Proposed Idea | iConquerMS.org

These ideas have been proposed by the community but no analysis has been initiated.

Is there any research specific to trigeminal neuralgia ongoing or being considered? What meds seem best for the condition?

What is the best treatment for MS patients who experience nighttime foot-twitching?

What causes MS-related fatigue to be so severe that it affects thinking, coordination, speech, and even the ability to sleep?

Could skin conditions/allergies, eg urticaria, be a symptom and possibly part of the Prodrome of MS?

Could MS symptoms be managed through hormone replacement, adjustment, or augmentation?

Does a CD20 b cell deleting DMT increase your chance of getting long COVID?

Are MS symptoms linked to specific lesion locations, and could these links be identified through a comprehensive database of MS MRI images?

Can right hip flexor problems caused by MS be helped with physical therapy?

Do diets or supplements aimed at improving mitochondrial health have the potential to help with MS fatigue?

Does Wellbutrin improve MS fatigue?

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