No diagnosis chronic pain
Hi everyone I'm new here. I would love some advice/comments on what I've been dealing with for around four months. It's a long story thankyou if you read and respond.
Around the end of January I started getting intense burning pain on the top of my legs and middle of abdomen. No rash or Marks on the skin just intense pain. I tried ibuforen, lidocaine gel, advil tylenol nothing helped. Started with primary care doctor she said to use lidocaine gel and ordered blood test. Blood test results all fine except for slightly low vitamin d deficiency. She said to start vitamin d pill I have been for months levels gone up and no relief in pain. Then went to pain clinic they did cortisone injections directly to abdomen. The injections gave me a horrible reaction that I ended up in the er for. Started on predisone and benadryl for 10 days. Once allergic reaction was gone same exact pain. They started me on lyrica made pain worse. I went to a dermatologist who said that it had to be nerve pain bc theres no rash on the skin she said to go to a neurologist. I went to him he did blood test ct scan and everything normal. I'm at a loss š I've been on lyrica, gabapentin, tropokendi, cbd cream from neurologist, acupuncture/herbs, chiropractor and laser treatment, muscle relaxer and tramadol. I'm not on any medications right now everything seems to make it worse. And creams I put on my skin break it out horribly. I'm at a loss and so miserable. This is such a mystery and no doctors can help me. I want my life back š !!!
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Hi Ginger....thank you so very much for your reply! I will be going to the MN location. Itās nice because itās only a 7 hour drive for us. I will definitely write down a brief history and who Iāve seen and whatās been done. Thanks again 😁🙏
Thanks a million, @richman54660....itās great to have support and appreciate you sharing your knowledge and experience with me! Thereās always more I learn and am grateful to have folks like yourself that have also walked in my shoes. Far too many doctors here have basically told me itās all in my head....well, I sure wish they could feel what I feel...then theyād know, itās not in my head. Thanks again!!
@mrea Forgive me if I missed this but, have you ever been seen by a neurologist or will Mayo MN be your first experience seeing one? I'm real happy for you finally going!
@rwinney Iāve had a neurologist for many years. Itās funny, but even with just a brief conversation with Mayo, they immediately scheduled me for their Department of Neurology....Iām really impressed!
Super! Every Neurologist is not built the same, as you may have heard already through this forum. They each have different levels of expertise and knowledge. Did your current neurologist offer you a skin punch biopsy?
@richman54660 I had to smile! When I moved up here, my hematologist oncologist sent on her records to my new oncologist, who I had picked out before the move. He is Mayo Clinic trained. They received 99 pages by fax, before I had even made the appt!
@mrea I have a bag that goes along with me. I admit to OCD tendencies, fair warning. In this bag are copies of all lab work for last 5 years, sorted by provider, plus chart notes. A separate folder has all biopsy results, scans, reports, etc. sequenced chronologically and indexed on first page. While it sounds to be overload, because I have a rare mix of issues, things can be and have been pulled from my bag during a dr visit, without having to go request/lookup.
@mrea Wishing you a safe drive to your appointment. I hope you let us know how your experience goes.
Ginger
@gingerriley I will absolutely let you all know how it goes 😁. Iām kinda getting excited....who ever thought weād get excited about seeing doctors 😂
@gingerw Now, I have to smile! You are my kind of girl. I too have a little OCD and have an accordion storage file system that can travel (if not too heavy for me to carry -haha).
me too back several years worth
👍🏼