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You all are great! Thanks! I got one message from some one to remind me to break long posts into paragraphs. I have to remember that. Often I'm a bit overwhelmed when I post. God! I published two books and a pile of articles and forget the basics of writing when I'm out of it! I'm sure I'll visit here often. Every day gets a little better. In a sense, I'm coming out of the trauma closet as well. I never sought help before, therapeutic or in this kind of forum. I've had a good life. By the way, we do not regret adopting her. Our love will not go away. but this has been the hardest few months of our lives. It's quite a test of our...I don't know..Committment? Character? Abilty to remain sane ourselves? One thing I do know: she is suffering far more than us. It puts things in perspective. I have to remember that when I start whining.
 
(((Old Dreamer)))

Welcome to the forum. I'm sorry you and your wife are having to cope with this. I imagine you are both in a kind of shock with what you have learnt. I'm glad to hear you are in therapy and are able to talk yhrough your feelings.

There are some great articles on the home page and also some recommended reading which may help.

And just letting me here that we're not alone is a big help.

Knowing that I am not alone was a huge realisation. Before I found the forum, I was convinced I was mad and that no-one else could possibly feel this way. However here I have found support, love and friendship. The posts are so good, almost inspirational and with good humour.

I wish you and your family well. Please take care of yourself as well.
KP
 
Thanks! We're doing the best we can. My wife's down with the flu so I did the week's shopping and errands and took a two mile dog walk. Amazing how that relieves stress!
 
you've had a time of it all right. i can somewhat sympathize/empathize. You see, my son is the joy of my life. When he was born - took me a long time to have him for alot of reasons, along with miscarriages - it was not your average experience. We found out at 32 weeks that he had spina bifida. over the next few weeks, there were ultrasounds, trips to hospitals, specialists, transport teams, etc. and me getting ducks in a row. My marriage was strained and voila. time to give birth. That morning in the delivery room, there were 15 people besides me and it was daunting. when my baby was delivered, he didn't cry - no one expected him to live - over the next few weeks there were many episodes of life support, surgeries, clergy, unintentionally cruel remarks and intentional ones as well - and I woke up to a whole new world. As much joy as that world is to me, I have had to take stretches of time off work to deal with my son's illnesses and my own fatigue. He didn't sleep through th enight until he was 11 years, 2 months and 3 days old - yeah, I remember it that well because I spent the whole night poking him to see if he was 'okay'. over the years we have dealt with 6 hour status seizures on a frequent basis, many ICU stays, j-tube insertion, developmental delay, legally blind, non-verbal, wheelchairs and the fittings and doctors adn therapists and and and.

His father and I are divorced and we've been on our own since he was 4 for the most part. anyway the point I was rying to make was that they are worth it and through the trials, through the tribulations, through the sorrows and joys, that one little smile or knowing you did something worthwhile today is the fuel that keeps the engine running. just try and turn the motor off occasionally - for everyone. a birdfeeder and a great book - and chocolate of course can sometimes reset you a little.
 
I am sorry you have had such a hard time. It always makes me feel bad to hear about Supporters because it is true that you suffer as much as we do. I hope we can all heal together as much as we can!
 
Hi Old Dreamer, it seems that everything I do today is a bit rushed so I apoligize for this. Just thought you might like to google the book "Trauma Stewardship: An Everyday Guide to Caring for Self While Caring for Others", by Connie Burk and Laura Van Dernoot Lipsky. I own a copy of it on file and have been trying to find enough time to read more and more of it, but so far no luck. What I have read though, maybe helpful to you, as so far it's a very good relevant book, but not directly similar.

I figure right now that if I don't share it's title with you, for you to keep in mind to read, or get your hands on to perhaps read then, I will probably forget too. I had wanted to read the whole thing first, before recommending it.

I just thought of something there is a website called Bookshares dot org for the low vision and blind and even though one cannot access those books without such needs, they can go there and search the libraries and perhaps get an idea on what this book is all about, if not doing the same thing elsewhere. But, I'd like you to at least know of this book.

Please Take Care, hang in there.

My Best Old Dreamer,
Hope
 
Thanks Hope. I have ordered a few books. This will go on the list. My daughter uses Bookshares quite often. She can read with Zoom Text and we bought her a Versa last winter. I'm hanging in there. She's in the midst of a crises now. I don't even know when we'll be able to see her again. When you're the trigger, just seeing me hurts her and causes a panic. We see our therapist Thursday. I hope to get some news, but l feel better. I've begun to accept how sick she is is and that there is nothing we can do about it. I saw something she wrote about me. Its wasn't nice..it also wasn't her. I've looked at a lot of her written work. Its not even her style or vocabulary. Disassociative Identity Disorder is quite a beast. I miss the daughter I knew. I know she is in there. I just hope she comes back. Without this group I'd feel a lot more alone. But my wife and I and doing much better.
 
Hi Old Dreamer,

I like your user name also but admit having a problem addressing anyone else from probably my generation as 'old'. :) Vanity!

I've only just caught up with your thread and story, and wished to at least say a belated welcome. I'm glad the group is helping in all the stress at your end. Yes, I suppose finals must but be adding to things considerably-my daughter is navigating them at the moment as a student but she has what, 5? Even with one going 3 hours it still can't be quite comparable to having to wade through how many classes worth of grading papers.

Your comment a few days ago about your dogs made me smile, too. It's just not easy being able to keep a sense of humour when PTSD introduces its various chaos into one's life but gosh, it's helpful. I did once run into someone who was a 'cat person' who claimed their cat was depressed and under going treatment but couldn't quite bring myself to ask further enlightenment!

I'm not a Carer, so probably will not be hugely helpful but did wish to say at least welcome here. I do hope it continues to be a support for you in all this as you help your daughter and heal with your family. And no, I'm certain it's not at all odd for a non-sufferer to celebrate therapy day. Now that you mention it, I'll have to ask my husband since it seems very likely he'll have the same response some days.

Take care,

Anni
 
Hi Old Dreamer

In answer to your question about Therapy days, as a supporter, I have to say no it is not odd. I used to have a list of issues for my husband to discuss with his therapist, as well as somethings that had happened since his last appointment for him to take with him.

It had to be done this way, as he would forget most things, but was I relieved sometimes when therapy days came around. Mainly as it would not be "ME", who had to deal with his issues, on that day. Very much less of me dealing with things now, more hubby dealing them with better himself.

Hope this helps some.

Amethist
 
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