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It may be that you just got sick - either a virus or food poisoning. If it's a virus, you'll just have to wait it out and see if you feel better in a few days, but you also might want to change out the food/broth/whatever you're eating for a different batch (not from whatever you are currently eating/drinking - go to a different store and buy a different brand of everything) and seeing if you still get the same symptoms. If it's not food poisoning it might be a sensitivity to a specific brand of something you're eating before you get sick. It sort of sounds like some of the symptoms of reactive hyperglycemia: https://en.wikipedia.org/wiki/Reactive_hypoglycemia I'd also caution you to not lay down within 30 minutes of eating or drinking anyway as it can cause you to get reflux in the early days. It wouldn't likely be what is making you sick tho. It honestly sounds more like you caught a flu bug or something like that more than anything related to your surgery.

I would for sure take the initiative and call. You are having the surgery and you are paying the premiums. Had I not continually called I would have never known that, the office sent my claim to BCBS of Texas and not BCBS of CA. Be proactive not reactive.

For post WLS patients the hypoglycemia after booze would be reactive, and it can cause you to pass out. Alcohol is extremely carb-dense, and its liquid so it will be absorbed very quickly, your body will respond in kind by releasing tons of insulin into the bloodstream. The booze will past through your digestive tract extremely quickly and the insulin will lower the glucose in your bloodstream by far more than you can handle. This problem gets compounded if you haven't had much to eat or drink, as in water, not booze, in the prior few hours. At any decent concert one can be there for hours.. even worse if they're burning off energy standing, walking, moshing, etc., and not sitting, out in the heat, it only gets worse. Sometimes people need to learn the hard way that their bodies can't take much post-op.

Oh, I guess I wasn't clear - I have no interest in the lap band. I've been doing lots of research and I'll be honest - I never thought I would ever be considering WLS. It wasn't until recently that I had even heard of VSG and what I've read about it makes me think it is a very viable option. I guess it just bums me out to realize that even though it seems like I am a prime example of someone who could be greatly helped by VSG (BMI of 48.something with high blood pressure, high cholesterol, pre diabetic, depression, and a history of sudden cardiac death in my family) but my insurance doesn't care about all that and would rather take a reactive rather than proactive approach to my health.

I see a Endocrinologist for my Hypo Thyroid. He has me on Armour Thyroid. It is a Natural Medication made from the Thyroid of a animal. I was skeptic at first. But the other Meds did not work on me. So I thought, what have you got to lose? Anyway it is GREAT Stuff ! I feel wonderful ! I'm awake ! and the Vitamins with choline in it helps allot, then add in the Protein shake, and I am ready to Rock n Roll all day long :party:

Talk to your endo. You won't be having many carbs but you can still bolus if you need to and dose for your carbs. I bet you won't need much and you may have hypo episodes while you are coming to grips with it. You may end up off insulin over time. Lots of type 2 basically leave the hospital in remission. I'm not on insulin but I'm on metformin and fully expect to be able to get off it. My latest A1C was 5.6.

Yes, we do get into it here sometimes. There are posts and comments that cause our hackles to rise. We are from different states, countries, cultures and have different values systems, experiences and opinions. We respond to different approaches in different ways. Some of us need a "kick in the pants" or "tough love" and respond well to that, others are more responsive to a gentle hand and softer words. There is no one size fits all in these forums, which is what makes it stronger for the differences. One thing is obvious to me at least, and that is we all share a common experience and passion. We are planning to, or have been through vsg surgery and we are at times scared, excited, thankful, ashamed, proud, angry, apathetic, and countless other feelings. This is an emotional process. It is mentally stressful. It is academic in our search for information. It is very physical. For some it is even spiritual. We do not have to agree on everything. We are here to share our thoughts, opinions, experiences and questions. Since it is a public forum, it is also open to anything from anyone at anytime. That may be more challenging for some than others when they read a response that they interpret as offensive. Some react strongly, others are not as emotionally invested in what others have to say. There is no right or wrong way to feel about this. We do all need to remember that we are working through a framework of a shared experience, though we may process our thinking about it in different ways. Definition of Reactive Thinking Reactive thinking is crisis-based thinking, coming up with solutions after problems develop. Reactive thinking responds to the situation. A reactive thinker often spends too much of his time fighting fires. A reactive thinker is easily blindsided by circumstances. A crisis-driven reactive thinker may be more prone to feeling stress. Definition of Proactive Thinking Proactive thinking, on the other hand, involves foresight. To be proactive means to think ahead, in anticipation of future changes or problems. It means covering your bases to include all possible scenarios. A proactive thinker will have several contingencies in mind. A proactive thinker sees the likelihood of crises before they happen. Ref: http://www.ehow.com/...e-thinking.html

Have you spoke with your insurance company yourself to find out exactly what they require? It could be that your Dr.'s offices records alone are enough to meet the requirements. If you know for a fact that they require more than can be submitted by the Dr.'s office, contact them and ask where the additional documentation can be sent. If there is any question it will speed things up to be proactive and do it yourself than being reactive and allowing the office staff to do it after a denial. If you send it yourself, don't forget to copy, document who you speak with, who and where you mail it to, and mail it with delivery confirmation, after faxing it to them---double up! Good Luck---sounds like the ball is rolling...just as the big ball is ready to drop--here's to a great year for you!!! Cheers! Kat

Hello: I read all the posts through page two, and I just wanted to add my two cents to the pot. Lots and Lots of good advise has been given...... I along with MANY here was the "fat" girl with the skinny sister. I started my period at age 9 and hid it from everyone including my mom for 3 years, because I was mortified of being so different. I played sports while young but was always one of the biggest girls on the team..... On the outside I was self confident, popular, involved... but on the inside I was miserable ALWAYS aware of my fat.... crushed when talked about or rejected.. because I started my period so early I WAS EXTREMELY HORMONAL... I would have major mood swings and since no one but me knew I was on my period.. I just was reguarded as a terror. (this is me thinking back on those years) Later at a realitively young age of 22 I was diagnosed with hypothyroid, as a matter of fact the endocrinologist made me come in 3 times because he thought the test was done wrong due to the fact of me having the thryroid of an 80 year old man... he was suprised I was functioning. Also I was diagnosed with PCOS.... both factors make it very hard for me to lose weight... and slimfast.. well I GAINED on it... because of the sugar. Eating Low Carb is the only way I can lose weight, and once I'm banded it will be THE way I continue to eat... and most of the stuff in your pantry is LOADED with carbs, including the fruit. Someone mentioned the MEXICAN doctor who does the band on teenagers, and my doc is working with a 16 year old now (in Kansas).......... the band is NOT easy, NOT a quick fix, and she would still be able to gain weight if she continued to eat the crap.. which as any inventive person can soon find.... that is why she will need to be emotionaly ready to do it........ I agree with others who say to BUILD her up from the inside.. she needs the self esteem, but also she needs to find something that will help her to shed some pounds.. enough that she sees the difference and feels the power of having control, and I'm betting that if she cut down the SUGAR... (ALL FORMS OF SUGAR) she would start losing...... and go check out those trendy clothes sites.... a girl DOES need some cool stuff to fit in even if It may be a little pricey. Most of all GOOD LUCK oh and I might mention... I was infertile, (both hypo and PCOS) factors... I was blessed at the age of 33 with a child, due to following a LC eating plan..... all this makes me more at risk for things like breast cancer.. so getting her checked out now is vital........ I hope some of what I said helps a bit.

I ended up with emergency surgery. Leak reappeared and spleen abscess reactivated. My surgery was 5.5 hours. The stomach leak was fixed. Spleen fused to liver and pancreas so my spleen was removed along with a small piece of liver and pancreas. Due to the way sleeve was done they were able to just snip off a leakey piece of stomach. So far i am doing good.

They discovered I have 1 biggish nodule in the left lobe and multiple littler in the right, still at the "Watchfully Waiting" stage, Lefty is just a little under operation level, haven't gone Hyper yet, but I am still losing,weight , so I'm not that much Hypo either, although more. there than "normal" , but then most facets ofv me didn't fit that description so Why would,i expect my Thyroid to be Any different?

I had bypass and I dump on sugars mostly. I agree with the above posters. I have an early warning system of seeing halos and then spots before my eyes. I find it helpful to get protein quickly to cut the sugar reaction. It happens 15-45 minutes after eating the offensive food. I’ve also had a delayed sugar reactive episode from eating a cup of ramen. It was 2 hours later and felt like dumping. Basically, your body will tell you what you need and what to avoid.

My friend, I would be concerned about adding a weight suppressant right now. Didn't you just recently start another new med? I think I would ask if THAT med might be revving up your appetite. It's weird how meds reactive so differently within individuals. Until you can find out about the med and its possibilities pertaining to you new appetite, I wouldn't be adding anything new. I'll always side on "changing the existing recipe" before "adding another ingredient". Decisions, decisions. Why do we always have to be making them? Prayers going up for you---and me.

I don't need a scientific study to prove that garlic makes me fart. I'm smart enough to realize that I'm reactive to certain substances or foods. MSG gives me headaches and I'm sure there are millions of other sensitive people that react to it as well. I’m not about to put that stuff in my body after all of the articles I’ve read. Scientific studies can be very tricky. First of all, who do you think funds the millions of dollars for these studies?!? People interested in making money. Bottom line. I don't know if there are any reputable studies proving it's dangerous or not but if there isn't, it's because there isn’t anybody who will make any money from proving it's unhealthy. I'm sure there are plenty of studies that show it's not dangerous and I wonder who paid for THOSE studies... Hmmmmmm.... The companies who put it in their food maybe? Follow the money trail... If I cared about your opinion I might take the time to find out about scientific studies but I don’t so I won’t…. I trust my doctor, I trust my nutritionist / naturopath, I trust my chiropractor and yes, I trust the millions of articles that try to get through to people about how dangerous it is and what it will do to your health in the long term. To those of you that agree with the rude and condescending post above, read the article again before you jump on the denial bandwagon... Maybe a little slower this time? It doesn't say that MSG MADE you fat. It states that MSG contributes to obesity. BIG DIFFERENCE. If you choose to eat it, that's your choice. If you choose to remain ignorant of the dangers, it's another personal choice you are free to make. After all, ignorance really is bliss in most cases. I'm just sharing information that I believe in and consider valuable. The smart ones will do their own research and trust their own instincts. Whether you agree or not is totally up to you but I'm not about to be intimidated and/or discouraged from sharing information. If you don't like it or don't like me, please click on the next post. I'm here for support, not drama.<BR style="mso-special-character: line-break">

You may have already done considerable research about RnY. But there are some very significant medical complications and side effects with the RnY that the sleeve doesn't (usually) trigger. For instance, * significant malabsorption and anemia issues requiring very serious Vitamin, mineral and other supplements for the rest of your life (more than with the sleeve) * reactive hypoglycemia -- as many as 72% of RnY (bypass) patients have it; it ain't a minor thing at all. "Reactive hypoglycemia is a late complication affecting up to 72% of RYGB patients although it seems to occur also after SG, in about 3% of the cases." See http://clinicaltrials.gov/show/NCT01581801 * more complicated surgery and more surgical complications with RnY than with gastric sleeve That's not to say that there aren't some diagnoses / patients for whom gastric bypass is the better choice. But IMHO you should choose bypass ONLY if you have those diagnoses. The choice between bypass and sleeve is not a simple 6 of one, half-dozen of the other proposition.

Does having no thyroid at all = hypo? I've wondered about that. I'm losing pretty well so far on pre-op diet. 9lbs in 10 days. But thats on all liquids except a lean dinner. 9lbs is a big deal since it would normally take a year to lose 5 just to gain back 15. The struggle is real with no metabolism. I gained 70 my first year after having it removed. I'd give anything if modern medicine would figure out how to do a transplant.

Apologizing in advance for the length of this post but here goes my 'deleting my online profile' story: So...I met a guy on Zoosk in the spring of 2015. No attraction on my part, and every time we went out, I said to myself that I would end it. Problem was...I really enjoyed spending time with him. Eventually we did become a couple and I hid my profile rather than delete it. Glad I did because after nine months of dating, he blindsided me and dumped me. We were not in love and I'm fairly certain in time, the relationship would have limped along till one of us made the move to end it. But because I wasn't prepared, it hit me like a ton of bricks and brought up all kinds of rejection issues for me and well.....you ladies know how this part goes...what did I do wrong?, why was I not good enough?, yada yada yada. What I did know when the relationship was over, was that I wanted to be with someone so crying hysterically, I resubscribed back onto Zoosk and JDate, which I had also shut down but not deleted my profile from. To my complete surprise, I met a man on JDate in June and we have been having a great time together. This relationship is nothing like with the other guy. This new one and I have so much in common and we enjoy talking about all kinds of things and doing so many of the same things. I wrote on another thread that he might be the lid to my pot and so far, it's going gangbusters. I know he deleted his profile from both Match and JDate a few weeks ago and knew that I had not. It wasn't that I was dating anyone else...I just wasn't ready to shut it down again. Last night I went onto Zoosk because I was getting email notifications from them and on a whim, went onto the site. Just for the heck of it, I looked up former boyfriend's profile...which he had not reactivated when I first went back onto Zoosk..and sure enough, he popped up this time. I looked at his profile..his new profile by the way...and the updated pictures on it. And that's when I knew...time to shut down my profile. It's not that I don't hope he finds someone...I'm not that petty. I just know more than ever now, that he's my past, and it's time to focus on my future..and with this new man in particular. Now...if I could just figure out how I managed to send old boyfriend a friggin' friend request on FB, it would be great. I swear I have no idea how I did that, but I did. I can't unfriend him now...not after sending that request...even by accident. Oh..and why he accepted that request is beyond me. But if I'm lucky, he'll see the pictures of me and the new guy, and delete me from his feed...

I'm a diabetic, and yes it does sound very much like how I get when I am having a hypo - I think you should go and get checked out for this as its not good to let it go on. Also buy yourself some dextrose tablets and take 3 or 4 of those when you are feeling like this - if it makes you feel better quickly, you will also have your answer... Take care. this isn't something to be ignored.

Let me start with a History of what's going on: Oct. 21, 2009 I had lapband surgery. I have lost to date 134lbs. I am at 350lbs right now. I know I am morbidly obese, and I am trying to work on that issue. I was enjoying life when losing the weight, and walking and exercising enjoying my new founded mobility. I was trying to eat right, but with lapband my diet consisted of mostly Protein. I was doing great and was happy with life...Then in March 2010 I went to the Beach for Spring Break and had a great time. In the beginning of April I noticed a redness on my cheeks that felt tight. I thought it was a sunburn left over from spring break. It never went away, and it started tingling. I went to my PCP and she said it was Rosacea. I used the metrogel, and it didn't go away. I went to two other doctors and they said maybe allergies. One gave me nasonex and the other just said use topical ointment like neosporin. I did everything nothing happened. In the middle end of April 2010 It started tingling and the numbness/tingling started going down my face. My mouth, cheeks, and jaw felt numb and tight. the numbness/tingling progress to the scalp, forehead, and extremeties arms, legs, fingers, feet, toes. It spread to the middle of my upper shoulders in where it is tight. My chest seemed to get tight also. I went to a neurologist due to having these weird sensations in my head and the rest of my body. occassionally feeling burning sensations on my toes and scalp. They did the general neuro test. Then they did an MRI of my Brain and Cervical Spine. They stated that it came out normal. THey stated they believed it was not MS. They did other blood work, and tested me for ANA which came out negative, and then B-12 was 174. I was even tested for diabetes and the glucose test came out negative. My first neurologist stated that the neuropathy was due to B-12 deficiency. I had the series of 7 shots. then I was advised to go back to my Primary Care Physician to get b-12 injections once a month. During the time I had to wait for the first shot I advised my neurologist I was still having the systems and they did not alleviate. I took it upon myself to take sublingual B-12 5000mg daily to try to get rid of the numbness and tingling throughout my body. I finaly went to my PCP for the first shot. I gave her a list of all my symptoms still. She did a whole blood work also and said everything was fine. She even did another ANA which came out negative again. The only thing that was off was my Vit. D which was at a level of 23-24. So I am taking megadose of vit. D for four weeks. I tried to tell my PCP what was going on and she just said go back to your neurologist. By this time I am dealing with anxiety and deprssion of what is happening to me. I have never been sick like this. I have had Hypothyroidism for six years, and then asthma all my life. I was diagnosed with sleep apnea prior to the weight loss surgery but I stopped using the cpap because after the weight loss i was able to sleep better. All doctors believed noone of this was what was causing the numbness/tingling throughout the body. So at this point I decided to go to another neurologist Dr. Sara Austin in Austin, Texas I told her what was happening, and gave her all the results. SHe did another neurological exam, and even did the EMG test where she poked needles into the peripheral nerves to see if there was damage. That test came out normal. Along with her other blood work. she did a CBC, an tested me for other vit. min. deficiencies which all came out normal according to her. She also stated I do not have MS or Guillen Barre. I asked about Lyme disease and she said I did not have that either. She just recently ordered another lab work to check for Fabry's Disease, ERS blood test, and another test called a Rheumotoid Factor. I don't have those results yet. I am just looking for answers. I asked my Lapband team if it could be the lapband and they stated No it was not. They took out some fill out of my band so that I could get more food in, thinking that the parenthesias was caused by malnutrition etc. I still have the numbness and tingling. My b-12 levels went from 174 to 1700 when my PCP tested me again. She stated I did not need to be taking any more B-12. I told her that I was taking the oral supplements but again that seemed to fall on death ears. My Endocronologist recently said I had switched to hypo to hyperthyroidism. which is weird so she lowered my synthroid level to .150mcg two pills a day. it was at .175mcg two pills a day So I am confused on what is going on with me. I will list my symptoms below, Maybe you could help or Guide me in a direction I need to be guided in. I would really appreciate your help. I know this was long but its been a long five months. I need answers and I need resolutions. Symptoms:</SPAN> Head - burning sensation on scalp occassionaly. Feels like I have a cap on somedats. tingling/numby. I do have a few pimples on the scalp but not sure if itsjust due to sweat or something else. Forehead - Tight the numbness seems to travel down my face underneath my eyes. Like a pulling sensation to. Face - cheeks numb/tight. around the mouth is tight and numb. I don't have any lost sensation it just feels numb and tight. Lips - Tight/numb sometimes burning tingling sensation Mouth - an ulcer on right cheek that has a clear bubble doesn't hurt. Upper Teeth numb. Vision - blurred vision occassionaly. Went to Optamologist and said she didn't see anything like pseudo tumors that could cause this. Neck/shoulders - tight and numb/tingling Chest - tight and red. Feels numb also. breast - feel tingling/had a recent mammo it came out fine Arms- Right side feels more numb/tingling than left side. sometimes get burning sensations. Small red dots on upper arms not sure if they have always been there or if its just started. Arms - Forearms feel tingling/pull. Burning sensation on wrists occassionally. Elbow Joints - when squeezing touching very tender and slight pain Fingers - Pointer fingers seem number than the rest, but again no sensation loss just feel numb. Joints feel stiff Stomach area - Feel tingling around lapband and on the right side feel burning sensation/tingling down right side of stomach to abdomen frequently. Kidneys - I think I feel an ache in them. I seem to feel sore, and feel tingling in that area. Burning pulling sensation sometimes in the front. Abdomen - again burning/tingling sensation across belly button area and ovary area. Legs - right let feels heavy and numb. Its had edema for a couple years now. but never has been numb or heavy. Left leg tingling numb frmo buttocks down. Right leg the same. Even my genital areas get tingling numb. Toes/Feet - burning sensation on toes. stiff. but no sensation loss on toes or legs. no weakness or balance problems that have been found. recently felt I was dealing with some mild vertigo but did not know if it was the Neurotin Dr. Austin prescribed me. 800mg three times a day, but only taking it at night due to having to work. My prescriptons include: synthroid .150 two pills once a day Neurotin 800mg I only take at night Hydroxzine 25MG...as needed for anxiety given to me by my old PCP I was not depressed or suffering from anxiety prior to all of this happening. I was on top of the world. I was enjoying losing weight and doing things I had not been able to do. Then I hit this brick wall, and I feel like crap. I don't feel fatigued just tired off all the tingling, numbing burning sensations. I'm tired of my body feeling foreign. Has anyone had this occure with their lapband. I'm scared and tired. Everyone tells me not to take the band out. ....I'm so confused on what's causing this. I don't know what other options to persue.

Hi :smile2: I'm scheduled for surgery in January and I'm just curious how those with hypo-thyroidism are making out with their lap-band...? I know how slowly I lose weight NOW with it - (I also have type II Diabetes controlled by metformin). I'd love to hear from all of you that have this thyroid disorder to see how you're making out or how you've made out... Thanks renee

Hi, I also have hypo, I had to crush the meds for the first couple of weeks, and wasn't really sure they were totally effective being crushed. But I did not see or feel any major differences losing weight. I am losing 1-2 pounds a week which for me is fantastic. I'm still very exhausted though, but I guess that will take time. Good luck and let us know how it turns out.

My date is scheduled for RNY on August 4th and as thrilled as I am I can't help but feel nervous. I keep changing my mind between the sleeve and the bypass all day long for two reasons. I'm afraid of Reactive hypoglycemia as a possible RNY side effect and not loosing enough weight with the sleeve. I know I'll be fine and that it's probably cold feet. Overall I am excited and thrilled that it's a bit over a month away.

My oldest daughter has it. It was brought on by the birth of her first child 4 years ago, she is 40 so she had her babies late. They medicated her than her thyroid went the other way. But she no longer has the buggy eyes. Her doctor said many times it is brought on my some sort of trauma to the system in her case it was having a baby. She did have to have invetro to have her 2 babies. However it does run in the family, she has a cousin on her dad's side who also has it. Strange thing in all of this is my other two daughters have hypo thyroid, So they all 3 have problems with their thyroid and I do not and their dad did not.

@ - I am so sorry to hear this! I know how miserable that is. Glad you have a beta blocker on hand. If it helps, even when I only adjusted by 1/4 of a pill per week (ie only 37.5mcg pet week, I felt better pretty quick - within a couple of weeks). Are you scheduled tiniest again in 6 or 8 weeks? 100mcg per week is a pretty. If adjustment and I don't want it to make you hypo and not catch it. Keep an eye on your symptoms and try to wait out the 8 weeks before retesting. Again so sorry you are miserable. It will stabilize eventually! Hugs!! Sent from my HTC One M9 using the BariatricPal App

Sorry you are going through this. I was hyper thyroid and went to hypo thyroid so they changed my meds but only by a 25mcg and I make them check it every month to see if I'm on track don't wait. However, I think it is why I have stalled in my weight loss no loss or gain for 3months