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DiscussionAutoimmune? Undiagnosed and don’t know where to go next
Autoimmune Diseases | Last Active: Oct 12 11:44pm | Replies (166)Comment receiving replies
Replies to "I have been actively fighting something for over 4 months now, since June 22nd. I apologize..."
@heatherdoney74 I’m so sorry you are going through this. I have had many of the symptoms you have described but not all. I have Sjogrens Syndrome, Lupus, Myasthenia Gravis and Rheumatoid Arthritis. The debilitating pain is so awful and people who don’t have it don’t understand. Hang in there and don’t give up fighting for answers. After the birth of my three children and going thru menopause the last three years have been the absolute worse and most painful times for me. Seems like hormonal changes have played a big role in affecting my diseases. Start documenting everything and make a three ring binder of your different doctor visits. Call and get copies of the office visits and put in your binder. Do whatever you can to get to Mayo Clinic. I have gone to the one in Rochester and I’m sure they can get to the root of your issues and figure out how to manage your pain. I know you feel like you can’t go but try to.-see if a fam member could go with you. I fought my hardest to get up every day. I was either going to be in pain in bed or in pain doing what I needed to do. Either way, I was in pain. Drink lots of water, stay away from artificial sweeteners. Caffeine triggers migraines for me. Are you vitamin deficient-has your PCP checked that? What’s your GFR (kidney functions)? I had trouble breathing that kept getting worse and it ended up being acute kidney failure. Keep fighting for answers. Praying for you.
HEATHER, My thoughts and Blessings go out to YOU! What you have is how I found Mayo Connect! It was in June of 2018 it hit me with a Monster Headache! I won't go inot all the details but they very much go along with what you went through! I've gone through Stage IV Colon cancer, severe Brain Injury, but nothing was worse than what this is!!
I went through every test and examination in our entire Hospital structure! They could find nothing! Finally watched a program on Professional Golfer Jimmy Walker. He and his wife finally after 20 + visits to doctors around the country. Finally came up with Lyme Disease! Started doing research like you and learned what you have learned.
There are several Good Web sites that explain alot about the Disease. BASICLY THERE IS NO CURE, ONLY CONTROLLING THE MISSORY!
In my case I had all the same symptoms you have, lack of energy, balance, Lyme Brain Fog and many other symptoms! My Worst Symptom was the Headaches. They were 24/7 in most cases.
Finally out of accident my PCP and I stumbled on to something to help. I took Oxcyconone periodocly for Burcitus in my right hip. I found the headaches went away!
I found by taking one when I wake up and then one about 2:30 PM I was functioning Great. So that's what I do!
I take a couple of herbal supliments to help certain symptoms.
(I don't even tell anyone what I take, so I won't be considered a Opiod Addict!)
My PCP is a very old school dr. and understands what I have been through! If I go to another dr. I get the lecture about Opid Abisie.
In my research I have found important info.
Lyme Disease mirrors other dieases. Fibromyalgia, lupus a,d West Nile! All of which there is really no cure for.
Since I still run my own company not working is not a option!
But I have found if I schedule an hour of down time in the early PM it really helps me function thoughout the day.
Stress is also a Big Factor! I just got through 3 weeks of Stress and fatigue and felt like Crap!
I spent this last weekend doing nothing and catching up on rest. Feeling really good now! You can reverse the over doing it by rest.
Please let me know if you have any other questions!
I would be Glad to Help!
My Blessings to You!
PS, I forgot one other thing, my last visit with a dr. recomended either Yoga or TaiChi! My YMCA has a Silver Sneakers Yoga Class that has really helped! The last thing is about every 45 days I have a Full Body Massaage using CBD Oil. Really is an energy Booster!
Sundance(RB)
Listen to your Body and not doctors! I know that sounds Crude, but many on Mayo Connect will agree.
My Best wishes for YOU!
Sundance(RB)
Will do. Thanks again so much!
Hello @heatherdoney74,
I tend to agree with Becky's (@becsbuddy) suggestion that you have your records sent to a large medical center like Mayo or a university medical school. These types of medical centers tend to be multi-disciplinary, which means they have teams of doctors from different specialty areas who work together for hard-to-diagnose problems. Many of us on Connect have had hard-to-diagnose problems and have eventually found an answer. It does take determination and persistence. So please keep advocating for yourself and looking for answers.
Will you post again?
Hello @heatherdoney74, Welcome to Connect. I know it can be quite discouraging seeing so many doctors and not being able to get a diagnosis and treatment that helps. I'm glad you are searching for answers and learning as much as you can about your condition. I'm tagging our moderator @ethanmcconkey to see if we should move your post to the following discussion where it will receive more visibility and you will meet others who talking about Lyme disease.
> Groups > Autoimmune Diseases > Lyme Disease
-- https://connect.mayoclinic.org/discussion/lyme-disease-1/
Have you thought about getting a second opinion at a large teaching hospital or at Mayo Clinic where a team of different specialists work together to diagnose your condition?
If you would like to seek help from Mayo Clinic, contact one of the appointment offices. The contact information for Minnesota, Arizona and Florida can be found here http://mayocl.in/1mtmR63.