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Hypochondriac Here!

Elijah

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Elijah Newbie
Elijah
Posted

I will try to make this post as short as I can. I was diagnosed with Cystic Fibrosis when I was born, in the last decade or so I contracted diabetes, and I have recently been diagnosed with osteoporosis in my hips. But the reason why I'm posting here is because I have been on some form of ant-acid for over 30 years. I've tried everything to wean myself off of Zantac from drinking apple cider vinegar, to trying mastic gum. But my stomach still hurts during the night, but during the day it doesn't really hurt, it just seems to sap my energy.

After eating a meal, my stomach growls intensely, and I have to take a gargantuan amount of digestive enzymes with my meals to avoid having gas, and no matter how many I take, I still have some.

I'm wondering if alot of my problems arise because of what I put into my body. Since I see enough drs already, I kinda frown on seeing anymore, so does anyone think it's a good idea to go on a gluten free diet for awhile to see if some of my symptoms subside? My gripe is that gluten free food isn't too cheap, and due to my CF, I have to maintain my weight.

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Candicep Newbie
Candicep
Posted

I truly believe that many diseases and problems that people have are related to what they ingest in some fashion. That's my opinion anyway. It won't hurt to try gluten free for a while to see how you feel! You dont have to buy all the prepackaged stuff to test this out. I started on gluten free brown/white rice and different kinds of sauteed vegetables/unprocessed meats. You can eat more cheaply that way for now until you see how it works for you.

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      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
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