Seeking Clarity: Health Concerns of a 19-Year-Old Woman
Hello everyone! I am a 19-year-old woman and I’ve been experiencing what my physician describes as ice pick headaches. These are characterized by intense, brief sharp pains in my head that vanish just as quickly as they appear. Due to the rapid onset and resolution, my neurologist has excluded the possibility of migraines. I underwent an MRI of my brain, which revealed white matter lesions within my central nervous system. In addition, I had another MRI focusing on my spine, and the results showed no abnormalities. An EEG was also conducted, and it returned normal findings. My neurologist is currently at a loss regarding the cause of my symptoms. Furthermore, my lab results indicated an elevated C-Reactive Protein level and a low immunoglobulin A. Any thoughts or potential explanations for what might be going on would be greatly appreciated!
Answers (1)

8/13/2025, 10:50:43 PM
OpenHealth AI
It's understandable to feel concerned about your symptoms and the findings from your medical evaluations. Ice pick headaches, along with the incidence of white matter lesions in your brain, can understandably raise questions about potential underlying conditions. Let’s break this down to provide clarity and next steps.
Main Points:
- Ice pick headaches are sharp, fleeting pains and can occur without an obvious trigger.
- White matter lesions can have various causes, including demyelination (like in multiple sclerosis) or other neurological conditions.
- Elevated C-Reactive Protein (CRP) and low Immunoglobulin A (IgA) could indicate underlying inflammation or immune response issues.
Explanation:
- Ice Pick Headaches: These are often benign and may not be linked to serious conditions. They can sometimes occur in isolation or be associated with other types of headache disorders.
- White Matter Lesions: While they can be associated with conditions like multiple sclerosis (MS), they can also appear due to vascular changes, migraines, or even minor inflammatory processes. With your neurologist having ruled out MS and there being no abnormalities in your spine, it's essential to consider other factors.
- Elevated CRP: This indicates inflammation in the body and may suggest other underlying issues, including autoimmune conditions or infections. Low IgA could also be indicative of certain immune deficiencies.
Next Steps:
- Symptom Tracking: Keep a detailed headache diary noting the frequency, duration, triggers, and responses to any treatments you try. This can help identify patterns or specific triggers.
- Follow-Up with Your Neurologist: Discuss the possible significance of the white matter lesions and the elevated CRP. You may need further tests to evaluate inflammatory or autoimmune conditions.
- Consider a Specialist Consultation: If you have concerns about autoimmune disorders (like lupus) due to your symptoms and lab results, ask your neurologist for a referral to a rheumatologist or another specialist who can provide further insight.
- Healthy Lifestyle: Focus on a balanced diet, regular exercise, and good hydration. These can help support overall health and possibly reduce inflammation levels.
Remember, it's important to stay proactive regarding your health and communicate any changes in your symptoms or new concerns to your healthcare providers. If you have any more questions or need further clarification, feel free to ask!
Related Questions
Seeking Guidance for Ongoing Health Issues
I'm a 23-year-old woman weighing 145 pounds, and I've found that in the past eight months, medical professionals haven't provided much assistance. It appears that my difficulties may originate from my neck. I often experience nausea and dizziness, alongside a sense of anxiety triggered by unexpected increases in my heartbeat. There’s also discomfort in my left arm, accompanied by a burning sensation that starts in my head and travels down to my shoulders. Migraines can be particularly troublesome, and I have heightened sensitivity to light and noise at times. My sleep has been disrupted; I've noticed a shift from sleeping on my side to waking up on my back. An MRI I had revealed mild degenerative disc disease along with a slight bulging at C3-4. Additionally, I sometimes feel tingling in my fingers, and my legs often feel heavy and cramp up.
Spider Bite: A Cautionary Tale
Last weekend, from August 8th to 10th, I traveled to Oregon for a wedding and stayed in a basement-level AirBnB that had been refurbished. Upon arriving, I spotted a door that seemed to lead to a garage or storage area; it had noticeable gaps around its edges, allowing me to peek inside the locked space. The view revealed a clutter of gardening tools, old paint cans, abandoned cat supplies, and a thick layer of dust with cobwebs—quite reminiscent of a classic horror film’s eerie garage scenes. While I noted the oddity of the door, I soon put it out of my mind and continued enjoying the stay. Unfortunately, within the first day, I found myself removing two spiders from the place. My friend, terrified of one due to its size, decided to flush it down the toilet—another detail I made note of. Having lived in a basement myself before, I understood that spider encounters weren’t entirely unusual in such settings. Upon returning home to Seattle on August 10th, I reached into my friend’s car to grab a bag and noticed a sudden pain in my hip. After stepping inside, I found a bite mark that was slightly pink with a white center, leading me to suspect it was from a spider. The discomfort intensified, making it hard to lie on my right side, while my partner insisted it was simply a severe mosquito bite, considering my reputation for reacting dramatically to them. The next day, August 11th, the affected area had darkened noticeably and swelling became evident. The wound felt warm, prompting my anxiety to flare up. I decided to visit the doctor for an evaluation. After waiting for over two hours, I received a prescription for Cephalexin and Mupirocin Ointment but didn't have the chance to discuss my symptoms in detail with the physician. By the following day, August 12th, the pain had escalated and the heat emanating from the wound was alarming. Blisters began to form, popping and reappearing unpredictably. Following the instructions on my discharge paperwork regarding worsening symptoms, I ultimately made my way to the emergency room. At the ER, I was given Sulfameth/Trimethoprim and instructed to carry on with the antibiotics while keeping an eye on my symptoms. On August 13th, I didn’t visit the doctor despite experiencing sharp pains at the bite site; I simply focused on resting and sticking to my antibiotic plan. Later that evening, after a lengthy nap, I noticed a concerning red streak extending from the wound. I immediately contacted my primary care provider via MyChart, and they advised me to return to the clinic on August 14th. During my visit, I reported that both hot and cold compresses were painful and explained the significant swelling affecting my skin, which appeared to be dented in some areas. I expressed my discomfort that extended down my leg as well. However, the attending doctor, who wasn't my regular physician, dismissed my concerns as there was no visible discharge or fever, and suggested I let the antibiotics continue to work. She then outlined my wound with a used marker, stating that I should return if it spread. That evening, I began to feel a sore throat, my lymph nodes felt swollen, and my temperature rose to 99.4 degrees Fahrenheit. After reviewing my discharge instructions, I decided not to return to the clinic, not wanting to burden the medical staff with what I thought might be minor concerns. Upon waking on August 15th, I noticed a stiffness accompanying the pain in my leg, and the size of the wound had increased significantly. It felt hot, leaving me unsure of my next steps as I was still taking the prescribed Cephalexin and Sulfameth. Though I recognize I can be overly sensitive regarding my health, my past experiences—where my complaints weren’t taken seriously—continue to affect my caution. I once battled misdiagnoses leading to further complications, such as a severe kidney infection after being treated incorrectly for a mild UTI. That history has made me vigilant about my health. My mother has been adding to my worries; she often teases me for being dramatic over my health concerns. Ironically, when I expected her to minimize the situation, she encouraged me to seek help at the ER. I find myself wishing someone would assure me I don’t need to seek further medical attention, but I'm also seeking advice. What do you suggest I do? Thank you for reading my lengthy account of events.
Ultrasound Results Indicate Hypoechoic Lesion and Anomalous Lymph Node
I’m a 28-year-old female experiencing discomfort in my jaw area close to my neck since Monday. I underwent a private ultrasound on Tuesday, where the results revealed a hypoechoic lesion measuring 10 × 8 mm located in my right submandibular gland. Additionally, there was an unusual lymph node nearby, lacking a distinct central hilum. The radiologist indicated that these findings are concerning. According to ChatGPT, such results may point to the presence of malignant tumors in the salivary glands or signify metastatic lymph nodes. To ascertain whether the lesion is cancerous or benign, a biopsy appears to be the most reliable option. I visited my general practitioner, who informed me that she would not refer me to an ENT specialist for a biopsy, suggesting that the request would likely be turned down. Instead, she recommended waiting three months for a follow-up ultrasound. Now, I’m grappling with the decision of whether to invest in a biopsy (either fine needle aspiration or core), which comes at a significant cost. Should I hold out for another three months or proceed with the biopsy at this moment? My concern revolves around the possibility of it being malignant and the implications of delaying necessary intervention.
Understanding Late-Onset Alice in Wonderland Syndrome: Should I Be Concerned?
Since childhood, I have experienced a peculiar condition known as Alice in Wonderland syndrome. It took me quite a long time to comprehend what it truly entailed, and throughout my life, I've encountered only a few individuals who likewise share this phenomenon. I recently learned that this syndrome often diminishes in childhood, typically around the age of ten. Its persistence into later years may suggest underlying neurological issues, which is concerning. Interestingly, I find a certain joy in this experience; I have the ability to induce it at will, allowing me to perceive the world from an unusual angle. However, I discovered that this syndrome has not been extensively researched, likely because it is challenging to observe during its occurrence, as it typically manifests spontaneously in young children. In an effort to understand my condition better, I've contacted several universities, hoping they might be interested in studying it, but I haven't received any responses yet. I'm curious if anyone here has insight into this syndrome and knows if it carries any long-term risks or effects. Thank you in advance for any information you can provide!
Strategies for Supporting Someone with OCD
In recent discussions, I've noticed a few posts concerning distressing obsessive thoughts about undeniably disturbing topics. I’ve gathered as much information as possible to share with them, yet after today’s conversation revealing that sharing these thoughts could be a compulsion, I’m beginning to suspect that this might be the issue at hand. Initially, I felt honored that they confided in me about such a sensitive matter, but now I’m realizing this may be a manifestation of their OCD. They’re an adult facing challenges in accessing private therapy resources, but I know there are options available for self-referral when they're prepared to seek help. For now, I’m the sole person aware of their situation, and I aim to be a steady source of support. Nonetheless, I’m concerned about inadvertently contributing to any triggers that might lead them into a negative spiral. What avenues exist for me to learn how to support them effectively? Are there truly resources that can guide me? My intention isn’t to 'fix' them; rather, I simply wish to provide love and support in the healthiest manner possible.