Does anyone have other auto immune diseases

I do not but I am sorry to hear about your pain and depression, I truly am sorry. I read that exercising and drinking lots of water lowers risks of blood clots maybe that can help. Of course you would need extra water since you have no colon.

I am so sorry you are going thru this.  I do feel depressed and angry because I have always been sick my whole life even when I was a younger child.  Today I was very depressed.  I wanted to help my husband with our rental and I became so tired and sweating to death.  I just don’t get it.  I think the part I hate the worse is the severe exhaustion.  But I do get migraines and severe neck pain.  I do have IC and I do believe it’s an auto disorder. My joints hurt but haven’t went to check it out.  It’s not that bad yet.  I sometimes feel I traded one thing for many others.  But I had pre cancer cells thru my whole colon so it all had to come out.  I guess I get pissed because of all my health issues also.  Some of my friends don’t get it either.  But we are all year to support you and help you thru this.  If you’d like to be penpals thru computer let me know.  I hear your pain though.  Tired of it all.  

I forgot to say that I am having problems with my jpouch also.  I have cuffitis.  Just tired of the urge to push.  

I also have been sick since I was a child I just didn't know it. I thought I was normal. You really need to get your joint pain checked. The sooner you find the cause and great it cause it will only get worse. I also have cuffitis. I have also had depression since I was about 10. I am not angry though. I just am confused as to why. Very depressed and sad. I am not the person I used to be and that makes me sad. It was determined by the Drs that I was gonna have cancer but they didn't know when it would happen.  I chose surgery as I was told it would cute me. I was bleeding a lot and in a lot of pain so I believed them. My Drs lied and I ended up trading one problem for 15 other problems.

I also have severe fatigue which limits my activities. I am so sorry you also so sick. I understand what it is like wanting to help family and friends but can't most times because of exhaustion and pain. 

I would like very much to be your pen pal. Therapists have never worked for me but my Drs are pretty much making me. She is specialized for U/C and crohns.  I think what will be best for me is to talk with others like me. I appreciate you reaching out to me and I look forward to getting to know more about you.

I know it's tough. I suffer from severe depression, endometriosis and interstitial cystitis.

How are you doing with all of that kangaroo?

I sent you a pm.  Thank you 

Nadine2012 - Thank you for asking. The major depression is a huge problem and I don't know what to do. I have the IC and endometriosis pretty much under control with meds.

Nadine2012.    I sent you a private message so we can be pen pals.  You should be able to find it up at the right corner and click on your account.  Look forward to talking to you.  Thank you. 

I have a lot of problems as well, started with colitis, then had surgery for it. After that had a reversal, got ileus after reversal. Shortly after that got knee inflammation and was diagnosed with arthritis. Had rectoscopy and doc told me that I have Indeterminate IBD, now I'm on Ramicade and just another day doc told me that I have antibodies. I don't know when will I have reversal surgery. Also my abdomen gets hard and bloated after eating. So I understand your problems

I am so sorry Nadine, I understand...it is way too much to handle at one time let alone at any time.

Yes, I have also been sick since birth...first surgeries and colostomy at age 2. Closed by age 3 but the damage was done to my colon/rectum. Joint and severe back pain since kiddihood. 

I've got severe food allergies, EDS, a congenital deficiency in collagen that means that my body does not build the glue to hold ligaments and skin together when injured. I am stretchy and pop out of joint constantly, do not heal post-op or post-accident and my spine is very curved...I also have a k pouch. It falls off of the wall regularly, I get hernias like others get colds and things just happen. My mom took DES and the rest is history.

That is my normal. 

Yes, I get angry sometimes that I need to work 5xs as hard as anyone else to get half as much result. Surgery means 6 weeks of sutures and another 6 with murphy-ties and 1 year to heal (or hell)...Keeping a job is hard, I am self-employed so that helps a lot but my job requires that I take public transportation and that adds a measure of difficulty to the mix. 

Depression? Occasionally...usually when I cannot find a surgeon to fix something...or when I am housebound. Less so since menopause (I believe that hormones had a lot to with the depression)

My dad taught me to always keep active and busy and never give in or give up. Busy minds/busy hands. I am an exerciser, doesn't matter where I am or what is wrong...I keep my body active...that helps my mind too. 

I cook & bake a lot for my family even if I can't eat it. 

I write, when all else fails, I keep my mind active...

As long as I am doing something else, I do not think about me and my pain, that is my only secret...I avoid meds at all costs but require a minimal dose of antiinflammatories/pain meds 2xs/daily for life of I cannot tie my shoelaces!

That's life. 

I would have loved to be born normal, but that can't be changed. I would have loved to not know so much pain or surgery but that can't be changed. I would have loved a loving and supportive family but...I had my dad and uncle...they were the best. 

What I can change is how I feel about it all. I scream in the shower sometimes, I workout until I drop, others. I teach and that is the best gift ever. 

You need to find your happy place where you do not feel your pain so much. 

Your mental escape...

That's all I've got...

Sharon

I have inflammatory airway disease and CSR (central seruos retinopathy) in my eyes (which may be an autoimmune disorder but the cause is unknown) as well as inflammatory bowel disease. 

 I too add my empathy to your situation. None of us got dealt the best health cards and we have to sacrifice time every day to compensate.  I agree with Sharon wholeheartedly. Although I no longer work I do volunteer. I find helping people who are less fortunate than I am allows me to put any problem in perspective. Exercise is critical, especially if you have fibromyalgia, which like you I have.  BTW, there are medications for fibromyalgia that are extremely helpful.

It’s very difficult for others to understand what  any of us have gone through. That’s why this site is like family for me. When I have a problem I do a search and am more informed, which helps me understand and cope with the problem. 

CT barrister: bummer of a disease to have with Covid! Hope you can stay well. 

Is Inflammatory airway disease same as asthma??? I have asthma.

Asthma is one inflammatory airway disease. There are many others such as bronchiactasis, sinusitis and allergic and non allergic rhinitis just to name a few.

@CTBarrister posted:

Asthma is one inflammatory airway disease. There are many others such as bronchiactasis, sinusitis and allergic and non allergic rhinitis just to name a few.

Oh I see. Do you take meds for your airway disease? I take Advair, Albuterol, and Montelukast.

Thank you everyone! I truly am sorry you are sick. I don't wish this on anyone. Maybe for a few hours so they understand...!o!. I still work full-time and it is real hard. I am soooo tired and in a lot of pain. I can't afford to not work for a year until it more trying to get on disability. How do all of you manage?

@Lauren Of Emerald City posted:

Oh I see. Do you take meds for your airway disease? I take Advair, Albuterol, and Montelukast.

Fluticasone Propionate (steroid nasal spray) and Azelastine HCL (antihistamine/anti-inflammatory)

@CTBarrister posted:

Fluticasone Propionate (steroid nasal spray) and Azelastine HCL (antihistamine/anti-inflammatory)

Cool! I see we are both taking steriods. Be careful about preventing osteoporosis while taking steriods. I take calcium and vitamin D supplements to prevent it.