Orlistat :: What To Eat And Avoid?
Oct 19, 2009
I'm fairly new to Orlistat having started beginning of october having not much luck on diets as I luuurve my food. But I had decided to go to my doctor and ask for help and she recommended I try these tablets.
I've struggled a couple of times trying to find the right foods but i'm slowly getting there i certainly have cut down on eating all the crap and stuff i love to eat but without totally having to give it all up by changing my fat/calorie intake. I have experienced the overload of fat once and it was not pretty lol, I will not be having a pizza for a while thats for sure. Its definitely a trial and error process just finding what foods work and wot doesn't for me and how much i can eat of it. I for one know these tablets are a god send as it stops me from having all those fatty lovely tasty foods that i know I shouldn't be eating and more of what i should be.
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Should you avoid alcohol with these tablets, or is small alcohol consumption ok with them ?
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I am on 45mg of Mirtazapine. I had quite a lot to drink on Saturday night and I know the info on the leaflet says avoid alcohol. I had a terrible day today with really low self esteem and suicidal thoughts. Has anyone else had similar experiences. I guess the answer is not to drink alcohol whilst on this medication.
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I have now had diverticular disease for the last 12 years and have a flare up every 6 months. I have apparently 6 pouches in my colon. I still do not know what foods to eat and to avoid. I have from my own experience stopped eating certain foods. I do not eat anything with seeds in ie some fruits have seeds so the only fruit I eat is melon pineapples bananas. The doctors say you should have a high fibre diet then they say do not eat seeds. I have just discovered that I should not be eating rice. How about baked beans should I eat these or not? Please could someone tell me as at the moment I am going mad not knowing what I should be doing.
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I've sorta solved my bleeding hemorrhoid problem. I had the right idea with bulking up on fiber, but the wrong type. Whole flaxseeds and chia only worked 50% of the time. As I was purchasing anything with fiber, I happened across a POWDERED texture flax . Its when I finally got around to using that is when the bleeding STOPPED. I also take a psyllium seed husk supplement and eat fiber rich foods like shredded wheat, spinach, string beans, red potatoes, etc. I've also discovered other exotic fiber packed foods like dried japanese persimmon slices, that do a great job. Stool comes fast, bulky, and like a shotgun blast most times. Sometimes the stool is so bulky and wants to come out so fast that the hole isn't big enough, so I have to be patient and ease it out. So fast that the tissue is almost clean. An occasional small red streak or faded red spot on the tissue, but, dude, the entire toilet bowl was red before powdered flax . So I've made a complete 180 from tissues soaked in blood.
I'm elated that the hemorrhoids are under control. But with that being said, there's still a list of certain foods in the back of my mind that I know must be avoided...they seem to overpower the fiber plan and cause bleeding no matter what. I just ate that food that ONE time, that one day, but the bleeding may last several days to a week before suddenly stopping, and everything returns back to normal. Foods like this I've learned to avoid:
Orange Juice
Iced Tea
Coffee with cream and sugar
The lemon garlic dressing on Boston Market's Mediterranean Salad
These foods, especially, override my fiber plan to irritate whatever, and I can bleed for several days until it runs its course. Looking at it outwardly, these foods seem to have sugar and acidity as a common characteristic. BUT YET...I can consume other similar sweetened foods and NOTHING happens! The tissue is clean and bowl clear! I eat candies
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I was diagnosed with SVT years back and have had 2 ablation ops with no success. Too near my AV node. Exercise is the main catalyst for an episode with myself(rapid heart,sweating,have to stop, feel faint) but have the odd flutter and increased heart rate at any time. However i have stopped drinking Caffeine and what a difference. I have not had any episodes whilst out running for about 3 months now( used to be every other run) and have confidence in entering 10k runs and completing them without having to stop. I am going to start playing squash again and really test out my hypothesis.Also, i am not noticing my heart jumping or bouncing during the day now. Just wanted to share this with others as stopping caffeine as really benefited me. I check all labels on soft drinks and obviously no coffee or tea.
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I'm currently 38 weeks & 3 days. the doctor wants to induce me at 39 weeks & 2 days due to avoid doing csection b/c of her size. is there anyway I can naturally go into labor?
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I am told by a cousin that it is "in our genes" My dad had it and now my aunt has it both on father's side.
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I finally received Atrovent and a nebulizer yesterday and I may be crazy or just overly excited but I think I can tell a big difference already. Pharmacist said it was fast acting. Anyways, was going to clean house and light candles like normal and didn't know if there are certain smells I should avoid. Other than the obvious, smoke, fumes, etc. More like fragrances.
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So I'm 25 weeks and so far no stretch marks, my doctor said I'm gaining weight slow and steady like I'm supposed to and that's best way to prevent stretch marks. I know they're hereditary, I've read tips online but I was wondering what you ladies used and what works so I can try some new things even though I will probably still get them in my third trimester.
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I'm almost 24 weeks with my first baby :) Although it hasn't happened yet, I was wondering if any of you other expecting mothers have found something that makes you not get bad stretch marks?
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I'm slim person. In order to gain weight, I'm focusing to various type of diet. In my food, I've used maximum amount of tomato because it's taste make my meal special and I love it. However, I've heard that tomato is mainly used to lose weight. So, I'm worried regarding the usage of tomato. Really it doesn't let to gain weight ? Is it beneficial to avoid tomato for gaining weight ?
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Since being diagnosed with PMR Sept, 2014, I've tried to follow an anti-inflammatory diet as closely as possible. One of the things I've incorporated in my diet & take as a supplement is Turmeric. That word happened to catch my eye as I scanned our newspaper this morning and saw it mentioned in a medical help column. I read the question and answer and learned something I didn't know about Turmeric not being a good choice for people who take blood thinners. I thought I would share this with you as I've noticed many people on this forum mention that they are on Coumadin or warfarin.
Here's the text I read:
Blood thinner users must avoid turmeric
Q. I have a lot of arthritic pain, so when you mentioned turmeric for joint pain, I thought I would try it. In three days, my nose was bleeding. I take the anticoagulant, Coumadin, so I was concerned. My prothrombin time was sky-high.
I had to go off the blood thinner for five days to get back to normal. You should warn your readers about this interaction. Having your blood too thin can be extremely dangerous.
A. Thank you for the reminder that anyone on warfarin (Coumadin) or other anticoagulants should steer clear of turmeric or curcumin.
Although this spice has anti-inflammatory properties, it also can magnify the effect of these anti-clotting medications.
Prothrombin time is a measure of how long it takes blood to clot.
This interaction has not been well studied and is not found in the official prescribing information for warfarin. Nevertheless, you are not the first person to report a serious bleeding problem with this combination.
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I used to use headphones a lot... but my research showed that significant hearing loss has troubled most headphones users so what can I do about it? Like putting a carved block of foam inside???!!! C'mon, guys, help me out, giving up is not an opinion, not when listening to music...
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I have had 2 miscarriages in the last 7 months, my doctor believes that is an issue with low progesterone. I am currently 3dpo, my doctor wants me to wait until I get a bfp to start my progesterone suppositories, but I keep reading that if I wait that long it might be to late. Should I begin the progesterone suppositories now or wait until my bfp like my doctor advised me to?
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Take selenium supplements and avoid gluten
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Finally got my diagnosis of ulcerative colitis today. I'm vegan and eat a lot of fruit, veg, beans etc. and have read that a lot of these can worsen your symptoms, are there any other vegans out there who know which foods I should avoid?
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I am 26 years old and have never had children, I was suffering from panic attacks from my pill so my nurse told me I should try the non hormonal copper coil. I had it fitted at 3pm on 03/03/2014, BIG mistake, by 3.30pm I was having severe cramps which i thought was normal as I had read they can be quite painful. I rolled around in agony for hours by 2am the following morning it had become so bad my partner called for an ambulance. I was taken to A&E a doctor examined me to tell me that she could not find the strings of my coil, she sent me straight to a gynecologist where they told me that my womb had been perforated by the coil and I had to have it removed as it could cause permanent damage. I would never recommend any women to have the coil it is dangerous and so painful words can not describe what I've been through.
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I had the surgery at 3.30pm yesterday and felt amazingly clear until about 4am when the common runny nose and tickling sensation started to build and at 4.20am I sneezed. I kept my mouth open as advised but my tongue clamped to the back of my teeth so not sure it helped. So much mucus and blood came out and it set off a few seconds of a nose bleed, it's now 8.45 am and I'm concentrating 100% on not sneezing again but it's so hard. My nose is filling up with clear, runny allergic mucus and I don't know what to do.
Anyone else had this?
PS I've wikied how to prevent sneezing and used all go their tips on pinching and pressing, etc!
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Since college and then 7 years afterwards, I was lacking a period. Then one day it came back. Wanting to know what happened, a gyno doc diagnosed me with PCOS. Also, the years without a period causes hyperplasia(crowded cells in the uterine lining, the form I had has a slight risk of cancer.) I was treated with provera pills to force a period for a while and the hyperplasia was reversed. I was also diagnosed with mild diabetes and I'm on metformin. When my doc found out I was sexually active and on metformin he encouraged me to be treated by depo provera. Also affecting things I take a drug called trileptal. Trileptal prevents most hormonal birth control from working and it is suggested depo to be given more often while on trileptal.
Anyway the problem is I'm started to get periods when I didn't before on depo and I'm acting all hormonal when I am not suppose to. It's so bad I'm getting breakthrough bipolar symptoms right before these periods. But my gyno says there is no way that is happening and my psych symptoms have nothing to do with the depo because hormone fluctuations are impossible on depo.
I want to go off depo, but my doctor is insistent that if I go off it my periods will stop again and I'll get hyperplasia again and get cancer. But there is no sign of my PCOS and I'm bleeding on depo, now that my pcos is treated why would my periods stop and the hyperplasia come back? I didn't take the depo and a main reason is I'm thinking about a child. Why would he push depo so heavily? Should I get the shot?
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My wife ( in her 60's) went to the NHS GP with cystitis and after a urine test, was prescribed Trimethoprim. Less than twenty four hours later she started to experience abdominal and back pain. She persisted with the Trimethoprim but the pain intensified.She said she had never felt so ill in her life and her skin was fiercely hot.We called NHS Direct and they questioned whether my wife had been to the gym, advised to drink plenty of water and to drink a particular fruit juice. She drank the juice and was almost immediately sick. Then, to help matters,the battery failed on my newly purchased thermometer.Later on Sunday night she felt really bad, couldn't sleep, couldn't drink , her body felt it was on fire and felt sick all the time. We then read the Trimethoprim leaflet that said these tablets should not be taken if there is a kidney complaint.I was on the verge of taking her diet to A&E at three o'clock in the morning.
First thing on Monday morning I got her to the surgery again and in spite of telling he receptionist how urgent the situation had become, we had to wait one and a half hours before having a consultation with ( another) doctor. By now the full urine analysis indicated a kidney disease against which Trimethoprim was ineffective and was given an alternative antibiotic - which (five days later) has now cleared the signs of the kidney problem. She has been ill for about two weeks, lost half a stone and can only eat small quantities of food - but at least she is eating again in small quantities.
After all this, I suggest the kidney infection developed very rapidly shortly after the first consultation and :cry: Trimethoprim failed to tackle that problem. Now the side effects of the Trimethoprim have only just subsided we realise that the constant nausea, burning skin, sleeplessness,
body aches were due to the Trimethoprim. Coupled with the kidney pain, it explains why she has never felt so ill in her life. We would never entertain taking Trimethoprim ever again.
Should you suffer the symptoms of cystitis, I would recommend the full nature and extent of the problem is diagnosed without a four day delay,
the correct antibiotic is taken, don't take the advice of NHS direct without a second opinion and avoid Trimethoprim.
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