tag:blogger.com,1999:blog-7595668649977089723.post1504825884312358600..comments2023-08-17T06:36:32.663-04:00Comments on Me and Mr. Jones: Invisible BoyJessihttp://www.blogger.com/profile/06476329539093288552noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-7595668649977089723.post-32757255422551738622014-10-11T06:00:41.210-04:002014-10-11T06:00:41.210-04:00Oh Jessi. I'm so sorry to hear you're suff...Oh Jessi. I'm so sorry to hear you're suffering in this way. I have a friend who has EDS, so I know a tiny bit of some of the struggles you face, and I also have an illness that have questioned whether it even exists because I don't always have physical symptoms. It's certainly tough. I'm praying for you and your family so much right now. xxAnonymousnoreply@blogger.comtag:blogger.com,1999:blog-7595668649977089723.post-84264840945346937982014-10-09T23:08:41.474-04:002014-10-09T23:08:41.474-04:00I'm sorry to hear that you most likely have ED...I'm sorry to hear that you most likely have EDS. I will be praying for you and your brother. Although I don't know what it's like to live with EDS, my husband has ulcerative colitis...a different chronic illness, but also unseen with stuff like joint pain, etc. in addition to ulcers in his colon. Anyway, that's all to say, I know how hard it is on him when he has flare-ups, but nothing is visible to the eye. People like to see diseases. But there are hard ones to live with that aren't obvious...to the bystander. Hannah H.https://www.blogger.com/profile/05634161187881955410noreply@blogger.com