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kevin
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crohns
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nicolamast@aol.com
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Clarzie
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Crohns
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UK
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clarza@msn.com
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Scots Highlander
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Crohns
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I've had Crohn's for 14 years and am Lactose intollerant. I've been lucky and haven't had any operations. Currently on Mercaptopurine long term. Looking for comments on food/medication/holiday destinations from other sufferers. Feel free to email me
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Inverness, Scotland
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ian.simpson7@tesco.net
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 Rachel |
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Chron's and Ulcerativ collitus
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Hi my name is Racheland I am 19yrs old and have known about my thing for just under a year. Eva need to chat?
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Nottingham, U.K.
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rachel_elliman@hotmail.com
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samantha
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crohns
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i have had crohns for nearly 10 years now, havent been too bad with it really till the last 2 months which have been hell. emailme if ya wanna chat about crohns or anything, i am a part time worker in a restaurant. I have a husband and 2 boys Ashley aged 9 and Joseph nearly 4.
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i am from chippenham in wiltshire in the u.k
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samweeler@aol.com
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Anita  |
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CD
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Hi all i have chrons disease since i was 23 now i am 33 but i am out of remission my doctor wants to do surgery i am hell of a time with also i have ibs i am singel no man wants to date me becasue of this i am on ssi. i cant work if u want to talk email me.
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jvena@wi.RR,com
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Dave
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Crohns
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44 years old  Crohns since 1983 (1988 diagnosed) 3 resections - last one in 2002. Seem to have tried most drugs, currently on Methotrexate course of jabs 02/04 Welcome chat from anyone who wants to talk
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Bedfordshire UK
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Lloydees@btinternet.com
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crohns
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hi! my name is kevin - 46 years old , divorced with 2 girls (11&13) have had crohn's for about 25 years - had an ileostomy 2 years ago , doing much better.... live in houston,texas and work for the city.would like to hear from anyone out there...
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houston,texas
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kfritz@houston.rr.com
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Hi my name is Leia stevens, im 19 and live in Kent, UK. i have had Chrons disease for 3 years and theres still a lot im unsure of! i am a very bubbly person and i love to smile everyday-i enjoy driving, geting out in the sunshin (when its here!) and talking, i love logic and adventue games and i hope i could meet a few new people who dont worry that they will catch chrons from me! it would be nice to speak to someone who understands! feel free to mail me any time at cheeseobsessed@htomail.com thanks! Bye
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Crohn's Disease
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I was diagnosed with Crohn's this year and the hardest thing is other people. They say i'm always complaining. They don't know what Crohn's is and i'm not sure how to explain it to them. Can anyone help
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iamjenn_gray@hotmail.com
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joanne
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palmer
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crohns
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15 years old 16 on the 13th of july. i have had crohn's sins the 11 of july 2002 have 2 dogs have now got a bag had that on the 28th of march 2003 love shopping and good on cloths
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derby in the uk
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crystle0@hotmail.com
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 Hi There Im known as Spiritman Or Just Plain Bernie..I had my Operation last September having an abscess removal from the large intestine and a partial bowel removal also..and a Colostomy/Stoma enplacement..so I now have a new friend named Skippy who lives in my pouch just like the real Aussie Kangaroo does? It takes a while to adjust to this new and wonderful creature, but to get use to it is a must for all of us pouch bearers wether we like it or not, at first the protrusion seems to want to be the boss like getting in the way when bending over, or allowing strange aroma's into the air when it suits itself to do so, or on a more serious note to allow certain fluids to leak out at the wrong time and place! Yes there will be a time when you will have to make allowances for this, but believe me you will adjust in time to all its little wonders and tricks it like's to perform for you, so be aware and not afraid of your ostomy protrusion because yours truly has been there and done it, and so have many who are comrades in arms.. Or should that read Pouches??? If you would wish to email me you are very welcome to do so.. Thats why we are all here for, to make friends just like I have and be to be reassured that that life can be as nomal as it was before your operation........I do wish you well.........Bernie ( Spiritman )
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Colostomy/Stoma's
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spiritman@ntlworld.com
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Vicky  25 Years Old
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Crohns
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I was diagnosed with crohns in 2003 and have it in both my large and small intenstines and have been on steriods on and off for nearly 2 years, recently been told by my specialist that i am going to have an operation to remove part of my bowel. has anyone had this operation i am really scared.
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Pontypool. South Wales
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vickyfrancis38@hotmail.com
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.John
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Crohns
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My teenage son has been diagnosed with CD and is just recovering from a Christmas relapse. Road to recovery well in sight
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john.short@blueyonder.co.uk
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Shona (weeyin)
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CD
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I was diagnosed in 1988 when I was 12. I feel as though this illness took away what should have been the ' best days of my life'. I am single and do not have children. I have tried to be positive as that is the only way to deal with this illness and have not let it interfere with my life, well as much as I can. I had 2 small bowel resections in 1994. I recently had 2 infusions of remicade, but had a severe reaction to the second one. Now it is just a case of 'wait and see' before I receive any more treatment. If anyone wants to talk, feel free to contact me.
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Glasgow Scotland
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shonpon@hotmail.com
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helen
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crohns
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i really need to chat to anyone with ibd i dont know anyone else who is ill with this and i need others to talk to. i am 37 with 2 children and have had chrons for many years i am about to stop work as i am scared and not able to get into remission
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lee.dixon@Tesco.net
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Di_uk
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Crohn's
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di-weston-2@hotmail.com
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I'm 43 and have had Crohn's for 24 years. I've had 4 resections, the last of which was 9 months ago. I'm currently going through a flare up and it looks as though I'll be having my 5th resection sooner than I thought! Feeling crap at the moment but if anyone wants to chat feel free  |
UK
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di_weston_2@hotmail.com
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Kerrie
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Crohns
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Hi, my name is Kerrie, I'm 19 years old, and have only been diagnosed with Crohn's disease a few months ago (November 2004). I am waiting to have an operation to have part of my bowel removed. Feel free to email me, would be good to talk to someone else with Crohns. Kerrie xxx
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kerriej85@hotmail.com
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kat
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crohns
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22yrs old, 2 children,crohns problem patient
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topchick22@msn.com
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Crohns
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pauley48us@yahoo.com
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Diane
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crohn's
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had crohn's since 1994, had ileo Feb 2006.
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from the north west
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lenordee@hotmail.co.uk
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Helen
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CD
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helenmcd2@hotmail.com
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Rachael
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Chrons
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hi im Rachael and im 14 nearly 15 i was diagnosed with chrons in feb 2005 and ive been on the horrible drinks, steriods, and something else which i cant remember and i am now on infliximab. i would like someone to talk to about it 
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titchy91@hotmail.com
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Diana
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Crohns
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michelle
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crohns
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 Ive had crohns for 5 years its not to bad which is good. I have 3 children 2 girls 8 and 4 and a boy of 9 months.live is good at the moment and I wish every one a happy one too 
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uk
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youngfreeandsingle002@hotmail.com
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Hi!! My name is Saffron I dont know any other people with Crohns and I would like to share stories and tips.
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Crohns
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Hi my name is Saffron and I am 31. I was diagnosed with Crohns when I was 19 however, they believe I have had it since I was 14 just misdiagnosed. I have had one surgery and did well for 1st year and now I am struggling again. Any great meal ideas would be appreciated. I have never really spoken with other people who have Crohns so I would love to chat about common things (problems and solutions).
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San Diego, California USA
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mcamacho28@msn.com
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AMANDAFAVER@HOTMAIL.CO.UK
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crohns
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AMANDA
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CROHNS
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AMANDA
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AMANDAFAVER@HOTMAIL.CO.UK
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Lia
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Chrons
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was diagnosed in january this year, have since had conlonscopy and fistulectomy. am now in full remission, no meds only herbal support from my naturopath, no lingering signs at the mo.
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I live in sunny Auckland, New Zealand a small hop from the beach and a ferry ride from work.
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liavanbaaren@hotmail.com
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Jennifer
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Crohns
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I'm 21, was diagnosed at 3 been in and out hospital many operations, had a colostomy aged 10, now have an ileostomy instead.
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Scotland
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jennifer101418@yahoo.co.uk
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Lin .
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CD
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I am 42 and had Crohn's since 1980 and I also have a Ileostomy. I have had many operations and attend St. Marks Hospital ona regular basis. I would like to correspond with other Crohn's sufferers. I have had a difficult time with the disease as it has affected my life in many ways. I have been to hell and back so I can relate to almost anything to do with this terrible disease. So if you would like a genuine friend please get in touch .
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UK
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singleton1917@aol.com
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Tom [;{> AKA Tomkat,
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Crohns
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CD 32+ years, Ileostomy/colostomy since april '86.
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Northwest Indiana, Near Chicago
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tkillorat@yahoo.com
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(r)Gemma(r)
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Crohns
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I was diagnosed with CD in February this year after a year of feeling unwell (was told i had IBS at first).. i could thank my GP, GI Consulatant and the nurses in the hospital enough for the help they have given me!!
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Bonnie Scotland
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Gemma638@hotmail.co.uk
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(r)Gemma(r)
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Crohns
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I was diagnosed with CD in February this year after a year of feeling unwell (was told i had IBS at first).. i could thank my GP, GI Consulatant and the nurses in the hospital enough for the help they have given me!!
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Bonnie Scotland
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Gemma638@hotmail.co.uk
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another scots lad
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crohns
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colitis
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iv had crohns and colitis for about 8 years now and have been though an op (rh hemicoloctomy) at the end of sept. on all kinds of drugs andim still in remission and thats after my op! been in the highlands i had to go to my local hospital, total waste of time!! the so called expert kept telling me i was stressed out! what a joke like, went back to my doctors and said that i wanted to go elsewhere, so i went to Aberdeen Royal. i was there for a week getting all sorts of tests(to which my local hospital had done) and they found that i had a narrowing of my colon and that i had to have emergency op. so all in all its better to get a second opinion if you are having no luck with your docs. if you want to get in touch plez do neilfisk@hotmail.com |
sunny inverness
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neilfisk@hotmail.com
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Gemma scanlon
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crohn's and colitis
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UK
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caseyrose25@hotmail.co.uk
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Lisa
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crohns
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I am 33 year old woman with 3 girls. I have had crohns since I was 15 years old and suffer with related arthritus, I have had 2 operations and am currently on the list for another one, would love to talk to anyone.
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Letchworth. Herts
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llisa666@hotmail.com
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Sandra
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CD
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Hi my name is Sandra and i only got CD in the last year ..been on steroids etc .I also have a son with a rare inflammatory bowel disease , multiple food allergies, sever reflux , blind loop and bacterial overgrowth and joint problems .He is 13 and artificially fed ......I would like to hear from anyone
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Northants UK
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anyakisses@hotmail.com
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Carole
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CROHNS, ulcerative colitis, mennieres disease
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I was diagnosed whith crohns and mennieres in 2000. I have never had any remision but amfortunate enough in that I have not so far needed any operations. I was diagnosed in 2005 with ulcerative colitis. I do not work, I have THE BEST hubby and 3 fab kids. Apart from the pain in the butt, ha ha, life is a laugh.
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BARR,SCOTLAND
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CAROLEMcCLYMONT@aol.com
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Carl
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cd
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36 yrs old Had CD for about 4 yrs. Currently on loperimide, prednisalone and Questran. Had a hemi collectomy in Dec 2000
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Llandudno North Wales
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carlharrap@hotmail.com
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Robin
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Crohns
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I am a Nurse and have CD for 2 years
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Texas, USA
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robin78c@yahoo.com
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JENNY SHIMMIN
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crohns
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am 15, 16 in september .i have had crohns since march 2002, i have been on loads of treatments but i now have an ileostomy ( have hadone since january of this year )i went for a colonoscopy and my colon perforated and i ended up with a bag , but it is the best thing that has ever happened to me !!! i just thought i would post a message on here to see how every one else has coped with a bag , i am so glad i have had it done as i am so well at the moment  . even though it was a bit of a shock at first . some of the treatments that i have been on include... azathioprine , tubefeed ( 9 weeks twice ), antibiotics, map bug treatment, skandishake errrrrrrrrrmmmmmm....... TPN also ad helicobacter pylori .lol ave been on more but i cant remember them at the mo. n e way will be happy to hear from anyone .
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BURY
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jenshimmin@msn.com
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Claire
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Crohns
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 Diagnosed in March 03 after removal of gallbladder op but think I have it about 10 years. Currently taking azathorpine, budesonide and Vitamin B12 injections every 3 months. Feel a bit shitty most days and very down. Can't get used to feeling absolutely knackered. Can't eat vegetables, fruit, anything with skins on or red meat. Would love to have any advice from other suff erers...... |
Wolverhampton, West Midlands
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clarza@blueyonder.co.uk
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Sarah
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Crohns
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I found out that i had corhns in june 03 it has been hell and there are still things going on that i cant talk to freinds about cos they dont understand if you want to chat then feel free to email me
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Greenwich
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Cheekylady44@hotmail.com
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Sarah
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Crohns
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I found out that i had corhns in june 03 it has been hell and there are still things going on that i cant talk to freinds about cos they dont understand if you want to chat then feel free to email me
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Greenwich
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Cheekylady44@hotmail.com
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Sarah
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Crohns
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I found out that i had corhns in june 03 it has been hell and there are still things going on that i cant talk to freinds about cos they dont understand if you want to chat then feel free to email me
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Greenwich
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Cheekylady44@hotmail.com
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Christie
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Crohn's disease
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 21 year old female from Canada with Crohn's. Have had two surgeries so far for my Crohn's. If anyone would like to chat feel free to e-amil me! christie@crohnszone.co.uk |
Canada
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christie@crohnszone.co.uk
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