Seeking Assistance with DMSO-Related Issues
Greetings, everyone. (I am a 34-year-old male, standing at 1.86 meters tall and weighing 70 kilograms.) Since February 2024, I have been enduring what seems to be a partial, yet irreversible impairment, which I suspect—though I can't confirm—might have resulted from my use of DMSO while walking barefoot in a vineyard. Is there anyone here who can offer guidance on how to move forward after dealing with this for such an extended period? I've visited the hospital on two occasions, where the medical staff attributed my symptoms to possible drug use; however, all relevant tests returned negative since I do not consume any drugs. Presently, I have only received an ambiguous diagnosis suggesting multiple sclerosis. I appreciate any assistance you can provide.
Answers (1)
8/18/2025, 3:41:45 PM
OpenHealth AI
I'm sorry to hear about the challenges you've been facing. It sounds like you're dealing with complex symptoms that are deeply affecting your life. Here’s a structured response to help guide you forward.
Main Points:
- Your symptoms may be related to the DMSO use, but a clear diagnosis is crucial.
- Understanding your condition and managing your symptoms can help improve your quality of life.
- Actionable next steps include self-monitoring and lifestyle adjustments, as well as exploring support options.
Explanation:
DMSO (dimethyl sulfoxide) is often used for its anti-inflammatory properties but can cause side effects or reactions, especially if absorbed through the skin. Your suspicion of it being related to your symptoms is not uncommon; however, without a formal diagnosis, it’s challenging to pinpoint the exact cause.
Multiple sclerosis (MS) is a neurological condition that can cause various symptoms, including fatigue, mobility issues, and numbness. If you've received an ambiguous diagnosis, it's crucial to seek clarification on your symptoms and their management.
Prioritized Next Steps:
-
Symptom Monitoring: Keep a detailed diary of your symptoms. Note when they occur, intensity, and any factors that may influence them (such as activity, diet, or stress levels). This information can be valuable for healthcare providers.
-
Nutrition and Hydration: Maintain a balanced diet rich in antioxidants and stay well-hydrated. Foods such as fruits, vegetables, whole grains, and healthy fats can support overall health.
-
Physical Activity: Gentle, non-strenuous exercise can help maintain mobility and reduce stress. Consider activities like walking, swimming, or yoga, which may also aid in relaxation.
-
Mental Health Support: Chronic conditions can take a toll on mental health. Engage in stress-relief practices such as mindfulness, meditation, or simply talking to friends or family about your experiences.
-
Seek Specialist Input: If you haven’t already, request a referral to a neurologist who specializes in MS or similar conditions for a more thorough evaluation. Having a formal diagnosis can guide your treatment and management strategies.
Please take care, and remember that it's okay to seek help from professionals who can provide the support you’re looking for in dealing with your symptoms. You're not alone in this journey, and there are paths to improve your situation. Let me know if you have any other questions or need more information!
Related Questions
Understanding Post-Surgical Pain After Ganglion Cyst Removal
I’m 17 years old (female, though I prefer He/him pronouns) and I have Ehlers-Danlos Syndrome (EDS) along with Dysautonomia. Currently, I’m not taking any medications that might impact my situation apart from an SNRI and birth control to manage cramping. Around a month ago, I underwent surgery to remove a ganglion cyst located on my dominant wrist (the right one). This cyst had been present for roughly three years, and despite my doctor attempting to aspirate it, the procedure was unsuccessful due to its firmness, leading to surgical intervention. This cyst significantly limited my wrist mobility. Now, after approximately four weeks post-surgery, I can say that my wrist is mostly improved. The scar is healing fairly well, and I’ve regained about half of my wrist’s mobility compared to the left one. Yet, I still experience significant pain when I move or apply pressure on the area that housed the cyst. Is this pain considered normal? Additionally, my fingers are in constant discomfort, and my wrist seems to dislocate frequently. Due to my EDS, I am accustomed to joint pain and dislocations, but this particular pain feels more severe than what I usually endure. When I brought this up with my surgeon, he dismissed my concerns, stating that such dislocations are common for individuals my age. However, I experience dislocations at least twice daily, and the process of resetting them creates such a loud sound that I've been asked to leave classes to avoid disturbing others. Is this normal? Could it be related to the cyst? Moreover, about four days ago, I noticed a small lump forming on my wrist just above the surgical area. When I consulted my doctor about it, he informed me that it was a benign fatty tumor and assured me it wasn't a serious issue. However, I've never encountered anything like this before, and while the lump is not painful, soft, and relatively small, I’m puzzled about its sudden appearance. Why did this occur, and what could explain my doctor’s nonchalant attitude towards my symptoms? I understand that experiencing pain and limited mobility after surgery is not unusual, but given my doctor’s dismissive approach towards my concerns, I felt compelled to seek insight here as well. He often seems skeptical about the symptoms I report, making it difficult for me to fully trust his evaluations.
Seeking Answers: Unexplained Symptoms
Profile Information: - **Age**: 15 - **Gender**: Female - **Height**: 5'3 - **Ethnicity**: Caucasian **Medication Regimen**: - Lisdexamfetamine: 40 mg daily - Famotidine: 20 mg, twice daily - Cetirizine: 40 mg daily I have been experiencing persistent pain for as long as I can recall, even before I started taking any medication, so I am skeptical about the drugs affecting my condition. Below is a compilation of my symptoms that I can remember offhand. My family has been advised on multiple occasions to consider testing for Mast Cell Activation Syndrome (MCAS) due to the alignment of my symptoms with the condition. My latest physician conducted laboratory tests to evaluate my tryptase levels without an initial baseline measurement. This was taken roughly 1.5 hours post-flare-up, which came back low. Consequently, she concluded that I do not have MCAS, but after researching further, I found that low levels do not definitively rule it out. I am reaching out for guidance—can anyone assist me in understanding my situation? **Presented Symptoms**: - Persistent hives - Facial flushing - Cognitive fog - Recurring headaches - Abdominal discomfort - Irregular bowel movements (ranging from diarrhea to constipation) - Anxiety attacks - Low blood pressure - Episodes of dizziness - Rapid heartbeat - Chronic fatigue - Episodes of fever - Severe joint pain - Night sweats - Bloating - Elevated sensitivity to sunlight - Intolerance to heat I frequently experience multiple symptoms together during flare-ups, with at least one flare occurring daily. The hives tend to emerge 1 to 3 times each day, primarily triggered by sun exposure and heightened emotional states, although at times they arise with no apparent cause. These flare-ups can occur abruptly, lasting anywhere from 15 minutes to several hours.
Three Weeks Post Gallbladder Surgery - Is It Infected?
Patient Profile: - Age: 35 - Gender: Female - Height: 5 feet 4 inches - Weight: 160 pounds - Ethnicity: Asian Issue Duration: 3 weeks Location: United States Relevant Medical History: Approximately three weeks ago, I underwent gallbladder removal surgery. Recently, I have observed a slight amount of cloudy fluid emerging from the surgical site over the past few days. Just moments ago, I noticed a possible pus discharge from the incision. While there is no significant pain, I do feel mild soreness when shifting my position. I have not experienced any fever or chills, and there is no unpleasant odor coming from the wound. Should I continue to clean the area with soap and water, or would it be prudent to seek immediate medical attention at the ER for a professional evaluation?
Should I Seek Medical Attention?
At 22 years old, I am a female who has been on medications like duloxetine, lamotrigine, and hydroxyzine for several years. I have managed to keep my Graves' disease under control, but I have reasons to believe I may also be experiencing symptoms of POTS (Postural Orthostatic Tachycardia Syndrome). Last year, I was scheduled to consult a neurologist regarding hand tremors and the possibility of fibromyalgia. Unfortunately, I could not continue my treatment after relocating and losing my health insurance. Just 15 minutes ago, I fainted. Prior to that incident, I was feeling unwell—dizzy, my vision was blurry, and I experienced a whooshing sensation along with heat in my ears. My face and arms also felt tingly. After fainting, I experienced a heavy, aching sensation in my head, and I still have a headache now. Additionally, I’ve been waking up with headaches for a couple of days. I want to know if it's advisable to go to the emergency room. It's important to note that this isn’t my first fainting spell; I had one incident years back, which helped me recognize the signs when it started happening. At that time, I was lifting a heavy bed frame, and when I began to feel faint, I tried to sit down but stood back up to assist, and that’s when I lost consciousness. I’m unsure how long I was out, but I initially thought I was just sleeping before realizing what had happened when I regained awareness.
Seeking Clarity on Medical Notes
Greetings, I’ve chosen to use a throwaway account to keep my medical details private from my main one. My daughter, a 3-year-old with cerebral palsy, is prescribed baclofen, gabapentin, senna, and occasionally, Miralax. She is raised in a smoke-free and alcohol-free environment. Recently, my daughter has exhibited instances of staring and being unresponsive, which we discussed with her pediatric neurologist. These episodes occurred multiple times over three weeks. Concerned about potential seizure activity, we recorded some incidents and shared them with the doctor. He advised us to schedule an EEG, which was set for the soonest available time a week later, while instructing us to call if more episodes occurred. When another episode took place, we reached out to the neurologist, who practices at a children’s hospital approximately two hours away. He recommended that we go to our local emergency room. Upon arriving there, the attending physician reviewed her history but seemed skeptical. After a lengthy wait and attempts to clarify our situation, the on-call neurologist eventually came to see us—although he showed little interest in the video evidence we provided. He proceeded with an EEG that lasted only 15 minutes during which my daughter did not have any episodes. Unfortunately, this neurologist was rather abrupt and seemed dismissive, ultimately sending us home without satisfactory answers. Now, I find myself puzzled. In the EEG report, the neurologist mentioned something called a "teddy bear sign." As I had never encountered this term before, I did some research and discovered that it may suggest that seizure activity is not genuine if the patient is in possession of a stuffed animal or similar item. Is this a legitimate observation? My daughter indeed had her beloved baby doll, which she takes with her everywhere. I fail to comprehend how this could be relevant or why it might indicate that her potential seizure activity is fabricated. I plan to reach out to her primary neurologist to gain deeper insight into the meaning of this "teddy bear sign." Thank you for your help!