Please help me, I'm struggling to want to continue….

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Gabes-Apg
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Post by Gabes-Apg »

its semi normal... the mucus is an indicator of inflammation.

try not to get tooo overwhelmed by all that is in the the toilet bowl.
things will improve, its about progress.... not perfection.
Gabes Ryan

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carolm
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Post by carolm »

Martha,
I'm sorry you are feeling so distressed but I certainly understand it. When I had my biggest flare that lead to a diagnosis I had to eat no sugar, no caffeine, low fat, low (or no) fiber, no raw vegetables. Think "eat simply"-- baked chicken with carrots or a lean roast with potatoes.. you get the idea. Go completely gluten free and dairy free. Be aware that some of us..me especially... are also reactive to soy. I finally stopped gurgling when I eliminated soy.

Did I read that you are on probiotics? Probiotics very rarely work for us. For most of us it creates more problems. You don't need them-- your goal is to reduce inflammation so your body can work correctly. Probiotics won't help you there. Diet changes will. Some people (including me) also take Claritin or Allegra or some other antihistamine to help fight inflammatory reactions. If my allergies are amped up, I'll add Benadryl at night. If you have GERD or nausea, an H2 blocker antihistamine, like Zantac will help.

Hang in there. You are not alone and most of us have been very, very, sick in the beginning but with the knowledge and support here we gradually get our lives back.

Carol
“.... people will forget what you said, people will forget what you did, but people will never forget how you made them feel.” Maya Angelou
MarthaE
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Post by MarthaE »

Thank you Carol. I'm full of fear and I'm so tired. Appreciate the kindness
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Heady
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Post by Heady »

I started here April 1st, and have blood work booked for tomorrow to check for Selective IgA deficiency, vit.D,thyroid,hormones&blood sugar. Sel IgA def. could change whether Enterolab tests will be accurate. I am still awaiting the book I ordered thru amazon. Hopefully it arrives soon.
I try to tackle one day at a time. I have tried some pepto bismol but found it made my tinnitus worse.
We all have our own individual MC Journey. There is a lot of info in previous topics throughout this entire site worth reviewing. We are all here for each other.
Rest,relax & know that the healing starts here.
I wish you well in your quest for health.
Diabetic DX June 2012
Diverticulosis/ MC DX Feb.2014

I am thankful for my struggle because without it I wouldn't have stumbled across my strength.

What are you willing to let go of so you can live the life you know you deserve?
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Post by JLH »

:welcome: Sorry you are having such a rough time.

Buying Tex's book would help you get information faster.

Check out LDN, too.

:bigbighug:
DISCLAIMER: I am not a doctor and don't play one on TV.

LDN July 18, 2014

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Post by Leah »

Welcome Martha.
I know this is so scary and difficult, but try to stay calm because stress can make our symptoms worse. The mucus is pretty normal for active MC. You may just have too much fiber in your diet ( i am a certified personal trainer/nutrition specialist) . When it come to vegetables, you are best off right now with carrots, squashes, and maybe green beans. Sweet potato works well for most of us. White rice is gentle ( but some of us have to give up all grains). Many of us can eat potato, but others can't do night shades. Try to eat fresh foods only and high protein. The protein helps heal.

If Entocort isn't right for you, maybe the Pepto protocol will work ( while you work on the diet). It's up to eight chewables a day for 2 months. It works for some. Not all. Be prepared for your BMs to be black if you try this.

Staying hydrated is very important. Keep a food/bm journal. It can be very helpful.

OTC antihistmines help many of us ( including me). If it turns out that they help you, then you should look at eliminating high histamine foods. Mushrooms and spinach can be a problem.

Buying Tex's book is a good idea. It really helps in understanding this disease.

Please know that this can get better. It takes a lot of detective work, cooking, planning, and patience…. but all your hard work will pay off. After 6 months, i was down to one BM a day. After a year, I was able to add some things back into my diet. Now, two years later, I am gluten, soy, and dairy free, but I live a normal life otherwise. There is hope!

Ask anything. Take a deep breath. We are all here for you :)

leah
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Post by brandy »

Hi Martha,

I had a lot of brain issues while I was on Entocort that I thought would be better on the lower doses but I still felt lousy on one every third day. I knew the last day I took Entocort was the last day that I would ever take Entocort and I have never knowingly consumed G, D, or S. The extreme Entocort side effects keep me on a healthy diet path every day of GF, DF, and SF. If you think you still need the help of pharmaceuticals folks have found relief using the above list that Gabe listed.

Brandy
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Post by MarthaE »

Ok sigh…. just want to thank everyone for the kindness and support. Was laughing today because I actually had a small slim firm movement. Nice to laugh. Not sure why things shifted butt :) I need to keep better food supplement/journal. Called mom to inform her of my form, such strange joy, gotta know she loves that But I will take it! Did the MRT blood testing today and looking forward to checking out the entrolab testing. Is bone broth a good idea to heal the gut? I keep reading that it does, but wonder if others have had success with it. Hope to some day figure out my triggers. :pigtail:
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Gabes-Apg
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Post by Gabes-Apg »

Woo hoo!!! Progress !
Definitely worthy of a happy dance when you poop starts to resemble normal.


Bone broth worked really well for me for healing and I still have it/use it for cooking 4+ years later.
Start simple with chicken. Or beef. Make sure you don't react to that item.

For me in Aus, lamb is half the cost of beef, so my bone broth is lamb and chicken.
Lamb also freezes and reheats better, so my stews are a mix of lamb, veal and pork

Only thing I add is Himalayan salt.
Bone broth has about 60-70% of the amino acids our bodies need.
plus natural source of gelatine and animal fats

Take your time, the journey is about progress..... Not perfection.
Gabes Ryan

"Anything that contradicts experience and logic should be abandoned"
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MaggieRedwings
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Post by MaggieRedwings »

Great progress Martha - only 1 is sometimes a highlight. Welcome belatedly.

Can I ask what side effects you had from Entocort? I also incurred side effects and had to stop it.

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Jeanemcl
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Post by Jeanemcl »

Martha,
Hang in there...it does get better. I was on Endocort the first time I was diagnosed with CC and it worked like a charm. I was healthy for 3 years. Then I started with flares. Endocort worked again but the flare came back in 3 months. Then the stuggle began. Endocort was not working as well and I kept getting sick. Finally, found this forum, had lab testing and cut out gluten, soy, and cassein. Struggled for another 3 months, tried some probiotics and health food supplements (worked briefly) and then tried Questran and Elavil. I think the combo of meds, diet change and time finally worked and I have been been much better. I read labels, try not to overeat, watch my sugar intake and eliminate anything with soy, cassein, and gluten. I try to get enough sleep and keep stress at a minimum....pretty talk order, but it has worked. I struggled with patience and fear kept creeping in. I know that didn't help, so I tried to work with that...meditation and exercise. I am down to 1/2 pkg of Questran every 3-4 days and that seems to be working for me now. The people on this forum were so helpful and it was a "safe" place to go when I was discouraged. Good luck on your journey...
Jean
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Post by brandy »

Martha,

I forgot to mention I spent about $3000.00 on food allergy testing that my GI doc wanted done. Ended up being useless and not covered by my United Healthcare.
Suggest invest in Tex's book, see upper right hand corner, @$25.00, invest in Enterolab stool tests @ $400.00 and will tell you if you need to be GF, DF, SF or EF.
And, finally some people if they are still struggling invest in MRT testing, @$600.00. I didn't have to do that one. Just a thought. Brandy
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Lesley
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Post by Lesley »

Martha - I was desperate when I found this forum.

Everything people said is right. I cannot eat chicken, so if you find you are still not getting better when eating it try lamb, which is much more digestible.
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Martha
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Post by Martha »

Welcome, Martha, from another Martha.

I don't have any insights to add to what has already been said, but I do encourage you to totally eliminate gluten, dairy, and soy from your diet. And the Enterolab tests--the best $400 I spent! My insurance wouldn't cover it, even though they didn't blink an eye at the more than $600 per month for Entocort (which worked very well for me). But just having that assurance that I really did need to cut out those foods was helpful emotionally.

Love and hugs,
Martha
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coryhub
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Post by coryhub »

Hi Martha-

Don't be scared about mucus stools as it is very common as fats are not digested properly causing fatty malabsorption. You might see oily, mucus, or floaty stools among other things. You did not say whether you were eating gluten-free or not. That's the biggest piece of advice I would give you. Remove gluten and processed foods from your life. You survived a brain tumor, and I'm sure you will get your MC under control. It takes some time, research and patience. Tex's book (above, top right hand corner) has a wealth of information and I recommend it.

Best,
Cory
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On and off Entocort(Currently Off)
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