New diagnosis and I'm struggling

Posted , 9 users are following.

I have been diagnosed with fibromyalgia, after seeing various medical professionals for over 3 years, had various treatments, paid thousands to a chiropractor, and tried so many meds. Now because there's nothing they can do it's fibromyalgia. I work full-time and my employer is not supportive at all, I'm in pain I just can't describe and feel like my life is not worth it. I have thought about death lots in this last year, and nobody understands how I feel. I guess I'm just trying to reach out, I hate the pain I hate my life!

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  • Posted

    Just remember that you're not alone...We walk the same unpredictable path everyday.

    Hugs🤗

  • Posted

    Welcome to the site. Everyone here knows and understands your pain and frustration. There are good days and bad. This is a place to vent as well as to get advice.

    Most of us are elated when we get diagnosed at first because we have a name for it and now people will realize we are not crazy or making it up. Then reality sets in. People still don't understand what you are going through. While the testing phase and habitual doctor appointments has ended you now have to find a treatment plan that will help you. We are all different and you will read about different meds, supplements, and treatments here. It's like getting a diagnosis. You have to keep going until you find one that works for you. Don't give up. We are here if you need us!

  • Posted

    Oh you poor dear! We all can understand your anguish and pain. But please don't take this as a life sentence! It is a manageable condition and you will definitely find ways to cope. I have had this condition for over 30 years now and I can still find things to be grateful for in my life despite trials and disappointments. You will have better days, I promise you. Flare ups often come after some extreme stress or emotional upheaval. Please remember that there are people in your life who genuinely care about you. It is true that in the business world, bosses usually do not show genuine compassion or empathy. They just see a production issue and profit. So don't get discouraged because of your boss's insensitive attitude. Many with FM have to face this situation. You are not alone as Emma mentioned sweetie. So many are struggling with this chronic condition among other issues. Just try to be kind to yourself and be balanced in your expectations. You must recognise your limitations. You need to realise that this is a chronic condition like many others, such as Lupus, etc,  and you need to state that as a fact. It is recognised in the medical journals and the research is going on. So never apologise or be afraid to state your needs and limitations. Inform yourself regarding any program or govt assistance that can help you in this regard. Never despair my dear! Things always seem dark when we are in pain and feeling worthless. We all go through those times. But this too shall pass. Just take good and gentle care of yourself as you would a beloved friend. No doubt you have lived through some very trying times in your life and many distressing situations like many FM sufferers. The body can just cope with so much. So not surprising that we end up developing these kind of conditions. You can do this! One day at a time. Never presume that things will not work out. Life has many twists and turns. Tomorrow is always a brand new day. Sending you some warm gentle hugs! Maggie xx

    • Posted

      Thank you Magbie2me,I'm actually sitting here crying reading the comments, I just don't know what to say. My family don't really understand, and just think I'm being miserable, I find it so hard to get into relationships because I don't have a social life anymore and then I think who'd want to be with someone who is limited. I just want the pain to go, I want to feel confident again and I want to stop taking medications that make me feel rubbish.

    • Posted

      You sound like an amazing and courageous person sweetie. Depression often goes along with FM. I don't know if you are taking an antidepressant but that may be of benefit to you. I cannot give you any advice on medication since I have never taken any except for Ibuprofen when I get a migraine. I have approached the condition holistically with some supplements and mainly nutrition. Organic Collagen powder has really helped with my pain. I drink green smoothies with Kale, Spinach, a bit of banana or blueberries, carrot, chia seeds for omega 3, a bit of Maca powder to balance hormones, probiotic, and rice milk or almond milk. Other ingredients can be added as well. I add this all to a NutriBullet and drink it every morning. I have learnt that nutrition deficiency can cause a great deal of symptoms. B complex is an absolute necessity for us since our nervous system is greatly affected. Doing our best to balance our bodies vitamin and mineral needs can have a major impact. That is what has helped me cope and manage this condition all through the years. Keeping a 'feeling' journal has helped greatly as well. Getting out our emotions helps us to reason better and think more rationally. Give yourself the support you need sweetie. Family cannot always relate. Learn to value and respect the amazing person you are. Warm hugs! Maggie xx

    • Posted

      Thank you Magbie2me, your words mean a lot along with everyone that has taken the time to comment. I was prescribed an antidepressant more to help me sleep, but it made me tired more than usual, and with a full-time job it was hard. I have spoken to a counsellor looking at ways to deal with the stresses, didn’t really help. I am willing to try alternative methods and gp doesn't mention B complex. I've been in pain for so long, just wanted some relief. Thank you for your very kind words.

    • Posted

      Oomph like Maggie I can't take meds and have had to try other methods. Have you tried sam e? It has helped with my mood and doesn't leave me with the side effects of antidepressants.

    • Posted

      My pharmacist has suggested drinking a glass of ginger water and to go back Monday, he noticed all the strong meds I was taking so has suggested trying other things, so I am willing to try.
    • Posted

      You have to watch your liver and kidneys with taking a lot of meds. I know you are worried about having to go to the bathroom with urgency. I had stress incontinence. It's frustrating and embarrassing. Thanks to this site I had cut out caffeine soda and it made a difference. Apparently it was aggravating my bladder. I now start the day off with green tea with mint and ginger and then a green drink. It has helped with stomach issues, inflammation, the function of my liver and kidneys, not to mention minimized the incontinence to a rare occasion from a multiple times a day occurrence. There are many supplements that help but you will need to talk to your doctor and pharmacist to see if there are any interactions.

  • Posted

    Hi Oompa, I understand everything your talking about. I have also had feeling of suicide because the pain is unbearable. I have 3 kids and a husband and I thought about how me taking my life would effect them. I cried out to God because I had a strong feeling of suicide. I look up scriptures to help me. I read (My soul find rest in God my hope is in Him.) This verse helped me. I also ask for referral for a psychologist and was referred christian counseling to try to seek ways to help cope with pain. I wasnt look for a pill but ways to cope and someone to listen. The pain is horrible but your life is worth it. What gets me through is knowing someone is worse off than me with no limb, not able to take care of themselves. I use inspirational music so I sing through my task the pain is still there but it occupy my mind. I use scriptures to encourage me. It's depressing going to the doctor office and being in pain 24/7.

    I was in pain and working for almost 1 yr before diagnoses. I was working full time and had to stop working because I weak. I tried aqua and physical therapy and I was still in pain. Never lower than a 5. I was of work from Nov 2014 to Aug 2015. I worked at a job last stressful but I was still in pain I was give Cymbalta, Lyrica,Gabapentin. Not effective. i was diagnosed with fibromyalgia in Aug 2015. My Rheumatologist referred me to the pain clinic I had steroid injections, butrans patch which help for about 1 month with some pain. I been on Norco, fentanyl patch you name it. Still no pain relief. I worked in pain using icy hot and biofreeze which helps cool the area. I had to use it a least 2x a shift. Still in pain. All my test are normal . Shows at little inflammation. I tried stay active and exercise regular and again had to icy hot just to exercise. Stay horrible pain all the time. Pain in neck, shoulders,back,hips, knees, inner ankles and heels. If cold my hands are stiff and painful. I have been in constant pain 24/7 since Nov 2014. I want scream and cry. I feel miss understood. I feel like the doctors are insensitive and not hard enough. All my doctors are giving up on me. Read my recent discussion and you will see why.

    • Posted

      Thank you kikirae,I've looked to God often but nothing works, tried lots and just getting fed up

    • Posted

      I'm fed up with pain and doctors and ineffective too. Don't lost hope. I have read through other that it takes our professional to help get the help they need sometimes. Try looking for new Rheumatologist and check their reviews. I know persistent payoff. I been trying to get into U of Michigan because doctors do not what to do. I have been begging my neurologist for help and very insensitive to my pain and conditions. My Rheumatologist referred but I call for my appointment. I was given 6/16/17. Way too long. I finally call 2 days ago ask my rheumatologist office to call they give them May 22 and than my rheumatologist call yesterday and I call today. I been in horrible pain, barely able to walk and do basic task burning and tingling all over my body. Migraine daily sharp pain in my etc... Everyday something new. May health has declined so much on 6 months its unreal. I understand I leave the doctor office crying and disappointed every time. Hope I get answers I need. Just wanted to share to encourage you to keep hope and seek other options for care if you not getting treatment and answers you need.

    • Posted

      Thanks kikirae for the reassuring words. Something has to give. I hope you feel better too.
    • Posted

      I thought I put U of M called me today. Mr rheumatologist told them to put me 1st on there cancellation list. I have been calling almost everday the last 2 weeks. Prayer and persistent.
    • Posted

      Thank You praying for answers from U of M in 2 weeks.

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