We should do something together, please consider.................

 

Dear Blog readers and Lipoma sufferers

I think it is the time to consider the question if we should  constitute the Lipoma-Tumor Foundation Inernational (LTFI) to bring not only my but also other people's experiences and knowledge, and not only from the patient's view but also from the medical point together and really start further research and investigation into the major problems
a) why people are suffering with Lipoma-Tumors
b) how we can help to treat them
c) what can be done to prevent new growth
d) to get Lipoma-Tumors recognised  by WHO

These are the major questions, and when I look into my blog how many readers are be interested to read my stories and more, from which countries these are coming, I think that it is time to do more. Over 80.000 people around the globe, with the majority of  19 countries in Europe, Asia, China and America are suffering under this symptom.

My success in treatment to get rid of them and the prevention of new Lipoma-Tumors over the years, should be taken as a positive sign, that it is possible to provide help.

What you could do in the first stage?

You can become a member of the LTFI
When there is enough interest, several organisational questions should be answered.

From my knowledge it is very much important to promote these problems and take off the shyness and the stress of high number of people and motivate them, as let them hanging alone with there physical problems!

We have today several other organisation, such as cancer, diabetic etc etc, why we should not form a LTFI to help us.

Please, if you belief or like to sponsor this, please make your comment here or send me an email; klausg@amnet,net.au

I'm positive that had happened to me, can be also done by others!!!!


Kind regards

             

                                  

 

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