|
View Poll Results: Have you been dxed w/an autoimmune disorder? | |
Yes (please specify which below), but close relatives have not been
|     | 45 | 56.25% | |
No, and close relatives have not been
|    | 17 | 21.25% | |
No, but I think I have one or more (specify which below)
|    | 9 | 11.25% | |
No, but my parents or siblings have one or more (specify which below)
|    | 6 | 7.50% | |
Not sure
|    | 3 | 3.75% |
 | | 
06-29-2008, 03:32 AM
|
#46 (permalink)
| | Registered User
Join Date: Feb 2006
Posts: 12
Points: 1,077.42 Bank: 0.00 Total Points: 1,077.42 |
Psoriasis.
My psoriasis didn't start until age 20 - the year my period stopped. I'm 25, and years 24 & 25 (the worst years of my PCOS) my skin was the worst. I'm on two immunosuppressant drugs to try to clean my skin. Nothing worse than being fat and having your whole body covered in red scaly patches!
__________________
Me: 25
DF: 30
Together since 6/14/03 over 5 happy years!
To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
Engaged 9/30/07, will be married 5/30/09 in a big bash!
Diagnosed: 12/05
Meds: Byetta (IR), Synthroid (Hypothyroid), Raptiva (Psoriasis), Methotrexate (Psoriasis), Folic Acid (Psoriasis) | 
|  | |
06-29-2008, 04:16 AM
|
#47 (permalink)
| | Registered User
Join Date: Sep 2001 Location: iowa usa
Posts: 403
My Mood:  Points: 9,623.03 Bank: 0.00 Total Points: 9,623.03 |
i have fibro and my dads sister died of lupus
__________________
me 28
dx 1993
dx with
diabetes type 2
fibromyalgia
cts
miagrines
oxycodone for pain
mirena
yahoo: kissablesweetie50530
msn:
To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
| |
| | |
06-29-2008, 05:31 PM
|
#48 (permalink)
| | Registered User
Join Date: Jun 2008 Location: Washington, DC
Posts: 6
Points: 174.75 Bank: 0.00 Total Points: 174.75 |
alopecia areata -- diagnosed 20 days after starting to take metformin  | |
| | |
07-01-2008, 10:45 AM
|
#49 (permalink)
| | Blessed
Join Date: Oct 2004 Location: Piedmont Triad of NC, USA
Posts: 17,224
My Mood:  Points: 233,838.87 Bank: 98,421,747.15 Total Points: 98,655,586.03 |
One of my cousins I was sure has PCOS. She still doesn't have a diagnosis yet, but I spoke with her sister last night. The one I hadn't suspected has a lot of health issues including fatty liver, fibromyalgia, endometerosis and post tubal ligation syndrome among other things. I wonder if she has PCOS, but I did encourage her to get checked for liver and insulin problems yearly. She is also worried about her daughter and son because of their weight and sugar cravings.
__________________
Romans 12:12
Be joyful in hope, patient in affliction, faithful in prayer. | |
| | |
09-15-2008, 12:46 PM
|
#50 (permalink)
| | Registered User
Join Date: Mar 2005
Posts: 1
Points: 24.45 Bank: 0.00 Total Points: 24.45 |
I was dx'd w/Multiple Sclerosis in March 2007 | |
| | |
09-15-2008, 01:24 PM
|
#51 (permalink)
| | Registered User
Join Date: Aug 2008 Location: Vancouver, WA
Posts: 295
My Mood:  Points: 8,090.89 Bank: 0.00 Total Points: 8,090.89 |
Endometriosis (some say it is autoimmune, some say it isn't) and getting tested for Chronic Fatigue. I had a really bad bout of mononucleosis when I was 19 and it will flare up from time to time (at least it seems that way... the jury is out about some of the complications that come along with the epstein barr virus). I have a lot of symptoms of many different autoimmune disorders but Dr says none of them are *severe* enough, but I'm pushing to figure it out before things do get bad so I can take steps to help myself. | |
| | |
09-15-2008, 04:45 PM
|
#52 (permalink)
| | Ruler of Rainbowland
Join Date: Aug 2008 Location: the Carolinas
Posts: 85
My Mood:  Points: 2,462.67 Bank: 0.00 Total Points: 2,462.67 |
Hashimoto's Thyroiditis (auto-immune hypothyroidism) here. My mom and her brother have it too *sigh*
__________________
ME = 28, DH = 24
Cyster since 1995, Diagnosed 2006
5'6" / 125lbs
Taking: Cyclessa/Velivet BC
| |
| | |
09-16-2008, 04:45 PM
|
#53 (permalink)
| | Registered User
Join Date: Sep 2008
Posts: 11
Points: 224.34 Bank: 0.00 Total Points: 224.34 |
Hashimotos, raynauds, RA, and Menieres disease. | |
| | |
09-18-2008, 12:43 AM
|
#54 (permalink)
| | Kayaker
Join Date: Oct 2007 Location: NW Washington
Posts: 530
Points: 12,158.62 Bank: 1,302.73 Total Points: 13,461.35 |
Langerhans Cell Histiocytosis
__________________
Me 30, DH 29, married since 2003.
Langerhans Cell Histiocytosis Survivor
To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
Forever converted menstrul cup user!
To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
| |
| | |
09-18-2008, 07:56 PM
|
#55 (permalink)
| | Registered User
Join Date: Sep 2008 Location: I live in the state of Pennsylvania.
Posts: 7
My Mood:  Points: 313.23 Bank: 0.00 Total Points: 313.23 |
I have Lupus (SLE) and Fibromyalgia. The aches, pains, and sleepless nights really take a toll on the body and mind. I know that my dad has arthritis from an old injury but no real autoimmune disorder. I have little to no contact with my birth mom but do know that diabetes runs in her family and she gave me severe thyroid problems (she and all 7 of her sisters had thyroid problems...since she walked out when I was 9 months I had no clue to watch for it and after more than 10 doctors missed it I almost died). I have only recently received the PCOS and IR diagnoses and hope that some weight loss and of course more meds will help. | |
| | | |
Posting Rules
| You may not post new threads You may not post replies You may not post attachments You may not edit your posts
HTML code is On
Points Per Thread View: 1.00 Points Per Thread: 15.00 Points Per Post: 5.00 | | |
| |
