Hi everyone
I joined this forum just to talk to someone as I am feeling terrible. My story is long an complicate but to summarise quickly,
about 4 years ago I got gastritis from antibiotics and steroids for asthma. This lead me to develop a hypersensitivity of nerves in
my stomach. This mean I could not eat anything apart from boiled chicken and rice and at the odd piece of carrots. This went on for 4 years with various flare u9s resulting from anything from trying new foods to trying to come off protein pump inhibitors. I had maybe over 20 forceps and they would prevent me from standing and walking also, quiet complicated to explain. I would have to ear every 2 hours and missing a meal would leave me with vain, reflux and breathless. Anyway, 5 weeks ago I had a severe flareup one much worse than before, it actually started when I changed my honey winch gave me a small flare up and I tried to get off my PPI.medication. This time I had a sensitivity issue much worse than ever before, I also developed gastritis.
This time I could not eat even chicken and rice, I could not eat anything apart from porridge oats gluten free.. Alco I would have to eat hourly and because of the vain I could not sleep I would end up earning 20x a day for last 6 weeks almost.I also had to eat them semi dry as eating them wett would hurt me and cause breathless and asthma attack.
This is my story so far, I am also very malnourished right now. I am low on many vitamins, this time now and I also have has to take my protein pump inhibitors at much higher dose than before and recommended doses, pantoprazole 40mg x 3 daily. I did this to save my life.
My problem is for about 1 week I am started first to get blurred left eye, I thought it was protein pump inhibitors and I changed it to nexium 20mg x 3. over the next 3 days my blurred eye got worse so this made me suspect it might not be the PPI medication. I started to get dry mouth in the evening and mostly at night. It made eating porridge so difficult and to swallow porridge as I usually it eat very dry and rely on my saliva to lubricate it.
the problem is now my doctor/family suspect I am possibly diabetic. TAHIS IS NIGHTMARE SITUATION FOR ME as I can only eat porridge and I eat about 30g every hour with tiny bit water. I can't eat meats as it puts me in unbelievable pain in stomach and makes me breathless. The diabetic diet involves no carbs or about 230g of carbs but I am eating about 1000g+ of carbs a day. I could possibly reduce my meals to 20g of oats but have to eat every hour. I don't know what to do. I can't stop earning ots and if I do cont8nue I could up blinds or with other diabetic complications. The only thing I am not doing is urinating a lot. Someone said to me the large amount of oats could be making you dehydrated but I tried drinking 2 -3 titles of water but my dry mouth did not stop.
I am confused and scared. I recently did a nerve block for the pain but it was not successful. I can't tolerate the other pain meds and waiting for pain consultant to recommend next thing to try which is RF ablation of the nerves to kill them. But they take my case so casually its funny at best.
My whole mid section is so sensitive that I can't walk for longer than 2-3 min at a time before having to lay down.
any diet or diabetes advice would be greatly appreciated as my situation is scary.
thank for reading this long wall of txt.
I joined this forum just to talk to someone as I am feeling terrible. My story is long an complicate but to summarise quickly,
about 4 years ago I got gastritis from antibiotics and steroids for asthma. This lead me to develop a hypersensitivity of nerves in
my stomach. This mean I could not eat anything apart from boiled chicken and rice and at the odd piece of carrots. This went on for 4 years with various flare u9s resulting from anything from trying new foods to trying to come off protein pump inhibitors. I had maybe over 20 forceps and they would prevent me from standing and walking also, quiet complicated to explain. I would have to ear every 2 hours and missing a meal would leave me with vain, reflux and breathless. Anyway, 5 weeks ago I had a severe flareup one much worse than before, it actually started when I changed my honey winch gave me a small flare up and I tried to get off my PPI.medication. This time I had a sensitivity issue much worse than ever before, I also developed gastritis.
This time I could not eat even chicken and rice, I could not eat anything apart from porridge oats gluten free.. Alco I would have to eat hourly and because of the vain I could not sleep I would end up earning 20x a day for last 6 weeks almost.I also had to eat them semi dry as eating them wett would hurt me and cause breathless and asthma attack.
This is my story so far, I am also very malnourished right now. I am low on many vitamins, this time now and I also have has to take my protein pump inhibitors at much higher dose than before and recommended doses, pantoprazole 40mg x 3 daily. I did this to save my life.
My problem is for about 1 week I am started first to get blurred left eye, I thought it was protein pump inhibitors and I changed it to nexium 20mg x 3. over the next 3 days my blurred eye got worse so this made me suspect it might not be the PPI medication. I started to get dry mouth in the evening and mostly at night. It made eating porridge so difficult and to swallow porridge as I usually it eat very dry and rely on my saliva to lubricate it.
the problem is now my doctor/family suspect I am possibly diabetic. TAHIS IS NIGHTMARE SITUATION FOR ME as I can only eat porridge and I eat about 30g every hour with tiny bit water. I can't eat meats as it puts me in unbelievable pain in stomach and makes me breathless. The diabetic diet involves no carbs or about 230g of carbs but I am eating about 1000g+ of carbs a day. I could possibly reduce my meals to 20g of oats but have to eat every hour. I don't know what to do. I can't stop earning ots and if I do cont8nue I could up blinds or with other diabetic complications. The only thing I am not doing is urinating a lot. Someone said to me the large amount of oats could be making you dehydrated but I tried drinking 2 -3 titles of water but my dry mouth did not stop.
I am confused and scared. I recently did a nerve block for the pain but it was not successful. I can't tolerate the other pain meds and waiting for pain consultant to recommend next thing to try which is RF ablation of the nerves to kill them. But they take my case so casually its funny at best.
My whole mid section is so sensitive that I can't walk for longer than 2-3 min at a time before having to lay down.
any diet or diabetes advice would be greatly appreciated as my situation is scary.
thank for reading this long wall of txt.