ChronicBabe Forum

An online resource for young women with chronic illness

Helping you live an awesome life in spite of chronic illness!

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Forum Rules - Please Read!

1. Offer solutions and suggestions anytime you can. We want to build a supportive, positive community. If you're just here to complain, there's no room for that...please take complaints somewhere else.
2. Be nice. ChronicBabes are all about finding solutions, not starting arguments. Respect different points of view - you just might learn something.
3. Please don't use profanity, and we will immediately ban anyone who says anything racist, homophobic or otherwise inflammatory. Got it?
4. If you want to post a photo or two (not 10!) of yourself or something that inspires you, great - but don't use the photo or video section to advertise your business or you'll be banned immediately.
5. Have fun! As with all things ChronicBabe-related, we want the Forum to be a place where you can enjoy yourself, get fresh ideas, meet cool people and connect in a positive way. That will happen because you make it happen, so go for it!

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A few words on thoughtfulness

We are a community, which means there are many of us, all from different backgrounds and experiences. When we talk on the forum, we bring unique benefits - and biases - to the table. Please use care when responding to another member's question or statement; she (or he) may be going through a hard time, or may come from a different perspective. Try to be as factually accurate and respectful as possible, and remember that medical advice from another member should never take the place of a health care provider's advice. XO Jenni

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You're here! We are so happy. Some tips:

Welcome to the ChronicBabe Forum! As of today, we have nearly 1,700 members! YES!!! And, we're growing faster than ever. Join the conversation...and be sure to "friend" Editrix Jenni!

If you're brand new to discussion forums, read this first. As you get comfy with our group, personalize your page and add a profile image (even if you want to be anonymous, give us something nice to look at!) You can add photos that will play in a random slideshow (many members already have, and they're great pics!), or videos for other Babes to watch (we have a bunch already!). You can create a Group within the community (maybe on a specific disease, or a goal you have) and you can chat with other members in our chat room (you can participate any time you're logged in.)

Like the Forum? Grab the Badge on the lower right-hand corner and post it on your blog to help spread our message. Because we're so new, there might be little issues; if you have things you would like to see, please email Jenni by visiting ChronicBabe.com/contact. PLUS: Please read the FORUM RULES (to the left) before you dive into the conversation. Thanks!

Latest Activity

Eden Knox joined Elizabeth Wakefield's group
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Sleep disorder Babes

For Babes with all kinds of sleep disorders - let's chat about our issues and how to live with and/or overcome!  This is a picture of me - not at my best!
7 hours ago
Profile IconEden Knox and Yuli Jacobson joined ChronicBabe Forum
7 hours ago
Casilia Smith posted photos
yesterday
LeeFrances Sweet posted a blog post

Thoughts on My New Lyme Disease Diagnosis

So this week I got word from my newest doctor that I have a diagnosis. I have late stage Lyme disease. My tests last summer came back abnormal but my primary care doctor wouldn't follow up on them. I found a chronic disease specialist the next state over. They redid the tests which came back abnormal again but inconclusive again. So they sent them out to Igenex in CA for more thorough testing. That was last month and I just got the news that the tests were positive, not only for Lyme but for…See More
Sunday

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    ** Disclaimer **

    Babes, we are not doctors. Nor are we lawyers. In fact, we're just a bunch of women (and a few men) who are sick and want to share resources. So please be careful what you do after reading medical advice here. Always speak to your health care professional before trying a new medication, supplement, exercise routine, etc. ChronicBabe.com and its staff are not liable if bad stuff happens to you, and we would hate for bad stuff to happen to you! So be smart, savvy, and do your own research. XO Jenni, the Editrix

    Blog Posts

    Thoughts on My New Lyme Disease Diagnosis

    Posted by LeeFrances Sweet on May 19, 2013 at 11:30am 0 Comments

    So this week I got word from my newest doctor that I have a diagnosis. I have late stage Lyme disease. My tests last summer came back abnormal but my primary care doctor wouldn't follow up on them. I found a chronic disease specialist the next state over. They redid the tests which came back abnormal again but inconclusive again. So they sent them out to Igenex in CA for more thorough testing. That was last month and I just got the news that the tests were positive, not only for Lyme but for…

    Continue

    Chronic illness and relationship FOMO

    Posted by Samantha Joie on May 8, 2013 at 8:37am 0 Comments

    I have to admit that every time I come on Chronic Babe I feel very inexperienced. Everyone else has such great ideas and after about six months I'm still a little clueless by my fibromyalgia diagnosis. One of my biggest frustrations, though, is my love life. It sounds trivial, I know, but any woman who has been or is in this situation knows that love and moral support are priceless.

    The problem is, I always have a tendency to fall in love but then wonder "What if the next guy is better?"… Continue

    panic

    Posted by amy rose on April 15, 2013 at 6:46pm 0 Comments

    after a mild panic attack this weekend, i decided i needed to reach out to people in similiar situations as i. i am so young and everyone tells me i look so healthy, yet i cant open a bottle of water or paint anymore because i am loosing the function of my hands. after my hands started to go was when my depression began because my creativity felt so pent up. all of my old stress relievers now cause me too much pain. im just trying to find my place in this world as i enter the career field and… Continue

    How do you cope when life seems to pass you by and you cannot participate like you use to.

    Posted by Julie Schreiber on April 11, 2013 at 8:05am 0 Comments

    Do a lot of you feel like your missing out on life-that it's passing you by-when your chronically ill and cannot participate like you use to? How do you handle guilt that others  tend to put on you when you cancel, yet again? How do you get through to people that your illness is holding you back and your not cancelling to be anti-social? How do you get others to recognize your illness is "real" and try to get emotional support? Dilemma. The past 3 years have been really hard for me in these…

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    Meet Our Moderators!

    We have four main moderators on the Forum. Contact them with questions about etiquette, membership, tech support, or anything else that's confusing. Rachel is our lead moderator; Helen does a ton and she's on U.K. time; Amy is our chief spam banner (she's great at spotting them!). And of course Editrix Jenni is also here for you. 

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    Jenni Prokopy created this Ning Network.

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