Living with JDM
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Learning to thrive, not just survive with JA. Today I am excited to feature a guest post from my dear friend Herchel, a fabulous blogger and fellow JA parent. Since I am a mom with teen juvenile arthritis patients, I thought she could provide great perspective regarding issues surrounding pain. I am Herchel Scruggs, of Gym Craft Laundry,. It took me much longer.
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Living with JDMDESCRIPTION
This is a blog about my family and the emotional, medical and financial stress that we have gone through together. This is about being the Mother of two children that have two very different medical issues. One child has cerebral palsy CP the other has Dermatomyositis autoimmune disease or JDM for short. This blog is mostly about my daughter with JDM. There is no cure for this very rare autoimmune disease and any info that I can find or share is appreciated.CONTENT
This web page jennasjdmstory.blogspot.com states the following, "Friday, October 17, 2014." We saw that the webpage said " We all have our own ways of dealing with things and someone might look at the way I deal with things and not agree? The one thing that I cant do is take away Jordans cerebral palsy or take away Jennas dermatomyositis, panniculitis, pseudo tumor or the depression that goes along with all of this! You want so much for your kids to be healthy and happy." It also said " These are suppose to be the best years of their lives! I have looked in the mirror and asked why? I cant hel."SEEK SIMILAR DOMAINS
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Mais le plus souvent ont a des BD comiques .
Scientifiques et techniques et sciences humaines. 5ème Fête du livre de Quiberon. Pour vous désabonner cliquez ici. 6 973 références en stock.