Hemochromatosis patients stories, forum, tell your story you may be able to help someone else even if it is just to let them realize that they may also be at risk of this hideous disease leave a comment or just have a look around my site thank you and i hope I was of some help
mike winnubst
What a lovely weblog. I will certainly be back again. Please hold writing!
Admiring the commitment you put into your blog and detailed information you present. It’s good to come across a blog every once in a while that isn’t the same unwanted rehashed material. Wonderful read! I’ve bookmarked your site and I’m adding your RSS feeds to my Google account.
I dont know what to say. This blog is fantastic. Thats not really a really huge statement, but its all I could come up with after reading this. You know so much about this subject. So much so that you made me want to learn more about it. Your blog is my stepping stone, my friend. Thanks for the heads up on this subject.
Get It Now Risk Free!
I am going to make this decision a bit easier for you. If you have read the letter above then you are probably looking for some help in regard to this disease. I am offering assistance to anyone who wants to call, write or email me via the form on the forum page, so that you can be assured I am real person who suffers the disease and not just another hemochromatosis generic web site. They cater to every illness known to man and have a generic answer for all of them. I have personal experiences of just how horrid the disease can get. The longer you wait to take control of this disease, apart from thousands of dollars of specialists fees and tests which can become more invasive and undesirable, the greater the chance becomes of irreversible organ damage. Well, as you have stayed to this point reading this material and as your time is also valuable I would like to offer you a copy of my book in pdf format totally free. This book “How to find a Doctor” is valued at $25.95 .You can access this gift by going to the contact page and filling in your details. I will personally make sure that you get your free copy. You can even get my new ebook “A SIMPLE GUIDE TO HEMOCHROMATOSIS” totally free. All you need to do is read my book “How to find a Doctor” and let me know your thoughts and include your own patient story relating to how you were diagnosed, how you are handling the symptoms and if you have strange symptoms. Then I will send you the ebook ”A SIMPLE GUIDE TO HEMOCHROMATOSIS”. You can even steal them both from me simply by purchasing the product, downloading it and keeping it. I can”t take it back off you.I will stand behind the sixty day 100% money back guarantee. PayPal monitors and maintains this process.
Mike Winnubst
This is such a great resource that you are providing and you give it away for free. I enjoy seeing websites that understand the value of providing a prime resource for free. I truly loved reading your post. Thanks!
Great post I Agree with your leading points and think the title says it all, I loved reading and I will certainly come occasionally to read more of your writing. sustain the great work!
If you cant find help with what you are looking for here. check out the other pages.Contact me direct at puzzles@live.com or go to our contacts page most get an answer in 48 hrs contact me for a special book deal you
Thank you very much for it. I found, what i want
great post… I like the theme too
I guess you’re likely to be right on the subject of Hemochromatosis Forum and Blog. brbr I am not sure that absolutely everyone might understand it like that of course.
I’m still learning from you, as I’m trying to reach my goals. I definitely love reading all that is written on your blog.Keep the aarticles coming. I enjoyed it
I was recommended this website by my cousin. I’m not sure whether this post is written by him as no one else know such detailed about my difficulty. You’re amazing! Thanks!
We all hear so many stories; here is a quick one about misdiagnose.
If you suspect you have high iron [Hemochromatosis] read this
A Man spends life savings after wrong diagnosis!
A British comedian spent his life savings after he was wrongly told by doctors he only had three months to live.
Dave Ismay was so devastated by the initial diagnosis that he set out to complete his own “bucket list” and achieve his lifelong dreams, the Birmingham Mail reports.
The 64-year-old grandfather, who has performed both on stage and on television, had been told by doctors that alcohol abuse had left him with cirrhosis of the liver
after test results showed he had excess iron levels.
He was baffled because he hadn’t been a big drinker and had cut down smoking when he was 40.
Ismay, from Ashby in Leicestershire, decided to set out and complete his bucketlist — which included writing a book about close friend and fellow comedian Bob
Monkhouse, playing golf at an exclusive Irish golf course, visiting Australia and appearing in a pantomime.
“When you’re told you’ve got three months to live, it really focuses your mind,” Ismay told the Mail.
“I even bought a new Merc because I thought: ‘If I’m going to go, it will be in a comfortable car!’.”
Eight weeks after his incorrect diagnosis, and after splashing out $46,000 on the new Mercedes, Ismay underwent a full body scan test which showed he was in fact
suffering from the non-life threatening blood condition known as Hemochromatosis.
Be sure to check out our home page just look around and leave a comment
Mark A. Kendallsays: May 25, 2011 at 7:27 pm
I was wondering how long it takes to recieve the e-book and doctors list book?? I was credited for these product and have not received them yet. I would appreciate if you could send me my book quickly as i need help with Hemochromatosis and i am not stable financialy..
mike says: May 26, 2011 at 2:54 am
This is an automatically generated Delivery Status Notification. Delivery to the following recipients failed. mandmk@praiseyahweh.com
Dear mark I have been trying to foward you the book links but your email keeps failing contact me direct at puzzles@live.com.au and i will send you a bounce back e mail with your down load product link
mike winnubst
I have just posted marks reply
so others who have has experienced the same or who may have a similar advice .Please contact me if you think that you can help or post a comment
Shalom Mike…I pray you are doing well….I receiver your books….Thank You…….In your book on one page you say on things to avoid you have phytates,tannates(found in tea),phosphates, oxalates and calcium. You say all these help in the binding of iron and thus inihibitits absorbption…… I was told to drink green tea and have calcium with my meals…I do not understand( inhibits iron) and inhibits iron absorbption and binding of iron. My FIRST FERRITIN levels back on 11-02-2010 was 1890 with my iron at 229 after a series of 12 phlebotomies my ferritin level is 744 and iron is 205..my white blood cell cout is 3.0 now…. What do you know if any thing about wheat grass…or ip6???? My natural doctor put me on ip6 and i have been drinking wheat grass with fruit smoothies…… Blessings to you and yours…Mark… Shalom
ps.you can post this on your site if you want..
I am so pLeased that we were finally able to sort that out !
I can give my opinion but as I have said before I am not a doctor.
I can tell what I have done and been through and have researched also. In my eBooks are countless hyperlinks to expert medical information,(also on the bottom of some of these pages on site) it can be rather a daunting task to go into, but it’s there if you have a special problem. Mark mentioned green tea and I agree that the choice is preferably to normal tea and coffee. Wheat grass I will need to find out about. Your levels are still high so keep doing the phlebotomies. Fruit smoothies still have lots of goodness but a lot of vitamin C, so keep it in moderation or you will stay at the same ferritin level even with being bleed. The same with meat and alcohol they would be best eliminated till the iron –ferritin are at the correct levels. Then these can be taken in moderation as long as the phlebotomies continue if and when your levels climb up again. I get tested every three months and with what I am doing have not had to get bled for over a year now. I was 1150 and now I am at 50 so there is hope. There is some research to suggest that once you are lowing your iron ferritin levels, that high vitamin C doses will release the iron build up in the tissue. As it is only experimental it is not recommended yet and definitely not if you aren’t being bleed because it could lead to organ damage. Maybe this is what your doctor is trying to do on you with the smoothies. Absorption means the iron is taken into the blood and stored whereas inhibits prevents the storage process.
With thanks Mike
http://EzineArticles.com/?expert=Lewis_Freeman
here is a post visit my site
Hemochromatosis
Hemochromatosis is a condition that plagues countless people around the world. Not everyone that has it or knows someone who has it fully understands the nature and the gravity that comes with it. The illness is an often hereditary one that is characterized by an overload of iron in the body that causes a lack of energy, swelling, stiffness of joints, liver problems, hair loss, weight gain or loss, and many other symptoms.
A new book on the topic by Mike Winnubst aims to clarify and simplify Hemochromatosis since he suffers from it himself. His writings are not only from his experience but also serves as a guide for those going through the process.
This book entitled “A Simple Guide to Hemochromatosis” provides readers with a more knowledgeable approach because they are informed about how it is diagnosed, how to live with it, treatments both traditional and alternative, and many other great insights about it.
This is best for persons with a family history of Hemochromatosis since early detection is strongly advised. Even for family members, this book will be a great guide for caring for your loved one with the disease.
“A Simple Guide to Hemochromatosis” will even help you prepare for the illness when it comes and give hope to sufferers of the condition. Real life stories are also in the book which patients can relate to on a personal level.
This disease is not something you want to have unknowingly and especially if you or your doctors think it is something else. It’s time to be informed if you’re at risk for the disease or if you suffer from any of the symptoms that comes along with it. Avail of this book online for only $24.95 and we’ll also give you “A Simple Guide to Finding a Doctor” for free.
http://www.hemochromatosissite.com/symptoms/video just wanted to say back link this to my web site
http://www.highironlevelsedu.com
see hemochromatosis books
My Mother was one of the first women to be diagnosed with this here in Australia. My childhood was often spent with her having venesections. She later went on to have diabetes and significant arthritis. She died at 72 of Bowel cancer but it had quickly spread to her liver which was of course in a much more weakened state after so many years of this disease. I have 2 uncles with it and several cousins with it and have seen first-hand how it can impede someones life. I had genetic testing some years ago and know I am a carrier, which is a relief to know and work with. From my experience, the earlier we know about something, the easier it is to deal with! Just go and get tested, it’s only a little blood and then you can plan good care hopefully avoiding problems or take a breath and relax?!
Hkeow do I know if I have hemocrotis. I don’t have the money for a dr.my symtoms as I know are. I can’t sleep I’m shakey very no sexdrive mad about work I never had haves had them a week ago and can’t go to the dr cause I’m broke period maybe every 2 weeks
Hi there blue eyes you need to explain how you feel a bit more
What makes you think that you have hemochromatosis, age is a factor from 40s on ward signs strat to appear fatigue is the first then pain in the joints. Do yo have a family member who has high iron in the blood .do you come from northern european background
usa ,canada, african ireland singapore ,or pacific islands these countries are most at risk unless a parent has hemochromatosis most cases both must be a carrier (carry the geyne ) read mikes story or check out the symptoms list and match it to your own sorry you forgot to leave your name with thanks mike http://www.hemochromatosissite.com