Patient & Caregiver Stories Main Menu
(English) Stories by First Name: A B C D E F G H I J K L M N O P Q R S T U V-Z
All Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
Stories by Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms
Stories by Language: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish
Buggzy: Autoimmune Hepatitis, Fibromyalgia, Undiagnosed
I have long ago given up trying to find what is wrong with me.

Swallowtail Butterflies by Ione Bridgman, ISN Artist I am a forty-six-year-old mother of three children, and I have two grandchildren. This might seem like a tirade, but I am anxious to know if anyone has had a similar experience. I have been diagnosed with fibromyalgia, ulcerative esophagitis, Gilbert's syndrome, diverticulitis, peripheral neuritis, and trigeminal neuralgia. I lost all taste sensation for about eight months, at one stage, but all that showed up in pathology was an elevated erythrocyte sedimentation rate (ESR).

When I was ten, I got this huge, black blood blister on the roof of my mouth, which stayed for years. I had it x-rayed and they put it down as a mucous cyst, stating that it was highly unusual! Over the years, I have had blood blisters, the size of grapes, in my mouth. The doctors are mystified by it! I have also had blood blisters on my thighs, stomach, and chest as well as petechiae.

I have had surgeries for dislocated joints, a hernia, and removal of my gallbladder and tonsils. I have also had a nephrectomy because of kidney cancer, and sutures to hold my pregnancies. I lost my first two babies preterm and all my kids were premature.

My antinuclear antibodies (ANA) ranged between 1:40 to 1:640, and I have always had abnormal liver function tests as well as elevated serum ACE and ESR levels.

The only reason I have listed everything is in the hope that one of you may have had similar experiences. I know it sounds like a hypochondriac's diary, but I am really desperate to get some answers or to hear from others in the same boat as me.

~ Update ~

Since my first letter in 1999, I have had many unnamed illnesses. I am just getting over my third attack of trigeminal neuralgia. It is the most excruciating thing I have had to deal with. It lasted over a month this time and gradually subsided. My blood screens for this period were way off the chart. They showed extreme inflammation in my body. The doctor did not tell me the levels, but I had to go back for repeat tests.My hair was falling out by the truckload. I don't have any bald patches, just overall hair loss.

In May 2001, I developed three blisters the size of hardboiled eggs on my stomach. I foolishly burst them and copious amounts of fluid came out. The lesion had three points of hemorrhage on the surface, and it deteriorated into a severe ulcer. I had skin biopsies. Nobody offered a diagnosis. Nobody had any idea. Nobody had seen anything like it. Possibilities thrown at me included a burn and a white-tailed spider bite. The biopsies simply showed ulceration. Eleven weeks later with fresh dressings every second day, none of us is wiser, except that I have a huge, ugly scar.

At the same time this was happening, my left knee started dislocating again for no reason, and my problems with endometriosis began. I felt bamboozled by all these things. My serum iron levels were very low, but the doctor suggested that this could have been from the loss of all the fluid through the ulcer on my stomach.

My fibromyalgia has been really bad over the last twelve months, and I find I have to sleep often. The trigeminal neuralgia caused my blood tests to be extremely abnormal. Over the last two years, I have had two hysteroscopies for endometritis (not endometriosis). It seems that instead of being 2 cm., my endometrium is 14 cm.; all due to inflammation. My gynecologist just wants to wait and see if it sorts itself out.

Of interest is that they have found I have an abnormal Alpha-1 Antitrypsin (A1A) gene, supposedly passed down through my Danish heritage.

Since my last update, I have also had another liver biopsy, which showed inflammation, but no scarring. I have long ago given up trying to find what is wrong with me.

To Contact the Author
Buggzy
New email address needed.
Old Email: maurbug@joynet.com.au
Story posted 7-7-99
Story update 2-22-02
Story edited VH1: JTD 9-8-03
Email note posted 01-20-05 SLE

Story Artist: Ione Bridgman
Story Editor V1: Judith Devlin
LINKS
Antinuclear Antibodies
Bullous Pemphigoid
Cancer and Scleroderma
ESR
Fibromyalgia
Gilbert's Syndrome
Hair Loss (Alopecia)
Peripheral Neuritis
Pregnancy and Scleroderma
Trigeminal Neuralgia
Ulcerative Esophagitis
Voices of Scleroderma Volume 1
This Story is Featured in Voices of Scleroderma Volume 1
Voices of Scleroderma Volume 1
The story on this page is featured in the top-notch Voices of Scleroderma Volume 1 which features articles by top scleroderma experts, including Dr. Joseph Korn, as well as 100 true patient and caregiver stories from this website! The book delivers excellent information and support for scleroderma patients and caregivers. It's a great way to inform family and friends about scleroderma, too!
ISN Artist: Ione Bridgman
Ione Bridgman ISN Artist Ione Bridgman created original artwork to illustrate this page. She is 90 years old, and lives in New Zealand. Her lovely paintings illustrate many of our pages and the covers of our  Voices of Scleroderma Book Series .
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith Thompson Devlin is the ISN Story Editor for this story. She is also lead editor of the ISN's wonderful Voices of Scleroderma book series !
New Personal Stories
Mila: Morphea Now I am twenty-five years old, and that spot has grown throughout my right leg and on one side of my belly button...
(Español/Spanish) Mila: Morfea Hoy en día tengo 25 años y esa mancha está en toda mi pierna derecha y al lado de mi ombligo...
(Español/Spanish) (Update) Jeins: Esclerodermia Sistemica Difusa y Dermatopolimiositis Ya había escrito mi historia hace 3 años cuando recién estaba pasando por la enfermedad. Para quienes no lo saben tengo esclerodermia y dermatomiositis desde los 19 años.
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
More New Stories: November 2008
Submit Your Patient, Caregiver or Survivor Story in:
Arabic  | Dutch  | English  | Español  | Deutsche (German)
Italiano  | Polski  | Russian  | Spanish  | Turkish  | Other Languages
We will edit your story, create original artwork to decorate it, prepare it for the web, and post it on this site. Just fill out our simple Story Submission Form for your story, updates, or email address changes.
Keep on Surfing!
Go to Bwana: Keloids
Contact ISN. We are a full-service nonprofit scleroderma charitable foundation.
Email: isn@sclero.org or
Post in Sclero Forums!
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
USA
Toll Free Hotline in U.S.
1-800-564-7099
Direct Line
1-952-831-3091 (U.S.)

Donate in Memory to the nonprofit International Scleroderma Network at sclero.org. We will make a custom donation form and link for you, and send thank you's and acknowledgement cards. We list donors and events in our website and newsletter.

Please help raise awareness of scleroderma and related illnesses by mentioning and linking to the nonprofit International Scleroderma Network at sclero.org in conversations, speeches, web sites, and publications.

(We are also known as the Scleroderma from A to Z web site.)
© Copyright 1998-2009 International Scleroderma Network
All Rights Reserved