LUPUS STORIES ~ Chapter Fifteen ~

LUPUS STORIES ~ Chapter Fifteen ~

PRIVACY STATEMENT DISCLAIMER

LUPUS LINKS CHOOSE ANOTHER ROOM

Lupus Stories ~ Chapter Fifteen

If you are still without a diagnosis, confused and frustrated by the medical run-around, please read through the pages of Issy's LUPUS INFORMATION CENTER. There you will find answers to many of your questions and probably even some you've never considered. Contained within these pages are symptoms, statistics, little-known facts, and common mis-conceptions. There may even be something there for those of you who have already been diagnosed! I believe you will find it well worth your time. The Lupus Information Center is now available in Print Friendly Pages. A new section has also been added on Social Security Disability Benefits. Be sure to check it out before you apply!

I will post your responses to the Lupus Survey as they are received! Read your post and those of others. Make friends, learn more about your disease, share emotions, and know that all-important sense of belonging. Please share your story with us!

PLEASE NOTE!
I have recently discovered that I have not been receiving all of the responses to this form!! I always reply to each submission within 2-3 days. If you do not receive an e-mail from me within that time period after submitting your response, please
e-mail { IssyMissy } with your story. I don't want to leave anyone out! Thank you and I regret this inconvenience.

If you haven't yet, please be sure to see what you can do to help support
H.R. 762
Funding for Lupus Care and Research

If you are interested, you may read my own personal lupus story here.

I'm Really Not Crazy!

79) ~ Bev ~
"...I don't have any friends any longer, I guess through all these years of my being ill they got tired of hearing that I don't feel well..."
READ:

Bev's
Story

HERE!

80) ~ Susan ~
"... I try not to worry about my symptoms, but I sometimes can not help but worry about my health..."
READ:

Susan's
Story

HERE!

81) ~ Saundra ~
"...For some reason, I felt worse when I found out I had lupus than when I was told I might need heart surgery..."
READ:

Saundra's
Story

HERE!

82) ~ Janice ~
"...I also began to have migraines again that I hadn't had in years, but the most puzzling symptom was that it hurt just for anyone to touch me, even just to pat me on the back or grab my arm..."
READ:

Janice's
Story

HERE!

83) ~ Nancy ~
"...I have had pain for as long as I can remember. I had been telling my family doctor about persistant pain in my hands for years. He never seemed to never take me seriously..."
READ:

Nancy's
Story

HERE!

84) ~ Kendra ~
"...I am in pain every day, yet I don't want to burden anyone with this nor do I want their sympathy. ..."
READ:

Kendra's
Story

HERE!

Lupus Stories
Chapter Fourteen

Lupus Stories
Chapter Sixteen

~ OR ~

You may use the listing of ROOMS provided below to navigate to the various pages of Personal Lupus Stories, as well as any other room in the house!

Choose another room:
[ The Hall ] [ Site Map of Issy's House ]
[ Foyer ] [ Sign Guest Book ] [ View Guest Book ]
[ Living Room] [ Kitchen] [ Holiday Suite ]
[ Den] [ Sarah's Photo Album ] [ Wood Shop Designs ]
[ Bathroom ] [ Bedroom ] [ Personal Lupus Story ] [ Closet ] [ Top Shelf ]
[ Library] [ Patio ] [ Crafting Shed] [ Background Boutique ]
[ Lupus Survey ] [ Lupus Stories 1 ] [ Lupus Stories 2 ]
[ Lupus Stories 3 ] [ Lupus Stories 4 ] [ Lupus Stories 5 ]
[ Lupus Stories 6 ] [ Lupus Stories 7 ] [ Lupus Stories 8 ]
[ Lupus Stories 9 ] [ Lupus Stories 10 ] [ Lupus Stories 11 ]
[ Lupus Stories 12 ] [ Lupus Stories 13 ] [ Lupus Stories 14 ]
[ Lupus Information Center ]
[ MS Links ] [ MS Information Center ] [ Win An Award ]

Know someone who might benefit from reading our stories, or might like to share their own Lupus story with us?
Send This Page!

Find loads of Lupus Info, Help, Support, and more!

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This site is owned and maintained by Gayla Pledger. All stories contained within these pages are the © copyright of the author and used here with the express consent of each individual.
Please note that neither I nor the individuals sharing their lupus stories, are physicians. This area of IssyMissy's House is provided strictly for the purpose of sharing our experiences and feelings with one another as a means of support and validation. The opinions expressed here are strictly those of the person who gave them and should be treated as such. Lupus is a disease as unique as each individual and only your doctor can know what medications and treatments are best for you. Follow the directions of your own personal physician and always consult your doctor before changing or discontinuing any treatments or medications.
"IssyMissy" and "Miss Issy" are the trademarks of Gayla Pledger.
( © copyright - 1998,1999 ) ALL RIGHTS RESERVED.

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