Hi I was diagnose with MG at age of 37 in 1997 and I had the Thymectomy in 1998,it did work for me now i am in remision since July of 2004,I feel great and I think anyone that is diagnose with MG should go for it as long they are young and strong and have a great neurologist too,I had it change twice and help me alot,good luck to you all and keep in touch and updates on your recuparation.
I have cf and am finding myself bein admitted every coiuple of months. how frustrating. i’m noticing my body is slowing down but my spirit just wants to keep going! i need motivation to do things right!
I have been living with the effects of alopecia areata for 10 months now. I have been to so many doctors that I’m starting to feel like a guinea pig, and have actually been diagnosed with more problems then I thought I had in the first place. I have tried several medications and I’m sick of it all. I just want to live my life as my own and to stop all of this madness… but then again I really want my hair back.
My name is Denita, I am 42 yrs old and I was diagnosed with Ataxia in 1994. I am still intimated by it and have yet to come to terms with my condition. I guess that’s mainly because I still don’t understand it and I would like to. Please give me some information. It would be much appreciated.
Thank you
Denita.
I am interested in the body and diseases caused by whatever, mistakes, lack of supplements the body needs, & infections, fungus left untreated.
I am 14 years old.
My name is steve I have stuttered all of my life I am a good singerI have been in the music world a long time I am 6ft tall and 240 pounds I want to connect with people who stutter also mabe someone single.
well take care
steve
I was diagnosed in 1999 with hemangioma on my liver ay yhe age of 43, just would like to know more about my condition as it comes available. I would like to connect with people who may have same symptoms now or have had in past.
Hi, my name is Amy. I’m a teenager struggling with NPD. I am trying to figure out how to overcome it from a Biblical perspective. I’ve lost friends and practically pushed away my whole family. I’m not proud of it, and I want to learn how to change. I never wanted to be like this, but now that I am I have to learn how to deal. I just want support.
Last week my mom was diagnosed with follicular lymphoma and large b-cell lymphoma. Would love to know more about treatment options, including alternative treatment options.
my name is ashley and i’ve been living with cystic fibrosis for 18 years. i been having a hard time being around friends who dont understand it. they are more afriad then i get. i explained up and down to my bestfriends they understand alittle bit but also known me for years. there are new friends in my life, that im so afriad they will judge me for what i have then who i really am as a person. i can never finds ways to say it or why i take meds before i eat or seveal meds aday. i’ve been picked on as a kid for having this illness and im tired of being different then everyone else. its hard to not know anyone with cf to share storys with. mostly to have someone understand what i’ve been through or how i have to live day by day with cystic fibrosis…college is right around the corner nd that makes me so worried i wont make any friends. its really hard living like this i would like to meet some great people out there who have it and here there storys.
I HAVE ALOT OF MENTAL HEALTH PROBLEMS THAT RUN IN MY FAMILY. I BELIEVE THAT NPD IS THE MAIN PROBLEM .I WOULD LIKE TO KNOW MORE ABOUT IT AND HOW TO LIVE WITH FAMILY MEMBERS IN REASONABLE PEACE.
I am female of 30 years old I have been battling depression for about 15 years now I came across the site hoping to join here cause I feel that it would be a great place to learn and cope.
My father has Chronic Lymphocytic Leukemia. Interested in learning as much as possible about it.
3 months now recovering from celiac desease … thankfully a tolerable cure, how ever it does take an extra effort to successfully control. I’m in my late 50’s and now reflect on the many symptoms I’ve encountered over the years.
I am interested in this condition because i think i suffer from it and wants to learn as much as i can.
I’m Terri from Central GA USA. I’m 34, and I live with PCOS every day. I wake up everyday and I’m still fat, hairy, ugly and childless. Doesn’t matter what I do, I’m fat! Depression is unreal! I sometimes feel like a 55+ yr old lady going thru menopause. The mood swings, the cramps, oh the cramps. I know I’m not having kids. I have begged my GYN to remove it all since none of it works. Of course they say no! If anyone out there wants to another fat hairy friend, hit me up! haha
Much love to all of you cysters!
my mother has been recently diagnosed with breast cancer, i want to learn as much as i can about the condition in case she asks me something and I want to connect with people in the same or similar situation as me.
Hello, for several years I was told that I had MS. Until 2005, I was then told I had Sjogren’s, vasculitis, RA and was suffering from peripheral neuropathy, ataxia, depression, and fatigue to name a few. I now have crohn’s and Primary Biliary Cirrhosis of the liver. I would like to connect with others who have the same conditions associated with Sjogren’s and learn more about diet and what is helping others to cope better.
Hi Connie, Joyce here from Polk County. I would love to be a part of this community to share with others that have sjogens. 