Efexxor dosage increase nearly ruined my life!

I have been very quiet and too afraid to write in my blog. You see for the last 6 weeks i have not been able to do anything right. I turned 45 on May 13 it seemed very clear i had reached the end of my life as I knew it. I would forget my keys and glasses, I would forget to wash my hair in the shower. I would forget to pay bills or I would overpay forgetting they were already paid!

At work it was even worse. My job requires me to write communications to the management and executive levels of my company. I was thinking one word and typing another one, I was missing words, misspelling words, forgetting to do even basic tasks associated with my role. My bosses were so upset, my team mates were embarrassed. I wrote checklists for myself, I read what i wrote out loud, i slowed down, all in desperate attempts to fix myself!  I decided I was either aging far too early with alzheimer’s or their must be something neurological happening. The alternative scared me to death! Could I be going crazy?

I had no explanation for my confusion, I could not seem to apply any logic to fix it. I was on the road to losing my job and I was unable to stop that. I started realizing that if I lost this job due to the inability to do anything right , then I would NEVER even be able to get another job. You have to be able to do basic tasks consistently to be successful at any job. Therefore I decided I was likely heading to a life on disability.

I would have to break up with my boyfriend, how could i make anyone stand beside me when I am clearly going crazy. I would have to suggest my daughter go live with someone else , someone would have to take Toby for me too.  I couldn’t take care of myself how could i take care of others.

I spent nights crying aimlessly. I saw no answers, no chance at helping myself. One night last week i hit my bottom, so sure i was only a pain for everyone in my life I looked into the bottle of Effexor as I poured out 3 capsules and considered it it would be easier to just swallow the whole bottle and stop this madness right now.

For me this was a lightbulb moment. I remembered that in late April I had my Effexor XR dose moved from 150mg to 225 mg. I thought back over the month of May and realized that I had almost fainted 2 times, my blood pressure had spiked, I had the worst migraine of my life and I had a constant headache. I had shakes, I had excessive sweating, I had more anxiety not less, My skin picking was way worse.

I ran to my computer and typed in Effexor side effect – confusion….sure enough I found that the memory loss, the confusion, the excess sweating, dizziness and every other symptom of the month was listed under side effect or serious side effect.

I had gone to a psychiatrist in April. I wanted to finally work through all the survival techniques I set up as a child in an unsafe home to determine which were still valuable to me at 45 and which ones did I have to learn to let go of.

I knew I wanted to stop my skin picking, I wanted to stop shutting down when I felt stress, I wanted to learn how to love myself.

So the psychiatrist suggested I join a group therapy program that I will be starting in July, This will help to teach me how to regulate emotions correctly.

Then he suggested we increase the dose of Effexor to see if would help my anxiety and skin picking.  I told him i don’t like the drug. I had been on it since 2005 and gone between 75 mg to 150 mg depending on what was happening in my life.

In the end I agreed with him that we try increasing the one my body knows and then if that doesn’t work we could look at other drugs.

So June 11 I had a transient thought of suicide. for me this is always a warning sign that i am in over my head and i need help. I would never abandon my children, I would never take the steps to suicide. My mother tried to kill herself as a hobby in my childhood..images of her scraping a knife over her wrists daring my father to push down, the nights begging her not to swallow pills which she ignored and swallowed anyway. For me it is cruel to my family and not something I would ever hold over someones head to make them behave a certain way. Its just not in me to do this.  For me my mother almost normalized it , desensitized me to it. When I felt like committing suicide as a teen it was to hurt my mother, but i realized she wouldn’t even care. I considered it more seriously in 2005 and that is when i was put on effexor, because the day those thoughts come i reach out and request help .

June 12 I told my manager and my team leader that i had figured out I was having a bad reaction to the increase in my effexor dose. I went too the emergency room and they suggested i drop my dose back down to 150 and follow up with the psychiatrist to let him know it caused problems instead of creating solutions.

So this is a warning to anyone whose doctors want to put them on Effexor in doses over 200mg. A second level of changes to the brain occur here and you should make sure you talk through all of those changes and the potential side effects to watch out for with your doctor.

I will look to come off of Effexor in the next year , I also learned in my research that long term use of anti depressants can impact memory as well. I have been on this drug long enough. I know all about the withdrawl effects and I know it will have to be done slowly with the assistance of a doctor.

To all those I disappointed in the last 6 weeks i am so sorry, my brain has not been working correctly and I am happy to report that today on June 17 I feel like I now have all my abilities back and I am ready to take the world on again.  Happily stabalized at 150mg Effexor ….

 

 

 

 

Growing evidence of childhood fatty liver disease

I am seeing a number of studies and proof to support something I have known since 2008. Our kids are in serious trouble for their futures if they live on processed foods, soda pop and sauces coating anything natural. Finding those kids out there is a challenge. We have about 6 children in my fatty liver disease support group on Facebook ranging from age 2 – 18.  This is 2 girls and 4  boys which is not by any means a predictor.

Doctors DO NOT look for liver disease as a rule. They are NOT taught to look for the disease. They will blame the pancreas, gallbladder, IBS, Celiac Disease, Diabetes before they would even pay attention to elevated liver enzymes.  As a Parent you need to pay attention to your child’s symptoms and NOT be too quick to blindly trust the doctor.  Demand a blood test for your child. review the levels for AST and ALT and ask your doctor what the safe levels are for enzymes. As for an Ultrasound of the stomach.  If the liver has fatty deposits they will be shown in this test.  Ask for genetic testing they are now proving there are genetic links to fatty liver disease. I am not saying every child has a problem with their livers but I would bet my life at this point far more do then are being diagnosed. Studies say between 3 – 13% of kids have fatty liver disease. I suspect its closer to the 25-30% that is happening in adults.

These kids generally have homes where both parents are working. There are few home cooked meals because parents are stressed out and running between all the soccer, dance, skating, hockey, baseball games that kids are involved with. Or because they can’t get their kids away from the video games and their kids are picky eaters who will ONLY eat hamburgers, chicken nuggets , macaroni or other standard processed or junk foods.

The very sad reality is that these products are created by companies who know and love the fact that people get addicted to their products. If your kid eats it once and it has high fructose corn syrup in it there is no message to the brain to tell them that they are full. and there is no balancing of the sugars. This creates a fatty cell in the liver and your child becomes addicted to those products.

So when they are eventually diagnosed with Fatty Liver Disease or Diabetes or other metabolic disorders you will find you have a child who is trying to sneak foods, or find ways to drive you nuts until you give in. The problem is that they are actually ADDICTED to these products its like they are coming out of alcoholism or drug addiction. Everything in their body is telling them they NEED those foods.  You essentially need to accept that your child is in withdrawl

You have to be strong and fight for your child. This disease can and does lead to liver failure. Doctors and researchers have no understanding about this disease right now. They are all fighting to find the answers but we are dealing with it TODAY and don’t have time to wait for them. I am aware of 2 men in their 30′s who died of liver failure due to fatty liver disease. Neither of them were alcoholics or drug addicts. They were only in  their 30′s. I suspect you want your child to experience life longer than that!

This generation of children are the first generation which will live shorter lives. This is directly related to processed foods and additives and genetically modified foods. Our body’s DO not know how to process these chemicals. Our poor children do not stand a chance in this world of Monsanto versus humans.

If your child is dealing with chronic illness that doesn’t get better. Try getting rid of sugar! Getting rid of junk food, do they start to feel better? You will find after 3- 6 weeks of not eating those things or drinking sugary beverages they will feel healthier!

Parents please pay attention and do not go blindly into dealings with doctors. Get the right tests, keep all test results…you need to take this into your control for your kids sake!

Arbonne Body Care and Cosmetics – Fundraising for MetoWe Camp!

I have been lucky enough to try Arbonne products thanks to numerous amazing ladies I am connected with on social media. Arbonne® products are vegan-certified: their formulas are never tested on animals and do not contain animal-derived ingredients or animal by-products. Due to the growth in Metabolic disease and Non Alcoholic Fatty Liver Disease this is very important to me and to those I care for. The chemicals being added by other companies are hurting our bodies in a toxic world.

To read about the products go to http://www.arbonne.ca/products/index.asp

To read about the company go to https://www.arbonne.ca/company/manifesto.asp

Megan wants to attend A Social Innovation for Change Camp this summer. This camp offers an amazing leadership opportunity that will be able to help Megan bring back to our community through volunteer work and other humanitarian efforts. Megan will be working with industry professionals to help her learn ways to create tangible changes. To learn more about this camp go to Me to We’s website.

http://www.metowe.com/motivation-leadership/take-action-camp/ontario-take-action-academy/#social-innovation-for-change-fostering-creative-and-innovative-ideas-for-positive-social-influence

Megan is 16 years old and a junior at Sir Frederick Banting Secondary School The opportunity to attend this camp would mean the world to her as she looks towards a career in human rights law after fighting for 6 years with a chronic illness called Non Alcoholic Fatty Liver Disease that left me in various states of extreme sickness throughout that time. She has impressed Investor’s Group enough so that they have given her a bursary to  cover some of the costs, but with me as a single mother she need help to raise the remaining funds. Human Rights are a huge passion for her and she will  make a difference in both the local and international community.

Janet Auty-Carlisle is a great friend that I have not had the pleasure of meeting in person but I have known on Social Media for a good 5 years. Whenever there has been an opportunity to support Megan and I in that time she has always stepped up and been wonderful.

Now she is offering to give Megan a nice percentage of all sales in May for Arbonne products purchased online with Janet’s Sales ID.

So if you want to help Megan and you want to help your body by using non toxic products go to

https://www.arbonne.ca/shop_online/shopOnline.asp

Orders can be placed in North America, United Kingdom and Australia. You will need to enter the 9 digit id 115726215 to get the fundraising donation to Megan.

Thank you in advance from your liver and from Megan!

 

Baking Fundraising for Me to We Camp!

Megan Clermont described this perfectly I have adjusted slightly.

Do you like baked goods and helping out a good cause?

For the month of May my daughter will be baking a variety of home baked cookies, breads, and cupcakes with all proceeds going towards fees for a Me to We Take Action Camp this summer. Prices for these items range from $1-$7.50 with a total of $500 needed to be raised for the cost of attendance.

This camp offers an amazing leadership opportunity that will be able to help Megan bring back to our community through volunteer work and other humanitarian efforts. Megan will be working with industry professionals to help her learn ways to create tangible changes. To learn more about this camp go to Me to We’s website.

http://www.metowe.com/motivation-leadership/take-action-camp/ontario-take-action-academy/#social-innovation-for-change-fostering-creative-and-innovative-ideas-for-positive-social-influence

Megan is 16 years old and a junior at Sir Frederick Banting Secondary School The opportunity to attend this camp would mean the world to her as she looks towards a career in human rights law after fighting for 6 years with a chronic illness called Non Alcoholic Fatty Liver Disease that left me in various states of extreme sickness throughout that time. She has impressed Investor’s Group enough so that they have given her a bursary to  cover some of the costs, but with me as a single mother she need help to raise the remaining funds. Human Rights are a huge passion for her and she will  make a difference in both the local and international community.

If you live in the GTA of Toronto Ontario or Southwestern Ontario we would be happy to deliver the baked goods to you. Sadly we can’t do this beyond that geographical area.  There will be 2 days that deliveries will be made to the Toronto area. This offer is limited to the month of May 2013.

In order to support Megan in this amazing opportunity please go to the attached order form and fill out your information and order request and submit to have it sent to Megan.

https://adobeformscentral.com/?f=PbKTYKRgo2IZr23pmmLnIA

 

 

 

 

 

 

Finally 2013 looking much better!!

2013 has been a rough year personally with broken bones ruling my life! As of April 12, 2013 we finally got the news that Megan’s toe was healing and she would not require surgery

Over the last couple of weeks my rib has healed enough that I rarely feel the pain unless i am stretching that specific area.

I have seen Megan walking down the stairs without crutches, climbing up the stairs without having to crawl.

She is still reliant somewhat on the chair in the shower but is standing to wash most of her body and her need for me is reducing dramatically.

We have gone out without her wheelchair! We have replaced the air cast with very high quality doc marten’s to provide the added support for her foot. But at least she feels more human!

Alex returned from Halifax completing his first year of university it has matured him so much and he is flourishing in that setting.  I got to meet his beautful girlfriend Beth. They are perfect together and were together for most of this school year. Sadly Beth is from England and had a year in Canada which ends at the end of May when she will return home and the relationship will end. This relationship will likely be the one they both look back on and compare every other relationship too as they start meeting other people. I am so happy for them for experiencing this together and I know Alex will not settle for less than what he had with Beth and I hope the same for Beth. You both deserve happiness and don’t settle for less.

Alex has struggled with finding a job in the last year. This is not unusual for students, the economy is very very hard on young adults who are looking for work. The jobs they apply for are also being applied for by adults who are underemployed and need more money.  Alex started watching job ads and saw one for a Caulking company looking for a student for the summer. He contacted them and met with them and he has now officially started working for the summer at 14 dollars per hour which is awesome for a summer job and will make returning to university in the fall so much easier!

For Megan I am always watching for opportunities to enrich her life experience. As she is not in school very much due to health over the last 5 years i try to make sure there is always something to look forward to, always something to fight for.  In February I was looking at the WE DAY website and I found http://www.metowe.com/ On this site their were summer camps with leadership streams that would be so perfect for Megan. But they are 900 for a week and there would be no way I could pay for her to attend.  I noticed that there was a bursary option with investors group and I looked into that. Megan would need to write about why she wanted to attend the camp and what she hoped to get out of it. She needed 2 other letters of recomendations. I wrote one easily talking about why Megan deserves this and her school guidance counsellor also wrote a nice letter for her.

We forgot about it for the month of April , had no idea how many kids would apply for a bursary , whether there was any shot for Megan to attend. We focussed on getting Megan walking and her toe! On April 30, 2013 Megan got a voice mail from MetoWe for her to call them. Megan and I looked at each other and i know i caught my breath thinking would they call if She DID NOT get a bursary…talked myself into that they would want to thank every student for their efforts.

Megan called them on May 1. Not only had she qualified for a bursary she qualified for the highest amount they have ever given a student from Investors group! She was given 400 dollars towards the 900.00 cost of this camp.  This is going to be so incredible for Megan, It will be in August just before she returns to school and I know she will be so inspired! They are not allowed to bring electronics and have to focus on the program. This is the program she will attend

 

Offered weeks one (July 7-13) and four (August 4-10)

This program is designed for youth who are interested in tackling problems in a new creative way that can help foster positive social change. Social Innovation focuses on providing youth with the skill set of a successful “innovator” Youth will develop not only leadership skills and a better understanding of the issues the world is facing, but creative thinking, idea generation, and collaboration skills–all important for producing ideas that change the world.

This stream will:

  • Develop campers’ leadership  and life skills, including communication, collaboration, planning and decision making
  • Provide a  deeper understanding of the role that social innovation is playing in reshaping the way we look at social justice issues
  • Develop the skill set of a social innovator, including:  creating  social capital , networking, generating creative solutions to problems, coming to terms with and dealing with failure  and fostering the self-motivation to carry out and implement an idea
  • Creating a blueprint of a business plan that uses these skills to have a positive impact on the local and global community

Ideal for participants who:

  • Have an interest in business
  • Are creative, forward-thinking and solution orientated
  • Are passionate about a range of social justice issues

 

Stay tuned tomorrow as I share the ideas for how we will fundraise 500.00 for the rest of the cost of this camp in the month of May.

Brimming with Happiness here today!!

 

 

Austin’s Story – 14 year old with Fatty Liver Disease – Guest Post Cat Case

My Sons Journey to Diagnosis of Liver Disease

By C. Case©

At age 14 my son was diagnosed with Liver Disease. From the time he was born up until this diagnoses, I just knew something was very wrong with my son. He was born weighing 7 lbs 1. oz  after 8 weeks old his weight tripled and he was constantly hungry, and either had constipation or diarrhea. By age 3 he weighed 70 lbs. By age 6 he lost the weight as he also was diagnosed with ADHD and was on medication.

As an infant and toddler he ate fast and so much he threw up everything that just went in him, and I mean projectile vomiting. He also had digestive problems we went through so many different diagnosis it was spinning my head.  We went from formula allergies to wheat and lactose intolerance. My son had severe gastric reflux and he does have burn scars on his throat from it. My son started to get severe diarrhea, where I took him to the emergency room and they kept telling me it was just the stomach flu. I was like okay and went with the doctors order, but it just continued on.

My son started gaining back that weight even being on the medication for ADHD at age 8  He has had a gastroenterologist that he has been seeing since an infant on and off. It has been about 3 years since he has been back to see him as he ruled my sons problem to a wheat sensitivity, lactose intolerance and severe IBS. He has had a colonoscopy and endoscope and age 9. I was getting concerned as my son has put on a great amount of weight by age 11, he is now 14 and is 5’8 and weighs over 200 lbs. At first I though maybe diabetes since that runs in both sides of our family, but his sugar lever was elevated but not that much, then I am thinking he has an eating disorder, that was not it either, then I am thinking heart issue possibly? His heart is fine as well.

My son in the past three years has missed so much school from either vomiting uncontrollably to a severe case of diarrhea or constipation and cramps. He put on over 80 lbs since this time last year. He also has migraines associated with the above mentioned . He still has episodes of vomiting and having diarrhea or severe constipation and this year he was complaining about cramps and pains under his rib cage on his right side. If he ran in P.E. He could not go far as the pain and cramps became unbearable.  His disposition was always irritable, and just plain mean when he was having flare ups.

I took my son to the doctor last month for a check up as he was having bad migraines, and diarrhea, the doctor run a blood panel on him and his liver enzymes came back elevated, we waited to 2 weeks to go back and have it redone and it came back elevated ever more. She sent him for an ultrasound just last week and within 45 minutes, my doctors office calls and tells me the news that he has Liver Disease as in a NAFL and to lower his calorie intake and certain carbohydrates and for him to get out an exercise if possible and to stay away from certain foods. His Cholesterol is also high its at 245. Apparently his liver is not breaking down any of the fats in his system for some reason and is just sitting there,. I am surprised that his PCP did recommend him to see his gastroenterolgist or a hepatologist. So I will contact his Gastrenetologist for further assessments on the issue.

So for now my son is on a low fat, low carbohydrate diet, he is drinking a lot of water and is off soft drinks and he is making good choices in school for lunches.

 

Join our group on facebook https://www.facebook.com/groups/fattyliversupport/

Follow us on Twitter @fattyliverhelp

And join our website with patients helping patients at http://www.reversefattyliverdisease.com/

Marina’s Story – 14 Year old NAFLD patient

I met and started talking to Darlene who is Marina’s grandmother after she found my blogs about my daughter Megan. I have asked her to share the story of her grand daughter Marina.

It was Nov 1. 2012. Marina woke up for school and said her stomach hurt her. She generally never gets up at 5 am and for her to wake me up that early, I knew it must hurt her very badly because she is not a complainer.
She showed me where it hurt and it was like the top right side of her abdomen. She started getting ready for school and she was still in a lot of pain..so much so that I took her to the urgent care clinic instead of waiting to call her family doctor’s office. At the clinic ,they took Marina right back and drew blood, after examining her and with her being in so much pain, they reviewed the blood work wnich showed her (* white blood count was way off) they actually called an ambulance to transport her to Children’s Hospital.

When we got to the hospital…they hooked up an IV…started drawing blood and she was in so much pain she was crying. They did a CT scan and a Sonogram and took her right to the ICU. Her blood pressure sky rocketed..her blood count was way off…and she couldn’t stop crying about the pain. I was trying to act calm on the outside to keep Marina calm, but I was so worried …thinking…let this be her appendix so it will be solved quickly!

That would have been to good to be true. They call in the Gastroentologist and we were told the scan results were in and she had pancreaticitis. Marina just had to stay for a few days in the hospital …keeping a good eye on her in the ICU. No food to give her pancreas a rest with just an IV and lots of pain medication. So, I could breath again… she stopped crying cause the pain medications were working.They brought a portable toilet for her to pee in because she was hooked up to monitors.She was dealing with nausea but didn’t throw up…her blood pressure was high but they said it was due to the pain. To me, she looked so uncomfortable from the pain the whole thing,then she goes pee and what the heck her urine was brown like coffee. I almost passed out but I am still acting calm on the outside..she was groggy and I calmly asked the nurse why is her urine that color? Oh that’s ok, its just that her pancreas is inflamed and it needs to rest. Ok they are the medical experts… so for the next 24 hrs..she continued to feel nausea she was still getting the iv so she could let her pancreas rest, still urinating brown ,blood pressure high but a little lower with drugs,she did not sleep much and I didn’t sleep at all.

So 24 hrs go by and the doctors came in to make their rounds. I asked all kinds of questions…like what caused this what can be done why is her blood pressure so high…why is her urine so brown…they answered all my questions and said her pancreas got infected…they don’t know how…these things happen… no med for it just no food to rest it and the pee is brown because the pancreas and liver work together and the red blood cells are coming out in her urine because the liver is not working correctly because of the pancreas being swollen…its fine.

So two more days went by and she still was on pain medications but it was hurting less everyday…her blood pressure was returning to normal and her pee was a light brown….so they moved her to a regular room and had her start in liquids… they gave her soda POP…with sugar in it…coke, pepsi,ginger ale, they gave her pudding, ice cream, jello and these are medically trained doctors?. So I not knowing they were poisoning her liver, I was so happy Marina was holding it down. So after a day of sugar galore, her face started turning red,then purplish. Again I was calm on the outside falling apart on the inside. I Go and tell the nurse and they see her blood pressure rocket, her pain was coming back. They rush her back to the ICU. What’ going on?? I go to an empty room to call my daughter long distance to tell her help!. I was so weak inside my daughter (marinas aunt) and my son in law and my daughters best friend get on their computers they are searching reading, looking, talking, trying to save Marina.

I am sitting in marinas ICU room when a nurse…now this is extremely important to remember..THIS NURSE who was taking care of marina that shift…commented to me…who by the way NOT ONE DR. OR SPECIALIST SAID A WORD ABOUT to me…her liver enzymes are so high. So I freak out inside what? her liver enzymes are so high I am thinking no doctor or specialist said that to me!!! As far as they were concerned it was all only about her pancreas So now back home they start thinking maybe its not her pancreas maybe her liver is causing her pancreas to be sick!

Now keep that comment from my daughter’s friend in your mind along with what the nurse said about marinas enzymes
So I see my precious grand daughter is getting so sick again after she started getting better!

I go to the room where marina can’t hear the desperation in my voice and tell my daughter listen to this a nurse just said to me wow her liver enzymes are so high. I said why would she be concerned about that,all along the doctors and other nurses were saying to me…no its her pancreas, the other organs are just helping with her pancreas. So my daughter says mom let me talk to her doctor. And I took my phone and went and found Marina’s doctor and told her to please explain to my daughter about marinas health… 20 min the doctor hands me back the phone and my daughter says to me MOM..WHY ARE YOU TELLING US COMMENTS MADE BY A NURSE…GETTING EVERYONE WORRIED THAT MARINAS SO SICK..HER DOCTOR SAID HER LIVER IS FINE she just needs to rest her pancreas everything is fine!

so I am numb am half happy, half thinking no she is back in the ICU, I am in a mind set of total confusion. I’m thinking about what the nurse said and I have marinas mom stay with her and I went to a computer, typed in liver and Fructose in Google searched fructose, sugar, high fructose corn syrup, every thing I typed in about liver..dark urine pain. I start seeing all this about children…fructose ,liver, dark urine and I’m like what??. So I send all these links to to my family. My son-in-law said get Marina out of that hospital something is not right!

marina was so sick when she came here they didn’t put anything in her body meaning no sugar because they wanted her pancreas to rest and it was working her blood pressure went down her blood count was getting better her urine was lightening with every pee. Then since she was getting better they took her out of ICU and gave her all liquids and soft food high fructose pudding high sugar jello, sugar in chocolate milk The comment stood out in my mind….maybe its her liver that’s making her pancreas sick I said I am taking her home…The doctors said you can’t, no said marinas mom! I said OH YES I CAN I AM HER LEGAL GUARDIAN I took her home and put her on a strict no sugar diet and my family and I read everything about fructose sugar liver and by the next week when they did blood work…wow….was her body getting better not much pain at all pee turning yellow not brown no nausea, sleeping good Since then we have been very on top of marina walking for exercise..every day she has to walk… he set her up with drinking watered down cider vinegar every other day….and on the other days she drinks a spice with water… turmeric. Every label is now read for hidden ways of saying sugar!

Marina is an honor role student and is doing very well since we took her health into our own hands! Doctors are not taught enough about this disease and they don’t look for it and assume its other things. We blindly trust doctors with our lives and sometimes you just need to listen to common sense. If the sugar brought all symptoms back then there is something to consider getting rid of for your body!

This disease is hitting kids as young as 2.

Do not ignore it, if 1 in 3 north Americans has liver disease someone you love is dealing with it before it starts showing nasty symptoms like this.

Join our group on facebook https://www.facebook.com/groups/fattyliversupport/

Follow us on Twitter @fattyliverhelp

And join our website with patients helping patients at http://www.reversefattyliverdisease.com/

What Cooking Oils do you use? are they SAFE?

Cooking oil safety, there are so many that are making us sick! We have been tricked by so many corporations telling us things are heart healthy and good for our bodies and things to avoid that are blatant lies. This is another shocking reality that most of us have no idea about. Please read this article and then throw out any seed oils or veggie oils and all margarines! …buy coconut oils and real butter! use olive oil to mix in AFTER cooking not during cooking. Lots to learn in this article. I have to get rid of Canola oil in my house and look into getting something to replace it. I will have to stop using olive oil to cook as well. I already avoid Margarine like the plague! Its all plastics nothing is really natural in that! When will corporate america start caring about our health versus just the bottom line!

This journey into learning about Fatty liver disease has shown me such a scary side of corporate america!

http://authoritynutrition.com/are-vegetable-and-seed-oils-bad/

Join us on Facebook for a private group to discuss dealing with this disease!

https://www.facebook.com/groups/fattyliversupport/

Follow us on Twitter to keep up with the findings that are published! @fattyliverhelp

Join our website and register on our forums at http://www.reversefattyliverdisease.com/

Is Anything here Healthy?

Dr Robert Lustig – Sugar The Bitter Truth

I came across Dr Lustig for the first time on Youtube on November 1 2011. I was flabbergasted when I watched Sugar The Bitter Truth and I learned that high fructose corn syrup and sugar in general was directly related to Fatty Liver Disease and causing us all to be addicted to foods with it. I emailed him the next day and told him about my 15 year old daughter and the issues she had with her liver, extreme vertigo, fainting and insomnia. I researched him online a bit and found that he was a pediatric endocrinologist for 32 years. In that time, he had watched the obesity and metabolic syndrome rates climb, first to the level of epidemic , and now the rates in other countries qualify this as a pandemic. Worse yet, these problems are occurring in infants and toddlers, who clearly cannot be guilty of character flaws. He was the man I had been waiting for since 2008. The one who could help me understand my daughter who had been sick since the age of 11.

He replied to my email and I recall being in tears as he told me that he was performing liver transplants on kids younger than my daughter with NAFLD. He told me kids as young as 2 were showing up with their livers already filling with fat cells. This email and that video changed something in me. I became very passionate about making sure every parent understood that sugar is poisoning their kids. I would tell them my daughters story and beg them not to let their children live on processed foods.

I found out the next year that our children will be the first generation that will live shorter lives than us and that is NOT OK with me. I don’t care if you want to saddle me as a 44 year old obese woman with a liver disease that could kill me but you cannot have our children. This craziness has to stop.

Doctors in general do not understand the serious nature of fatty liver disease. They do not yet understand how it changes from NAFLD to NASH to Cirrohsis but it is happening very quickly and I have seen 10 people die due to that speed and not having the chance to get a new liver. The youngest was 30 years old.

So when I see that Dr Lustig is starting a Responsible Food Mission I signed up immediately This is critical for our future and the future of our children. If things don’t change in the way we manufacture foods soon I will see people dying in my liver support group at younger and younger ages.

So I am calling you to action.

1. Go to youtube and watch Sugar the Bitter Truth http://www.youtube.com/watch?v=dBnniua6-oM

2. Go to http://www.responsiblefoods.org/ and register for his mailing list and call to action we need to support him!

3. Buy his book Fat Chance. Trust me this is the man to believe no matter what else is being fed to your mouths and ears from corporations and lobbyists.

We need to do this together!

Join us on Twitter at @fattyliverhelp

Join us on Facebook at https://www.facebook.com/groups/fattyliversupport/

and join our new website at http://www.reversefattyliverdisease.com/

Fatty Liver Disease and Sleep issues

Many members of my support group on facebook complain of insomnia. it is clearly a symptom and can also be a cause of Fatty liver disease. The sad truth is that our livers heal over night. So if we are not getting to the REM level of sleep then the liver is not healing.

Fatty Liver Disease

There are two types of fatty liver disease, nonalcoholic and alcohol-induced. Nonalcoholic fatty liver disease is a condition where there is an accumulation of fat in the liver even if you do not drink alcohol or drink only a little. This type of fatty liver disease is common, and often has no complications or symptoms. However, it can cause scarring and inflammation in your liver. Alcohol-induced fatty liver is also an accumulation of too much fat in the liver. It is the most common type of alcohol-induced liver disorder. This causes your liver to enlarge, which may lead to discomfort on the upper right side of your abdomen.

Sleep disturbances like insomnia are common among people with liver disease. However, excessive sleeping, called hypersomnia, is also common for liver disease patients. Often, people alternate between insomnia and hypersomnia, which contributes to general fatigue. The exact reason for these sleep disturbances is unclear. It is possible that liver disease causes alterations in how the body makes melatonin, which is a substance that helps you sleep. Smoking, drinking alcohol or caffeinated beverages can contribute to sleeping problems too, as can some medications. Prednisone, interferon, ribavirin and propanolol are all associated with insomnia.

Cirrhosis

Cirrhosis is a diseased liver that is severely scarred. One of the causes of cirrhosis is nonalcoholic steatohepatits, which is the more severe type of nonalcoholic fatty liver diseases. Other causes include chronic hepatitis B or C and longstanding abuse of alcohol. The liver damage from cirrhosis can can disrupt the brain’s chemical pathways, which alters sleep patterns. “The American Journal of Gastroenterology” reported in May 2008 that the antihistamine hydroxyzine restored normal sleep patterns in a study involving cirrhosis patients suffering from insomnia.

Sleep Apnea

Another sleep issue that fatty liver sufferers can have is obstructive sleep apnea. Many people with obstructive sleep apnea are obese, which puts them at risk for fatty liver. Obstructive sleep apnea is a condition where your breathing stops and starts repeatedly while sleeping. Both insomnia and hypersomnia are signs of obstructive sleep apnea. A study in “Hepatology” journal published in June 2005 found that of the 163 patients with obstructive sleep apnea in the study, there was a significantly higher percentage of fatty liver disease in the most severe cases.

Insomnia is characterized by difficulty falling asleep or staying asleep. If you have insomnia, then you likely do not feel refreshed when you wake up in the morning. This is common among people with fatty liver disease. Insomnia can have many causes, from anxiety to poor sleeping habits, but fatty liver disease is also a possible cause.

Sleep is as important to your health as a healthy diet and regular exercise are. Whatever your reason for sleep loss, insomnia affects people both mentally and physically. The impact can be cumulative, with chronic insomnia likely to precede depression, anxiety, internal organ or chronic pain disorders. Additionally, lack of sleep slows your problem-solving skills and may cause someone to take unnecessary risks.

Variations on sleeplessness include problems falling asleep, maintaining sleep or experiencing non-restorative sleep. Because sleep rejuvenates the psyche and immune system, insomnia affects energy level, mood and overall health. The result of poor sleep is fatigue, which always perpetuates chronic illness. Long-term sleep deprivation increases the severity of chronic disease, including all kinds of liver disease.

When it comes to liver disease, the following are popular culprits for insomnia:

· Stress or Anxiety – Concerns about your health may keep your mind overly active, making relaxation and therefore a restful sleep difficult.

· Sleep Apnea – Affecting over 12 million Americans, obstructive sleep apnea interrupts the sleep cycle, resulting in poor quality sleep and fatigue. Additionally, French researchers have discovered that sleep apnea is a significant risk factor for fatty liver disease.

· Interferon Treatment – Interferon medication is the favored medical treatment for viral Hepatitis B and C. Although temporary, insomnia is a common side effect of interferon therapy.

· Cirrhosis – In people who have cirrhosis of the liver, histamine levels in the brain are often altered. In the brain, histamine regulates the sleep-wake cycle, so if levels of this chemical get out of balance, so do the person’s sleep patterns.

· Related Illnesses – Patients with liver disease often suffer from other related illnesses, including type-2 diabetes, obesity and hypertension – all of which can have insomnia as a symptom.

If a person’s sleep cycle is interrupted, the deepest, most restorative stages of sleep are never reached and the person will feel fatigued. By controlling the stages of sleep in your brain, some chemicals slow down brain waves, helping you fall asleep, while others stimulate brain waves, causing you to dream and wake. Alcohol disrupts these normal actions, ultimately hindering the quality of your sleep.

Conquering Insomnia : here are seven suggestions to encourage sound sleep:

1. Establish a sleep routine, retiring and rising at the same time each day.

2. Maintain an environment conducive to sleep by keeping your bedroom dark, quiet and cool.

3. Avoid caffeine, alcohol and big meals in the evening.

4. Try relaxing before bedtime with a warm bath or other soothing evening ritual.

5. Because fatigue typically causes restless sleep, break an unhealthy sleep cycle. Proven to increase energy levels by up to 40 percent without stimulants, try supplementing with to ensure adequate energy levels during the day for exercise and then restful sleep at night.

6. Do not have a visible bedroom clock. “Clock watching” often intensifies insomnia. Turn the clock face away from you or put it in a drawer.

Follow us on Twitter @Fattyliverhelp.

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http://www.facebook.fattyliversupport.com

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http://www.reversefattyliverdisease.com/