I have had breast cancer 2 times now and like to talk to other women who also have or had BC
suffer from this condition
I was diagnosed by a ct scan in aug of 2006 and have had problems ever since but the doctors in bc now say they don’t think that I have mp but they don’t know what I have . I have pain every day have lost 25 lbs( good) can’t eat meat or drink wine have rashes sometimes. have contracted every flu and cold this winter and my latest is they thought I had a blood clot in my swollen leg, now they are saying it could be vasculitis. My crp test is high and so is the d-dimer test. I have gone from having high blood pressure for 30 yr. to having low blood pressure. have boderline diabetes which is under control unless I am havin an attack. I am sick of being sick! the doctors here act as if this is all in my imagination. thanks for letting me inload. paulette
Well I am only 14 but have had alot of trouble with Celiac. My parents don’t understand the pain. I can’t gain weight and my parents who aren’t celiac don’t know its hard to gain weight therefor I get yelled at tons.
Well I am only 14 but have had alot of trouble with Celiac. My parents don’t understand the pain. I can’t gain weight and my parents who aren’t celiac don’t know its hard to gain weight therefor I get yelled at tons.
I have Sjogren’s Syndrome and alot of the related diseases and symptoms that stem from it. I don’t personally know another person who has it and would like to compare notes, as it were.
I myself have depression issues and would like some info. on this topic. Thank you. (petlover)
My name is Jenn. I am 32 and was diagnosed with SLE, RA, and Fibromyalgia. I am interested in chatting with people who are suffering from chronic illnesses and depression. My husband and I have been married 10 years, have a daughter 13, and son 9. I am trying to work, earn a college degree, and take care of my family as well as deal with the illnesses I have been facing for the past year.
I am a single mother of 2. I have an 15 year-old daughter and an 8 year-old son. I was diagnosed with SLE (Systemic Lupus Erythematosus) in 1994. Things are going ok.
My 16 yro son has been diagnosed with ADPKD, we are trying to learn as much as possible about this disease
My son is 26 with metastic Ewings. I am interested in trials, any info regarding overall care, comfort, pain management.
My name is Mandi my dad was diagnosed with PC 2 days after Easter this year…they said it was inoperableat this time due to being wrapped around the main vein in the liver he started chemo 3 weeks ago and now is going thru radiation, on Monday he will recieve his pump and then will be getting chemo and radiation 5 days a week for 5 weeks then 3 more weeks just chemo then back for another CT scan.
I am a 43 yr old lupus survivor. I am married with 2 adult sons , a daughter in law and a beautiful granddaughter.
I have been diagnosed with lupus, sojgren’s, raynauds,arthritis,depression,fibromyalgia, chronic pain,High blood pressure,diabetes…
I want to know more about these diseases/condtions and meet others that are dealing with all this.
I am a 40 yo that was diagnosed with Arnold Chiari Malformation and have not had very good support nor answers to questions because i have no insurance
I was diagnosed with this condition several months ago and want more information.
I was diagnosed with SLE many years ago. I have lived with Arthritis since I was 7. I am 35 years old and I have 2 children. I am married. I have kidney disease, CHF, Sjogrens, Crohn’s and Raynaud’s disease, to name a few. I want to learn more about how patients are being treated. I want to be able to help others with any questions that they might have.
I am 59 years old, mum of 3, grandma of 1. Suffering very badly at moment with aggressive RA - taking MTX, Celebrex, not getting much pain relief from this. Very bad shoulders, neck and wrists which are making life very difficult at the moment. Trying to move house as cannot manage stairs !!
Live in Shropshire, England in the Ironbridge Gorge area - very Victorian !! - Lynda
Hi , I am Toni, I am 42 ,married with 4 teenagers ages 18,18,16,and 14.We live in a small rural area in upstate New York, over by lake ontario .I have had RSD since 1995 when I was badly injured my left shoulder at work. Long story short, after 4 shoulder surgeries I am now left with degenerating arthritis in my shoulder and the RSD monster has set up house and decided to spread the the entire left side of my body.
I am intrested in groups like this one to enable me to speak with others whom actually understand what RSD is .(heck my regular family doctor has no idea what it is ugh!) I am looking for the support, knowlage, experience found in numbers. A place that we might come and find a comfort .
I have had Lupus since I was 22, and I am now 53yrs. old. I also have Fibromyalgia, and a host of other malady’s. I just like to keep in contact with people who have chronic illness and can relate to all the “bad” day, as well as enjoying a few “good” days, and having someone “really understand” that can offer support, and lend an ear for those days I feel like I need to “vent”.
hi, my name is sharon. i just found out about 3 months ago i have ic. i wanted to meet some people in my area to talk about it. who also have ic.