Sorry I've been MIA. This is a long catch up.

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Mrs. Poopy Jeans
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Sorry I've been MIA. This is a long catch up.

Post by Mrs. Poopy Jeans »

Hello to all, and a special howdy do to all our new MC Warriors. :grin:

Me? Mixed bag really. The food situation is great except that I may be giving myself too many choices. This is not one of my choices just the choice to be bad. Last week I was BAD and ate a hot pastrami sandwich, which is one of my most favorite things in the world to eat. Paid for it for two days.

Overall, I eat pretty strictly gluten, dairy and soy free. Alas, I still have D but not as often in a day and not as urgent......except after the hot pastrami fiasco. I have discovered that Earth Source Original spread is totally yummy and cooks and bakes very well. I tried rice milk. Yuck! Too watery. I was drinking Califia Almond milk and it is good but then I tried Silk Almond milk and Silk Almond Chocolate Milk! HELLO HOT CHOCOLATE! My two new favorites.

As I have mysterious neurological problems, it is really affecting my sleep. Either that or a cat in my lap sends sleep vapors and I find myself taking almost daily three, even four hour naps. Of course then I don't sleep at night and find myself going to bed around 1:00 A.M. The alarm goes off at 5:30 and I get up to get hubby off to work. He leaves and I get chores done but crash around 9:30A.M. and the cycle starts again. I have a Neurologist appt on the 19th in which I need to further clarify my missing brain matter issue, my pain in my lower back so that I cannot bend, my tremors in my hands, my balance issues and my sleep issues.

My spray Magnesian is a real help and I take 1000 units of vit D. I believe it is contributing to my feeling of well being along with my trusty 120 mg of Cymbalta.

Now this may sound really weird and ewwwww, but because most times when I sit, I don't know that I need to use the facilities. As soon as I stand up,however, it can be an urgent matter and it is then that the bathroom seems miles away as my mobility is compromised resulting in a messy mess. Here it is; I am seriously thinking of purchasing a sturdy potty chair with arms and a bucket and liner underneath so that I can get it done immediately. Is this just too gross? My shades are mostly pulled and I could dispose of the liner as soon as I'm through. In my case, as I'm sure this might be true for some of you, when you got sick, friends who said that they would always have your back, have slowly or quickly disappeared when faced with a "friend" who might be conceived as a burden, a drama queen/king or not worth hanging with because they have ceased to be "fun". This has happened to me for the most part, so I suddenly don't have many friends but plenty of acquaintances who have chosen to move on without me. So my point, it wouldn't be asthetically displeasing to have a potty chair in my living room because no one will see it but me and my hubby, and he's all for it. Goodness, my house is looking more like an assisted living care home every day.

I'll try to catch up with everyone as this next week approaches. I'm also going to look at making my own GF bread. That ought to be interesting. I have many G/D/S Free recipes on my on my Pinterest page that grows to more regularly.

TTFN
Sandi
Everyone poops.......
BUT NOT LIKE THIS!

Dx: Microscopic Colitis-Lymphocytic:March 2,2016
Onset: 2/2015.
Started GF/DF/SF: March 7, 2016
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Gabes-Apg
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Post by Gabes-Apg »

Sandi
so pleased to see an update from you, I was wondering how you were doing...

Glad the diet changes have helped, we all have hiccups and learnings along the way, and the reminder of consequences of stepping away from the safe eating plan is all the reminder we need as to why we need to stick with the safe eating plan..

with time, the magnesium and Vit D will work towards improving neurological symptoms.. progress not perfection. it can take a couple of months for deficiencies to be correct and start to feel benefits..

as to your situation with the potty chair - my thoughts are - LIVE LIFE FOR YOU!!!
the aim of what we are doing is to remove stress, and live life the best way we can despite the symptoms that are there. and with time and healing, the need for the potty chair in the living area may be a short term thing - if it will reduce stress and give you better wellbeing, that is very important at this stage of the healng journey.

take care
healing hugs
Gabes Ryan

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

Hi, Sandi. I agree with Gabes - do what you need to do! Sorry about your friends. I don't do as much with my friends as I used to do because so much involves eating out but I still see them. They're used to my bringing my own food to get-togethers, that seems to make things easier for everyone. You always find out who your true friends are when the going gets a little rough. I love your Potty People name. :smile:
Marcia
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My mission in life is not merely to survive, but to thrive and to do so with some passion, some compassion, some humor and some style. - M. Angelou
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Gabes-Apg
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Post by Gabes-Apg »

as part of living life for you

so what if you have assisted living aids around the house...
you have multiple conditions that are impacting your life. that is chronic illness.
admitting that you have chronic illness is not failure or giving in, it is acceptance. and with acceptance we can heal and improve.

this article may help
http://psychcentral.com/blog/archives/2 ... c-illness/
Gabes Ryan

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

Great article Gabes! Thanks for sharing!
Christina
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Erica P-G
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Post by Erica P-G »

So good to hear from you Sandi!

MC is a Yo-yo.....and it needs to be dealt with however is the most comfortable for each of us ;-)

So glad you are getting along, and figuring out what is working for you :-)
Cheers
Erica
To Succeed you have to Believe in something with such a passion that it becomes a Reality - Anita Roddick
Dx LC April 2012 had symptoms since Aug 2007
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