Not giving up !: How do you find the... - Cure Parkinson's

Cure Parkinson's

26,570 members27,876 posts

Not giving up !

zadok459 profile image
19 Replies

How do you find the balance between accepting your Parkinson's symptoms without quitting or giving up. Fighting cause so much stress and anxiety. It is if my body produces adrenaline automatically to prevent symptoms - which leave me tense. Any advice??

Written by
zadok459 profile image
zadok459
To view profiles and participate in discussions please or .
Read more about...
19 Replies
MBAnderson profile image
MBAnderson

That's a tough one. We go through a process of denial, anger, grief, eventually growth, and finally acceptance. It's a real struggle to achieve acceptance, but that may be the only way we can find a modicum of peace. We used to be somebody else, but now we are a PWP. Even so, you are still the good person you have always been.

Enidah profile image
Enidah

This is a fascinating topic and one that I have mulled over. I broke a bone in my foot the end of May and so consequently had about 8 weeks of forced relaxation. I thought all my anxiety came from PD but with this situation I realized a good deal of it comes from that voice in my head that says walk, hike, bicycle, anything to outrun the PD! Since this is a very real help in controlling symptoms I am left with that voice and keep moving as the anxiety to control symptoms motivates me. Perhaps one day I will sit down with a sigh and say, oh f*** it. But not yet, not today.

zadok459 profile image
zadok459 in reply toEnidah

Ver true - the noise in your head about regretting - keeping it up - exercising harder and faster. Notallowing you the inevitable - symptoms

Asbhai profile image
Asbhai

My experience shows that falling into some kind of addiction gives relief from stress and anxiety and Begin to live life in compartmentsAlso The state of affairs maybe they can as thewill of Almighty Almighty Almighty God

rebtar profile image
rebtar

If you find a solution to this, do post it!!! :-)

I get tired of pushing myself to do the things I believe I need to do, to stay healthy with PD. So far, it's worked pretty well, with slow progression. But it's tiresome. Feels like my freedom to choose what I want to do has been taken away. I've gotten a bit more flexible, on occasion doing less exercise that I usually do, or eating a treat I usually avoid. That has helped, being less rigid while continuing to do the things I believe are helpful. My anxiety has decreased, but isn't gone. I'm making a point of having fun as much as I can. After all, even if PD has given me a lot of work, I also deserve to have fun! I agree it's about finding a balance. You can't fight your symptoms. Fight as much as you like, they'll still be there. So finding a stance that's committed to your wellbeing, but not fighting? Something like that...

Despe profile image
Despe in reply torebtar

So true. My husband feels the same way. He is miserable because he can't have "junk" foods he had occasionally, but has to eat/do the right things to slow the progression of PD. He has high hopes that B1 is going to give him his life back, and I believe it's working. Patience is the key, but sometimes I feel so overwhelmed that I don't know what to do. I have done everything I could to help my husband.

Erniediaz1018 profile image
Erniediaz1018 in reply toDespe

B1 all the way... I've been on it just a few days and I've noticed remarkable progress. Especially the dyskinesia has almost completely disappeared. 😁

Despe profile image
Despe in reply toErniediaz1018

So happy for you! My husband doesn't have dyskinesia. He only has RH and L thumb tremors, and a scooped posture although not bad. Hopefully, B1 will correct all your and my husband's symptoms. Patience!

zadok459 profile image
zadok459 in reply torebtar

Very good advice - I find it such a tiring engaging illness -it occupies you from the moment you go to the bathroom to tying your shoe laces and the exercise you di to fight back the symptoms. It slowly steals from you.

ddmagee1 profile image
ddmagee1

Accepting it for what it is, keep moving, exercise, realize that one could have something much worse than PD ( like ALS ), stay positive, do not give in to negativity, and concentrate on what you are able to do, not on what you have lost or perceive to be losing! Reach out to others, who may need support. It is more of a blessing to give, than to receive. Find appreciation for the small details in life and know that you have the ability to not let this obstacle stand in the way of enjoying your life, as a person with PD.

jeffmayer profile image
jeffmayer

Do you exercise I find it a huge help cycling or CV work in a gym as regards to acceptance I think it just takes time unfortunately we have no choice we have to fight this shite condition and not let it win and beat you all the best

ddmagee1 profile image
ddmagee1 in reply tojeffmayer

Exercise, range of motion, and resistance exercise is helpful, for me. Additionally, Dalcroze Eurythmics.

alaynedellow profile image
alaynedellow

Indeed a tough one. You have to accept as a) have no choice and b) accepting makes it easier to deal with. You have to give up what was and go with what is. Peace is wonderful but sometimes elusive. Mannitol has been superb in helping to get rid of apathy which helps me keep up exercise- yoga is fab for mind and body. I believe in being compassionate to myself and not be harsh when its a tough day, when physically i done in i feed my brain with mental stimulation. Accept the new you with love. Good luck

zadok459 profile image
zadok459 in reply toalaynedellow

Thanks - good advice. I'm too hard on myself. I'm a former soldier - so weakness is difficult to accept and a 'mortal' wound difficult to ignore. BUT I'M ADAPTING - everyday is a learning curve

rch21 profile image
rch21

I have found that it is a fine line for me between accepting that I have this thing called PD and giving in to it. Over time, I have come to realize that the symptoms are just that - symptoms, not me. I exercise daily to try to keep some of them at bay (such as doing balancing exercises to retrain my nerves to maintain balance) and boxing to keep retraining eye-hand-foot coordination, etc. But I also have to remind myself that when my symptoms flare up in an off period, that I am not those symptoms - it is easy to lose confidence in going out to dinner, for example, if you knock over your water a few times and need help cutting meat. While in this case there are relatively easy work-arounds, such as order a pasta or casserole dish when out so it does not require cutting, there are things I have had to give in to like stopping driving that do not have such easy work-arounds.

This results in frequent re-examining my abilities, decisions, etc. and more risk of giving in. I guess, for me, it is a matter of both mentally and physically being aware of myself, accepting that there are some changes and will be more, but not giving in to PD and not letting the limitations define me - not always easy to do.

ddmagee1 profile image
ddmagee1 in reply torch21

Very well expressed. That's sorta how I handle it, too. PD does not define me.

janers profile image
janers

Thanks for posing this question! It's a great point to reflect upon. It's like life in general, accepting what it is and yet working for something better. Keep your chin up and your face towards the sun! Let the shadows fall behind you, and smile. You're beautiful just the way you are.

jeffmayer profile image
jeffmayer

exercise and fighting back I find are the only two ways of dealing with this horrible condition when I exercise I find the adrenaline it poroduces beneficial for me I do prefer cycling on the road I feel you can gauge your effort more rest afterwards is important just not to much otherwise I feel I will go backwards again undoing all the good I have just achieved by exercise acceptance is part of the process

zadok459 profile image
zadok459

Thanks I also exercise and walk every day. I've recently added photbiomodulation

Not what you're looking for?

You may also like...

On giving advice...

No spots today, apart from one on my face which has tele-ported me back to a time when I was...

My Dad Seems to be Giving Up...

I'm American. from California. I live in Scotland. (I know, I ask myself how I got there too, but...
CariCanRun profile image

Not PD?

I am the caregiver for my spouse who was diagnosed with PD in 2013. He, like others on here had...

Giving regular Thiamine HCl / B1 another go, stopping Sublingual B1.

Hi Friends! Just thought I'd bounce this off you. I used to take Thiamine HCl B1 as directed by...

Doom and Gloom Are Not Inevitable

Since being diagnosed five years ago, I have read virtually everything I can find regarding...
jimcaster profile image

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.