Thank you for visiting the ICN Support Forum. We are so happy that you found us! The ICN Support Forum is home to 50,000 patients who have participated in our 24/7 support system. However, to protect the privacy of our members, members of the public can not read posts unless you have registered first.
It's easy to register! Just click the "sign up" button in the upper right corner of the page. Make sure you use a correct email address because we'll send you an email to confirm that you are a real person!! We also screen all new applicants to verify that they aren't bots or spammers! If you have any problems, please feel free to send a quick email to: [email protected]!
Hello I'm new here and just wanted to say HI and this is a great site. I've been over every inch of it and was so amazed. As for me, I haven't officially been diagnosed, but I'm glad i have to place to come to to share urinary problems :p
Hi and welcome to the site. Since you have read a lot on here you will be that much more prepared to work as a partner in your care with your Dr. With IC that is a big part of your treatment, to know about the disease and work with your Dr. I don't know where you live in Texas but if you are needing a support group I know that there are for sure support groups in the DFW area and Houston and I think Austin. So we are fortunate here with our great medical care and with people willing to give their time for the support. Good Luck
Jolene
Jolene
"Life is what happens when you are making other plans" John Lennon
Jen's tips for great IC sex..http://www.ic-network.com/forum/showthread.php?t=22522&highlight=jens+tips[/url]
Newbie Angel...I will be happy to answer any questions or just listen. Email me at [email protected]
"IC Angel Volunteers are not medical authorities nor do we offer medical advice. In all cases, we strongly encourage you to discuss your medical treatment with your personal medical care provider. Only they can, and should, give medical recommendations to you."
I'm new, too. We're in the same boat. I just had the bladder hydrodistention done and I get my results next week at the post-op appt. I think I have it but we'll wait and see. They think I've had it since I was a kid because of the symptoms I've told them about. I just started seeing a urologist this year, but I should have seen one a long time ago. I've had stupid symptoms since I can remember but thought everyone did, you know. I wouldn't want another kid to go through that. It's not right. Anyway, welcome. I hope we can help each other.
"Life is 10% what happens to you and 90% how you react to it"
Hi Justice and welcome to the family, you are not alone here. Plenty of help, and advice, and compassion, when needed. Keep us posted as to how you are doing and good to have you on board, take care and welcoming hugs Iris hi grouphug
Today and every day you are loved, so don't be anxious about tomorrow, God will take care of you tomorrow; Live one day at a time.
Comment