Tumid Lupus with SLE Symptoms?
Hi! A couple years ago I visited the Mayo Clinic, which ultimate led to a biopsy and tumid lupus diagnosis.
Since then, I've also gotten the SLE label. While I don't have positive ANA, I have every SLE symptom under the sun (including tendinitis, painful joints, R.A.-like nodules and deformed finger joints, MS-like symptoms/spasms/muscle weakness, hair loss, 0 in both eyes on Shrimer's test, tachycardia/flushing, some high creatinine readings, history of colitis/lower G.I. bleeding, vasculitis bruising, looped capillaries, blah blah blah).
I've done CellCept (which helped a lot but caused me to puke all the time and lose 50 pounds). I also (miraculously enough) qualified for Benlysta and still go for once-a-month infusions. It doesn't last as long as I'd like, but it's changed my life. (I literally live for the first 2 weeks of the Benlysta cycle). 🙂
I understand tumid lupus is fairly rare, and that only 5-10% of tumid lupus patients have SLE symptoms (and almost none of those have positive ANA). I'm wondering if anyone else out there fits this profile? If so, I'd love to compare notes. Thanks!
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Yes, I fit the profile and it's been a roller coaster of a ride. Doctors, many really don't understand that it mimic so many other things. Wasted thousands of dollars on tests. Understand there is no easy way to state everyone has same profile. We all have similar symptoms and depends of doctors knowledge of Tumid Lupus and or SLE. Then it's the side effects from chemicals they put you on also. Someday I hope they will find a better test then ANA for those of us that don't show positive, yet have all the symptoms. .
Hi @pennyjo33, Welcome to Connect. Thank you for joining the discussion and sharing what you've learned. I'm tagging @mnkennedy, @pdesar65, and @lanakaymedina to see if they are able to share any information or suggestions with you.
Have you done any research on diet to help with your tumid lupus symptoms? From what I've read there is no special diet but there are some things to avoid and try.
Lupus Foundation - Diet and nutrition with lupus
-- https://www.lupus.org/resources/diet-and-nutrition-with-lupus
I have had Tumid lupus since age 14yo. I am now 44yo. My daughter has SLE with a positive ANA. I have a Negative ANA. I also have all the signs of SLE and googled it and came across your post. I may have a diagnosis of SLE from my Rheumatologist I'm not exactly sure. But I am going to Birmingham to another Rheumatologist for further testing. My joints and muscles hurt me daily. I am taking Enbrel and Plaquenil 200mg twice daily. I have noticed some improvement. But in 2018 was admitted to the hospital with severe anemia and no major cause of blood loss. I had been treated for what my GI Dr. Said looked like a bad case of Crohn's disease and a duodenal ulcer which was superficial. Ive had kidney issues since my teen years also. Your case sounds so much like mine! I had been looking at benlysta online and it sounds like a good one. I do hope she will tey me on this drug also!
Helllo @tdani75, Welcome to Connect. It sounds like you have a lot of experience dealing with Tumid Lupus. I can't imagine how hard it has to be to have the disease at such a young age. I think it's a good thing to learn as much as you can like you are doing and become a better advocate for your health. Have you discussed the new drug Benlysta with your doctor? Here's more information in case you haven't already seen this one.
Lupus Foundation of America - Benlysta: What you need to know
-- https://www.lupus.org/resources/benlysta-what-you-need-to-know
I'm tagging @pennyjo33, @lanakaymedina, @jessicanpayne and @seesawer who may have some suggestions or helpful information for you.
Hello @lexonpark, Since you mentioned you have been diagnosed with Lupus I'm wondering if your question might have more visibility in the following discussion where other members may share your symptoms.
> Groups > Autoimmune Diseases > Tumid Lupus with SLE Symptoms?
-- https://connect.mayoclinic.org/discussion/tumid-lupus-with-sle-symptoms/
You mentioned the ultrasound showed benign lymph nodes. Did the doctor give you an explanation? Just wondering if benign means a tumor on the lymph nodes or just swollen lymph nodes which can be a symptom of lupus.
Living-Symptoms of SLE - lupus
-- https://www.lupuscanada.org/living-symptoms-of-sle/
<p>Found some Nodes in my neck. Had an Ultrasound Benign Lymph Nodes. Anyone with Immune Diseases have this experience. I have also Been Diagnosed with Lupus.</p>
Hi @lexonpark you may have noticed I moved your post to this discussion that @johnbishop mentioned so that you can connect with others who have similar experiences. Simply click VIEW & REPLY in your email notification to get to your post.
I'd like to repeat John's question and ask if a doctor has given you an explanation for the lymph nodes?
I received my results when I went for my IVIG. So busy talking about my experience with Gammaguard (was getting Gamunex) that we didn't talk about the Ultasound report. Will make an appointment with my Internist and Rheumatologist. Will also speak to my Hematologist on my next visit.
Hello @ejlm, Welcome to Connect. I know you must be terribly frustrated trying to figure out what's causing your symptoms. From what I have read, one of the symptoms of Lupus is the butterfly rash across the face.
Mayo Clinic - Lupus Symptoms & Causes: https://www.mayoclinic.org/diseases-conditions/lupus/symptoms-causes/syc-20365789
PubMed also has some information that you may find helpful here: The Butterfly Rash and the Malar Flush. What Diseases Do These Signs Reflect?
-- https://pubmed.ncbi.nlm.nih.gov/1824645-the-butterfly-rash-and-the-malar-flush-what-diseases-do-these-signs-reflect/
I'm tagging our moderator @ethanmcconkey to see if we should move your post to the following discussion where it will receive more visibility.
> Groups > Autoimmune Diseases > Tumid Lupus with SLE Symptoms?
-- https://connect.mayoclinic.org/discussion/tumid-lupus-with-sle-symptoms/
@ejlm have you thought about getting a second opinion at a major teaching hospital or Mayo Clinic? If you would like get a second opinion from Mayo Clinic, you can find the contact information for the Minnesota, Arizona and Florida campuses here http://mayocl.in/1mtmR63.
Thank you John for the suggestions:) I have thought about the Rochester mayo but have not looked into what I would need to do to be seen there.