OpenHealth Q&A

Get answered by medical professionals

New Developments in Symptoms from Topamax

6/28/2025, 1:20:21 AMMale25-34

A 23-year-old female, currently prescribed Pristiq and Topamax, has been diagnosed with Persistent Postural-Perceptual Dizziness (PPPD), cervicogenic dizziness, and vestibular migraine. Upon increasing her Topamax dosage from 50 mg to 75 mg, she began experiencing unusual neurological symptoms that are not documented in the medication’s side effects. Following her concerns, her physician recommended she revert to her previous dosage of 50 mg to assess any changes in her condition. However, it has been two weeks, and her symptoms appear to be intensifying. According to her physical therapist, who claims to have no previous experience with such symptoms, she is reassured everything seems normal, yet she feels increasingly distressed. She is reaching out to see if anyone else has encountered similar issues and questioning whether these symptoms may arise from a structural issue related to vestibular migraine or be a byproduct of the medication itself. She describes an intensely vivid internal buzzing feeling, and notes a peculiar sensation where her neck, back, and legs feel unusually flexible, as if her spinal column is moving up and down within her body as she walks. Additionally, she feels as though her heels are sinking backwards into the ground, creating an odd walking experience. Moreover, there is a distinct sensation akin to her brain or skull vibrating; this does not feel like the typical brain zaps often reported, but rather a feeling of awareness of internal movement within her skull that becomes more pronounced when she turns her neck. Lastly, she frequently experiences tingling in her legs, accompanied by nerve pain radiating down both her arms and legs.

Multiple SclerosisFibromyalgiaCOPD

Answers (1)

Cony

6/28/2025, 1:20:42 AM

OpenHealth AI

It sounds like you are experiencing some very concerning and unusual symptoms following a change in your Topamax dosage, and it’s completely understandable to seek clarity and support. The combination of your ongoing conditions like Persistent Postural-Perceptual Dizziness (PPPD) and vestibular migraine, along with the new neurological symptoms, is understandably distressing.

Main Points:

  1. The symptoms you're describing—internal buzzing, unusual flexibility, and sensations related to movement in your body—may be linked to either medication side effects or the underlying conditions.
  2. It’s important to monitor your symptoms, evaluate any possible patterns, and share these observations with your healthcare provider to guide decision-making.

Explanation: Topamax (topiramate) can have side effects, including some neurological symptoms, but what you're experiencing may not be typical. It’s good that you've reverted back to the previous dosage under your doctor's guidance, but if your symptoms are intensifying, they should be taken seriously. It’s not uncommon for medications to interact in ways that can amplify certain sensations or symptoms when treating conditions affecting the nervous system.

Given that you are feeling more distressed and the physical therapist is unable to provide reassurance based on experience, it’s wise to take the following steps:

Next Steps:

  1. Keep a Symptom Journal: Document your symptoms' duration, intensity, and any triggers you notice. This will help both you and your healthcare provider understand the patterns more clearly.

  2. Communicate with Your Doctor: Schedule a follow-up appointment to discuss these ongoing and intensifying symptoms. Bring your symptom journal to provide a clearer picture of your experiences since adjusting your medication.

  3. Review Medication: Discuss the possibility of lower doses or alternatives with your healthcare provider. There may be other options or adjustments that could reduce side effects while still managing your original condition.

  4. Consider Additional Support: If you continue to feel distressed, consider seeking a second opinion from a neurologist or a specialist in vestibular disorders. They may provide insights or alternative treatment strategies based on their experience in this area.

  5. Focus on Self-Care: While you’re navigating this challenging time, prioritize aspects that promote your well-being, such as gentle physical activity as tolerated, mindfulness techniques, and staying hydrated.

Your symptoms are significant, and keeping an open line of communication with your healthcare team is crucial for feeling heard and finding the right treatment path for you. If severe symptoms like strong numbness, severe headaches, or any changes in consciousness occur, seek immediate attention.

Related Questions

Concerns Regarding Potential Polycythemia Vera Diagnosis

25-year-old male | Occasional smoker | No significant health problems I find myself in a complicated situation with conflicting opinions from various healthcare professionals regarding my potential diagnosis. In January, my complete blood count (CBC) displayed the following results: - Hemoglobin (HGB): 17 - Hematocrit (HCT): 50 I visited a hematologist (referred to as Hem-1) who recommended that I undergo testing, including an erythropoietin (EPO) assessment and a myeloproliferative neoplasm (MPN) reflex panel. The results were as follows: - EPO level: 6.6 - MPN panel: All tests returned negative for the mutations tested (Jak2 V617F, Exon 12, CALR, MPL, BCR/ABL1). Hem-1 advised me not to worry excessively and suggested donating one unit of blood, with plans to revisit around late June with updated results. Yesterday, I received my latest results, which indicated: - Hemoglobin: 16.2 - Hematocrit: 48.3 Although I intended to discuss these findings with Hem-1, he was unavailable, so I saw another hematologist (Hem-2) who presented an intriguing interpretation of my situation. Hem-2 explained that while I do not exhibit signs of MPNs, my normal EPO level suggests that secondary polycythemia can be excluded (since EPO would typically be elevated in such cases). He concluded that my condition might signify a primary variant of polycythemia vera (PV). Additionally, I noted that before these recent events, my blood work from 2021 showed values of Hemoglobin: 16.8 and Hematocrit: 49. This raises a question: if I indeed have PV, why have my levels not escalated over the past two years? Furthermore, can an EPO level of 6.6 genuinely rule out smoking as a contributing factor to my blood counts? I would appreciate any insights into my situation!

DiabetesCOPDEndocrinology
Male25-34
12 minutes ago

Concerns About My 4-Year-Old’s Health: Ear Issues or Something More?

My four-year-old has been grappling with numerous viral infections since January, which has resulted in persistent fever, often reaching 38.0°C, particularly affecting his head and ears, while his underarm temperature remains normal. Recently, I’ve noticed shifts in his behavior; he appears more irritable and prone to tantrums. During these episodes, he tends to sweat excessively, even before becoming visibly upset, and he seems less energetic than usual. One major concern is his sensitivity to sound. He frequently covers his ears or expresses discomfort regarding various noises, not just loud ones. While he can tolerate boisterous music or playful sounds from toys and instruments, he cannot endure the soft hum of our air purifier. He actively plugs his ears or switches off the device. Occasionally, he finds my brother’s deeper voice unsettling, but his reactions seem inconsistent as he often covers his ears randomly in response to quieter sounds. This auditory sensitivity seems to be linked to everything else occurring. He has been treated for ear infections on two occasions, as his symptoms originated with one of these infections. Following this, our doctor referred us to a pediatric specialist, who advised disregarding the fevers and not constantly monitoring his temperature, which I have complied with. Despite conducting various blood and urine tests, we still lack clarity on his condition. The physician is now considering a test for celiac disease. After this, though, I feel a bit adrift. I have a hunch that mold in our home could be contributing to his issues, but it seems there’s no straightforward way for doctors to test for it. I once visited a naturopath for myself but found the experience underwhelming; however, I’m wondering if that might be the only viable avenue if he is indeed suffering from a mold allergy. Yet, I hesitate to spend money on tests that don’t have solid scientific backing. He does not exhibit coughing, but he occasionally breathes loudly through his mouth and experiences nasal congestion, coupled with snoring and frequent teeth grinding, both day and night, along with eczema. Now, I am left questioning: - Should I leave his condition unchecked? - Should I consult a naturopath next? - Is there something crucial that has been overlooked? - If he were still facing issues with his ear—inner or middle ear—would a physical examination be sufficient for diagnosis? - Could previous ear infections have engendered complications that are undetectable without an MRI?

AsthmaMultiple SclerosisLupus
Male25-34
22 minutes ago

Struggling with Unexplained Health Issues

Hello all, I'm a 27-year-old male grappling with a perplexing illness that's persisted for roughly five years without a clear diagnosis. Despite undergoing nearly every conceivable medical examination—including two colonoscopies, two endoscopies, various MRI scans, X-rays, CT imaging, urine tests, a gastric emptying study, and numerous prostate evaluations—I have largely received normal results. Some conditions identified include the presence of polyps, diverticulitis, and bilateral hydronephrosis, alongside distention in both my liver and kidneys. My predominant symptoms revolve around gastrointestinal distress, urinary complications, and joint discomfort. A year ago, I underwent gallbladder removal surgery as well. Currently, I experience significant abdominal pain, nausea, and a drastic weight loss of over 100 pounds. I oscillate between constipation and diarrhea, deal with fissures and hemorrhoids, and have both internal and external hernias. I’ve also noticed painful, frequent, and urgent urination, while the joints in my legs often feel rigid, affecting my gait. Additionally, I endure persistent back and neck pain that can become quite severe. Recently, I’ve been experiencing sensitivity to sunlight, as my pupils seem unusually constricted. Out of the blue, I’ve also started developing bruises and rashes on my arms and legs without any clear cause. I’ve consulted various specialists including gastroenterologists, urologists, neurologists, and a rheumatologist, yet most have dismissed my concerns. Standing at 6 feet tall, my lowest weight has been 118 pounds. I can’t shake the feeling that my tattoos lead some professionals to suspect I'm merely seeking narcotics. It's frustrating; I can’t carry out daily functions like a typical person and often hear the term "hypochondriac" directed at me. The reality is, I wish this were just an exaggeration of concern. I do not consume alcohol or drugs. My current medications include lamotrigine, Effexor, and Abilify. Where do I go from here? I've attempted to seek second opinions, but many doctors are booked for months, and most do not accept state insurance. For the last two years, I have struggled to maintain employment for longer than 90 days, which hinders my ability to access health insurance. It creates a frustrating cycle of gaining state insurance, losing it due to income fluctuations, subsequently losing jobs, and then reverting back to relying on state support. Living just outside Philadelphia, I would deeply appreciate any advice or recommendations for a doctor willing to see me sooner rather than later. I am exhausted from feeling trapped within the healthcare system and yearn for an improved quality of life. Thank you to everyone who takes the time to read this.

LupusCrohn's DiseaseCOPD
Male25-34
22 minutes ago

Reaching Out for Assistance

I find myself in a desperate situation and could really use some guidance. I'm an 18-year-old who generally leads a healthy, active lifestyle. However, I've been battling pinworm infections since childhood. When I was around 12, I confided in my mother about my condition, and she provided me with medication, but unfortunately, it was ineffective—likely due to my lack of proper hygiene at the time. Eventually, I stopped discussing the issue with her and learned to cope with the discomfort on my own. These persistent parasites have significantly affected my well-being and mental health over the years, and even now, at 18, I continue to struggle with them. Despite maintaining good hygiene—such as keeping my nails short and refraining from any unsanitary habits—I'm still plagued by embarrassment and feel unable to seek help from others. It’s crucial that I find a way to eliminate them myself, as I am at a loss for how to proceed. I truly hope someone can offer me advice or support on this matter.

Multiple SclerosisInternal MedicineRheumatology
Male25-34
22 minutes ago

Seeking Answers for Ongoing Health Struggles

I find myself in urgent need of a proper diagnosis to achieve true relief rather than merely addressing symptoms. I’m unsure of the process, so I’ll outline my symptoms in hopes that someone might offer assistance. My health began to decline after experiencing a bullseye rash from a tick bite at the age of 17. I am a 36-year-old woman, standing 5 feet 8 inches tall and weighing 190 pounds. My medical history includes diagnoses of fibromyalgia, chronic Lyme disease, and migraines. Currently, I am taking several medications, including Emgality, Maxalt, Frovatriptan, Ambien, Benadryl, Midol, Zofran, and Phenergan, as needed. I experience daily headaches interspersed with occasional migraines. Additionally, I suffer from stomach cramps that might be related to IBS and persistent joint pain. Heat sensitivity has led to the emergence of a butterfly rash, which may trigger seizures that are not classified as epilepsy. Muscle weakness and sensations resembling growing pains are common, alongside the peculiar feeling of muscles vibrating or twitching simultaneously. I may be dealing with POTS, as I have an elevated heart rate believed to contribute to my seizures. Cognitive issues are increasingly concerning; I’m faced with memory lapses and persistent brain fog. I produce an excess of histamines and contend with debilitating fatigue. My neck’s range of motion is severely restricted, and I sometimes experience sharp, burning pain at the base of my skull. Typically, my body temperature hovers around 96.7 degrees Fahrenheit. My pupils are uneven and have unusual reactions to light. A spinal tap indicated the presence of MS, yet no lesions were found on my brain. Other findings include an empty sella, inflammation in the vein of my left temple and mastoid, and abnormal menstrual cycles often accompanied by ovarian cysts. Cognitive decline is a significant concern, and I might be facing Addison’s disease. My sleep patterns fluctuate between insomnia and excessive sleep. I have undergone treatment for Lyme and Rocky Mountain spotted fever, diagnosed seven years apart. The Lyme disease test was conducted several years after the appearance of my bullseye rash, while the RMSF diagnosis was incidental; although the infectious disease doctor stated it was caught early. I am acutely aware that I may be missing other symptoms, mainly due to memory challenges, and many of my issues tend to wax and wane. The neurological symptoms are particularly distressing and frequent, followed closely by joint pain. Unfortunately, my doctors seem to dismiss the possibility of any condition beyond migraines, despite my history of trials with multiple preventative and acute migraine medications. Most have adverse effects, but Maxalt occasionally provides relief, and I'm scheduled to start Botox treatments in three weeks. I long for my life to return to normal and seek to address the underlying causes rather than merely coping with symptoms. Currently, the only explanation offered is post-Lyme syndrome, with little hope for further action. Thank you in advance for any guidance or insights you can provide.

LupusFibromyalgiaCrohn's Disease
Male25-34
2 hours ago