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How Do You Defend And Protect Your Own Happiness?

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Meli

Silver Member
Hello All,

I'm having difficulty balancing the things I do to relieve stress and placing the right amount of focus on my family. I don't want to isolate myself from my family, nor do I want to force myself to endure too much stress at this point in my recovery. We are in the early stages of awareness to the disorder, and I feel like I require a lot of time to myself. I'm honestly not avoiding my family by doing so, at least I don't feel like I am. I'm not anxious about being around them, and I'm not dying to leave their company either. I've just switched gears, and started doing what makes me happy. It has made a huge improvement in my mood lately.

I just can't relay that need properly or find the right reason to give my family. I don't want them to think I'm hiding, but then again, I am wanting the the time alone to recharge. I absolutely avoided them in the past; shut myself off in a room and suffered anxiety at the sound of their footsteps outside the door. But that's just not the case now, and they just don't believe me.

Any advice would be helpful,
~Meli
 
Many of us feel a tremendous amount of guilt when it comes to our families but you must do what is right for you. Honesty is key and if you are close to your family and they are being supportive they should understand. Have they educated themselves about this disorder? Sometimes if YOU are trying to educate them about it they will not fully understand. I would encourage the members of your family that are close to you to and are effected by you having this disorder to read,read,read about PTSD and the effects it has on the sufferers and the carers involved.
Hope this helps.
Peace to you and yours Meli
J
 
I agree that is really is about their willingness to educate themselves and try to exercise a lil understanding for your situation. I can say I've lost family over this disorder. Some by choice (because I've realised just how much of a negative effect they've had on me, thus I've walked away), and others via their own unwillingness to even understand it is a disorder.

On the flipside - It's also revealed to me who is there for me. My Mum for example - I have had a couple of times where I have had to cancel lunch or a visit because I've been in too anxious of a state to really be out. She knows now not to take it personally when that happens. I try to give her as much notice as possible and she doesn't ask questions. She wont quiz me for half an hour about 'why?, 'what's wrong?', 'should I worry?', etc (which in turn would increase my guilt over cancelling, and thus, my anxiety). She just accepts that I'm not having the best day and that I feel the need to withdraw and that it will pass. I'd like to think she doesn't worry anywhere near as much about that since going out of her way to educate herself and understand why.
 
...Honesty is key and if you are close to your family and they are being supportive they should understand... Sometimes if YOU are trying to educate them about it they will not fully understand. I would encourage the members of your family that are close to you to and are effected by you having this disorder to read,read,read about PTSD and the effects it has on the sufferers and the carers involved.

Hi SuperJen,

I'm sorry to have waited so long to reply. "I am trying to educate my family", and it's not working for the most part. I'm telling my carer when I get triggered or stressed out, and he doesn't believe me because he can't see it. I'm very good at hiding outward symptoms, but that doesn't mean they aren't happening, or that they aren't affecting my thoughts and actions. He says I'm playing the PTSD card now, and exploiting it.

The thing is that I'm being accountable for what I do about my symptoms. Like if I'm on guard and being touchy, I tell him, with the utmost honesty, but I'm actively trying to stop doing it too. I'm not saying "Just let it go if I blow up", I'm saying "There's potential for me to blow up, and I don't want to; please help me avoid that". The truth is that some things that a carer does will trigger symptoms, and I don't know how to tell him about those things without him getting extremely defensive. I've even taken the words "what you did or said made me do something" out of it. But that's not working either.

I'm at my whits end on this one, and after the barrage of insults and slams about it this week, I'm feeling pretty bad about the situation and myself. I've tried so hard to do the right thing, and am failing miserably with him. I don't know what to do.

Boy did that sound whiney and desperate! Lol!

Thanks for responding, and I apologize again for taking so long.
~Meli
 
Ooops, I got confused, or didn't pay attention well enough. I'm so sorry JLINE. The previous post is for you, and I accidentally addressed it to SuperJen. Please forgive me, I "am" paying attention to the content.

Sincerely,
~Meli
 
To SuperJen,

Yes, mother's are marvelous. Mine is a gem. Even before I knew I had PTSD, she never questioned anything; no mood, no reaction, nothing. She's such a trooper, and believe me, I've given her H*LL!! I love my mom soooo much! I couldn't tell her that for 20 years, but I bit the bullet last year, and blurted it out. She about fell over, and then promptly started bawling. Life is good, huh? I tell her every day now, and it isn't a problem at all. I blamed her for not being able to protect me while my father was abusing me. It was stupid, but I understand why I did it. Now that I've changed that, done the right thing, I couldn't ask for a better friend. Well, she was my best friend before, but there's so much more to the relationship now.

I'm getting all kinds of negativity at the moment, but I'm hanging in there, and not letting it dictate how I feel about myself or my progress. I'll just keep doing the right thing, and cut some breaks I suppose. I have to make boundaries though, I know that. I won't tolerate name calling, and blaming me for everything. I have to stand up and make sure I don't slip back into depression and violence.

FOR EVERY BAD THING I DO, I DO 5 MORE GOOD THINGS! I'm sticking to that!!
~Meli
 
Hi Mali ,

I can see where you are coming from in this post , not with mothers and fathers , But with my Son and my Aunt. Im not ery good at replying to posts and saying what i ''think'' ect but ill give it a go for you
smile.png


''I don't want to isolate myself from my family, nor do I want to force myself to endure too much stress at this point in my recovery. We are in the early stages of awareness to the disorder, and I feel like I require a lot of time to myself''

A while ago i felt and still do feel somtimes that i dont spend Enough time with thoes close to me and i worry
That the people who care about me will think im ''giving up'' on them or dont actually want to be around them. I see this in a few ways (ill attempt to explain)

  • If too much time is spent arround family/loved ones at this time i could ''freak out'' and possibly upset them , at this stage in my/your recovery you will and do need space to Help yourself and learn how to deal with the ptsd and the moods it can put you in. So Part of me thinks , ok im not spending so much time with them at the moment but the time im using to myself is to help myself heal and to give my self the space and time i need so i dont ''hurt'' or upset them and so im less likley to get upset by things when im with them. So that when time is spent with them it can be fullfilling and hopefully peacefull as ive had some time to myself to work on my issues , then when im with them i can try to focus on being happy and being in the moment with them . (ok that sounds a little jumbled sorry) - I think ''you'' time is really important , Trying to explain to others the need for space and why , i think can be difficult howether.
'' I absolutely avoided them in the past; shut myself off in a room and suffered anxiety at the sound of their footsteps outside the door. But that's just not the case now, and they just don't believe me.''

  • Im not sure what to say to this , But i have the same issue with my Aunt , if i dont come over for dinner or if i sit quietly she thinks im avoiding her and she thinks i dont want to be in her company.....trying to get them to understand that infact ,no , your just finding peace within yourself for a short time . is really difficult.
sorry 4 how jumbled this is ,,,, im not sure it is written right or if it makes any sence , if it dosent tho ...... Keep going , your a lovely brave strong person and i am happy to have met you on here,

Sarah
 
im verry sorry i meant to write ''hi Meli'' . . ahhh thats better .

That's funny, I actually go by "Mali" as well. My grandfather calls me that, and so does my friend in Arizona. I have so many different names.... hee hee!

Thanks for the reassurance that I'm not being a butt for taking "Meli Time". I just still don't know how to get on neutral ground with my family concerning the issue. They don't seem to understand that effective "Meli Time" means no interraction at all for a while. They still come in to make requests that I spend time with them, or question why I'm hiding in the first place. If I tell you where I'm at, and I close the door.... am I really hiding? Or am I recharging my taxed mind in private to better benefit everyone; including myself?

They just don't understand that even being in the room with me can be stressful. And they can't see why I need to be truly alone in the first place. I feel pressured to please people, along with anxiety that I'm not pleasing them (i.e. not talking enough or not giving affection like they want). That in itself is exhausting, but they aren't strained like I am because of simple social activities. It's internal, and only shows up in the end; when I'm in a mood they can't figure out how I came to, and neither can I.

It's frustrating, but I believe I'm doing the right thing for myself and my family by enforcing my guidelines for "Meli Time". They need time to themselves too, but the two needs are no where near the same.

I understood your jumbles, hee hee! It feels good that I'm not the only who has this need, and I'm not the only one who has trouble explaining it to their families.

I see you online, but I have to finish up here, and go make supper. I'll be on later, I think. Depends on whether or not I get some alone time this evening. :-)

~Meli
 
Hi Meli,

Sorry for taking so long to respond. PTSD is not curable as far as studies have shown but we can learn to live with it....If your carer says you are playing "the PTSD card," he clearly doesn't understand the effects and seriousness of this disorder. You both sound frustrated and confused, not a fun place to be in for anyone. There are many carers on the forum that go to their own therapist. I would highly recommend he sees someone. Remember, he needs support too.

Not sure if you are in therapy but it has helped me tremendously. Medication is a personal choice but it has certainly improved the quality of my life as well as staying away from alcohol and pot...

I hope this helps Meli
Peace
 
Thank you for the campassion Jline,

Sometimes simply hearing that someone wishes to relieve my pain, whether the percieved cause of that pain is rational or not, is the most healing and comforting act that someone can do. I have a very hard time relaying this to my carer; hence his comments about "playing the PTSD card".

My carer wanted to discuss symptoms, needs, and accountability again last night, and I engaged willingly. I was doing good controlling my symptoms of blaming others and self-guilt all the way to the end of our discussion. I was proud of myself, but I knew d*mned well that it was absolutely neccessary to take a "time out" afterwards. As my carer and I like to say, although I did well, "My bucket was full to the brim" and dangerously tipsey. Early in our discussion, we were interrupted by my grown son, and we "ceased fire" where the discussion had gone awry. Thank Thor for my son's random appearance.

As we sat there in his company for 15 minutes, I half dissociated (still hearing the conversation, but not interpreting it in any way); staring at a TV image that was not registering in my brain. What was going on inside my head was introspection, and I was giving no thought to either of the men in the room. I began to realize what I was really thinking in the last few moments before my son arrived, and noticing the physical symptoms that I had been ignoring in the heat of the moment. It's so hard to wrap my head around the fact that these things are happening to me without my knowledge of them at the time.

Rage had been building inside of me, and I didn't even know what the h*ll I was so angry about. I recognized, during that spontaneous time out and before continuing the discussion, a "me" that was very familiar. While in introspect, I felt like I "was" that 15 year old girl who sat in front of her mirror... hating herself. I realize now, in fact, that I may have been having an episode of "feeling as if the truama were reoccuring in the present time". I honestly felt like I was her, all those years ago. Expressing this fact, to me, is a tool that allows my carer to make a positive difference when I'm not able to. To him, it is me "being the victim" or "playing the PTSD card". My carer feels as though I am blaming him or reacting to him because of what someone else did to me. I get that, and how it could feel as though I were doing that. But the honest truth is that I don't consciously feel that way about his contribution to my episodes, and it's extremely hard to relay that fact and have it understood or trusted. I do almost feel like I'm Skizophrenic at times because I revert to very specific "Meli's" due to different triggers and my multiple traumas.

I wrote down my symptoms and emotions while my son was effectively pausing our discussion. I felt confused and out of control, and I wanted to review my list when I could be more rational. Two hours later, when I read what I had wrote, I was shocked. Some of the things I had written were inconceivable to me after I had gained control again. I actually could not physically remember feeling that way just a couple hours before. The symptoms had come and gone without any mental retention of them. It scared the hell out of me, and made me aware of just HOW helpless am I against this disorder. Of course, all the feelings of being broken and unloveable rose to the surface, and added to the already existant fragility of my psyche because of this realization. I became extremely vulnerable to a break down..... and proceeded to have one a short time later.

I did spend some time to myself after our discussion, and I felt proud of myself for not loosing it. I was getting ready to turn out the light and go to bed, and struggled to decide whether or not to tell my carer and say goodnight. I thought about what I needed; total isolation; and I thought about what he needed; reassurance that I still loved him and cared about the effects on his life. I decided to go to his office and say goodnight in person.

He was on the forums, and immediately wanted me to read his response to something I had asked about there (along with another reader who was confused about it as well). One comment in his new post caused a major negative reaction in me, and I carefully corrected the technicality, thinking I could still remain in control of myself. Bad move! I would have preferred now that I had left it alone. It wasn't important. His response to my correction (as it seemed to me while in the moment) was him saying that he knows better than me what I'm thinking or intend to say in my comments.... I yelled.

Following that short disruption to my otherwise commendable behavior, my carer came to our bedroom and expressed his love and compassion for me. And here is an example of full blown PTSD; because he did that, I was able to let down my guard (the rage, the tough ugly exterior, and survival instincts), and show him what was really going on inside of me; what I was denying to myself in part, and what I was not aware of as well. One of my closest friends (also a survivor of rape) told me "Melinda, I'm sorry, I love you, but you front". And I do, all the time. I'm not tough at all, and inside I'm as fragile as a china doll. I promptly let the waters flow when I saw the love on my carer's face. I don't do that often; I'm embarassed by my weakness. I couldn't breathe, I couldn't think, I couldn't talk, and I couldn't bear the thought of being touched (another reason I front because people want to hug us when we cry). I was completely out of control, and in the deepest darkest abyss that was second only to the times I've considered suicide. I hated myself, and saw no future whatsoever.

My carer tells me that I should show him that more often, and I don't know what I think about that statement. That is an extremely terrifying place to be, and if I don't use some of my coping mechanisms (anger and numbing), I'm afraid that I will hurt myself or someone else. My point to all this is to express how volotile and dangerous this disorder is.

I will post my list of symptoms in an appropriate thread at a later date. I do not feel strong enough to address that purpose right now. My eyes are swollen, and I need time to recuperate. I have devised a process plan for this very thing;

Trigger/Episode
Realization
Mental Processing
Relaxation

To me, it's obvious that every episode demands this process in this order. The most important step, to me, being "relaxation". Without the time to let ourselves relax both physically and mentally, we cannot feel healthy. If we cannot feel healthy and rested, we cannot move forward out of a state of constant turmoil and stressors. Our episodes linger far longer than our carers realize.

~Meli
 
Hi Meli,

In the forum section under "Post Traumatic Stress Disorder" there is a thread called "I believe PTSD is curable" check it out if you haven't already. The eye patch therapy some of us do is described in the thread as well as some other things people have tried. It sounds as if you are having flashbacks....I suffered for a long time with those, they are just horrible and you feel like you can never be the age or person you are today. Eye patch therapy stopped my anxiety and flashbacks completely. I am not saying I am cured but I am able to stay in the world of today instead of constantly flashing back to when I was younger and traumatized. I am able to learn how to be the person I am today now that I am not in the pasts shadow all the time. Give the eye patch thing a try....trust me it does work. Be patient and kind to yourself.

Peace to you and yours Meli
 
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