|
View Poll Results: Have you been dxed w/an autoimmune disorder? | |
Yes (please specify which below), but close relatives have not been
|    | 36 | 55.38% | |
No, and close relatives have not been
|    | 15 | 23.08% | |
No, but I think I have one or more (specify which below)
|    | 8 | 12.31% | |
No, but my parents or siblings have one or more (specify which below)
|    | 4 | 6.15% | |
Not sure
|    | 2 | 3.08% |  | |
04-28-2008, 11:10 PM
|
#31 (permalink)
| | PCOS Dancer
Join Date: Mar 2008
Posts: 9
My Mood: Points: 414.31 Bank: 0.00 Total Points: 414.31 | I have psoriasis, as does my sister. I also have eczema and when my psoriasis flares up, the eczema tags along.
Has anyone noticed a connection with flare-ups in their autoimmune disorder and flare-ups with their PCOS?
I've noticed that I tend to get more patches of psoriasis when I'm suffering with the most amount (and most painful) cysts. During the time when my ovaries are almost normal, my is often completely clear. |
| |
04-29-2008, 07:20 PM
|
#32 (permalink)
| | flower in the rain
Join Date: Dec 2007
Posts: 62
My Mood: Points: 3,072.42 Bank: 0.00 Total Points: 3,072.42 | I have vitiligo (although thankfully its limited to a fairly small area on my arm at this point) and I'm currently undergoing testing for what my doctors suspect is some sort of autoimmune issue that's affecting my joints and muscles...
__________________ Grace To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
PCOS - dx July 2005 social anxiety disorder fibromyalgia - dx July 2008 current meds: Yasmin 18 year old English major Bisexual cyster I love my 3 cute lil furbabies!!! To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts. To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
"I don't... make friends easily. I'm awkward and am bad at small talk and generally don't like people I don't know... but I made friends with you......" (-Erica Hahn on Grey's Anatomy) |
| |
05-15-2008, 07:39 PM
|
#33 (permalink)
| | Registered User
Join Date: Jul 2007 Location: Maine
Posts: 2
My Mood: Points: 324.96 Bank: 0.00 Total Points: 324.96 | U.c. I have ulcerative colitis, diagnosed last year. No history of it in the family  |
| |
05-17-2008, 12:17 AM
|
#34 (permalink)
| | The Flying Cyster
Join Date: Sep 2003 Location: Alaska
Posts: 125
My Mood: Points: 17,533.63 Bank: 0.00 Total Points: 17,533.63 | I've had Crohn's disease for years. I also have rheumatoid arthritis, but it didn't come into play until after treatment for metastatic thyroid cancer, and from what I've heard, a lot of cancer survivors end up with RA.
__________________ "Women are meant to be loved, not understood" - Oscar Wilde
~ We are never given more than we can't handle. ~
Me (25) To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts. Patrick (25) |
| |
05-17-2008, 12:19 AM
|
#35 (permalink)
| | The Flying Cyster
Join Date: Sep 2003 Location: Alaska
Posts: 125
My Mood: Points: 17,533.63 Bank: 0.00 Total Points: 17,533.63 | Quote:
Originally Posted by KeyGoblin Has anyone noticed a connection with flare-ups in their autoimmune disorder and flare-ups with their PCOS? | I most certainly have! I have more pelvic pain, bad complexion, and increased hair growth when I'm having a severe Crohn's or RA flareup.
I can't help but wonder if the pain caused by the autoimmune issues causes stress, which then causes a chemical reaction that worsens the symptoms of PCOS?
__________________ "Women are meant to be loved, not understood" - Oscar Wilde
~ We are never given more than we can't handle. ~
Me (25) To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts. Patrick (25) |
| |
05-17-2008, 03:02 PM
|
#36 (permalink)
| | Addicted to watermellon
Join Date: Oct 2004 Location: NC, USA
Posts: 16,885
My Mood: Points: 210,239.62 Bank: 46,375,066.28 Total Points: 46,585,305.90 | My cousin was just diagnosed with either lupis or fibro. She is now dying of NAFLD. Be sure to get periodic liver screenings for you and your close relatives. It could save a life. |
| |
05-17-2008, 07:26 PM
|
#37 (permalink)
| | Registered User
Join Date: Mar 2008
Posts: 30
Points: 846.23 Bank: 0.00 Total Points: 846.23 | hashimoto and celiac |
| |
05-17-2008, 07:31 PM
|
#38 (permalink)
| | Registered User
Join Date: Aug 2006
Posts: 1,220
My Mood: Points: 6,739.59 Bank: 126,737.42 Total Points: 133,477.01 | Alaskaflygirl, If you have an autoimmune disease, sometimes you end up with two. My son had crohn's disease and his doctor is keeping an eye on him. She says that he could get RA or something else too...
I have psoriasis and it flares up with I'm stressed out and when my sugar levels aren't in control...which is most of the time...
__________________ DX 1994-told to lose weight by GYN,Suffered 12 years before seeking treatments: REDX 2006 by a family doc sent to endo July 31, 2006 and glad I went; Byetta, 2000mg Metformin, fish oil, 1000mg calcium, Vytorin, baby aspirin. Type 2 diabetic and high cholesterol dx March 05, psoriasis dx 1992. Married 19 yrs 2 kids: girl 18 yrs old and boy 16 yrs old. |
| |
06-04-2008, 02:23 PM
|
#39 (permalink)
| | Registered User
Join Date: Mar 2007 Location: Madison, WI
Posts: 12
Points: 450.84 Bank: 0.00 Total Points: 450.84 | Crohn's and PCOS I have been Diagnosed with Crohn's disease and chronic Pancreatitis with secondary RA.
My doctors have all said that there must be a link between the PCOS and autoimmune disease especially since my Pancreas is being affected by both.
FYI for anyone else battling IBD, I take Humira for Crohn's and it is helping me stay off of Prednisone. It may seem like a scary drug but it has given me my life back. |
| |
06-04-2008, 02:30 PM
|
#40 (permalink)
| | Registered User
Join Date: Mar 2007 Location: Madison, WI
Posts: 12
Points: 450.84 Bank: 0.00 Total Points: 450.84 | Quote:
Originally Posted by alaskaflygirl I most certainly have! I have more pelvic pain, bad complexion, and increased hair growth when I'm having a severe Crohn's or RA flareup.
I can't help but wonder if the pain caused by the autoimmune issues causes stress, which then causes a chemical reaction that worsens the symptoms of PCOS? | I am totally with you, same thing happens. When it rains it pours for sure. Is it a flare causes the PCOS to act up or the other way around? Sometimes I feel like PCOS gives me a flare. |
| |
06-04-2008, 04:05 PM
|
#41 (permalink)
| | Registered User
Join Date: Jan 2006 Location: St. Louis
Posts: 22
Points: 1,323.93 Bank: 0.00 Total Points: 1,323.93 | Lacking insurance, I am currently undiagnosed. However, I want to get myself checked out for Selective Immunoglobulin A Deficiency (Selective IgAD)-- which is not an autoimmune but an immunodeficiency disorder--as well as Celiac's Disease once I get insurance. These two occur often together and I display the full set of symptoms as well as similar symptoms through my mother's side (it seems to prefer maternal transmission).
However, without testing, I obviously can't say for certain.
**Important Note for Anyone Who Suspects Celiac's Disease:
You should also get yourself checked for IgA Deficiency as you're getting checked for Celiac's, because if you test positive for Selective IgAD you may get a false negative for Celiac's using the traditional blood test. SIgAD can affect antigliadin levels which are the typical indicator of Celiac's. So a different type of test would need to be used to make sure it isn't Celiac's. |
| |
06-23-2008, 04:22 PM
|
#42 (permalink)
| | Registered User
Join Date: Jun 2008 Location: NC
Posts: 26
My Mood: Points: 656.04 Bank: 0.00 Total Points: 656.04 | I have celiac and PCOS. My mom has miltiple auto-immune issues. I checked the first one. |
| |
06-23-2008, 07:57 PM
|
#43 (permalink)
| | Allergic to PMS
Join Date: Aug 2007 Location: Shawano, WI
Posts: 231
My Mood: Points: 2,348.49 Bank: 2,065.38 Total Points: 4,413.87 | I checked 'not sure'. I've been dealing with elevated WBC Count, specifically neutrophilia, for a little over a year now. 6 months of testing with a hematologist, and still haven't figured out what's wrong. I have a standing order for Prednisone at the pharmacy. Any sign of a cold, I have to take 5 days worth to keep it from turning into bronchitis or pneumonia again.
__________________ ~35 ~ PCOS/IR ~ LAVH due to fibroid, kept ovaries ~ |
| |
06-26-2008, 10:31 PM
|
#44 (permalink)
| | Registered User
Join Date: Feb 2003
Posts: 699
My Mood: Points: 1,569.66 Bank: 0.00 Total Points: 1,569.66 | I have hashimotos thyroiditis. My sister has celiac. My mom and grandma also have hashis. I think I may have chronic fatigue syndrome and am going to the doc to hopefully rule it out.
__________________ To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts.
To view links or images in signatures your post count must be 10 or greater. You currently have 0 posts. |
| |
06-29-2008, 03:26 AM
|
#45 (permalink)
| | Registered User
Join Date: Feb 2006
Posts: 12
Points: 970.42 Bank: 0.00 Total Points: 970.42 | Psoriasis.
The psoriasis didn't begin until the year my period went bye-bye... age 20. I am now 25 and years 24 & 25 (when my PCOS has been the worst) my psoriasis has been out of control. Nothing like being fat AND having crappy skin!
__________________ 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) |
| |  | |
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 | | | | » Subscriptions | | | |