I am 27 years old ,married and have one daughter. I would like more information on anxiety and depression. i have been dealing with this for several years now and I’m just realizing what it is im going through.
I have suffered from depression since I was a teenager and it really sucks!
I have HS and just want to have people to talk with who know exactly what I am living with here.
Is the above a typo? I am living with fnhl. It has spread 2x since dx (4/05). I have not had treatment, am on W&W. Am very sick, depressed, tired, don’t sleep and I am sick of people telling me that, " You look fine!," or “You’ll be fine!”. Just had my tonsil out so it could be biopsied, it is lymphoma. Iam gr1/2, stage 4. want to talk to others in the same boat. Barbara D
So that I will not go back into a deep depression and try suicide again.
Hello - I am a 43 yo man just coming to terms with depression and aniexty. I had a severe panic attack about a year ago, received treatment, thought I was fine. I relapsed badly a month or so ago. I am just beginning to accept that depression and aniexty have been with me my whole life. I recognize these feelings from growing up (not a particularly happy time for me). I am hoping to learn more by connecting with others as well as break the isolation that comes with depression. I feel like someone stole my life. I am praying that the meds that helped me the first time will help me again.
Also, I just want to say that I feel for everyone who feels pain like this. It sucks.
cause i suffer with depression and i dont have a dr or insurance to seek medical care for it, i would like to meet people who understands what i’m going through so they can encourage me with this
Hi my name is suzan and im interested to know more as most times i feel so isolated on many different levels.It would be re-assuring to learn more or to meet people in the same situation so we as human beings can identify similiar feeelings and converse openly with out judgement and with out fear.
Kind Regard
Suzan x
i was diagnosed with bipolar last year…after being misdiagnosed for ten years…and am looking to meet other people with the same condition that i can speak with and compare treatments and therapy, to see what may work best for me.
I have just been diagnosed and want to find information resources and also ask questions of those who have more information on this than I do.
my uncles sister just had a double lung transplant which, saved her life. she is an avid researcher of ways tomake cf patients lives more livable especially in the advanced stages of the disease. i want to know more!
My name is Bridget, and I am helplessly and hopelessly depressed/anxious, and have been for over 7 years chronically/severely. I have no insurance so I have no access to regular counsel or medication. I have a couple of friends that i can confide in, but I am just plain sick of life and no words of advice will pull me out of this. I’m hoping that maybe there will be like-minded people on here that can relate to me…
Wuts good, this is Nicole Miles I’m a 23yrs old African American Women who lives in Delaware. Unfortunately I have severe form of O.I. I use a power wheelchair to get me to and from, whether it’s to go to work, or to the mall basically where ever I travel I have to use my wheelchair at all times because I can not walk. I am joining this group to meet others that live a similar life as mine. I really need to speak with someone that can understand where I’m coming from, Far as being black with this disease, being young with this disease, dealing with this condition on a day to day basis PERIOD! And I believe that this I.O. community could help me make friends and assist with all those areas I just mention.
I have ATN, I’d like to learn more about the condition, potential treatments, and I’d like to talk with anyone else who has this problem.
I have lupus and I have been abandoned by my husband and I am in dire need of HELP!!
I have battled with it my entire life and an married to a bi-polar
I’d like to meet other people living with this condition.
I sustained a back injury which left me unable to walk without braces, or control my personal functions. Very embarassing.
well i’m interested in knowing more about AoCC… when i was 38 weeks pregnant of my 2nd child ( a boy ) i had an ultrasound done at the hosp and it seemed like a cyst on my baby’s head but they couldn’t tell me what it was… when my baby was born i told the Dr i wanted to make sure what was it on my baby’s head, he took a sonogram on his head but still wasn’t sure what was it exactly, he decided to do a catscan and told me agenesis of corpus callosum was found!
I was shocked to learn I have PPS…told I was cured in jr. high-1963.I’m having a hard time coming to accept it.Does it get worse at such a fast rate for every one or is it just me?I was diagnosed 8-05.Once I started getting my Soc. Sec. Dis. I became ineligible for Medicaid, and I don’t become eligible for Medicare til 5-08.I can’t afford to go to the polio dr. for treatment or help. I am declining rapidly.Anyone else in my situation?What do you do?Comments or advice-e-mail:Kori G at johnandkorig@yahoo.com. Thanks.