IS THERE A NUMBER FOR ANYTHING: We all don't... - PSP Association

PSP Association

9,232 members11,334 posts

IS THERE A NUMBER FOR ANYTHING

Auddonz profile image
14 Replies

We all don't know what the next day will bring for any of us with or without PSP. Since my honey got rid of the UTI and his med Sinemet were raised from 25/100 to 25/250 and changed as when to take then. He takes them 3 times a day whole and then a half for the 4th dose. Turns out to be 4 times a day, 4 hours apart. Then of course there is his blood pressure meds, and something to calm him, diazapan at night to help him sleep. Prilosac to protect his tummy. No lose of balance now, just tired from being in the hospital twice, 2 rehab facilities, one of which almost killed him. Now if I could only convince him to do his exercises, that would make me happy. Also trying to convince him his walker is his best friend besides me :). Fingers crosses things stay this way for a while but none of us know. He will be 78 in June. The 2 plus months since he was diagnosed made me a basket case but having him sleeping next to me in a hospital bed makes me very happy.

Written by
Auddonz profile image
Auddonz
To view profiles and participate in discussions please or .
Read more about...
14 Replies
Yvonneandgeorge profile image
Yvonneandgeorge

Hi Audrey glad all is going well, and you have Don home love to you both Yvonne xxxxxxx

Auddonz profile image
Auddonz in reply to Yvonneandgeorge

You have no idea how happy I am to have him with me. Love back to you both, xoxoxo Yvonne

NannaB profile image
NannaB

I'm so pleased things have improved for both of you. Long may it last.

X

Auddonz profile image
Auddonz in reply to NannaB

TY NannaB X

jimandsharynp profile image
jimandsharynp

Check out the long range effects of Sinnmet on the internet. There are some very bad effects. In my opinion, if you aren't seeing results from using the drug then stop usage (check with your neurologist). Jimbo

bubbie profile image
bubbie in reply to jimandsharynp

hi there jim. sorry we never connected when you came to boca. alan is still hanging in. very hard lately with swallowing and having trouble sleeping.he coughs pretty much all night. last night I had to go in to our other bedroom to get some sleep. we lost a member from our group this week. it made me so upset. she and alan had this horrible disease together. spoke to her husband and he was glad she is in a better place. so so sad. how are you doing??? please write back and let me know. I guess I have no choice but to keep on going on for the sake of my kids and grandchildren. I miss them a lot. I am going to ny. on june 11th for a few days so that should give me a lift. be well and take care. bubbie

jimandsharynp profile image
jimandsharynp in reply to bubbie

So good to hear from you. Yes, sleep can be an issue. Sorry about the other person passing away. A break to NY will bolster you a bit. Keep in touch. Email a photo to jim.pierce@gmail.com and I'll do the same back to you. Jimbo

Auddonz profile image
Auddonz in reply to jimandsharynp

Everything we put in our mouths even an aspirin, has a side effect. For now it seems to be helping him and I am happy, so is he Jimbo

Peter3 profile image
Peter3

Jim is quite right in his comment about Sinemet. This condition brings enough problems without the added risk of side effects of a drug that is helping the person.

abirke profile image
abirke

Yah we took B off Sinemet. Didn't seem to produce any positive results. I can't remember if there were any terribly negative results.....just maybe nothing.....But on the bright side he is home and though it's alot of medicine getting and cojouling to exercise you are both together. That's how I feel about being with B.

AVB

laroux profile image
laroux

My hubby has been on sinnemet since he was wrongly diagnosed with Parkinson's about 4 years ago. It was increased several times after he was diagnosed with PSP, it's been a god send for him, without it he has severe rigidity accompanied by unbearable pain. I guess you just have to weigh out the positive and negative.

joan

Auddonz profile image
Auddonz in reply to laroux

Totally agree Joan. Everything has its side effects but he is doing so much better now. He couldn't move before by himself, getting in and out of bed was a nightmare. What dosage is your husband on? Audrey

laroux profile image
laroux in reply to Auddonz

he takes 100mg/25mg, I believe 3tabs 6 times a day. Pretty high dose, but there have been studies to say if the effects are not adverse then it should be safe (within reason). The increase was gradual and has been beneficial. I know if he doesn't have it he can't move either and cramps up terribly.

joan

Auddonz profile image
Auddonz in reply to laroux

Joan, I believe that the pills taken throughout the day rather than just 3 times a day makes a difference. It did with my husband and he doesn't remember any of it when it was bad. He had a UTI as well, which did a horrible job on him. Emailed the Dtr that finally diagnosed him and he said it will effect them terribly which it did. BTW, PSP is in the Parkinson's family and happens to be the worst one you can have. He has been getting up in the middle of the night because he is hungry which does worry me. He has lost a lot of weight since this started. PSP itself or the meds, I just don't know. He has serious heart issues as well along with high blood pressure. Senior years really difficult. He is 77 and will be 78 in June. But having him home and mobile with the med makes him happy and me as well.

Audrey

You may also like...

Restlessness. Anything that can be done to help?

of days, he is constantly crossing and uncrossing his legs, sitting down, standing up (losing his...

Is there anything to be thankful for in PSP?

had only one UTI during her years with PSP. No hospitalization for Pneumonia from aspirating. No...

Is there anything that helps with hallucinations?

For about a week he asks us continuously to help him stand up.Then he walks to the door and he...

is there anything more i can do

Hi im new on here but mom has psp and my dad and i are her main caregivers just this last weekend...

disabled rooms in good hotels seem to be very few in number

rooms if we are to get away and have similar facilities liek a thome lol Jill :-)