Parkinson’s: When Is It Time to Get Outside Help?

Parkinson’s disease is a particular type of nervous system disorder, which is a progressive type and affects movement. When it comes to the symptoms, in some cases, they appear gradually, and also, in some cases, they are barely noticeable.

Tremors are really common. However, the disorder commonly causes slowing of movement or stiffness. During the early stages of this disease, the individual’s face might show little or simply no expression.

When the patient is walking, their arms might not swing. Their speech might become slurred or soft. As the condition progresses over time, the symptoms of Parkinson’s worsen.

It is true that this particular disease can not be cured, but medications might significantly enhance the symptoms. In order to regulate some particular regions of your brand and to improve your symptoms, doctors occasionally might suggest surgery.

Taking care of the patient is a challenging job. Here we will guide you with that.

When Is It Time To Get Outside Help?

In order to understand the answer to this particular question, one must understand and also balance the needs and wants of both the person who is suffering from Perkinson’s and the caregiver of the individual.

When it comes to Parkinson’s, every individual does not want an extra hand, even when you actually require it. It might be really hard to accept this reality and also deal with the emotions this particular thing brings up.

However, as the care of your loved one requires change, you have to re-evaluate your requirements for help on a continuous basis.

In every individual, Perkinson progresses in a different way. During those initial days, you might need assistance in picking up groceries now and then. But as the disease advances, your requirements might evolve to going for a daycare service or a home health aide for some hours at a time.

Eventually, with every passing day, full-time home care or an experienced and skilled nursing faculty might become necessary.

Be Realistic

A lot of people make promises of always taking care of their loved ones all by themselves, at home. In case you also have made this promise, you might not have properly understood all the responsibilities a caregiver entails.

In the late stage of Perkinson’s, a number of individuals can not help with their own movements or daily living activities. It means heavy lifting along with myriad other tasks that you are responsible for. In case you have to break your promise, you might feel like a traitor.

Eventually, you might lose your physical stamina and strength and can not keep your promise. You also can lack the technical skills for providing the kind of care your loved one requires.

So, ultimately, when everything becomes really difficult, you are failing to balance your own life with your caregiver responsibilities, or at the time when your physical burden is more than your capability, it is time to get outside help.

Start Small

When Parkinson’s is unpredictable, it could be really hard to plan for help. Here, you do not know what every day or every hour is going to hold. In case you are putting it off for really long, you could start to feel overwhelmed.

In order to begin with, pick a time of the day, particularly for a helper to visit, which is the most convenient for you. It can be a specific yoga class you have been missing or are willing to try. Schedule help so that you become capable of doing it a couple of times a week.

When you are progressing to get assistance for more days in a week or longer hours, we will advise you to try to maintain some elements of your routine. This way, you will not feel like you are giving your complete control.

Final Talks

When you are making the decision of seeking support from your caregiver, you need to be sure about the impact of a caregiver change on you. In case you are changing the caregiver, especially when the individual is suffering from Perkinson’s, the situation might get worse.

Research shows that non-professional caregivers who are just introduced to Perkinson’s caregiving routine might worsen the scenario, and the patient might react differently;y with the treatment and therapies.