Skip to main content

Dating: "So I have CF..."

"I have CF..." just say it!

So I have read some questions about relationships on a couple of the CF online communities and I've noticed lots of CFers have different attitudes when it comes to dating and when/how to tell a guy you have CF. Ha, it’s never easy... some respond with questions and some says "it’s cool". lol. You never know. But the sooner you tell them, the sooner they can accept it and learn how to deal with it, and you will be able a healthy relationship.

I am by no means an expert on relationships. However, here is my opinion and advice to fellow CFers, so they do not make the same mistakes I did.

I dated a couple guys in college, but I didn't stand up for myself (when it came to meds) and would always agree to go out (late at night) or travel to visit friends for a weekend. I wouldn't pack my therapies and I wouldn't take my pills in front of them. Basically, my health always suffered. I dated a few guys I had known since High School and it was easier (I didn't have to "hide" anything), but I still would put my health on the "back burner." My last relationship was the worst for me medically. My last boyfriend would hang out with me from the time my classes ended until like midnight...I would miss my therapies for the day and by the time he'd leave I would be too tired to make my stomach feeding. People started saying I looked thin, etc. and I did. I weighed myself on my parent's scale and I had lost 20 lbs. in two months... I had clinic in one month. The relationship ended and I worked hard on my health. I got my weight back before clinic, but realized I was not at a point in my life where I was ready to be in a relationship. I decided to stay single for at least a year and work on my health and figuring out myself (that was in 2010).

Cfers: Never, be scared to share or tell your BF/GF about your health. It will only harm your health and the relationship.
I look back at who I was a couple years ago and I can't believe I let relationships, plays, and other activities interfere with my health. You DON'T have to choose between social life or health! I can't give advice on how to deal with CF and a relationship, since I'm still single. I know from my mistakes what I should have done. Taking the time to figure that out made me tougher and even more determined to keep my health an active part of my life! I'm soo glad I understand better how to balance my social life (play practices, meetings, CIDF, church events, etc) with my Cystic Fibrosis!

And my hometown may seem boring, but it has given me a chance to figure it out before heading to Grad School. I'm so thankful for it. Now the only place for me to look is forward! Starting with my 5K goal! Then later on...Grad School.

BOTTOM LINE CFers: I found it hard going from hometown to college (everyone in my hometown knows). If I cough in my hometown, nobody notices. But if I coughed in Champaign, I'd get stared at and disgusted looks. It’s tough, but don't let it bother you and ESPECIALLY don't let it hinder you. Keep on top of your health and you can balance it with your social life. I promise! It just took me a little longer to figure it out!


*Added Nov 2014 - 2 more posts on dating: Click here to read my perspective & my boyfriend's

Comments

  1. I'm so glad you figured it out... and I know what you mean about not telling someone because it is (1) embarrassing and (2) a sensitive subject even in a healthy relationship. I have to say that I think this happens to A LOT of people in relationships... putting their health on the back burner. Even people who don't have CF or a mental illness or a terminal illness or something of that sort. People just tend to "let things go" when they get in a relationship, for various reasons. I think that it is perhaps the result of being/becoming co-dependent in the relationship... which is never a good thing... but sometimes happens without you realizing it. I have to keep a pretty strict regimen too, with the food I eat, when I eat, how much I eat, how much I work out, when I work out, taking meds, getting the appropriate amount of sleep, not stressing myself out too much, etc. It's all a very intricate matter in my life... and most men don't get it! Unfortunately, "getting it" doesn't seem to be enough to make a relationship last. They also have to be willing to "work with it" and stick by your side.

    The way I see it, if you are strong enough to assert yourself for your needs and wants, THE RIGHT GUY will be right there with you encouraging you and helping to make it possible... NOT trying to monopolize your time and energy for his own benefit. But that's just my point of view, I'm sure there are other viewpoints out there lol

    ReplyDelete
    Replies
    1. Yes, I agree! (ps. it nots like my past BFs did anything wrong, I didn't tell them I when I needed to do meds). You are right about it having to with the right balance though. And yes, "the right guy" will understand about your eating/working out/stress, etc. Just like "the right guy" will try to understand/ and eventually understand my CF. There are plenty of guys like this, in fact a lot of my guy friends are perfect exmaples! :-) Glad you enjoy the blog and can relate so much. Love hearing from you!

      Delete

Post a Comment

Popular posts from this blog

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec...

Beginning of the Year Troubles

Normal "beginning of the year" troubles for Andrew and I only really consist of one topic: Our Deductible [please no Obama, or government bashing] I've always had high deductibles ALL MY LIFE (no matter who was president). The problem is I hit my deductible within the first week of January. In the past I have always prepared for this and since I was still on my father's insurance (up until last year) he typically paid the bill (at least for medical stuff). And in the future Andrew & I won't have such an issue with this. We will be able to save and plan ahead for the $3,000 (for my deductible, his is another $3,000). However, this year was more difficult. We saved all 2013-2014 for our wedding & honeymoon, plus had our deductible saved too. But Real Estate was a pricey career to start, I've put almost $5,000 into it (classes, dues, licensing, exam, advertising, etc). So needless to say our deductible disappeared, thanks to my new career. Wh...

Updates Galore!

Big News, Big Times, Big Change: I had my post hospital Doctor's appointment on April 21st and it went well. I posted a video on my CF facebook page. My weight is back on track, heading up. Also, my lung function was around 55%, so that's almost my baseline. I got to take my needle out that night. OH BOY!! I loved being needle free! Whoohoo no more IVs!!!!! In the last week I have been super busy with a few different things. 1. Work. I have a new client AND I had all my post licensing webinars & exams this last week! 2. More CF Foundation Volunteer work. I held a presentation in my home town, where I discussed CF, the different mutations & severity of classes, as well as fundraising for great strides. I talked about the history of the CF foundation, care centers, and more about our local IL CF fundraisers. Overall, it wasn't a big turn out, so I was a little bummed. My hometown has always supported my CF cause, so it was disappointing not to have a good numb...