Have been diagnosed with depression 2 years go and panic anxiety go along with it, have know for a very long time that I’ve been depressed and haven’t dealt well with it, now I am taking medication and would like to take next step and speak with other people and/or get some counseling Thank you
Had melanoma 10 years ago, but never seem to be free of it, even though I am supposed to be. Cat scans are always coming up with new spots to be investigated.
i’ve suffered through manic depression, otherwise known as bipolar…i have now crashed and am in depression mode. i’m do depressed i don’t know what to do…i have crying spells i’m unmotivated to do anything and life seems so hopeless
Hi! My name is Andrea, I’m 33 years old and live in Charlotte, North Carolina USA. I was born with pseudohypoparathyroidism, and was diagnosed with it in the early 1980’s. I am interested to meet new people with the disorder, and I also would like to learn more about it. I do know some about it, but not very much. If anyone has questions for me, please feel free to ask.
I have had chronic, recurrent depression for over 25 years; among other problems. Other communites aren’t active at all, some of them. I am also interested in other areas.
I have had RLS since before they really were talking about it. It is one of many issues I have to deal with. I also have fibromyalgia, IBS among other things
I m a Distant Pranic Healer, Distant Energy Scanner and Pranic Psychotherapist.
I treat all kinds of physical, mental and emotional disorders without meds, without touch. without pain and without presence.
I remove coronary blockage, brain tumor and stones etc, sucessfully.
I m director to “Depollutionize Yourself & Be Transformed” program in which the entire human system is made free from all kinds of toxins, pollutants and waste materials without any effort with the help[ of latest breakthroughs like "Depollutionizing Chamber"
I conduct depollutionizing camps, worldwide, at the request of any group or organization for general mass.
Hi-
I am the parent of a wonderful daughter who was diagnosed with iritis almost 2 years ago. I was seekinginformation about this condition because I had never heard of it and found not many people had.
I have this condition and have never met another person with it, so this community is very interesting.
I like to chat with others so I can learn how to deal with my situations, I had other chats and it helped me a great deal knowing Im not the only one that down. Maybe I can get some feedback on this site.
I came down with Bacterial Meningitis in 2001 just one day shy of a month after the 9/11 attacks. I’m fully recovered but with long lasting physical scars. I’m hoping to meet more people who have come through such tough times and still remain okay.
hi, I am Michele, a mother of 3 with my youngest being born with bilateral clubbed feet.
I’ve been struggling with OCD since SIX YEARS OF AGE… at a time, BEFORE anybody HAD A NAME FOR IT, or, KNEW ANYTHING ABOUT IT; except for “Dr. Freud”… who thought that: “it HAD SOMETHING TO DO… with TOILET TRAINING in MEN!!!” But then… with “Dr. Freud” IT’S ALL… either ORAL or ANAL!!! 8-)))
In addition… i’ve: BEEN “FEATURED” on ABC TV’s 20/20… i was the SECOND HOARDER… that they EVER HAD ON THE SHOW… nearly 15 YEARS AGO!!!
i’ve been the “resident expert”, in numerous online support groups… many, based in England… and some, in the midwest…
i’ve also been on DOZENS of SSRI medications… some, with DISASTEROUS OUTCOMES (suicidal ideation, extreme weight gain, dehydration, worsening of conditions, etc, etc)… and, CBT programs… with LITTLE or NO positive results!!!
and now… i’m here!!!
We have a 16 month old daughter, Maya with an hemangioma on (in) her upper lip. She’s had it since about 3 months old. Nothing has really worked and so now we are awaiting a plastic surgeon appointment.
Hi. My name is Alisha. I was diagnosed with moderate neutropenia last year (ANC about 1.0). Before the diagnosis, I had never heard of neutropenia before. I am not taking the Neulasta, but may begin treatment shortly due to recurrent infections.
I’m happy to talk with anyone with neutropenia. It’s good therapy to make a connection with those who you have something in common with.
My wife has had CFS for seven years I am her carer and work full time. I am very interested in research in the CFS area.
I have started a petition at ipetitions to urge governments to redirect CFS psychology research into CFS biology research so that real progress can be made.
My petition is at:
Just ignore the request for donation. Your signature will still be registered if you don’t donate.
I have FSGS/Nephrotic Syndrome with MCD
Hi,
I have Protein S Deficiency & many other health problems. Both genetic & not genetic.
I have 100% blockage of the Superior Vena Cava from a blood clot that has been there for 7 years.
Recently (May 29th) had surgery to remove a mass in my neck (benign!!) & it was tricky keeping my blood thin but not too thin for surgery. I am healing well.
I look forward to chatting with others.
Hugs, RustyLady
Hello ,
My name is Patricia i live in Maine. I have had rsd for 10years in my left foot and leg spreading up my other leg due to surgery on my foot. This disease has totally ruined my life. I had to stop working, my income has dropped i am on ssd. The pain and burning is unbelievable sometimes cant deal with it. Cant do things i used to like get down aon floor and play with my grandchildren. Oh by the way i am 55yrs old and i have 5 grown children and 12 grandchildren. They are waht keeps me going.
hugs Patriciai had a5 years old chiled with fragile x