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| | Notices | Welcome to PTSD Forum. Post Traumatic Stress Disorder (PTSD) is a life threatening, debilitating disorder that can break down a sufferer’s body through anxiety and stress. Further it poses a significant suicide risk resulting from the brains neurological imbalance and chemical depression. Sufferers often live in denial, thus this community is aimed at helping PTSD sufferers help themselves through others experiences, guidance and education. We are here for the sufferer, spouse and families surrounding PTSD. Spouses and family are too often forgotten in this equation, and often they receive all the worst that PTSD has to offer. If you're involved in any way with PTSD, get registered and help yourself now. Non-active members will eventually be deleted. If you are not a sufferer, carer or someone within the mental health industry, and active, then there is little reason for you to be a member of this forum. Non-active members with zero posts are deleted periodically during the year. |  | 
02-08-2006, 08:34 AM
| | | | Join Date: Aug 2006 Location: Fort Lauderdale, FL
Posts: 1
| | New Person - I Have PTSD and Lupus I'm Helen. I'm 28-years-old. After being in and out of various, mostly ineffective therapy for years I was diagnosed with PTSD last spring due to childhood/young adult abuse (sexual and domestic). I also have systemic lupus- I was diagnosed in 2003. My husband (we have been friends most of our lives, married this past December) is a God-send to me in helping me manage my PTSD symptoms. Because I also have lupus, no one will prescribe me medication (the 'malpractice fear' in this country is a large cause of this). So I self-medicate with vitamins and St. John's wort. I was in psychotherapy but my therapist stopped her practice so now I'm looking for another one. I alternate between feeling good, feeling okay, and falling apart. Today is one of the falling apart days.
I live in Fort Lauderdale, Florida, USA. (I know some people are angry at Americans but please don't hold it against me- I'm a pacifist.) I've yet to meet anyone with PTSD and lupus, so maybe I can find a kindred spirit here. | 
02-08-2006, 09:18 AM
|  | | | Join Date: Jun 2006 Location: midwest
Posts: 960
| | Hello Helen. Welcome aboard. I don't have lupus, but I do have ptsd. In some ways, we're on the same search. My ptsd was caused by repressed memories returning in my early twenties. Aparently, it's rare, and it's controversial. I have found people, though, here at this website. It makes a huge difference.
I hope that you do find someone here that you can connect with. One thing is for sure, we are either going through it, on the other side of it, or have a friend/spouse going through it. It is a really tough journey, but worth seeing it through. I'm glad you've found us. We welcome you... | 
02-08-2006, 09:19 AM
|  | | | Join Date: Jun 2006 Location: midwest
Posts: 960
| | And I forgot to mention, I'm an American too. I live in the midwest, where it is pouring at the moment.... | 
02-08-2006, 12:00 PM
|  | Administrative Editor PTSD | | Join Date: Sep 2005 Location: Melbourne, Australia
Posts: 7,426
| | Hi Helen,
Welcome to the forum. Don't worry, I won't hold being a yank against you... :) Americans are the majority here already... so the rest of us our out numbered I guess. Good to hear that your looking for a new therapists... very great news, and even better that you have a supportive husband to help you. We all need that at times... | 
02-08-2006, 02:56 PM
|  | | | Join Date: Jul 2006 Location: Pennsylvania
Posts: 305
| | Hi Helen. Welcome to the forum. I haven't been here long but I quickly came to realize that this is a place where we can finally feel "normal" and where everyone understands what we're going through. We don't judge, rant, or rave, but we do babble, write our autobiography, laugh at ourselves, and ask for (and get) advice.
You mentioned that you have lupus. While I don't clinically have lupus, I do test positive for the ANA, although I don't present with any of the other symptoms. This came about 3 years ago after I had chicken pox (for the 2nd time! Yeah, I am one of the lucky ones who actually DO get it twice in one lifetime!); I wasn't feeling well and the doc ordered almost every blood test available.
I do have Hashimoto's Thyroiditis which is an autoimmune disorder. My doc watches me pretty close because once a person has one autoimmune disorder they tend to have others.
Of course, after all I've been through, nothing would surprise me.
So welcome. Sit back and relax. Yell, scream, laugh, smile. Above all, remember to breathe...
Kim | 
02-08-2006, 03:37 PM
|  | | | Join Date: Jul 2006
Posts: 72
| | Hi Helen..Welcome! Nancy here in southern VA. About 20 minutes form the NC border. We are almost neighbors! I was in ft. Lauderdale last year. It was winter time and I soaked up the sun. Loved it!
I hope you stick around and join us on our journey of recovery.
Nancy | 
02-08-2006, 11:17 PM
|  | | | Join Date: Oct 2005 Location: Melbourne, Australia
Posts: 443
| | Hi Helen,
Welcome aboard. I'm with my husband, we Aussies seem to be outnumbered here at the moment. That's cool with us, we don't care where you come from or how you got PTSD. We are happy to have you here and help provide the means through which you can get support. | 
03-08-2006, 12:28 PM
|  | | | Join Date: Jan 2006 Location: Canada
Posts: 960
| | Welcome HelenAngel!!
Nope, I don't have lupus, (I'm actually about to google it right now... I'm not familar with that condition)
But I do have PTSD, along with a couple other disorders (just to make my life more exciting, lol)
Take care of yourself and I look forward to hearing more about you :) | 
03-08-2006, 11:06 PM
|  | Administrative Editor PTSD | | Join Date: Sep 2005 Location: Melbourne, Australia
Posts: 7,426
| | You won't like what you find YA, as Lupus is basically a breakdown of the immune system, and basically your internal system starts attacking itself. Not pretty... | | Thread Tools | | | | Display Modes | Linear Mode |
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