to as Love. I notice that there are times that you sign off with a different name, is there a special greeting that you prefer so as to not leave anyone out in corresponding back and forth? I know the importance of acknowledging all who may be attentive to words. For each and everyone holds a very special function to the system. Please take care, I look forward to your response,Bob…
To Camigwen, I just came across your March 11th update, sensing a lot of frustration with job seeking??? I can relate to this, although I am on a small pension I have been sending out resumes to switch over into casework or casemanagement. Not much going on here in the line of success. I will pass on a word of encouragement though, your ability and some of your talents are reflected in your site. I don’t know what you are seeking in employment but have you considered advertising your talent on youtube?? Sometimes it is just plain old location,location, location. You do have a lot to offer. Best wishes Bob…
Good point, sorry ,anonimity slipped my thinking. Nomad is the same way. I had heard that some people were advertising their skills on the web in order to gain employment. We have’nt figured out how to market a book without getting public with it. Your talent is apparent, please be encouraged , I know that does’nt pay the bills. Camigwen is an interesting name, does it hold a specific meaning? Sorry if that is too personal, just curious. I know alot of Nomad’s different alters had meaningful names. Please take care , aaI look forward to your response. Bob…
Bob,will sign off for a while,I will be proceeding to chemo & a kidney transplant in the near future. My best of hopes to you all in your future. Later Bob…
Greetings Cami& All, This is Bob, Starting dyalisis August 11th,Got a P.D. catheter put in last week, that hurt. I hope you are all doing well and progressing with your journey. I am now 3 months into the wait for a kidney, they tell me that the usual wait for this region is 1 year. They also say that dyalisis will make me feel alot better. I did just return to my part time job yesterday, did I tell you that I did patient transport for a pschyiatric hospital in the midwest?? We serve ages 3-21,and are becoming a nationally known facility. I do admissions and discharges mostly in Missouri, Oklahoma and Nebraska. It is probably the best retirment job ever. I get to get kids to a place where they can get help, and take them home when they are ready. Thanks for thinking of me, I will get along one day at a time. Please let me know how you all are, I think your blog is great. You All take care, Later Bob…
Greetings again to Camigwen & All, This is Bob again. I had a thought to a previous bit that I wrote you concerning your writing, The Writer’s Market, the book probably available at a Library, has resources of magazines,periodicals looking for articles short to long to fill their publications. Just a thought but you do have a talent. Hope things are going well for you all, Bob will be okay, I’m a survivor…





i go through cycles of believing i am d.i.d. on a ‘not believing cycle’ right now, so it is easy to read what others go through.
Thanks for sharing your experiences. I enjoy your sense of humor. You are a delight.