aenigma20.blogspot.com
Laser Hair Removal with Hidradenitis Suppurativa: July 23rd - More Laser Hair Removal
http://aenigma20.blogspot.com/2008/07/july-23rd-more-laser-hair-removal.html
Laser Hair Removal with Hidradenitis Suppurativa. THIS IS TO DOCUMENT MY JOURNEY THROUGH LASER HAIR REMOVAL TO SEE IF IT HAS ANY AFFECT ON MY SKIN DISEASE HIDRADENITIS SUPPURATIVA. Thursday, July 24, 2008. July 23rd - More Laser Hair Removal. This time I actually remembered to look at what kind of equipment is being used. A Palomar StarLux 500. Is being used. I'm not sure what the number mean, but on the display the settings she was using was 34 /20. Some Pictures of my HS. HS Video with Pictures. This p...
textualfury.wordpress.com
February | 2014 | Textual Fury
https://textualfury.wordpress.com/2014/02
The Almighty Corkscrew of Justice. Andrea ’s Buzzing About:. Astrid ’s Journal. Brilliant Mind Broken Body. Day in Washington Audio Blog. Despite all the rage I am still just a rat in a cage. Http:/ mattkailey.wordpress.com. Life in the House That Asperger Built. The Phrenologist ’s Notebook. The Vitality of Matt. Autism Society’s page on Asperger’s. Day in Washington Audio Blog. Mayo Clinic Definition for PTSD. Nueropathy Information and Support. Oral Allergy Syndrome Information. How do you handle it?
textualfury.wordpress.com
Glamour Secrets | Textual Fury
https://textualfury.wordpress.com/glamour-secrets
The Almighty Corkscrew of Justice. Andrea ’s Buzzing About:. Astrid ’s Journal. Brilliant Mind Broken Body. Day in Washington Audio Blog. Despite all the rage I am still just a rat in a cage. Http:/ mattkailey.wordpress.com. Life in the House That Asperger Built. The Phrenologist ’s Notebook. The Vitality of Matt. Autism Society’s page on Asperger’s. Day in Washington Audio Blog. Mayo Clinic Definition for PTSD. Nueropathy Information and Support. Oral Allergy Syndrome Information. How do you handle it?
hsratt1962.blogspot.com
My Life & Journey with Hidradenitis Suppurativa: What's It Like To Have HS?
http://hsratt1962.blogspot.com/2005/10/whats-it-like-to-have-hs.html
My Life and Journey with Hidradenitis Suppurativa. This is my personal journal about living with a chronic illness called Hidradenitis Suppurativa. While this journal has info about this disease, I am also including some of my personal thoughts on current event issues. Wednesday, October 05, 2005. What's It Like To Have HS? People with HS are sometimes asked "What's it like to have HS? What’s It Like To Have HS? Answering the question our loved ones are asking. And how many ways have we all answered it?
hsratt1962.blogspot.com
My Life & Journey with Hidradenitis Suppurativa: Disability Tips (Part 1)
http://hsratt1962.blogspot.com/2005/10/disability-tips-part-1.html
My Life and Journey with Hidradenitis Suppurativa. This is my personal journal about living with a chronic illness called Hidradenitis Suppurativa. While this journal has info about this disease, I am also including some of my personal thoughts on current event issues. Wednesday, October 05, 2005. Disability Tips (Part 1). Can be a daunting experience for anyone. Here are a few starter tips that may help you. Try to get your doctor to document very well. Size and location of lesions, exactly what supplie...
hsratt1962.blogspot.com
My Life & Journey with Hidradenitis Suppurativa: Disability Tips (Part 2)
http://hsratt1962.blogspot.com/2005/10/disability-tips-part-2.html
My Life and Journey with Hidradenitis Suppurativa. This is my personal journal about living with a chronic illness called Hidradenitis Suppurativa. While this journal has info about this disease, I am also including some of my personal thoughts on current event issues. Wednesday, October 05, 2005. Disability Tips (Part 2). Follow-up to "Disability Tips" : The initial application. Http:/ www.ssa.gov/. When would you say you became disabled? Do you have copies of your medical records? The interviewer will ...
hidrosadenit.blogspot.com
Venter på et mirakel: Masser af energi :-)
http://hidrosadenit.blogspot.com/2009/12/masser-af-energi.html
Venter på et mirakel. Jeg har lavet denne blog for at dele mine erfaringer med dig. Jeg har haft hidrosadenit/hidrosadenitis siden puberteten, dvs. mere end 30 år. Som mange andre med samme sygdom gik der mange år inden jeg fik den rigtige diagnose at vide, og jeg har prøvet behandling efter behandling med tvivlsomme eller svigtende resultater. Nye biologiske midler giver håb, men også problemer. Nu venter jeg på miraklet. Onsdag den 23. december 2009. Masser af energi :-). Masser af energi :-).
hidrosadenit.blogspot.com
Venter på et mirakel: august 2010
http://hidrosadenit.blogspot.com/2010_08_01_archive.html
Venter på et mirakel. Jeg har lavet denne blog for at dele mine erfaringer med dig. Jeg har haft hidrosadenit/hidrosadenitis siden puberteten, dvs. mere end 30 år. Som mange andre med samme sygdom gik der mange år inden jeg fik den rigtige diagnose at vide, og jeg har prøvet behandling efter behandling med tvivlsomme eller svigtende resultater. Nye biologiske midler giver håb, men også problemer. Nu venter jeg på miraklet. Torsdag den 19. august 2010. Abonner på: Indlæg (Atom). Skriveri - om HS.
hidrosadenit.blogspot.com
Venter på et mirakel: oktober 2008
http://hidrosadenit.blogspot.com/2008_10_01_archive.html
Venter på et mirakel. Jeg har lavet denne blog for at dele mine erfaringer med dig. Jeg har haft hidrosadenit/hidrosadenitis siden puberteten, dvs. mere end 30 år. Som mange andre med samme sygdom gik der mange år inden jeg fik den rigtige diagnose at vide, og jeg har prøvet behandling efter behandling med tvivlsomme eller svigtende resultater. Nye biologiske midler giver håb, men også problemer. Nu venter jeg på miraklet. Lørdag den 25. oktober 2008. Fredag den 17. oktober 2008. Abonner på: Indlæg (Atom).
hidrosadenit.blogspot.com
Venter på et mirakel: februar 2010
http://hidrosadenit.blogspot.com/2010_02_01_archive.html
Venter på et mirakel. Jeg har lavet denne blog for at dele mine erfaringer med dig. Jeg har haft hidrosadenit/hidrosadenitis siden puberteten, dvs. mere end 30 år. Som mange andre med samme sygdom gik der mange år inden jeg fik den rigtige diagnose at vide, og jeg har prøvet behandling efter behandling med tvivlsomme eller svigtende resultater. Nye biologiske midler giver håb, men også problemer. Nu venter jeg på miraklet. Mandag den 1. februar 2010. Abonner på: Indlæg (Atom). Skriveri - om HS.