Hi, Barb,

I looked for FUSE Ointment but could not find it. Could you please provide where you found it on the internet? Would truly appreciate it!

Thanks,
Jen

I just found this! I must have overlooked it. Sorry! 🙂 I saved your number..thank you so much for reaching out to me! I'd love to text you someday soon 🙂 when is the best time for you??

No I'm not seeing ANY doc right now...I'm mad and frustrated with doctors that I've seen so far...so I'm taking a break!! 🙁

I told my husband the same! 🙁
I have noticed VERY MUCH that old injuries (which I have a lot of!) hurt more now...well a change over the years. But I've been in THE MOST pain since I had my last child and during pregnancy even 🙁 she is 13 months old

UPDATE-
After having a nervous breakdown at the beginning of December and being hospitalized for a week. I am now getting the medical care and treatment that I have been looking for!!!
I am driving 2 hours one way to get it, but I finally found the doc that is AWESOME and willing to listen and she is very thorough and I am very confident that I am in the right hands FINALLY!! My pain in now being managed by taking Nurotin...600mg a day...Tramadol...and a few other non narcotic meds...im glad that I'm not having to take Vicodin to live through the day..although I know If I had the Vicodin I wouldn't feel much pain at all, but at least I can tollerate the pain most of the time now. I also am very aware that my emotions are linked to my pain...when I get upset my pain increases IMMENSELY so I try deep breathing and to stay calm..I know it will take so time to make this a reaction so I don't even have to think about it...but it will be well worth it!!
Thank you all for sharing your story and giving your advice!! It's so "nice" to know I'm not alone in this 🙂
My heart, thoughts and prayers go out to you all!!! <3

I have been had anemia since high school, chronic neck pain and left shoulder pain since August 30th of 2000 from a car accident, kidney disease since 2004 (I had enclampsia with my 4th and last child in 2000. My immune system hasn't been the same since), Fibromyalgia and Chronic Fatigue Syndrome since about 2005. I use to love excercising, staying active with my kids, working, I loved life! In 2006 my body became extremely wore down after my husband walked out at the end of 2004, my mom died in 2005, 7mo. after she died I was dealing with a custody battle, and a rebellious teen that I was praying would live to see adulthood. I say all that to explain that I understand pain, fatigue and stress to the max! I have had doctors say I'm too young, I have heard the same line you have too, still do, "You don't look sick" while they have this look that I must be doing better, when I have progressively gotten worse with time. I know they mean well because they love me, but it can be disheartening, because it makes me feel like they just don't get it! My usual reply is to say" thank you, I'm glad I don't look sick", while I politely smile. I can pull it together for a couple of hours and put on my game face, but I'm done after 2 or 3 hrs out of the day. I take vicodine for the pain. I have taken the same dose for 11 yrs. and I take the 3 pills I'm perscribed for the day. Even with such a large medical file I had to be persistant and keep going back to the doctor to get that 3rd pill after being in nearly constant pain for the last 7 years! Doctors or so worried about addiction they would rather let you suffer and try every other med out there first rather than give you what YOU know what works. Mean while people with our condition suffer. I know they're not all like that because I had a fairly good doctor, but when she left I got stuck with a P.A. that wasn't listening and I was losing hope and feeling disrespected as a human being, so I quit that company completely and went to a different one. I explained to the new doctor that I know my body after years of being sick. I know my lab #'s, I know my pain level, I know when stress is affecting me worse, and I know I'm not addicted because I don't think about my meds unless I'm hurting which of course is anytime I'm active, but my dose is the same dose as when I first started taking it, plus there are 24 hrs in a day, 2 pills are not cutting it. I use to cry from miserableness at the end of the day, that 1 more pain reliever helps make it tolerable. I always have about 3 to 4 days left of medicine when it's due to be refilled unless I have had an episode where the pain is beyond keeping it controlled, then I have to take more, that hasn't happened in a few months. I also explained I have taken every medicine they recommended! Cymbalta, Lyrica, and several others. Some gave me weird thoughts, NOT cool! I quit those immediately! The Cymbalta worked for the pain and anxiety, but it also made me gain weight. After a couple of yrs of being on it, and then going off, I lost weight and my blood pressure came down to normal. High blood pressure can shut my kidney's down. I can't take anything else at this point that I'm aware of.- I am so frustrated with the medical community, it makes me sick. They need to listen to their patients and quit assuming they know best for every person. They're human and make mistakes daily just like us. When I saw your original message my heart went out to you because my oldest daughter who is 22 now has mild scoliosis, degenerative disc disease in her neck, she get's migrains daily, and she aches all over at this point. She has a 14 mo. old boy too, so she can't always rest like she needs to. She is also having trouble finding a solution to her pain issues. My suggestion to you is to be persistant in finding a doctor that will listen to you, even if you have to find a different one. (As exhausting as that is). Also avoid foods that cause inflammation. I was feeling better when we were eating organic, I was avoiding soda, and junk food. In general you feel better. Magnesium, calcium, and vit. B is suppose to help with inflammation and stress. My husband and I started researching vitamins and organic foods, as well as people who have had similar issues have shared with us what works for them. Some of them said excercise helps them, but I crash when I excercise. However speaking from experience, pushing through the pain and miserableness does help keep your muscles from deteriating. I found that out last year the hard way. I hope you find what you need to help you in your situation. I know our bodies don't react the same to everything, so you have to find what works for you and don't give up on finding a doctor that will have compassion for your pain and give you the right pain reliever.

Thank you so much for sharing!! I appreciate all that you've been through and all of your advice!! I think I found a doc who can finally help me...we will see 🙂

Back in the olden days...lol, when I first went to a Dr for my pain,he told me I needed to go see a psych because there was no such thing as Fibro. I told him he could go see a psych for not believing that people were actually suffering from Fibrocytis(that's what they called in the olden days). !! I really have to stress how much excercise helps. Sure it hurts as you're doing it, but the pain from the excercises and the Fibro is helped for maybe 3-4 hours, then it's do it all again. That's why I see no sense in going to a Chiropractor, all that money because I'd have to go 4-5 times a day to stay out of pain! The reason the Dr touched you is there are 19 Trigger points on your body that are painful to the touch. That's about the only way Fibro can be diagnosed. I hope you find some freedom from the pain.

PS, thank you WorkHorse 1 for mentioning the breathing for help with pain. I do deep breathing techniques for pain about 5 times a day. Breathe in deep through the nose and exhale slowly through the mouth. It's amazing what all this helps, even Panic Attacks!