Forum Replies Created

  • Brenda Reese

    Member
    May 16, 2023 at 6:01 pm in reply to: Do you struggle with urinary control?
    1. I agree. Diapers ARE a poor AND expensive choice. At some point, we will try the catheter. He IS on Medicare, so glad they cover the catheters!
  • Brenda Reese

    Member
    May 16, 2023 at 5:57 pm in reply to: overwhelming as a caregiver

    Marjorie, thank you for your response. My husband takes Magnesium citrate 409 mg with each meal and I have to insert 2 glycerin suppositories every morning to help him poop. I bought him Miralax, but he won’t take it. I believe it would work, if he would take it!

  • Brenda Reese

    Member
    May 16, 2023 at 3:42 pm in reply to: overwhelming as a caregiver
      <li style=”text-align: left;”>My husband was diagnosed in 2016 with stage 3 PD, but he obviously had symptoms well before that. We have tried manitol for his constipation. I don’t see that it helps much with any of his symptoms, but I keep giving him 1 tsp in his OJ each morning. He has sleep issues, urinary issues, hears music that is not there, is mobile but slow, masked face, weak muscles, mind not always clear. But he is not depressed. He is a minister who had to go out on disability at age 62. He knows that I will take care of him and that the good Lord will take care of us. I did worry about our future when he was first diagnosed, but I decided that worrying was was futile and drained my strength to deal with the situation, so now I just take one day at a time and ask God to help me with whatever I face each day. We are dealing with slow progressing PD. So, he might outlive me! Anyway, God has been faithful to us and we have a good church family. Our children live 2 states away, so they do not help me, but church family is here for us.
  • Brenda Reese

    Member
    May 16, 2023 at 2:52 pm in reply to: Do you struggle with urinary control?

    My husband has PD. He goes to the bathroom 3-4x per night. He has urgency issues from time to time. He does not want to wear diapers, so he has wet the bed a few times. Ugh. His urologist has not been helpful in dealing with this issue. He just says to wear diapers. 😫

  • Brenda Reese

    Member
    May 16, 2023 at 2:41 pm in reply to: Horew does the heat effects effect you?

    My husband has Parkinson’s disease. He cannot tolerate the outdoor heat either. He just “wilts”. He has to come back into the house in the air conditioning.   In the winter, he gets too cold. Sometimes, I am content with the indoor temperature and he is either cold OR hot! The neurologist says that goes with Parkinson’s disease impact on the sympathetic nervous system. No suggestions were given on how to handle outdoor heat. 😟

  • Brenda Reese

    Member
    July 5, 2022 at 3:18 pm in reply to: Fainting

    My husband takes 4mg Fludrocortisone at breakfast to combat dizziness that would lead to fainting. If he still feels lightheaded, he sits in his recliner for 15-30 min with eyes closed. Then, he is usually able to function alright the rest of the day. He is stage 3 PD, age 69. Diagnosed early 2016, but had symptoms probably 10 years before diagnosis.

  • Brenda Reese

    Member
    March 22, 2022 at 8:09 pm in reply to: Who are you in relation to your person with Parkinson’s?

    Theresa, you just described to a “T” exactly all the things that I do. My husband was diagnosed with PD in 2016, already stage 3. I believe it began around 2004. Nearly every morning when I wake him up, he says “Are you my nurse for the day?” Of course, he is just teasing me, but sadly, I am nurse and much more.  It is frustrating to not feel like a wife. ~Brenda R.