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.
This blog is for the many women who suffer from Endometriosis,it's also for the men/women whom suffer from other Invisible/Chronic Illnesses who need an outlet to talk and vent. I have suffered with Endo for more than 15yrs. Let's connect, share things that help and those that don't. I hope to aid in sharing knowledge, regaining your faith, motivation, inspiration, and hope. Thanks for Visiting & Subscribing!
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