Caring for someone with Alzheimers disease is not a simple task and each day can be filled with new challenges as the persons abilities change. The Alzheimers caregiver must be fully aware of the effects of the disease and to react to certain things that will happen either occasionally or daily, depending on the severity of the disease. Patience is the key element for an Alzheimers caregiver and even then, there is the chance of depression and feeling of being overwhelmed with the responsibility.

Communication is a key ingredient for the Alzheimers caregiver and is usually better to short simple sentences when talking to the patient. Do not use baby language or refer to them in the third person. Use their name often and keep the tone soft and gentle. It is also better to remove any distractions in the room that may take the patients attention away from the conversation. When they try to respond, be patient and do not interrupt, regardless of how lone they seem to be taking, however if they appear to be stuck on a word gently suggesting the word may help, but if they argue do not insist on being right.

Bathing and dressing can be a simple task or an extreme challenge for an Alzheimers caregiver as some patients enjoy it and have no trouble at all, while others may find it a terrifying experience. The Alzheimers caregiver should try to schedule the activities at a time when the patient is usually calm and agreeable. Be gentle and calm and allow the person to perform as much of the function as possible.

Confusion Can Be Exacerbated By Tone Of Voice

When finished with the bath and trying to get the patient dressed the Alzheimers caregiver will be wise to forego complicated fasteners on clothing and should avoid strings or belts altogether. Again, keeping a calm, smooth tone to the voice can help the patient better understand instructions and prevent them from getting flustered if they have trouble understanding or carrying out the instruction.

Eating can also be challenge for the Alzheimers caregiver, as many times the patient may have lost the memory of their favorite foods. Meal time should be the same time every day with the patient allowed to feed themselves as much as possible, but if their coordination is such they may hurt themselves with utensils, then they will need to be fed. Small bites, and slowly to give them a chance to chew and swallow without feeling rushed can make the meal time go smoothly.

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