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-   -   Can't take it anymore . (https://www.neurotalk.org/peripheral-neuropathy/186198-cant-anymore.html)

lined_in_silver 04-19-2013 07:49 AM

Quote:

Originally Posted by Mads (Post 974658)
Hi featherbullet,

Bless you ,I know how you feel -exactly. Lifes just been stolen away from us!. Just something that has helped me a little so thought id message you is having a fast acting med to top up and for surges in pain (breakthrough or spikes). As well as oxycontin , i have oxynorm (its fast acting sister). I assume your oxy is slow release - i find that doesnt cover the pain sufficiently.
I also take lyrica.I also cant function if i take too much - its horrid stuff. Have you tried topiramate?

A cream im trying is suppose to ease nerve/itching pain etc... Its Capsaicin cream. Ill let you know how it goes( prescription only).

Oil of magnesuim - i spray on joints - cant really say if its helping but anything is worth a shot.

Also im now on methadone for pain . It has helped a little.

Stay strong. As we read on site things can stabilise and even get slightly more tolerable

God bless x


Hi, I just saw this now. Oops.
I have tried everything you mentioned!! ( capsiacin cream,magnesium oil,on lyrica)
I was on instant release oxycodone. Now I'm only on the patch and yesterday all that they would give me is clonidine for withdrawals. At my pain clinic they prescribe minimal narcotics. They feel that you should find other ways to deal with any breakthrough pain.
Horrible huh?? However...I am ready to get my mind back again. I feel very dumb..and clouded. Quite sick often..can't explain it. Just not ME


I feel OK today. :)


It seems

lined_in_silver 04-19-2013 07:51 AM

Quote:

Originally Posted by ginnie (Post 976042)
I know the pain of being rejected for disability. I went three go rounds before it was granted. Also weened off morphine, so I certainly know about percocet and the withdrawls with that. Your doc. should have given you something to ease your way off the drug. I received kolonopin. Have hope that the sensations will not last, and that there are other medications that have less bad side effects.
Hope you have legal reps. for your claim. don't give up feather, it will happen. Most people I know have indeed been rejected a few times. I know how devestated you fell however. This system of ours, makes us suffer too much. You will be in my thoughts and prayers. ginnie:hug:

Thanks ginnie..it seems that we have similar situations. Trying to get disability is a lot tougher than I had imagined. I do have a lawyer working with me now. Were looking at another 6-7 months before I can go in front of the social benefits tribunal :/
I have klonopin, and it settles me a lot. But again, its addictive, so I try to take just .25 mg every other day as needed. You?
Hugs

PaulaJ 04-25-2013 10:57 PM

Don't give up
 
I totally feel your pain. I have been disabled since I was 24 and I am now 54. I just went through the most terrifying experience of my life. I realized I was having substantial blackouts. Periods of confusion got so bad that I no longer recognized my own name. My verbal output was totally scrambled although in my head I knew the answser I wanted to give it was not what would come out my mouth.

I have CFS, ADD, hypothyroidism, dysthymic disorder, chronic major depressive disorder, general anxiety disorder and of course, B12 deficiency and pernicious anemia which apparently as it has not been treated iin 10 years because of my insurance company denying treatment this is what caused my recent experience and possibly everything else.

At the ER they did a CT scan that proved no dementia or early onset Alzheimers but it took weeks in the hospital and weeks of out patient and advocating for myself to get my B12 levels tested. They are barely over 100. Now that I have an answer I finally have hope but I am here to find out what appropriate treatment should be to insure that I will get what I need to get well.

For me, faith has been what has gotten me thru. During that time that I did not even know my own name and thought it was 1916 I was writing on my daily forms give me B12 shots. Only God could have provided that information when I was in such a condition. It was not done and when I was released I continued to do my own research and got tested. Have faith. Get tested. Be persistent. You do not deserve to be feeling that way at your age, nor that way at mine for that matter.

I pray that you will find the answers and get the help that you need. Do not let the depression eat you alive and do not take no for an answer. Seek doctors that will listen to you and work with you. No one knows your own body like you do. I had to see several doctors over several years to get the tests I needed as I do not present normally. I also do not react normally to many medications. I just found this board and I hope to find some answers here. But, please do not give up. God has a purpose for all of us and you can get well. It just may take a lot of work and a lot of prayer and a lot of persistence and good doctoring.


Quote:

Originally Posted by featherbullet (Post 970783)
After 2.5 years of living hell, at 29 years of age .. After maxing out on narcotics and taking as much lyrica as I can function on, all the right supplements ,
Rest, time, tests , Losing relationships, friendships,putting immense strain on my family , being denied disability , and being terribly broke ...
I am out of hope , faith, and a will to carry on
I got the diagnosis of peripheral neuropathy.. But with no known cause.
In the morning, my hands are numb.. All of my muscles hurt and burn when I stretch. Burning from neck to feet .. That is relentless. I have tried all the lotions and potions. I can't just sit at home with ice packs all over me forever.
I'm not even 30.. Single , no profession because I had to drop out of school..
There is no hope. I have up on prayer ages ago.
Nobody wants to be around a whiny , negative person who is never happy and always in 24/7 pain.
I'm done. I'm just done. No desire to torture myself any longer.


Has anyone else ever dealt with crippling depression because of this horrendous disease?
Everyone I see on here is older .. No offence .. But my best years were still to come.


I had to get this out. Thanks for listening.


Stillfighting 04-26-2013 08:49 AM

disability
 
Sorry about your condition. I have two friends who are over 50 that are on disability. They both have severe pain issues, however. Both their doctors could only get them approved by promoting mental health issues. One with extreme anxiety and paranoia, the other with a learning disability and poor socialization skills. The second told me the other day that though he has severe back injuries from doing heavy labor. His doctor said that wasn't going to get him anywhere without the other. Sad to say but if you have to pull the crazy card, we won't judge you here.:D

lined_in_silver 04-28-2013 11:41 AM

Paula J-what a heart wrenching story. I'm so sorry. I am, however happy that you gave faith to hold onto and which led you to discover what ails you.
It is such a struggle to find answers. A LOT of trial and error. 2.5 years and counting for me.
Thanks for the encouragement.
I am sitting down with a pastor tomorrow who may help clarify my questions on God.
I lost all faith a long time ago. Praying never helped in any way.
I have 2 close friends in my life who want me to try to find God and have a relationship with him. We will see. I am skeptical.

Still fighting: I have to now wait at least 6 months for a court date to plead my case to the social benefits tribunal. Its infuriating that during this horrifying time, I have zero financial assistance. It is increasingly difficult in Ontario to obtain disability. Even with a hand written letter from my pain doctor, commenting on the neuropathy, cael tunnel, and psychiatric illnesses, they still refused me.:eek:
I have considered a psychiatric hospital countless times, but am afraid of many aspects.
I am tied into a lease at my apartment, for one. I truly am stuck.

The fentanyl has stolen my energy completely. I have hot flashes all day, as well as headaches. On top of residual pain and of course depression, anxiety, OCD, bpd..etc. its unbelievably difficult. Every minute of the day.

Thanks for reading...:grouphug:

ginnie 04-28-2013 01:47 PM

Hi Feather bullet
 
I do the same as you with kolonipin, as necessary, and not often. I sometimes put it bed side, then read and fall asleep not needing it. It is addictive. My doctor has watched me on this drug for about 8 months now, and she knows how far I can stretch it. Good for you feather bullet, to take as little as possible. I do this with pain meds too. I had hydrocodone, 90 pills, lasted from Dec. 5th until the last of last month. I think I did real good. I have stronger things, but have not used it at all. Take care of yourself and keep in touch. I am always here to listen. ginnie:hug:

lined_in_silver 04-30-2013 08:09 PM

Its extremely tempting to load up on drugs to dull emotional pain for me. But if I did that, I'd run out early and feel worse going through dangerous withdrawals.

Tried hypnosis today to quit smoking and it didn't work
I don't know why I bother trying to do anything anymore.

Thanks Ginnie. You're strong for stretching out pain killers. Its an easy way out.

ginnie 04-30-2013 08:18 PM

Hi feather bullet
 
You try, because the option is worse. It is human nature to give it your best shot. Thats all any of us can do. Been down that road of depression a time or two myself, and know how hard it is some days to drag my sorry butt out of bed. You keep giving it your all because you are a good person and truely hope for better results. Have you tried a physiatrist????? Treats the whole person, and may be a route to consider. You need a very compassionte doctor in your life, that can help you, when you feel so down. Depression always makes the pain worse. You are doing find, just talking here on Neuro Talk. this outlet, helps us survive too. Always glad to hear from you. Keep the effort going. I quit smoking cold turkey after two pack 30 year habbit. All it took was my father dying of thoat cancer. That will do it. Sometimes it does take a shock. Don't stop trying to put them down OK? try one day at a time. xxxginnie:hug:

littletexan77 04-30-2013 09:28 PM

Featherbullet, I joined this site specifically looking for people that were having the same issues that I was having - mine is lingering and worsening pain from an SCS implant back in Nov 30 last year. I did find a few people in my boat, but more importantly, I found a huge group of people that could relate to my pain, frustration, and depression. Knowing and talking to people that can relate to that part (despite the cause of their pain) was a huge help for me. Not a complete help, I admit, but a help. I will tell you something I've been keeping a secret until now. Last Sunday I called the suicide hotline because I snapped and the depression and loneliness took over. They helped me tremendously. Since then, because I really have no one here to turn to, I have learned to utilize the chat rooms. The depression and loneliness came back last night and I jumped into a chat room before doing anything else. I cannot express my thanks for the people that were there last night. Not only did I get hugs and support, they even had me in more back pain from laughing so hard before we were done. BTW, I will be 36 on Saturday - not too old, but probably old from your standpoint! I can still have a long way to go and another 50 or 60 years to live after I get through this bump in the road. Doc says mine will last about 5 years. It's a big, long bump, but it is just a bump none the less. I somehow hope my sharing something here helps make you feel just a little better, because a little better here and a little better there, really does add up! Good Luck, Best Wishes, and a big (HUG)

littletexan77 04-30-2013 11:52 PM

Just one more thing, maybe to give you an idea of where I am coming from emotionally, I started my own thread not long ago called "5 months since SCS implant and depressed" Not sure if you would care to read it, and I know there is a way to put links to these things, I'm just not computer savvy enough to figure it out! Anyway, keep your head up! (HUGS)


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