any agencies that provide assistance for overly expensive pd medication and Parkinson's disease | MyParkinsonsTeam

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Top 10 Search Results for "any agencies that provide assistance for overly expensive pd medication"

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Medication Cost Assistance
A MyParkinsonsTeam Member asked a question 💭

Parkinsons medications can be very expensive, and my parents' finances are starting to dwindle. What type of assistance is available for people who can't afford the medications but need them to live?

A MyParkinsonsTeam Member

possibly some resources here Needy Meds
https://www.needymeds.org/copay_diseases.taf?_f...

Anyone Else On Rytary?
A MyParkinsonsTeam Member asked a question 💭

Is it expensive? My doctor tried to give me a higher dose but it made me too ill. I was throwing up all day. Now îf my insurance would only approve ît! I can't imagine why they are balking unless it is over the cost. I believe it is a newer drug.

A MyParkinsonsTeam Member

Rytary costs us about $300/3mo supply

Home Care Providers
A MyParkinsonsTeam Member asked a question 💭

I am interested in knowing I advice regarding hiring home care providers. Have people been happier with the national chain type agencies versus smaller independent agencies versus privately hiring an individual? What was the hourly rate you had to pay? We’re you happy with the quality of care or disappointed? What worked and what didn’t work well? Thanks!!!!

A MyParkinsonsTeam Member

I am completely disheartened trying to find a solution for care. I wish I could retire and just take care of my dad myself as I enjoy caring for him.

CONFUSION
A MyParkinsonsTeam Member asked a question 💭

is there anything that can be done for confusion? take anything? movement causes MORE confusion.

A MyParkinsonsTeam Member

Sorry I'm not sure I understand the question ....... 😃

.. My Balance Has Gotten Worse And I Have Fallen . I Can No Longer Work In Garden Or Daily Walk. Has Anyone Heard About Service Dogs?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

There are agencies who provide support animals for people with PD. Please be careful, like many things, some businesses have turned there focus to making money, not necessarily providing support. Be… read more

Antipsychotic Drugs (Quetiapine) Can Be Harmful For People With Parkinson's
A MyParkinsonsTeam Member asked a question 💭

Antipsychotic drugs (Quetiapine) may be harmful for people with Parkinson's by Yvette Brazier March 22, 2016

http://www.medicalnewstoday.com/articles/308163...

Antipsychotic drugs that are commonly prescribed for people with Parkinson's disease may be causing additional harm, says research reported in JAMA Neurology. Around 1 million Americans are estimated to be living with Parkinson's, and physicians diagnose 60,000 new cases each year, according to the Parkinson's Disease Foundation… read more

A MyParkinsonsTeam Member

It seems the problem with Quetiapine is when it is taken with Levodopa, the first line treatment for PD. The two drugs will interact and often cause a serious problem. Please avoid taking… read more

Does Any One Have An Emotional Support Dog And How Did You Go About Getting One? Also Do You Recommend It For Someone With Parkinson's?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

There are no standards for an emotional support animal and no legal protection. You can't take them to places where dogs aren't allowed, though some people try. For many of us, all pets provide… read more

Rytary
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

I volunteered to resign to retire. I was not forced to retire !!

I Dont Know How To Do Anything About Help For Me, House, Finances, Everything. Who Do I Trust? What Do I Do As I Get More Panicky From Pd?
A MyParkinsonsTeam Member asked a question 💭

how do i pull my pants up and down too?

A MyParkinsonsTeam Member

Go to churches to see if they will help you. People have go fund me ads. The county that you live can have home health and can help with groceries. There can be clubs and agencies that can help. If… read more

What Medicare "D" Plan Can I Use That Defrays The Cost Of Azilect?
A MyParkinsonsTeam Member asked a question 💭

I need help with a Plan "D" plan for my first enrollment into Medicare. I'm going through/getting help through a non-profit to help find the best plans/best cost, but the Azilect seems to be a sticking point. The Plan "D" drug plan is going to cost more than my current copay with a commercial PPO. The issue is, as most of you know, there is no generic Azliect (Teva Labs got an injunction about a month ago preventing a generic to come into the US market). Any suggestions? Terry

A MyParkinsonsTeam Member

I actually got a separate plan from CVS that saved me a lot.