Interviews

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This page is dedicated to all those whom have shared their stories. Feel free to read through all of them if you have the time. Have a great day, I remain hopeful always.

Join Magdalena as she shares her story living with hemiplegic migraines, nonspecific connective tissue disorder, postural orthostatic tachycardia syndrome, inappropriate sinus tachycardia, scoliosis, kyphosis, chronic tension headaches, hypermobility syndrome, hypotension, mitral valve prolapse, heart murmur, chronic pain, chronic fatigue, depression, anxiety, OCD, and social anxiety. https://annawerrunblog.wordpress.com/2017/07/12/interview-with-magdalena/

Join Ash as he tells his story, “I am female to male transgender. I’m currently diagnosed with POTS, Ehler’s Danlos hypermobility type, Depression, Anxiety and I’ve had a spinal operation for tethered cord syndrome. I am also recovering from an eating disorder which exacerbated my illnesses, due to dysmorphia from the illness, and from having a gender identity that isn’t reflected in my birth sex.” https://annawerrunblog.wordpress.com/2017/07/10/interveiw-with-ash/

Karissa shares her journey, “I am 17 years old and from Ohio, America. I have Elhers Danlos Syndrome type 3, postural orthostatic tachycardia syndrome, eczema, mast cell activation syndrome, degenerative disc disease, scoliosis, and vocal cord dysfunction along with severe allergies. This can cause me generalized anxiety and sometimes even some depression.” https://annawerrunblog.wordpress.com/2017/06/24/interview-with-karissa/

Join Angela Arndt as she shares her chronic illness journey living with EDS, and fibromyalgia. https://annawerrunblog.wordpress.com/2017/04/13/interview-with-angela-arndt/

Join Laetitia as she talks about her journey living with EDS, Chrons Diseases, Dysautonomia, general anxiety, and fibromyalgia. Please be respectful of her and her journey. https://annawerrunblog.wordpress.com/2017/04/13/interview-with-laetitia/

Join Angela and she shares her care takers journey. Angela’s daughter Anneliese lives with Blount’s disease. Please be respectful of Angela, and Anneliese’s story. #blountsdisease https://annawerrunblog.wordpress.com/2017/02/28/interview-with-care-giver-angela/ 

Join Jerry (a father and a husband) as he shares his journey being a care giver. He takes on the role of being both mom and dad. His wife Bonnie is affected by VEDS also known as Vascular Ehlers Danlos Syndrome. Bonnie isn’t the only one living with disease. Please be considerate of Jerry and his journey, as he shares his story in his own words. https://annawerrunblog.wordpress.com/2017/02/27/care-givers-interveiw-with-jerry-wheeler/

Join Stephanie as she shares her journey living with EDS, Fibromyalgia, and body dystrophic disorder. Please be considerate of Stephanie and her journey.
https://annawerrunblog.wordpress.com/2017/02/27/steph-may-heads-shares-her-journey/

Join me as Kimmyn shares her story, her life’s journey and her illness told in her own words. She shares her illness journey and talks about Fibromyalgia, Lyme, Ehlers Danlos Syndrome, Mast Cell Disease, and POTS. #raredisease #fibromyalgia #eds #pots #mastcelldisease #lyme https://annawerrunblog.wordpress.com/2017/02/22/kimmyns-life-illness-and-journey/

Join Will as he shares his story of living with chronic migraines and his journey with depression. Please be respectful of him and his journey. #chronicmigraines https://annawerrunblog.wordpress.com/2017/02/22/interview-with-will-randolph/

Interview with Lyle Romans. My latest interview was done with Lyle. Lyle is terminally ill he has been diagnosed with the following diseases, terminal pulmonary fibrosis, dermatomyositis, small fiber neuropathy, depression, and anxiety. Please be respectful of him, his journey as you read his interview in essay form. https://annawerrunblog.wordpress.com/2017/01/21/interview-with-lyle/

Interview with Patricia Smith. This is the interview that was done with Patricia Smith, she tells her story in essay form. She shares her journey living with Systemic Mastocytosis, Dysautonomia, Dystonia, Eosinophilic, Eosinophilic Esophagitis, Type 2 Diabetes, Degenerative disk disease, scoliosis, and depression. Please be respectful of her and her story told in her own words. https://annawerrunblog.wordpress.com/2017/01/30/interview-patricia-smith/

Interview with Beth. Join Beth as she talks about her journey with fibromyalgia, PCOS, anxiety and depression. This is her story in her own words, please be respectful of Beth and her journey. https://annawerrunblog.wordpress.com/2017/02/13/interview-with-beth/

Interview with Dorsey Ross. This is Dorsey Ross’s story. Please respectful of him and his journey as he shares his story living with Apert Syndrome. Apert syndrome is a genetic disorder. https://annawerrunblog.wordpress.com/2017/02/14/interview-with-dorsey-ross/

Interview with Cindy. This is Cindy Belz story. She lives with EDS, gastroparesis, dysautonomia, Degenerative disc disease, chairi, spinal tumour, synriomygelia and synriobebelia. Please be respectful of her and her story told in her own words. https://annawerrunblog.wordpress.com/2017/02/10/interveiw-with-cindy-belz/

Interview with Pashondra James. This is Pashondra’s story as she shares what is it is like to live with EDS hypermobility type and vascular cross over type. She also talks about the following POTS, Dandy Walker Syndrome, Ménière’s disease, Mitral valve prolapse, Raynaud’s, and migraines. Please be respectful of Panondra and her story. https://annawerrunblog.wordpress.com/2017/01/17/interview-with-pashondra-james/

Interview with Bill. This is interview was done with Bill. This is his stroy in essay form talking about what it has been like to live with SCFE, Quervain Syndrome, osteoarthritis and iliopsoas impingement. Please be respectful of him and his story. https://annawerrunblog.wordpress.com/2017/01/16/interview-with-bill/

Interview with Angela. My interview with Angela. She talks about her journey living with Ehlers Danlos, Hyperandergic POTS, and Interstitial Cystitis. Please be respectful of her story told in her own words. https://annawerrunblog.wordpress.com/2017/01/15/interview-with-angela/

Interview with Laura. This is Laura’s story living it’s NEADS, PTSD, Lupus and EDS. Below are links to help you learn more about what she lives with. This is her story in her words please be respectful. https://annawerrunblog.wordpress.com/2017/01/14/interview-with-laura/

Interview with Heather M. This is the interview of Heather M. She shares her journey living with Fibromyalgia, EDS, autism spectrum disorder, delayed gastric emptying, Raynaud’s, GERD, MCAS, and dysautonomia. Please be respectful of Heather and her story as she shares her words. https://annawerrunblog.wordpress.com/2017/01/13/interview-with-heather-m/

Interview with Nycci. This is my interview with Nycci as she shares her story living with Endometriosis, prolactinoma, arthritis, Raynaud’s, migraines, depression, anxiety, insomnia, and ADD. Please be respectful of Nycci and her story as it is told in her own words.https://annawerrunblog.wordpress.com/2017/01/12/interview-with-nycci/

Interview with Sheri. This is Sheri’s story living with fibromyalgia and Raynaud’s phenomenon. This is her story in her words please be respectful.   https://annawerrunblog.wordpress.com/2017/01/11/interview-with-sheri/

Interview with Zoe. This is Zoe’s story. She bravely shares her journey living with Major Depressive Disorder and generalized Anxiety Disorder. ThIs is her story in her words please be respectful. https://annawerrunblog.wordpress.com/2017/01/11/interview-with-zoe/

Interview with Anna. The following is a interview with Anna a sixteen year old living with EDS, fibromyalgia, borderline personality disorder, autism spectrum disorder, anxiety and depression. https://annawerrunblog.wordpress.com/2017/01/09/interview-with-anna/

Interview with Adrienne. This is an interview I did with Adrienne, this is her journey, she describes her experience in an essay form. She shares her journey living with Ehlers Danlos Syndrome, and Postural Orthostatic a Tachicardia Syndrome. https://annawerrunblog.wordpress.com/2017/01/08/interview-with-adrienne-ferron/

Interview with Lesley Jeal. The first care givers interview I have done was with Lesley Jeal. I asked her a series of questions about her and her husbands life raising their son with Mitochondrail disease. Please be aware this is her story. https://annawerrunblog.wordpress.com/2017/01/08/care-giver-interview-with-lesley-jeal/

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