i suffer from major depresssion and anxiety and panick attacks which are under control at the present time i just wanted to talk to others that may be on the same meds as me and c what there sideffects were…
ey, my is Jonelle Burgest. I am mother of three teenage daugthers. Ive been depress after i lost my sister last year. Iam a change person. I need support because I feel iam going to lose. Iam meds, but its not helping me. I need support. I feel no one understands me. I wanna learn how too control my life again. I wanna connect wit that is suffering from depression like me.
I am a woman who wants to learn more about the conditions of others and help thoes who want the help.
Hi - I am going through a divorce along with being in a major motorcycle accident. Depression, anxiety and pain are all I seem to have to think about these days.
ok, i want to learn more about depression, i was told by a doctor i have depression,that was when i was 17, i am 27 now and my depression has got worse, i want to connect with people who have depression, likei do, so we can talk to each other and maybe together make the depression go away, or at leat not so bad.
I have depression,anxiety,insomnia and chronic pain. I want to learn how to deal with depression.
I am quite ill and have been for awhile. I am so Anxious or so depressed I can not get out of bed for weeks on end. I need help and do not know where to turn. I am Not Suicidal, but Ihave NO LIFE, only my bed. Everything given to me has not worked.
i want to talk with others that are in the same situation as me… i drink to be able to verbilize… i know im depressed but need to drink to verbilize
I would like to talk to others who live with chronic pain and diabetes insipidus.
I like many have Dercums Disease, being newly diagnosed of this rare but non cure, as of now. I am looking for others that are willing to stand it out, till there are cures either by the mapping of the genome, or a drug that either suppresses it, or cures it.
Hello! I have been told by two doctors that I have mctd, and I just want to learn as much as I can about this, and I hope to share with others about mctd…
Hi, My name is Daniel Hansen, I am a Doctor of Upper Cervical Chiropractic. I have seen many sufferers get well from all sorts of disorders such as: Trigeminal Neuralgia, Chronic pain, Migraine headaches, Asthma, Carpal Tunnel, Seizures, Meniere’s Disease, Bell’s Palsy, Fibromyalgia. My mission is to get sick people well. I am here for support and to care for those that suffer from terrible disorders.
Hi! I’m Sue. I was dnx’d with Lupus and Mixed connective tissue disease… Its not went into organ involvement as of yet. I also have Fm,Oa,Neuropathy in my legs,hypothyroidism,HB…some minor disk problems in my back and neck. I am full of it…Pain that is! lol
I am married and have 4 grown children…we have 2 small grandsons and also have 2 grandchild who will be born in November/December the Lord willing. (my sons wife is expecting and so is my youngest daughter) I am looking foward to meeting all of you!! Love,Sue
I experienced my first migraine at age 6, so I’ve been on this wild ride for more than twenty years now. But in November 2003, my migraines became much, much worse for no easily identifiable reason. Ever since I’ve been trying to find the right combination of preventatives and have a somewhat normal life. It is hard work being sick and trying to get well, but I’m hanging in there.
I blog about migraines and depression at http://migraineur.blogspot.com. Writing helps keep me sane.
Hi, my name is Sara and I suffer from Trigeminal Neuralgia. I have learned a lot about this disease since my diagnosis in 2003 and have made a lot of research in order to help myself as well as others cope with it. Right now I am in remission, but I have joined this list to see how I can be of help to other sufferers. One of my goals has been to create awareness among the medical community, because it seems not many of them are knowledgeable about TN.
Hello to all, I am 27 and have had Trigeminal Neuralgia since July 7, 2006 at 6am sharp. I have been diagnosed with both TN and ATN since July 17, 2006. I had a MVD procedure done August 28, 2006 and unfortunately was unsuccessful. I would like to find more people to talk to that have Trigeminal Neuralgia.
I was diagnosed with Rheumitoid Arthritis in 12/2003. Just prior, I was diagnosed with Sarcoidosis, and my Rheumitologist believes my RA is actually Sarcoid in the joints. I have tried many different protocols, but still have not been able to wean off Prednisone. I am now on Remicade and Methotrexate. I would like to share information with others who have had similar experiences.
I was diagnosed with Systemic Lupus in October 1992. Six months later I was diagnosed with Fibromyalgia. At the present time I am having a hard time dealing with this stupid disease. I am getting a second opinion tomorrow from a rheumatologist in another city. I feel my present rheumatologist just is not giving me adequate pain control and I do not feel my Lupus is under control. I feel my health is going down hill fast and my present rheumatologist just does not seem to be taking me seriously. I am hoping this new rheumatologist will be able to help me.
I have been diagnosed with TN for about 5 yrs now. I am currentlt on Carbatrol 300 mg 3 x a day and have been completly pain free for the past year. But from everthing i’ve read, nothing lasts forever, and am dreading the day the pain comes back.
I am the author of the only book on the first person experience of living with and struggling against trigerminal neuralgia.
My pain started in 1979 so my experience has encompassed most of the medications, therapies, and surgeries.
If this group is as supportive and helpful as the Yahoo group I would very much like to be a part of it.
Thank you.