MissAli,
I do that too sometimes, worry I've triggered someone. Then of course I wind up triggering myself. LOL. I've only been triggered a couple of times on this board, and I know it was just me being my overly-sensitive Borderline self. I got over it quickly and I can always come back and apologize if I've "vented" too much. Hope this doesn't sound cheesy or bossy, but please try not to worry about triggering me. I find that other Borderlines almost never trigger me.

I love my BPD friends. They are amazing to me. They are "my people."
Yes, and about my son, I recognized that he has created a lovely little co-dependent triangle for himself. He has a friend that is struggling with a mental illness (Schizophrenia) and all of his siblings have it. My son, being used to pwMI, has no troubles with it and has actually realized he naturally gravitates toward and understands people with emotional troubles. So, this friend kind of needs him a lot, and my son really loves him to pieces so is there for him a lot. BUT, his friend and my son's gf do NOT get along at all. Fight constantly. This of course puts my son in the middle, however, he also kind of uses his friend as "escapism" from his hard to deal with gf. It's complex, but I'm sure you get the gist of it.
Yeah, I do realize it's his defense mechanism, and since I am so into working toward excellent mental health, it's hard on me when he wants to avoid. Cause, well, I know that in the long run, you can't run away, you have to deal eventually. The Mom in me says, "NOooo, you need counseling." But the Mom in me also understands, he is just not ready to deal. Thanks for the nice words, too. I appreciate your support in that and the understanding that I am trying to be the best Mom I can given the circumstances. It isn't easy!
No, you're not being nosy. At least I don't think so. Funny you should mention boundary issues. LOL. Because I have them too, and didn't realize that was the cause of a lot of stress with friends and even people I would just meet. I guess I'd ask too many questions and turn people off. But the flip side of that is that in a way I don't get WHY so many people can't handle just talking - about anything. To me there are no taboo topics. I can talk about anything. I have a hard time understanding why other people can't do that. LOL. Like sex, for example. I have no hang-ups talking about it. It freezes others instantly. I am always left bewildered. It seems to me that if more people could just talk, instead of freezing at certain topics, the world would be a better place. Ah, me, the idealist Borderline.

Plus, I was raised by academics who encouraged me to talk about anything. I could talk to my Mother and my step-dad about any issue at all. Could say anything I wanted. So coming from that background, it has always puzzled me that in the real world a lot of people aren't like that. Sigh.
Anyway, no don't mind you asking. Nice that someone is curious. I have talked about my physical DX a lot on this site. The physical stuff triggers the BPD and vice versa. Hard to separate mind and body.
Now, just a disclaimer here: I suffer from OWS (Over-Writing Syndrome) so I apologize if it gets lengthy. I could write for pages, and sometimes that is way too much for people.
Well, there is little stuff: high blood pressure and cholesterol, which is exacerbated by stress of course. Have Pernicious Anemia (Vitamin B-12 deficiency). Have to do shots in my leg twice a month. I have IBS (Irritable Bowel Syndrome) too. Those are the minor things.
The big things are Scoliosis and Hidradenitis Suppurativa. Say what? LOL
I am sure you've heard of Scoliosis. Mine was so bad that after a year of bracing, they decided on surgery. My whole spine is fused as one bone. I have a metal rod in my back to support the fused spine. As a result of the fusion (done at age ten) I now have Osteoarthritis. This is an expected result of the fusion - happens once you get older - say 40's. Well I am there now. The arthritis is in my neck, spine, shoulders and hips. Very painful. My neck is curved in the opposite direction it should be as a result of another expected consequence of the surgery. Flatback Syndrome. This is when your hips, neck and spine do not line up like they're supposed to. Incredibly painful. Any and every position hurts. Walking, bending, lifting, sleeping, sitting, standing...you get the idea. I also have chronic Hip Bursitis. So walking is a hard thing. Some days I can only manage to hobble about the house with my cane. Ugh.
The Hidradenitis Suppurativa is a chronic, incurable sweat gland disorder.
So, sweating is bad for me. I am supposed to avoid all things that make me sweat. Ummm... LOL
My skin needs constant air flow. I can't wear pants, skirts, shorts, really anything on my bottom half, for very long, or the sores set in. My sweat glands don't work right and lucky me, because they don't work right I have three types of rare bacteria (non-contagious) that live on my skin permanently because they are literally attracted to the faulty sweat glands. So, if I get too sweaty, or don't get enough air flow, I get sores that last for days (under my breast, in my armpits and in my groin area). Lovely, eh? Sometimes they are small and don't hurt too much, but I have had them the size of golf balls and have had to be hospitalized for weeks at a time on IV antibiotics. The condition can be life-threatening if it gets into your bloodstream.
I am from NY and one of the reasons I moved to the Southwest was for the dry air. It does help my skin. But, silly me, I had no idea they use these things here called Swamp Coolers and not Air Conditioners. Swamp Coolers use water to cool. So, when you turn them on, they pump huge amounts of moisture into your house. Well, it doesn't take a whole lot to figure out that this does not help my skin at all. Exactly the opposite. Almost no one has A/C's in this area. So, once summer hits, it's sore season for me.
So, I spend all day taking pills. LOL. Pills for my skin. Pills for pain. Pills for my HBP, etc. All I do is chase pain and try to figure out how to prevent it. That's my whole day. And, what works for one ailment, makes another worse. Example: reading. It hurts to look down at a book because of my neck, so I try to sit in this weird position with pillows to try to more or less prop the book up so it's more at eye-level. Well, that makes the Hidradenitis worse because now I've just cut off air flow. It's a pain in the a$$ literally. LOL
Of course all this makes the BPD worse. I get "ragey" because I am in pain a lot. Get mad that SSI takes so long. Get upset that I can't have a normal life, never mind the BPD! I can't go for walks, go take pictures like I used to...all kinds of things. Gee, no wonder I'm so angry.
And then any trigger due to the BPD makes the physical pain worse.
I could go on, but I'm sure you get the point and how frustrating it is. That's the Reader's Digest version.

No, she isn't ignoring me. I think I do split with her sometimes, and also, I'm still trying to figure out who played what role in the development of the BPD. Of course, like many others, I was abused. In some ways she was abusive, but not in an obvious way. I know she loves me, but some of her actions didn't help when I was a kid. So I think I swing back and forth between believing she abused me far more than I realized, and then thinking I'm nuts for thinking that.
But I can count on her too much sometimes. She will let me vent for hours, which is not good for me, because then I don't learn to regulate my own emotions.
I know what you mean. I wear people out, too. For me it's the constant need to clarify and explain things to people. I always want people to understand, PRECISELY, what I'm saying. I can spend hours alone and not be bothered by it, but if someone doesn't get something that I'm trying to explain, I can also spend hours wearing people out by coming up with analogies and metaphors that drive people bonkers.
But, but, but - it's like THIS, don't you SEE? LOL