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I hope I'm not breaking any rules by posting here, but I just wanted to say this to you all:

Don't EVER give up hope- especially when it comes to something like a relationship. I've been with my girlfriend now for exactly 22 months today. And I have to say- I NEVER expected to find someone. I was 19 when we met, and though we were both single, it took me forever to ever ask her out. As all of you have mentioned, dealing with Crohn's was enough, I wasn't even thinking about a relationship. But as it worked out, she has become the most important thing in my life. And if I'd never gotten the courage to invite her to a simple movie one day, I'd be without her.

Now that doesn't mean anyone NEEDS to have a significant other. All I want to convey is that you DO NOT need to be at "optimal health" to spend time with someone. If your Crohn's is a little active, then deal with it! It's awkward I admit, but if the person is worth being with, they will understand. Even from the beginning.

Here's to hoping all of you find happiness- even if it doesn't at all involve a significant other. Learning to love yourself and to be comfortable with yourself is so vital. You need that before you should be thinking about a relationship.

I agree 100% with all you said except you have to love God too.But, hey that's me! I am happy you met someone who overlooks your health issues. To me, that is just part of loving someone and I mean it's even in marriage vows. People get sick, it's part of life. If you are that selfish of a person that you can't handle illness in your partner, then you don't deserve one! Just my point of view. My hubs has been through cancer with me and the surgery he took care of me recovering, and crohn's and back surgery, you name it. It brought us closer if anything. I appreciate him so much more for all he does for me and he appreciates me so much more because I could have died and my life was spared and we still have each other to love. How perfect is that?:heart::heart::heart::D
 
I'm so glad you found love and that your illness wasn't an obstacle.

Well, I doubt that the illness wasn't an obstacle, but it was an obstacle they overcame! Let's face it, it's not easy, but with the right person, it's definitely possible. (And even with the wrong person, it's not always, or even often, the biggest problem with the relationship).

Hope we all get the kinds of relationships we want, and sooner rather than later! :)
 
To everyone worried about someone not wanting to date you because of an ostomy (just came back and read stuff since pre-op a couple months ago), perhaps my perspective is different because I know any Crohn's patient runs the risk of waking up with an ostomy at some point down the road, but I totally don't think this would be a problem for someone who wants you for more than a lay - and even then...! I did my fair share of research before my surgery in april because I was very sick and the risk of my coming out with an ileostomy was elevated. I got lucky, but it looks like there are some 'solutions' for concealing the bag if it makes you feel more comfortable and confident. But really, as someone without an ostomy and who had a long remission, I can confidently say that any reasonable healthy person who likes you isn't going to bail *because of* our Crohn's or our bags if we have one. At least for me, and I think for a lot of people, finding someone you really like is so tough that once you find one, bailing because of a bag just isn't rational! It's hard when we're really sick (hell, I've been couch- and bed-ridden for a couple months now between surgeries and abscess drains), but we all need to remember that our illnesses are but one (albeit important) small part of our entirety as people, if that makes sense, and that the people we know see it as being a much smaller part of us than we do (which is why they act like such d!cks sometimes).
 
I think it is all too easy to judge a partner for not being able to cope with our illnesses or to even understand it.

Image being on the outside looking in, especially for a bloke. It's in a man's nature to want to 'fix' the problem and if they can't then they can feel pretty useless.

I'm not excusing anyone who uses an illness as a reason not to be with someone. But to be honest, if it was the right person, the illness wouldn't even be an issue.

I find that my illness and illeostomy bag is a great way to sort the men from the boys, without me having to look to hard. But, I always give guys a chance to get to grips with it, even if their initial reaction is bad, they are only human after all.

I believe my ex broke up with me because i'm stubborn and pig headed...and lets face it there is no cure for that either :ylol:
Whilst I am not a sufferer who has a bag, when I was ill the first time without a diagnosis I realized the various possibilities of what my illness could be and that if things couldn't improve then I may need a bag. I had a female work colleague who was always championing the rights of the disabled because she had worked in care. One day I asked her if she'd go with a guy with a bag and was staggered when she said, "no way!". Staggering. Despite not having a bag it really put me off her, just the thought that you could desert a person because they needed this surgery. I thought she showed herself to be so shallow.
 
Hi Guys! I jus joined this support group, and so glad I did since I'm single. I seriously think that I'll be single forever bc well let's face it, jus walking into a possible relationship its unlikely somne is going to willingly date a person with a chronic illness that is very stressful. To be honest, I wouldn't. So I can't even get upset at somne else for judging me. My symptoms are embarrassing as is and I've had to deal with it for past 16 yrs. Now. There's talk bout me being in a bag bc my disease is so far gone. *sigh Now my chances for meeting a good man got even more slim. I try not to dwell on it much. But it can get depressing at times around holidays and fun events. I have my family for moral support. However, meeting my soulmate and getting married and growing old with the one you love is a dream come true. But again, some ppl who are (healthy) can't find it how much hope do I have??
 
Hi all!
I'm not new to this group, but I haven't posted here before. I just wanted to share a little insight for others who may be struggling with the idea of being single.

I've had my heart broken so many times and have also done the heart breaking. It wasn't until recently, the last couple of months really, that I have come to accept single-hood. I came out of a deep depression (not related to Crohn's) and finally had this epiphany: that I am content alone. I enjoy being single. I have finally accepted myself for who I am. I think that is key to being single. You must be content with yourself first, regardless of disease. Do I want a partner that will support and love me unconditionally? Absolutely. Will I give up hope that it will happen for me? Absolutely not! I will always hope that I will find someone. But I've made the conscious decision that I'm not going to let myself get upset about being single. Eventually, I will find someone, but until then, I am going to continue on trying to be the best possible me.

It's taken a lot of inner reflection and self-acceptance to get to the point where I'm at right now. I just hope that everyone here can appreciate YOU for YOU because you are AMAZING just the way you are, IBD and all!
 
Don't get me wrong, I've learned to love my single life but I was jus thinking how nice it be to actually find a nice guy who is understanding and not grossed out by all the embarrising symptoms I get w my Crohn's. Lol but until then, I'm proud at how far I've come! :)
 
Had a few great dates and am now a little hesitant to make things romantic b/c of seton drain. The stress of dating and worry of what guys will think when we hook up is terrible! Wish me luck!

How did it go? I haven't dated for a while because I hated the thought of having to explain my seton drain, but I'm trying to just go for it now. Still a bit nervous about how/when to discuss it though.
 
Hi, I'm pretty new here too. I was diagnosed with Crohn's in 1975 when I was 13. I've been single much of my adult life. The few relationships I've had ended abruptly when I've ended up in the hospital ... or I've had a bad flare. Even some friends have disappeared when I've gotten sick. So I've resigned myself to being single. The friends who've stuck by me through it all are my family.
 
Hey everyone, it's nice that this group exists! I am 26 years old, but I have had Crohn's since I was 16. I have struggled with maintaining my relationships with friends and family members since I was diagnosed. Finding a nice guy?? Forget about it - at first it didn't bother me very much, as dating is not really a norm in my culture. I am still okay with being single, as I am just beginning to get my life back on track - I want to be able to actually enjoy the single life before I settle with someone. However, if fate comes by my way tomorrow, I am not going to resist :soledance:
 
Gotta join this group!
I really wish this was around when I was 12. I was really sick all through high school so I never dated. Got my ileo at 19 and started to live...but really avoided relationships. I just couldn't picture any girl being alright with this so I never gave anyone a chance. Been in relationships but never risked letting them go anywhere. Been totally fine with the single life. Recently I've started thinking it would be nice to have someone in my life. My family isn't that close and I've got good friends but it's not the same. I go to my appointments on my own. I take a cab to the hospital when I have a blockage. I often go into surgery and come out of surgery alone. If I'm only in hospital for dehydration it's hit and miss if I see anyone. In fairness I always down play what's going on. Mentally I'm stuck in that time when I was sick. I don't believe I'll ever get married. To top it off I need to move home because this flare is getting the best of me. I can't work and I've lost everything. Not a very eligible bachelor. I would be happy just to get back to being a happy single person. Wow, I've never said this to anyone before now.
 
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I can't believe I didn't find this support group sooner! :ywow:
It's a really good idea, so does anyone have any tips for a 26 year old single dad with low self esteem?
 
46, strait, female, mom x 4, grandma x 2, been single for about 2 years. Most days I'm glad I'm single, too exhausted to not be. Date? are you kidding? get dressed up and have a conversation with someone? That would seriously cut into my nap time! (risk having gas in public? no way!)

I'm not part of this group yet but I will be after the holidays but this post is so so true this would be me LOL
 
How do you single and dating folks deal with body image? I finally found someone I am interested in dating and who seems very interested in me as well. They are being very compassionate about my crohn's situation.

But I am realizing that I have developed some lower-body image issues. I have barely dated since I have been diagnosed and have only been intimate for a VERY short period since diagnosed. And when I have I tend to try and hide my body/cover it up more than I ever did before and I know it's because I am thinking of my crohn's. I don't feel comfortable showing/exposing myself.

Has anyone else single/dating experienced this? How do you cope/manage? What do you tell yourself to overcome the insecurities brought on by IBD?
 
I'll tell u this much. By experience, if he's into you he won't care bout scars. I don't have any. But I do have stretch marks really bad I can't wear a bikini ever again. I'm self conscious bout it. I hate them. But he loved it. I didn't understand I felt they made me ugly. And sometimes at night he would kiss them and say it shows that I'm a strong woman who bared 3 beautiful children and still got a rockin body! Lol. Well, he made feel better. U see, doesn't matter how you see yourself. If he likes you they se it in a different point if you. It's up to you to look at it from their eyes and not focus so much how you view ur body from your eyes. Guys like confident women. Be confident. Having Crohns is an every day struggle. Be proud how far you've come. And I wish you all the best with u and the new lucky guy! :)
 
No. no surgeries or scars. Just feeling a bit insecure about my body is all after all the illness it has been through. Thanks for the advice and support! :)
 
You mention the lower body though. If no scars is it about running to the bathroom? Or did your body proportion change due to weight loss?

Whatever the reason I think the same answer applies in most scenarios. If someone likes you for who you are and cares about you, it shouldn't make a difference in the world. I find from personal experience that my insecurities lessen once someone I'm with reassures me they don't see me any differently and it's confirmed through their actions and the fact that they stay with me.
 
I'm not gonna lie, when I was w my ex. He lived with me. And boy were there days I wished he didn't. Lol. Even though I have my own bathrm in my bdrm...didn't matter. There's no privacy w kids. They leave my bdrm door open. I'm doing my business right when he walks in. I wanted to disappear. I was so embarrassed. I don't care how much he'd cared. Don't nobody wanna be around that! Lol. Well, anyway. The urgencies and death smelling bathrm usage is all part of Crohns life. And like I mentioned befre. Even though we hate it and embarrassed by it. If they care, they are more than understanding its all part of our disease and have no control over it. It's hard. But that's why we have our own lil forum to vent to when it comes to dating! Lol ;)
 
I'm so glad I found this group. This is my First time being single and dealing with a major Crohn 's issue. Defiantly a different feeling. I'm currently in the hospital dealing with my second flare in 30 days. (Ended up in a different hospital last time was not treated aggressively enough)

Thank you guys for being here
 
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Hi. I have had Crohn's for almost 2 years. I don't have any serious symptoms yet. Just taking 8 pentasa pills a day with bleeding and going to bathroom about 12 times a day. I don't have bad stomach pains thank goodness.
 
What a great idea this thread is....as I sit here all by myself :rolleyes:
At least I have my cats.... 4 of them. I better get a boyfriend before I end up with 5 lol.
All joking aside now, I really miss having a boyfriend. Been single for 7 weeks now. The ex never came right out and said he was sick of me being sick, but I would be if I were in his shoes. The flare ups are bad enough, but even when they subside, the back and leg pain, restless legs, sinus problems,head aches and rashes never go away completely, some days are just a little better than others.
It would be nice to date someone with similar health problems because they would understand me.
But if I'm being honest, and a little selfish, I don't think I could handle it.
What about those rare days you actually feel half normal and your partner is sick. I have to live for those few days. And I can barely take care if myself most of the time.
I really miss having someone to take care of me when I need I.
My parents and friends are very supportive, but its just not the same.
 
Yea!! So glad I found this thread! I have been single all my life and have never been in a committed relationship (let a alone a date for that matter). I am 28 and have had Crohn's for about a year and half now. I had a colon resection back in February of this year and that put me into remission, but I also struggled with depression for a while during the recovery time. I still live with my parents because that is all I can afford right now. I work two jobs and still can't make enough money to afford my own place. My primary job keeps me very busy, but don't get me wrong, I love what I do, but I often feel isolated from my peers. The few friends I have are either married, or are getting married and I feel left out and they also did not give me a lot of support after I had my surgery.

I would like to start dating, but is seems like there are not many eligible men in my area. I have tried online dating, but it did not get anywhere. I also don't want to get "Catfished" either.
 
Hi All! Well, it happened. Im now carrying a bag. I had my colostomy surgery n Sept. I was having a tough time before with only my Crohns acting up. Now that my Crohns has been quit since my surgery I have to learn how to live my new life with this appliance. I kno how great it is that I'm healthy again. But its still some getting used to. I have to learn to feel comfortable with it. If I don't how can I expect another especially a potential bf to feel about it. What about those intimate moments. Oh, boy I think I'ma be si.glefor awhile...lol.
 
Hey, glad i found this group.

Been single for a while now. Was diagnosed at the tail end of 2008 and been on Remicade for the past couple years. Sucks not having anyone to be with when i go do my infusions. But i guess thats life. Definitely would like to find a potential gf that understands what i go through. Im from the bay area.
 
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This such a great forum, I was looking for something along the lines of single parent and I think this will work just fine. I have been recently diagnosed with crohns but have had it for a ling time. I am single and have been for about 4 years, I al so have 2 young boys 4 and 9, I have raised and taken care of them by myself.

this disease has not only taken a toll on me but it effects my children the most, most of the time I am to sick and in to much pain to do anything, my children want my attention so badly and I dont have much to give. I do wish I had a companion in life for me and my boys, but for now I will take working on the disease and my boys.
 
Sooooooo. I have a guy I am crazy about who is coming to see me in a few weeks....he has not seen me since I had my colectomy/ileostomy..... I need a pep talk. ...Yeah, he knows about it. But I don't think he has ever seen one and I don't think he is terribly comfortable with the idea.... It saved my life and is SO much better than living in Crohn's hell, but I still feel like a big freak and I already was shy in dating scenarios before all this. :frown:
 
Hello everyone! I just subscribed to this support group and I, too, am grateful for it! :)
I am 33 and single and am also caught in the battle between "hopeful and hopeless". I actually had a date tonight, but my flare up put an end to that. (thanks a lot Crohns) I was feeling a little sad and upset b/c it is very difficult to date in our situations. So I logged onto the forum and here was this support group... exactly what I needed. :) It is nice to see that we are not alone although it feels that way most of the time.

@nogutsnoglory thanks! I joined that prescription4love site you posted the link for. Gonna try it out and see how it goes.. fingers crossed ;)

I do a lot of online dating since I am usually way to exhausted to go out after work. I have used this site called plenty of fish and I usually make my title, something crohns related. It's a gutsy move, b/c I have encountered some mean people, but its cool b/c I just block them lol But I was surprised to see a few responses from people going through the same thing. I guess my point is... we have to be strong on a daily basis anyway, just to maintain, what could it hurt to put ourselves out there on regular sites and see who might be going through the same thing as us.. inspire a lil hope in ourselves and others. Hey and if it doesn't work, theres always a block option and a delete option lol :)
 
I'm glad to hear that you joined the site and definitely please let me know how it goes for you.

I think it's okay to put that you have Crohn's in your profile that way you can weed out anyone who might feel like that's an issue for them.
 
Sooooooo. I have a guy I am crazy about who is coming to see me in a few weeks....he has not seen me since I had my colectomy/ileostomy..... I need a pep talk. ...Yeah, he knows about it. But I don't think he has ever seen one and I don't think he is terribly comfortable with the idea.... It saved my life and is SO much better than living in Crohn's hell, but I still feel like a big freak and I already was shy in dating scenarios before all this. :frown:

Hey, that is so awesome for you. Hope it all goes well with your visit n the boy you're oh so crazy about. I'm in the same boat as you as to having a bag and thankful bc I feel heck of a lot better thank I did w/o it. As for your dude, idk, I guess I if I were you not to push it all on him. I'd wait for him to ask all the questions. But he didn't come to talk bout the bag I'm sure. Lol So let him see the real you have fun and enjoy all the things I'm sure you can do befre the surgery. I know I am!! :)
 
Hi! I'm 23 and single. I have had Crohn's disease since high school. I am really scared to go out on dates. I don't want to have an attack during the date or have to explain why to my date why I don't want to eat. Please give me some advice to help me out! I don't want to grow old alone.
 
Single momma of two young boys, 3 and 4.5
Some days are harder than others to gather the energy for myself never mind my two kids as well... Social Support would be great :)
 
There are several dating sites for people with crohns,UC,Ostomy not sure how good they are.


CrystaL Lee we could "what if" ourselves to death with possible bad out comes, stay positive and concentrate on all the great things that will happen when you find that special someone (and you will). It's not easy to take a leap of faith and go out but I've found most of the ladies I've dated are very understanding.
 
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I was single when I was diagnosed in 2012. Started dating someone shortly thereafter but the symptoms didn't help things. I had a temporary ileostomy placed in March 2013 and since then things haven't been good on the relationship front. Usually when women find out about what happened and that you have a medical appliance like an ostomy bag it turns them away.

I think this group will be great.
 
hi singles,

every article i try to find about sex and crohn's talks about how to communicate with your partner.... has anyone found anything on dating and sex?

im having a lot of pain in my rectum from three surgeries, and am totally self-conscious about the smell and sight of it. my sex drive has plummeted from the last two years living with these seton drains, and i'm so ashamed about it that i don't even try anymore.

anyone have similar experiences about losing your sex drive/being ashamed of your body? it would help to not feel so alone and depressed about this.
 
Let me tell you, I can't stand how I look with this bag. I didn't like how I looked when I was healthy, let alone how I look now. Dating has been non existent, but my drive is still high...prime of my life ya know lol.


hi singles,

every article i try to find about sex and crohn's talks about how to communicate with your partner.... has anyone found anything on dating and sex?

im having a lot of pain in my rectum from three surgeries, and am totally self-conscious about the smell and sight of it. my sex drive has plummeted from the last two years living with these seton drains, and i'm so ashamed about it that i don't even try anymore.

anyone have similar experiences about losing your sex drive/being ashamed of your body? it would help to not feel so alone and depressed about this.
 
I also can't stand how I look with the bag. Before the scars of previous surgeries bothered me but now I don't care about those. I'm afraid for anyone to see my bag I haven't pursued any relationships since I got it. I just flirt here and there to feel like I'm in the game but I'm too scared to deal with it.
 
I haven't been able to convince myself to getting into the dating game. I haven't had any surgeries, but I am still not in remission. I can't bring myself to try to date when I'm liable to spend the majority of the date in the washroom.

Hopefully one day all of us will find that special someone one day.
 
smack116 you're not alone I think we all get depressed about this wonderful benefit of have crohn's, won't be human if you didn't. I don't think being alone is a desired state for any of us. I've had an ostomy sense age 16 I'm 60 now in my younger years it really didn't hold me back from dating,it didn't seem to bother the woman I dated. I'm coming out of a twenty year relationship so it's back to dating although I don't think it will be as easy now as when I was 25. I've always found that developing a strong friendship helps reduce the stress, anxiety of letting them know about my crohn's, ostomy.

You have nothing to lose by stepping out and trying and everything to gain.
 
I really admire those who date freely without worry about the ostomy. The truth is it is what it is and if anything maybe will filter those who aren't open to it.
 
Divorced since 2004, no kids. Diagnosed with Crohns in 2005. Haven't been interested in any relationship since my divorce. Not because of Crohns (it's actually very mild compared to most cases I read about here), it's because my marriage was a very very bad experience. Stayed single and secluded to heal some scars and grew to prefer the single life. I don't look forward to growing old alone with Crohns, I would enjoy a companion to share my interests with but my heart got broken so bad that I have a hard time putting my trust into people. Tried a couple of dating websites but they practically ignored my preferences in my profile.
 
Anyone else search out terms like crohns, colitis on online dating sites? I rarely find anyone brave enough to publicize their disability, I certainly don't but I'd be more likely to message someone assuming we are a good match in other areas as well if they listed IBD or some ailment.
 
Hi Everyone, I have never posted in this group before but was advised to by one of the members.

I had posted on the stoma page that I had just got engaged. Susan said I should also write about it here as a lot of people with Crohn's and stoma's believe they will never meet anyone who will be able to deal with all the baggage we come with.

I first told my boyfriend on our first date that I had Crohn's, he wasn't in the least bit worried, although I was in remission and looked well then. After 2 years of being together I got sick again, I had to have a resection which he stuck by me through. A year later I had to have a total panproctocolectomy and end ileostomy, I thought my life was over and that he would leave me. He didn't, he stuck by me and helped me through everything. He also tried me to get to come to terms with my stoma every though I tried to ignore it was there.

I just want to say that no matter how sick you are or how bad you feel, you will come through it, it is very hard but the right person will want to be with you whether you are sick or not and whether you have a stoma or not :)
 
Thanks and I wish that for you as well. I found that when I was in a relationship that I was doing much better with my symptoms. I think the stress and lack of affection being out of a relationship makes my flare worse. I was in surgery very soon after my last relationship ended and I wonder if there is a correlation.

I'm 35 single have Crohn's and about 99 other medical issues. I guess I've found in the past that the people I've been dating or in relationships with have always been really pretty good about surgery... it's sort of like to a degree when anyone is in the hospital or has just had surgery there are sort of socital guidelines of what to do or how to try to help. And it's easy, they get to be the hero to their friends, your friends, the families (he's such a great guy, he's been at the hospital every day, he's been doing all the cooking and cleaning, he bought such beautiful flowers etc. etc.). I find it's the the regular day to day life of being in a relationship with someone who has Crohn's or other illnesses. They don't get it and they (not always their fault) say and do the wrong the wrong things and don't understand enough to understand why your weight fluctuates, or why your night table is a pharmacy or why you're too tired to go out even though you planned it weeks ago and you reservations someplace impossible to get into. They may care a lot about you, you may even love each other but it's like living in two different worlds and sometimes no matter how much you both care and try it's impossible!
 
I think I've dated once since my disembowelling. It ended quickly by my hand, it was a couple months after surgery and I was just finally starting to get over the ending of a long term relationship. She wanted far more than I was able to give that early on. She kind of scared me, should have seen the warning signs on the first date. I just kind of stopped dating after that. That was a couple of years ago.
 
I am 45 and divorced. I think it was one of the causes for it but she was to polite to say so. Dating someone who isn't in the medical field or knows what we have blows. Can we get a meet and greet or dating forum?
 
I am 45 and divorced. I think it was one of the causes for it but she was to polite to say so. Dating someone who isn't in the medical field or knows what we have blows. Can we get a meet and greet or dating forum?

That would be awesome as I am newly divorced and would love companionship with someone who understands the disease. This is what ultimately ended my marriage. Thanks for suggesting. : )
 
hi all, i live alone and was diagnosed with crohns in june. I have since started humira, but the doctor thinks its not working well.

what is really bothering me is she recommended i go to the emergency room and get a blood transfusion because my hemoglobin is at 8.1. im really worried about this process, any advice?
 
Ugh I know the feeling, I'm quite self conscious as it is but when I got diagnosed with crohns a week before my birthday I lost all my confidence mainly because I went down to 6.3 stone and all my bones were poking out but things are picking up I've put a stone on and getting my energy back. But as much as I would like to meet a guy who wouldn't be bothered about me having crohns I don't have the confidence to do it, I think it would just be easier to find a boyfriend who also has IBD. It would take a lot of the embarrassment away I know that much!

lol sorry for the rant!!
 
its ok, i dont weigh too much more than you did.
the transfusion went ok, i dont know how long it will last for.
 
Divorced since 2004, no kids. Diagnosed with Crohns in 2005. Haven't been interested in any relationship since my divorce. Not because of Crohns (it's actually very mild compared to most cases I read about here), it's because my marriage was a very very bad experience. Stayed single and secluded to heal some scars and grew to prefer the single life. I don't look forward to growing old alone with Crohns, I would enjoy a companion to share my interests with but my heart got broken so bad that I have a hard time putting my trust into people. Tried a couple of dating websites but they practically ignored my preferences in my profile.



Sorry for all your bad luck. Glad to talk more. Me - 59 w/ crohn's since 17 yo. Surgery in 1990 - felt great 24 yrs til about 6 months ago - flair up again. Busy active business owner in KS - USA. Tell me more.

Alan G.
 
I only had one relationship since I turned 21. That was my marriage at age 30 which officially ended when I was 34. I'll be 52 next year.
 
Sorry for all your bad luck. Glad to talk more. Me - 59 w/ crohn's since 17 yo. Surgery in 1990 - felt great 24 yrs til about 6 months ago - flair up again. Busy active business owner in KS - USA. Tell me more.

Alan G.

Married the WRONG woman and didn't recognize the warning signs. Single average income. No kids - thank God considering what she became. Turned into a Benedict Arnold and a master manipulator, the marriage only lasted four years. The person I trusted with my personal info used them against me, which damaged my trust in women. She forced me out of the house and changed the locks, which the judge ruled was cruel and inhuman treatment. During the two years of separation, she flew to her extramarital affairs on my dime without my knowledge and got involved in BDSM.

Since she wouldn't forward my mail, she had control of the finances - found out that she missed several mortgage payments, transferred her credit card debts to cards in my name, maxxed out all our joint cards. I finally filed a forwarding on mail in my name without telling her - one of the first mail I received was from a credit card company I never heard of, requesting more information to complete a credit card application. I learned that she had opened a credit card offer addressed to me, filled out my personal info, made herself authorized user, and applied for a $13,000 credit card. Had I never intercepted my mail those cards would had gotten into her hands without me ever knowing it. It took YEARS to repair the damage to my credit history.

It took FOUR YEARS to drag that broad into a divorce court. What should had been a plain-jane divorce case was dragged out by her exploiting any legal speedbump possible and willfully waiting until the last minute to respond to legal matters. The process servers could not find her, she was dodging them. Her motive - from her doctor's notes admitted as evidence - was to milk maximum "spousal support" entitled to her by state law. My lawyer laid all this out before a very impressed judge, who realized who the real victim was. Even my lawyer - who had 30 years in the business - said he had never seen a case that bad.

The two year separation and four year divorce process was LONGER than the marriage itself. It was terrible having six years of your life tied down.

I may had won my case but there was a lot of emotional damage to repair. I retreated to tranquil seclusion to heal the scars, which took years. Financially I had to start all over. Frankly I hesitated to write this post for a couple of weeks as I didn't want to re-open old wounds. It's safe to say I am officially over it because I didn't feel the anguish that I used to feel when I recalled those horrible years.

I gained a lot of wisdom from the experience. The few dating websites I tried literally ignored my preferences so they were a waste of time. Haven't dated at all since, it's just hard to learn to trust again. I had a few at work show an interest but red flags went up because I developed a stronger sense of smell (being allegorical here). So I ruled out an intimate relationship with anyone at work. As far as my Crohns (which I developed a year after the divorce), the only repulsive thing that shows is a scar on my abdomen.
 
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Wow Real MC That was a living nightmare. Wonder if the stress helped contribute to your crohn's I've always wondered what roll stress played with the disease. I hope you find someone that really cares about you and doesn't mistreat you. I can imagine the trust issue you would have with someone else I would probably never trust anyone ever again after that.
 
I didn't have Crohns during that ordeal, I developed it a year later following a really bad flu. That flu messed with my system - my smell became more sensitive (not being allegorical). Stress can certainly aggravate Crohns. No one knows what causes it, but there is a strong suspicion that it is connected with the influenza.
 
Wow, I'm so sorry to hear that too The Real MC....stress can cause a lot of health problems. Given that scenario, that's A LOT of stress. You know what might help is maybe joining a meetup, or just talking to folks online (dating site...but not actually dating lol). It might be difficult, given the scars this woman gave you, but you know what....scars heal, no matter how long it takes. Either naturally or mechanically, they can be dealt with. I find forums like this fill a certain void and I hope it does the same for you!
 
hi all, i live alone and was diagnosed with crohns in june. I have since started humira, but the doctor thinks its not working well.

what is really bothering me is she recommended i go to the emergency room and get a blood transfusion because my hemoglobin is at 8.1. im really worried about this process, any advice?

I had a blood transfusion in 2009. My hemoglobin was even lower than yours. I think mine was 5 or 6.

My doctor said to immediately go to the Emergency Room and so I did. I was in a hospital room overnight while I received two units of blood. I started taking two iron pills a day every single day after that ( over the counter ). I recently started seeing a new Primary Care Physician and he said that I did not have to take the iron pills any longer. I quit taking them per his recommendation. I hope that I don't end up in the Emergency Room again because he recommended going off of the iron pills. I get blood draws from many doctors quite often, so I am sure that if my hemoglobin was low they would tell me, right ?

I was a vegetarian in the early 1990's and I also donated blood quite a bit back then ( every 8 weeks ), so that is probably why I was anemic. I take B12 now for B12 deficiency. And I take vitamin D3 now too because of osteoporosis.
 
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Can I recommended a website ? Is that allowed here ?

I have Ulcerative Colitis. I also suffer from many other health conditions. One of the other health issues I suffer from is Major Depressive Disorder. I know that IBD and depression seem to live side by side with each other.

I currently participate in a website called www.depressiontribe.com. There are a lot of nice folks there. I have been reading, writing and chatting there for a few months now

I am single and I am 54 years old. I have had symptoms of Ulcerative Colitis since 1997, but I was not diagnosed until 2006. I have trust issues as far as relationships, even friendships. I have a hard time even exchanging my phone number or e-mail address to people. There are so many people out there that are not honest and they will take advantage of you in so many ways. At this time I am not even interested in a dating anyone. I just want a friend. Having a friend to spend time with would be great. Old age and bad health are bringing me down. I feel so much older than I am. ( Sigh ).
 
I had a blood transfusion in 2009. My hemoglobin was even lower than yours. I think mine was 5 or 6.

My doctor said to immediately go to the Emergency Room and so I did. I was in a hospital room overnight while I received two units of blood. I started taking two iron pills a day every single day after that ( over the counter ). I recently started seeing a new Primary Care Physician and he said that I did not have to take the iron pills any longer. I quit taking them per his recommendation. I hope that I don't end up in the Emergency Room again because he recommended going off of the iron pills. I get blood draws from many doctors quite often, so I am sure that if my hemoglobin was low they would tell me, right ?

I was a vegetarian in the early 1990's and I also donated blood quite a bit back then ( every 8 weeks ), so that is probably why I was anemic. I take B12 now for B12 deficiency. And I take vitamin D3 now too because of osteoporosis.

Hi Ann,

I wanted to mention something about the iron supplementation as I've had a lot of challenges with iron deficiency anemia. If you're able to, I would ask to have your Ferritin and Iron Storage Panel checked. Many times I had a good enough hemoglobin and blood count, but I had almost no iron stores, which makes the blood cells smaller even if there are technically enough of them. Since you needed iron in the past, you probably will continue to need it to maintain ferritin. If not, that can be shown with the test. There are two types of iron infusion options as well if the pills aren't effective.
My experience has been iron deficiency anemia is often overlooked and definitely not actively monitored. Hope this helps, best of luck.
 
Hi sk: Thank you SO much for the information about ferritin and iron storage panel. I just had a blood drawn one week ago for my Primary Care Physician. I am going to get a paper copy of those blood test results or I will call his office to get very specific information about the blood draw. I also have regular blood draws for my Urologist and Endocrinologist. I have no idea what each of these doctors are checking my blood for! I need to become way more informed as a patient. Also, my PCP AND my Endocrinologist are monitoring my B12 level and that is not neccessary. I now going to start asking more questions during my doctors visits.
 
PS: I had two blood draws on the same day for two different doctors. The lab techs used the same exact place on the inside of my arm to draw blood. How stupid! I still have bruises on my arm after one week !:ybatty:
 
Wow, I'm so sorry to hear that too The Real MC....stress can cause a lot of health problems. Given that scenario, that's A LOT of stress. You know what might help is maybe joining a meetup, or just talking to folks online (dating site...but not actually dating lol). It might be difficult, given the scars this woman gave you, but you know what....scars heal, no matter how long it takes. Either naturally or mechanically, they can be dealt with. I find forums like this fill a certain void and I hope it does the same for you!

Hi, I noticed not only do you have crohns in the same place I do but also you have been diagnosed for 2 years - about the same amount of time since I got really ill with mine.

How are you doing and how did things go for you...

Sorry to be asking but I just wondered if we could compare notes as I haven't noticed anyone else with it in the same place and approx 2 years like myself on here.
 
This is about the only company I keep these days. She was part of my last relationship ( a very young pup at that time), a relationship that saw me in hospital for asthma and an anal abscess. During both stays in hospital he would somehow manage to leave the gates open. I live on a four-lane highway, but the dog somehow managed to get across the street, be caught and taken to the local vet, who knew her all-too-well due to the regular epileptic-type fits she was having at that time.

He wouldn't collect her from the vet even after I was released from hospital ( I was still unable to drive) until I asked him to go get her, pretty please. She is a great motivator and muscle builder! I learned a lot about toxic relationships after I kicked him out and haven't really even thought about dating. I get my kicks gardening. You'll never know what a potato tastes like until you grow some.

p.s. The dog had no more fits after He left.
 

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Err hey, thought I'd pop in and look around. I struggle with the whole "friends" and "relationship" thing. I live with UC and even though I'm still quite young I often feel painfully isolated and unsure how to approach people. This probably isn't so abnormal, but a large part of me not getting close to anyone is just the fact that I identify as bigender and bisexual as well. And I'm not really open about either thing atm so I often end up in this situation where, by the time I see the look on the other person's face when I mention my illness, I just forget explaining the rest. I don't know a lot of people who personally have my illness in person, and as a teen almost in college, it just feels like I should have more of a social life than I do. But you know, it's hard not to feel self-conscious with all the scars and pain and all that shnaz. People can try to be understanding, but it's just not the same as knowing someone who goes through it too. Then there's the meds and...ergh being social is such a headache sometimes.
 
zombie penguin i know how you feel. im still in college as a transfer from out of state, i never knew many people here even before i got sick. crohns did some serious damage to my body. to be blunt, i worry about finding a girl who is not bothered by diarrhea.
 
Err hey, thought I'd pop in and look around. I struggle with the whole "friends" and "relationship" thing. I live with UC and even though I'm still quite young I often feel painfully isolated and unsure how to approach people. This probably isn't so abnormal, but a large part of me not getting close to anyone is just the fact that I identify as bigender and bisexual as well. And I'm not really open about either thing atm so I often end up in this situation where, by the time I see the look on the other person's face when I mention my illness, I just forget explaining the rest. I don't know a lot of people who personally have my illness in person, and as a teen almost in college, it just feels like I should have more of a social life than I do. But you know, it's hard not to feel self-conscious with all the scars and pain and all that shnaz. People can try to be understanding, but it's just not the same as knowing someone who goes through it too. Then there's the meds and...ergh being social is such a headache sometimes.

I am 54 years old and have a hard time trusting people. I FINALLY exchanged phone numbers with a neighbor here at my apartment complex today. I hope my decision was not a mistake. I worry about everything ! She and I always chat outside in the courtyard of my building. She is a very nice and outgoing person, but sometimes I think SHE trusts too many people here ! She is always the "welcome wagon" for new tenants and gets involved with them and their lives so quickly. I have lived here quite a long while but did not give her my phone number until today. I really need some friends here.
 
Hey, I think this group is a great idea.

I'm 24, I'm single I've suffered from Crohn's for 11 years in April, and I've never had a real date never mind a relationship.

To be honest I was coming on here today to talk about that, but then I found this and thought I'd post it here.

Long story short is, I'm close to giving up. Over my time I've been single, I've pushed myself out my comfort zone over the years, I feel like I missed some great years of my life due to a lack of confidence Crohn's had given me. When I had my teen years I didn't have many friends, or a big social circle, and I withdrew myself from the world as my confidence was so low.

However over time, I've became more and more confident. I've went to clubs in hope of finding someone, and that didn't work. I've tried meeting people through friends, but I wasn't really attracted to anyone my friends knew.

Over the last 5 months, I've tried harder than I have ever tried to meet someone. I'm not talking about going to more clubs etc. Right now my Crohn's is in remission, and I have been determined to meet someone. Mainly because I'm at an age where all the friends, I do have, are getting married, engaged or moving in together, and I spend every Friday and Saturday night by myself, just wishing I had somebody.

Now back what I have been up to in the last 5 months, I have just been going out, meeting people I find attractive in the street and saying hello, and letting them know I find them attractive and I take it from there, sometimes it will go well, and I'll get the number, and try and set up a possible date (which will obviously go nowhere) other times the girl may not be interested, or have a boyfriend etc, fair enough. I'd say I've done this a few hundred times and all I get is numbers...people agree to go on a date with me and cancel last minute, I dunno why. The girls I do get the number of, sometimes tell me I've made their day, and that most men don't have the balls to do this...it's nice to hear that, but if it goes nowhere, it doesn't really change my situation, as I've done this so much, I've actually ended up approaching woman I've already met.

I've up ended going to night clubs alone to meet woman, and like in the daytime some appreciate it, others don't, but it usually goes nowhere.

I consider myself average looking, some people tell me I'm good looking at work (I work in a female dominated office). However I can't seem to meet someone who is interested in me.

I've been on and off online dating for a number of years. Yet again in the last 5 months, nothing has come from it. Again, I've messaged so many woman on there, I've ended up messaging the same woman twice as I can't remember who I've already messaged.

That's my situation, I'm single, I'm 24, In what's meant to be "the prime" of my life. I've basically met every woman in a 15 mile radius of myself where I live and nobody is interested.

If you've read all this then thank you, but as of right now, I give up.

The only positive I can take from the last 5 months, is that at least I can say I tried.
 
Being single is such like a.... permanent state in my life that it didn't even occur to me that having Crohn's might present extra challenges to dating until I saw that this forum existed. That's so sad. :p

bro21, if I might give you some advice? Advice that, clearly, I don't follow, but I promise it's good advice and I should follow it. :p Clubs are the WORST place to meet people to date. Go to clubs to hang out with friends, have some laughs, make some friends, sure. Some of my best friends I've met out at clubs and bars. But the only people I've ever met to date at bars or clubs fall squarely into the "mistakes" category, y'know what I mean?

The best way to find someone to date is to pursue your interests, not to pursue people. I don't know what your hobbies are, but I can almost 100% guarantee there's other people around with similar hobbies and finding them, meeting them... The benefit here is, not only are you doing something you enjoy (thus making you more attractive because happy people are attractive!) you also already know you have a common interest with the people you meet there.
So don't give up yet, is the point I'm trying to make! :)
 
Bro: Don't give up. There is an understanding gal out there for you who will love you and accept you the way you are. You are young, so don't get dissappointed. There is that saying "Love will happen when you least expect it". So true ! I guess I am old fashioned in a way, but I really do believe that you must be friends with your future partner before anything else. Keep us posted. Good things are coming your way. : - )
 
I am bored and depressed. Been at home five days taking Flagyl and having diarrhea. Just was diagnosed with c-diff the other day. I am infectious. I have been home 8 days in a row now. I WAS going to a program 3-4 times a week for five weeks and I was thriving. I was going there for my mental health issues. I could socialize there and reinforce my coping skills. Going to a new GI tomorrow. What I have learned here about c-diff has not been too good. I was diagnosed with UC in 2006. Now that this Flagyl is causing diarrhea and is infectious, I cannot return to my program until the c-diff is gone. So now I am back to isolating, being depressed, watching TV and eating all day long. I have to be near a bathroom. I'm tired. I miss my new friends I was making at the program/facility I was attending. Here I am now alone in my apartment. Bummer.:boring:
 
Never thought I would be this lonely, can meet ppl, but then, how to explain, fatigue, arthritis all the issues. How to find a way to better, or just to get out of house.
 
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I hate to hear the question, what is wrong with u? I only weigh 100 lbs, so they say, u look so healthy! Healthy is stick thin and weak?
 
Hi Ann,

I wanted to mention something about the iron supplementation as I've had a lot of challenges with iron deficiency anemia. If you're able to, I would ask to have your Ferritin and Iron Storage Panel checked. Many times I had a good enough hemoglobin and blood count, but I had almost no iron stores, which makes the blood cells smaller even if there are technically enough of them. Since you needed iron in the past, you probably will continue to need it to maintain ferritin. If not, that can be shown with the test. There are two types of iron infusion options as well if the pills aren't effective.
My experience has been iron deficiency anemia is often overlooked and definitely not actively monitored. Hope this helps, best of luck.

Interesting, they check my hemoglobin and say I'm fine, did recently have 2 positive blood tests. Line up for yet another colonoscopy after 7 in 9 years, it's in the small intestines!
 
I am disabled, but everything that is wrong with me is on the INSIDE, so no one "sees" the health issues I have. I obese, but last year I lost 30 pounds due to changes in my UC symptoms. All my doctors thought it was great that I lost the weight. But I tried to explain to them that I was not TRYING to lose weight. Losing weight is a good thing for me, but to lose it because I am sick is not losing it in a healthy way. PS: Now I have gained 15 pounds back .Now I am sure my doctors will have something to say about THAT ?
 
Hi,
I am new to this forum. Not new to Crohn's.
I am 21 and was diagnosed at 12. I really haven't had the chance to do anything. I've been in the hospital 11 times for 2 weeks or longer each time.
 
I am 26 and a single mother of a 3 year old boy. I am undiagnosed but have been dealing with Crohn's symptoms my whole life and they have recently gotten worse. This is an amazing thread idea! I am happy it's not just me haha but it's hard to talk to guys knowing I have this issue. It's embarrassing lol not really good dinner topic. haha
 
nice to meet you Marley0724, it's hard to talk to anyone about crohn's sometimes I'm sure you will find a way, hope your son is doing well

hope all goes well with the scopy Hello2U
 
I am 26 and a single mother of a 3 year old boy. I am undiagnosed but have been dealing with Crohn's symptoms my whole life and they have recently gotten worse. This is an amazing thread idea! I am happy it's not just me haha but it's hard to talk to guys knowing I have this issue. It's embarrassing lol not really good dinner topic. haha
Yeah, I was invited to a barbeque at my apartment complex one day. I can't eat any of the food they were going to serve. So then I told them I have a Colon disease and that is why I could not eat the barbeque party food ( I did not want them to think I was being rude or unfriendly by not attending ). I was going to just go to the barbeque just to socialize ( but not eat). But a few hours before the barbeque I started getting grouchy about something else. So, I never did attend that barbeque. What am I going to tell people who offer me food, but I can't eat it ? Should I say, oh, by the way....I get diarrhea really bad from eating that ! I have Ulcerative Colitis and it really DOES affect my social life ( and traveling is almost out of the question too).
Have a good weekend !!
 
I mean, usually I just tell people "no thanks" for food that I can't eat and I only give further explanation if they ask. I figure at that point, it's their fault. If they didn't want to know they should've just let me say no. :p
 
Don't watch sad television shows when you are all alone ! I ate a bunch of candy. My sister sends me happy e-mails about her spending time with her grand-kids in Idaho. I am glad they are happy ? But I am all alone, so sending me e-mails about happy family time just makes me feel more alone and lonely. I know my sister is just trying to share with me part of her life. My parents are dead. I have no friends.
 
Crohn's, a curse of our evolving society. Life seems to be 3 steps forwards, 2 steps back. Then the Crohn's gets fully involved, and life seems to be nothing more than a black hole, sucking the life out of you. You get better, but you know that life around you, and those around you, are different. Why is this?
 
Everyone has their own demons and maybe it's not physical and maybe you don't see their suffering but nobody goes scot free in this world.
 
Thought I'd drop by with... idk if they're words of encouragement or what to call it.

I've been single my entire life because I struggle with social anxiety, and other facets of normal socialization.
I never reached out much to people around me in school, and when they reached out to me I didn't know how to respond, came off as hostile or reproachful.

After highschool I went straight to a quick course, small college where I hardly talked to anyone except my friend from HS I went with.

Immediately after I went straight onto disability and lived my life through world of warcraft and online forums where I came cynical because the online communities of many games and forums are predominantly hostile and negative.

When it came time to rejoin the world after I got my symptoms under control with diet, I suffered from a worsening of social anxiety. On top of that I've had chronic depression since trying Accutane in highschool.

I started making account on dating websites shortly before I started working again. I sent hundreds of messages and got very few replies. I didn't find it easy to create natural, organic conversations with people on these websites.

At work I made friends that reached out to me, and it made it much easier to leave me shell, but the social anxiety and also coping with Crohn's made things tough. Dating seemed impossible, restaurants and alcohol are strictly off the table to me, but I didn't give up anyway.

It took me 2 full years (at age of 25) before my first 'date' ever happened. After that a lot of my anxiety was lifted, and I've met over 6-7 girls now from various dating apps / websites. Obviously none of them really 'worked out' but that's how it is when your entire premise is basically "you're pretty, I'm pretty, let's meet and see if we click."

But in dealing with my Crohn's I've decided to just be upfront. I put right in my profile I can't do alcohol or restaurants, so if that's what's important to you then keep moving. Most people I talk to are at least willing to put that aside initially.

The girl I'm talking to right now I've known for a little over two months, I wouldn't say we're 'dating' but we hang out a lot on weekends. She enjoys going to the grocery store and pointing at stuff and saying "Can you eat that!?" and I'll read the ingredients and tell her all the reasons I can't. She's also offered to be an FMT donor if I ever go that route.

I went to some of her family events and they were asking me what I can and can't eat. I jokingly told them I'm a plant and I live off sunlight and water, there was an awkward silence before I explained that I have crohn's and they understood why I wouldn't accept food.

Idk if this will go anywhere / work out, just stay as friends or fizzle out since it's not that simple, but I just think it's important to focus on reaching out to people, keep trying, keep positive, and never forget to do the things that make you happy and fulfilled because that makes you the kind of person that other people want to be around.

Your Crohn's will always influence your life, but it doesn't have to define you, and you'll find people that won't let it define you in their eyes either.


This is a post I found on imgur the other day I think is helpful:
http://imgur.com/gallery/Llf5Tj9
The guy's wife left him after he became a paraplegic. His tattoo sums up his feelings on it:
"What lies behind us and what lies ahead of us are tiny matters compared to what lies within us."

Who you are will always prevail over what's going on in your life when you find the right people.

And if you're having problems with depression PLEASE seek help. Crohn's very likely causes or possibly RESULTS from the same chemical imbalances that cause depression. Some UC patients even go into remission on Welbutrin! You already have Crohn's you don't have to face depression as well.

I'm self medicating on tyrosine and 5-htp and when I get my dosing right it's profound.
 
Hey guys, just dropping in to say haaay! Lol well I'm still single. Lol. Idk what's wrong with me. I have talked to two guys who were willing to still date me with my colostomy due to my Crohn's and still suffer from my disease from time to time in a whole different way. I let them go. I just kept thinking yea they say that, but when I get a flare up and when I've gotten attached then they'll bail when I need them the most for support. I know it's not right to assume. How can I overcome this fear of rejection?
 
21 and never been in a relationship cos am too embarrassed of my bag! Ahh! Nice to know I'm not alone though haha
 
Dear InstantCoffee: I really enjoyed reading your post. You are able to put your feelings into words very well. Ten years ago I started to experience symptoms of depression and anxiety that negatively impacted every part of my life my from then on. I have Major Depressive Disorder and Anxiety. I take psychiatric medications and see a psychiatrist on a regular basis. My UC symptoms started in 1997, but I was not diagnosed until 2006. I am now 55 years old and "disabled" ( but I would rather say "retired"). I have a program available to me where I can socialize with my "peers". I thrive when I attend and find great comfort being around people "like me" ( who suffer from mental illness). But when I stay home I isolate and my confidence is low. Having UC effects every moment of my life. It is nice to be here on this site around folks who I can talk to about things like bowel movements, medications, abscesses. Have a good week everyone. Oh, here is a website I am a member of if you need someone to "talk" to.....www.depressiontribe.com.
 
Hey guys, just dropping in to say haaay! Lol well I'm still single. Lol. Idk what's wrong with me. I have talked to two guys who were willing to still date me with my colostomy due to my Crohn's and still suffer from my disease from time to time in a whole different way. I let them go. I just kept thinking yea they say that, but when I get a flare up and when I've gotten attached then they'll bail when I need them the most for support. I know it's not right to assume. How can I overcome this fear of rejection?

Every time you initiate something with anyone you risk getting hurt. I know how you feel though because I've gotten close to several people in just the past year or two only to have them push me out of their life when they're not interested anymore.

It hurts but you have to decide if what you're looking for will make it worth it.

I think it's also important we learn not to depend on others for support. Believe me I know as well as anyone how hard dealing with Crohn's on your own is. I've always felt like people around me were blind to my struggles because I've been able to keep my symptoms relatively controlled with diet, they don't understand that even on good days I still have Crohn's.

It's natural to want someone to share experiences with, and to help you with the bad ones, but it's always best to find satisfaction in the one thing you can't have taken away - yourself.

I am still working on this, and I know it's easier said then done. Part of it is rediscovering all the things that give us joy and realizing that it's all still just as great alone.

We also have to realize that as people with health conditions, being a support to us is kind of a big deal. A new person in your life may not be comfortable right away with it, it's going to take time before they're understand how to be there for you, and if you try to push it on them they may move away. Not because they're heartless, but because they're simply afraid of getting involved in supporting someone in a way they're not ready to.
 
Hi InstantCoffee! I think what you stated makes lots of sense. Especially the last part of it. I don't know how to explain to them how they can be there for me. Heck I don't even know how to deal with it. I just lock myself in a room and sleep it off until I feel better. That's not how I wanna deal with it if I'm in a relationship. I guess you're right. It all depends if my risk of being hurt is worth to get to know somebody and for them to know me and not my disease. Thanks! :)
 
Hi, I'm a single 52 yr old female, now iv been single for the last oh 22 yrs ish. . Well some of it through choice because I'd give up on finding a faithful man. Then when I thought there must be some out there, I kinda also thought, chances were id not find one. So iv become very independent, and totally non plussed about being in a relationship.I do still say never say never but hey ho, since having Crohns and surgery, iv barely had the energy to deal with my self never mind a man. But I know what you all mean, its nice too have someone care, that's not family as you don't always want to pour you troubles on them all the time. on a lighter note what's a women without a man...blessed lol. No offence intended to the guys it's just a wee joke :) hope we all find our Mr/Mrs right. Good luck n good health ...
 
Hi everyone. I'm a recently single mom. I've had Crohn's disease since I was 16. I turned 27 in June of this year. I have had two surgeries already. I'm looking to meet new friends who understand this disease. Hope everyone has a good day.
 
Ok don't start hating on me but there is a lot of talk here about being accepted. Im 30 and have this since I was 9. So 24 years of my life. I don't remember life without it, as a 'normal" ;) However, I also don't agree with looking for acceptance. For every scar you have they have an annoying trait. For every day you feel low they have a bad mood. There is nothing more demanding or more needy in you than there is in them. Stop looking for acceptance. If you accept yourself and know yourself then people know exactly what you need from them because you can show it. Anyone who doesn't take the time is a bullet dodged.

We're here for a good time, not a long time.
 

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