Which helps your pain the most?
Moist heat and baths - 14.3% - 1 votes
Ice - 0.0% - 0 votes
Supplements - 0.0% - 0 votes
Muscle Relaxers - 14.3% - 1 votes
Narcotics (Loritab,etc) - 57.1% - 4 votes
Exercise - 14.3% - 1 votes
Kagendo
Regular Member
Joined : Apr 2012
Posts : 49
Posted 4/23/2012 3:41 AM (GMT 0)
I am 23 years old and a newly-wed. My life looks nothing like my peers' and I've lost all friends my own age. I can't go bowling because it kills my wrists or go to the movies because medication sucks our bank account dry. I am a Christian and I continually look for the purpose in what happens. I don't feel bitter about my diseases. But I do try and make sense of it. One thing I struggle with, especially during flares, is finding purpose or feeling productive. Any suggestions? I read a lot, watch a lot of movies. But I absolutely love the outdoors and miss being outside. This week I have planted some herbs and watermelons. I figured it would be a simple little project to help me feel productive. But I don't want life to permanently be like this. I'm trying to get on disability but we all know thats a million hoops to jump through and my young age does not help. Also because of my age, doctors don't want to prescribe pain meds for me because they figure nothing is wrong with me and I'm just abusing them. I had a great doc but it just got too expensive. I need tips. On purpose, disability and pain. My hubby and I plan to move to Africa within the next five years. We'd go now but we really need to get my health somewhat stable first. Help!
Kagendo
Acheybody
Veteran Member
Joined : Nov 2008
Posts : 6036
Posted 4/23/2012 5:24 PM (GMT 0)
Hello, Kagendo, and welcome to the forum. I'm sorry you have to deal with this at such a young age, because it's no small matter (as i don't need to tell you.) I was only a few years older than you when I started having symptoms, so I know how frustrating it is.
I'm not one to say I know what the purpose for this affliction is, but it certainly does make us more compassionate toward others - how could it not? We know that people can be in great pain, and have severe suffering, and look "just fine," that tests can show someone is "perfectly normal," and yet be far from it. We also learn patience because - well - we don't have a heck of a lot of choice!
Kudos to you on planting a garden. That will lift your spirits! :)
When I was young, my doctor didn't want to prescribe pain meds for regular use, either, although I did have some for occasional breakthrough pain. I got by with a daily antidepressant for sleep and raised Serotonin levels - Nortriptyline. (Now I do take narcotics daily, but I have more going on, too. I still wish I didn't need them, and hope to come off of them all someday.)
Have you checked out Fibro 101, the second thread on this forum? There's so much helpful information there, on many pertinent aspects of this invisible condition. I hope you post often, and become part of the "family." We support eachother greatly, because we all get it.
Debbie
Kagendo
Regular Member
Joined : Apr 2012
Posts : 49
Posted 4/23/2012 5:31 PM (GMT 0)
Thanks, Debbie!
I was looking at your Diagnosis at the bottom. We are quite similar. Even with the hearing loss which is believed to be Menieres! That shocked me. My mother also has that. I've found that Mechlizine (sp?) works for me.
I am on a very low dose antidepressant (Trazadone) at night. I wonder often if I should be on something stronger. But my husband and I have just moved states and I'm on the hunt for a good doctor again so I'm in that horrible limbo. Praying for disability to come through.
So good to be understood.=)
Kagendo
MyselfRedux
Veteran Member
Joined : Dec 2009
Posts : 6232
Posted 4/23/2012 6:18 PM (GMT 0)
People have to find their own way through their life. Comparisons with others will only bring you down further. Your job is to build yourself up.
For me, personally, my job gives me a good deal of focus, even though I currently do not like it very much.
For the past three years, I have been pretty depressed, and have found it harder to find things to do that give ME joy. I certainly hope that the worst of the depression is past me. Find something to do every day. You do not need to give up the outdoors-that's defeatist thinking. You just need to find what you can do that will allow you the enjoyment as well as not be too taxing.
I do water aerobics, and bike with my partner. I love to cook. I read a good deal. I enjoy sports. TV and movies do not really distract me, since I am a terrible acting snob. I enjoy planting my herbs, feeding my birds, and doing battle with my squirrel.
jmw
Regular Member
Joined : Dec 2011
Posts : 161
Posted 4/23/2012 7:30 PM (GMT 0)
I voted narcotics (vicodin 5mg to be exact) but I found different things work depending on the amount of pain I am in. I take savella as well as several suppliments but those help control the fibro, not provide instant relief. I prefer using either a heating pad or my bed buddy to first try to bring some relief before taking a pain pill. Don't let this disease ruin your social life. If you can't go bowling you can still go and spend time with friends, even if its sitting there keeping score or playing cheerleader.
Springsun
Regular Member
Joined : Oct 2011
Posts : 59
Posted 4/25/2012 4:27 PM (GMT 0)
Hello Kagendo,
Your post Purpose?, caught my attention. A couple of weeks ago, I also posted a thread entitled - Purpose? I think it's on pg 4 now. I got some great responses from others who are sharing similar feelings. To relax and let life just be, is one thing which really helps and has always been a challenge for me, ill or no.
Congratulations on being a newlywed! How wonderful! :) I celebrated my 18th anniversary yesterday with my husband.
I am also applying for disability. I have been denied 3 times. I had a hearing before a judge last summer and re-applied starting all over in January. Good luck to you. It is a giant pain in the butt! I really believe in my heart though, that I deserve it. I think of it as, if I am approved, it will be a blessing for my family. No longer earning an income has been the most difficult thing for me in being ill. Not being able to "pull my own weight" as I have done my entire life. By earning money, I had determined my worth in the world. But, isn't this what we are taught? We become of value when we are successful? Which connects back to purpose in that many people believe who they are is what they do for a living. I have learned this is not true. I am still working on this, but have realized who I am or my purpose is not about money.
I love to plant a garden and flowers too. It takes me a lot longer now. But, I still plan to do it again this summer. The weather where I live has not been to good yet, only a few warm days sprinkled in. Most recently this past weekend, but it went from 50's to 80 and the quick change in temperature was too much for me. I could do little.
I am 50 however your question about purpose doesn't become defined by age. This illness is difficult at any age. I do not look like my peers either, or more importantly I do not look like what I thought I wanted for my life at this time. My youngest son is nearly grown and when I was your age, my children were little and I dreamed of what it would be like after they'd grown and left home. The plans, the traveling, the doing things one can't while raising children. All has changed. My plans that is... My plans weren't real though. They were only thoughts.
In the past couple of weeks really concentrating on this - my purpose - I have come to a conclusion that I am living my purpose. Is it crazy to consider this illness has come to teach me things that otherwise I would not have known?
I hope you can find peace of mind. I really needed to stop feeling quilt and trying to be something I can't. To accept my abilities for what they now are, so that I don't continue to keep letting myself down. Like I said... I am still working on this!!! I am trying to be more patient with myself and it's not easy. C is the new A!
My best to all!
Kagendo
Regular Member
Joined : Apr 2012
Posts : 49
Posted 4/26/2012 12:40 PM (GMT 0)
Hey guys! Thanks so much for the comments! And also for the poll....57% said narcotics work best...I totally agree but I can rarely get them. I want my doctors to understand that I want quality of life and I will take the narcotics risks to have that. Thanks also for the understanding and encouragement. Sometimes I think that what I need most is to be validates since so many people shoot us down or call us lazy or Docs ignore us. Pray for me...calling the doc again today to try and get refills.
Kagendo
(Fibromyalgia, Chonic Fatigue Syndrome, TMJ (with 3 surgeries), Hypothyroidism, Addison's Disease (maybe), Candida, Ulcers, Seizures)