Hello beauties,
This will be an ongoing post. This post shall provide knowledge about endo, lupus, lymesdisease, crohns, and any other invisible/chronic illnesses. Please feel free to post and let me know if I've left any out.
I believe this post will aid many sufferers because I've had so many ask me questions or have been told the wrong thing by physicians or told there's no aid or relief rather.
Every day I'll edit this post by adding info.
Please provide your knowledge or information in the comments section.
I thank you for your knowledge, stories, and or questions.
Remember we are not alone and the more we support one another the stronger we become.
Here's something to think about:
I'm wondering how many of us women suffer from #endo before a Dr tells us it's a benign form of cancer? Thank God for awesome specialist and reading materials. The more we know the better we can battle this.
I was diagnosed with #endo when I was 18years of age after suffering what I thought was a painful cycle. Many don't realize that severe pain during this time isn't normal, pain during intercorse, or being unable to stand/walk without feeling as though your legs may give out at any given moment. Also, many doctors that haven't studied this disease will tell you it's nothing but, it is, it's a benign form of cancer. I underwent chemo and countless medications. What's your story? Let's share our experiences and help others.
ReplyDeleteToday I found that even with taking a pain blocker at times it doesn't work. I think that's why I stopped taking it every day. It just like taking pain pills after awhile they don't work. What's your thoughts?
ReplyDeleteToday I found that even with taking a pain blocker at times it doesn't work. I think that's why I stopped taking it every day. It just like taking pain pills after awhile they don't work. What's your thoughts?
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