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Allopathic / conventional treatment of neurofibroma or neurofibromatosis (NF)or von Recklinghausen's disease involves the surgical removal of the tumors but the tumors have a tendency to come back. For symptoms like café au lait spots no treatment is given. Radiation therapy (localized treatment of tumors with targeted x-ray beams) may also be needed.
Sometimes the tumors are in such a place that they cannot be removed surgically. Tumors that cause pain or loss of function are removed on an individual basis.
In contrast homeopathy treatment can save you from the surgeon’s knife and the other symptoms of the disease can effectively be taken care of with homeopathic medicines.
Homeopathy is not against surgery but it often minimizes the use of this painful and terrifying procedure.
Diseased tissue (tumors) is not the cause of disease and its removal from the body will not prevent the recurrence of the disease after the surgery. Homeopathy treats the cause and not the effect. After the proper treatment not only diseased tissue will be healthy but the recurrences can be prevented as the vitality is raised by the homeopathic remedies.
The tumors start regressing in size and are gradually removed with the proper homeopathy treatment. Also the other skin symptoms, the spinal symptoms, freckles and so on can be managed easily with the homeopathic medicines.
Homeopathic treatment can be started on seeing the early signs of the disease like café au lait spots and its progress can be stopped in the beginning only.
Every family has typical "weak spots" in the health - some families have history of heart diseases, some of cancer, some of hormonal disorders, some of arthritis and so on. All these weaknesses are written down as potential in the genes, especially if both parents of the person have the same health disorders already expressed, or in their family health history. Chronic diseases which are repeated within the family are so often very difficult to solve, because people who carry them usually BELIEVE that inherited disorders are not possible to heal, consciously or subconsciously. For all such false believes the answer is the homeopathy treatment. Homeopathic medicines can take care of the predisposition to a disease. Homeopathic remedies strengthen the body to counter hereditary problems.
I have found in my clinical experience that homeopathic medicines often replace the conventional drugs and eliminate the need for heroic procedures. Ideally, homeopathy doctors are taking the best of the natural science to create a kind of care that will be commonplace in future.
There are 9 homoeopathy medicines which give great relief in neurofibroma or neurofibromatosis (NF) or von Recklinghausen's disease. However, the correct choice and the resulting relief is a matter of experience and right judgment on the part of the homeopathy physician. The treatment is decided after thorough case taking of the patient. Thus homeopathic remedies of neurofibroma or neurofibromatosis (NF) or von Recklinghausen's disease are designer made unlike allopathy in which all patients receive the same surgery or drugs although trade name may be different.
For online homeopathic treatment of neruofibroma or neurofibromatosis (NF) or von Recklinghausen's disease, you may fill in the consultation form at HomeopathicTreatment4U.com.
A neurofibroma or neurofibromatosis or Von Recklinghausen's Disease is a benign nerve sheath tumor in the peripheral nervous system. Usually found in individuals with neurofibromatosis type 1 (NF1), a genetically-inherited disease.
Neurofibromatosis (NF), or Von Recklinghausen's disease, is a genetic disease in which patients develop multiple soft tumors (neurofibromas). These tumors occur under the skin and throughout the nervous system.
In neurofibromatosis, a genetic defect causes these neural crest cells (neural crest cells are primitive cells which exist during fetal development) to develop abnormally. This results in numerous tumors and malformations of the nerves, bones, and skin.
Neurofibromatosis occurs in about one of every 4,000 births. Two types of NF exist, NF-1 (90% of all cases), and NF-2 (10% of all cases).
Both forms of neurofibroma or neurofibromatosis are caused by a defective gene. NF-1 is due to a defect on chromosome 17; NF-2 results from a defect on chromosome 22. Both of these disorders are inherited in a dominant fashion. This means that anybody who receives just one defective gene will have the disease.
It is interesting to note that only about half of all cases of neurofibromatosis show a family history of the disease. The other cases of neurofibromatosis occur because a specific gene spontaneously changes its structure (mutates). A person with this type of spontaneous mutation can then pass that gene onto his or her offspring. There is a 50% chance that a parent with neurofibroma or neurofibromatosis will pass the gene on to a child.
To be given the diagnosis of neurofibromatosis type 1 (NF1), an individual must have at least two of the following features. Some people with NF1 have only two, while others can have several of these features :
Six or more cafe-au-lait spots, or coffee-colored birthmarks, each measuring over an inch in adults (1/4 inch in children).
Two of more benign skin tumors called neurofibromas or one diffuse tumor of the soft tissue called a plexiform neurofibroma.
Freckles under the arm or in the groin region.
A tumor of the nerve to the eye called an optic glioma.
Two or more spots on the iris of the eye called Lisch nodules.
A problem of one of the bones such as bowing of a leg, with or without a fracture.
A parent, brother, sister, or child with NF1.
Individuals with neurofibromatosis type 2 (NF2) have fewer outward signs of the condition than individuals with NF1. To be given the diagnosis of NF2, an individual must have the following features :
Benign tumors on both sides of the head involving the nerves for hearing and balance, called acoustic neuromas or vestibular schwannomas
or
Family history of NF2 (a first-degree relative, i.e. mother, father, brother, sister, or child, with NF2) AND one of the following :
An acoustic neuroma or vestibular schwannoma on one side of the head before the age of 30, or
Any two of the following : meningioma, glioma, schwannoma, juvenile posterior subcapsular lenticular opacities / juvenile cortical cataract.
