Hirudal 250Iu Cream Health Feed

yes. it's safe. use them and try not to strain while passing stools. this will get alright after delivery

Cheek bone has soft muscles so its tend to get more time to heal and having more pain so apply ice pack on injured area and just consult physician if pain persist for long.

you may apply thrombophob ointment to dissolve the clot under the skin , automatically the blue green discolouration will go in a weeks time depending on the severity of clot.

Donot worry it's curable in Ayurveda ,first tell me since how many months you are suffer from, give me detail history, we are specialise in sexual disorder, please consult me in Private consultation. Or take our power plus package. Till then avoid masturbation and eat fresh foods avoid salty and spicy food article and do kegel exercise.

Adenoids need to removed by surgery and Mucopolysaccharidoses are a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called glycosaminoglycans.

Hi Prakash the disease occurs because of lack of some enzymes or their non functioning properly...

If it is completely absent then I don't know how much I can help but if it is because of their ineffectiveness I think homoeopathic medicine can help to certain extent...

In any case I will advise you to try homedicines...

At present there is no cure for any of the mucopolysaccharide diseases.Enzyme replacement therapy (ERT)has been approved by the FDA for several of the MPS diseases, but ERT has not been shown to be effective in MPS III. Bone marrow transplants have been tried on individuals with MPS III, but with disappointing results. Gene therapy, chaperone therapy and intrathecal enzyme therapy are a few of the treatments for MPS III where research is ongoing

The MPS Diseases. The Mucopolysaccharidoses (MPSs) are rare genetic disorders in children and adults. They involve an abnormal storage of mucopolysaccharides, caused by the absence of a specific enzyme. Without the enzyme, the breakdown process of mucopolysaccharides is incomplete.The life expectancy of these individuals is 10 to 20 years. Individuals with mild MPS II also have a shortened lifespan, but they typically live into adulthood and their intelligence is not affected. Heart disease and ...more

Mucopolysaccharide (MPS) and related diseases are Lysosomal Storage Diseases. These are rare, life-limiting, progressive, genetic conditions caused by the shortage of a particular enzyme.Currently, although there is no cure, Enzyme Replacement Therapy (ERT) and Haematopoietic Stem Cell Transplant (HSCT) are available to treat a few types of MPS and related diseases although for the majority there is only palliative treatment and care.

the tes is to see if he has The MPS Diseases. The Mucopolysaccharidoses (MPSs) are rare genetic disorders in children and adults. They involve an abnormal storage of mucopolysaccharides, caused by the absence of a specific enzyme. Without the enzyme, the breakdown process of mucopolysaccharides is incomplete. Mucopolysaccharidoses are a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called glycosaminoglycans.he age of ons...more