OpenHealth Q&A

Get answered by medical professionals

Concerns Regarding Chronic Low Protein, Albumin, and Calcium Levels

2/16/2026, 1:50:17 PMMale25-34

Greetings, medical professionals. I'm a 50-year-old woman standing at 5 feet 5 inches tall and weighing 138 pounds. Current medications include: - Adderall 30 XR once daily - Junel 1.5/30 Medical background: - Irritable Bowel Syndrome (IBS) - Primary lymphedema affecting both legs, left arm, and pelvis - Adenomyosis and endometriosis - Benign colon resection due to a leiomyomatosis tumor - Asthma I’ve been living with primary lymphedema since birth, and I'm wondering if it could be linked to my persistently low levels of protein, albumin, and calcium. Unfortunately, my doctors have not addressed this issue, and my gastroenterologist expressed little concern. I maintain a high-protein, low-carbohydrate, moderate-fat diet and am committed to daily exercise. Is there a way to elevate these levels? My most recent lab results from six months ago will be attached. Furthermore, I've noted that my foot wounds heal very slowly, which might be related to lymphatic issues or potentially low albumin levels. What guidance can you provide, or can you recommend someone who specializes in this area? This has been a persistent issue for many years, and I hadn't paid much attention to it until a filling in my primary care was alarmed by my protein levels. Thank you very much for your help! 🙏🏻

AsthmaArthritisFibromyalgia

Answers (1)

Cony

2/16/2026, 1:50:37 PM

OpenHealth AI

Thank you for sharing your concerns about low protein, albumin, and calcium levels, especially in the context of your underlying health issues. It’s understandable to seek clarity about how these factors might affect your overall health and healing, particularly with your lymphedema and healing challenges.

Main Points:

  1. Low protein and albumin levels can be linked to various factors, including malabsorption, chronic conditions, and dietary intake.
  2. Improving protein and calcium levels may involve dietary changes, nutritional supplementation, and monitoring your overall health.

Explanation:

  • Protein and Albumin: Albumin is a protein made by the liver, and it helps maintain fluid balance in your body. Low levels can be due to issues like malabsorption (which can occur with IBS) or liver function. Chronic inflammation or conditions like lymphedema can also affect these levels.
  • Calcium Levels: Calcium is essential for bone health and is influenced by dietary intake and absorption. Low levels can occur if you’re not getting enough calcium or if there are absorption issues, sometimes related to digestive health.

Next Steps:

  1. Dietary Assessment: Ensure you’re consuming enough high-quality protein sources (like fish, eggs, lean meats, legumes, and dairy). Keep a food diary for a week to help track protein intake and share it with a registered dietitian.

  2. Consider Supplements: Talk to a healthcare provider about possibly introducing a protein supplement (like whey or plant-based protein) or calcium/vitamin D supplements to your diet. These may help you reach optimal levels.

  3. Routine Monitoring: Since you’ve had low levels in the past, it’s wise to continue regular blood work to monitor protein, albumin, and calcium levels. Discuss with your healthcare provider when another test may be appropriate.

  4. Wound Care: To address slow-healing wounds, improve your overall protein intake, keep wounds clean, and maintain a healthy environment for healing. If wounds do not improve, consulting a wound care specialist can provide targeted help.

  5. Lymphedema Management: Continue managing your lymphedema with appropriate lifestyle modifications (like compression garments and elevation). Discuss with a specialist in lymphedema management for personalized strategies.

While I cannot recommend specific individuals, seeking a registered dietitian or a healthcare provider specialized in nutrition can be very beneficial. They can provide tailored guidance to address your specific needs and ensure all aspects of your health are being considered.

Please keep me updated on how you're doing and if you have any other questions!

Related Questions

Seeking Clarity on MRI/MRA Results for My Father, Age 58

Greetings, everyone. I’m reaching out on behalf of my father, who is 58 years old and recently underwent an MRI and MRA of the brain. We just received the findings, and I’m hoping to get some insight from those familiar with these types of reports. **Findings Overview:** - **White Matter Alterations / Small Vessel Disease:** The MRI indicates numerous T2/FLAIR hyperintensities located in both cortical and subcortical areas of the brain, particularly affecting the occipital lobes and the white matter around the ventricles. According to the radiologist, these alterations are likely related to chronic small vessel disease or previous minor vascular events rather than a current stroke. There is no indication of diffusion restriction, which rules out any acute issues. - **Signs of Gliosis and Initial Brain Atrophy:** There are signs of gliosis, meaning there may be scarring in the brain tissue caused by past insults or diminished blood flow, along with mild early-stage cerebral atrophy that may be attributed to his age. - **Ventricular Changes:** The third and lateral ventricles appear slightly enlarged; however, the fourth ventricle remains normal. Additionally, the subarachnoid spaces are normal, and there’s no evidence of any masses, bleeding, or midline shifts. - **Pituitary Region Assessment:** The examination of the sellar/suprasellar region shows no tumors or abnormalities. - **Cerebellum and Brainstem Evaluation:** Both are reported as normal. **Primary Concern - Aneurysm:** The MRA has identified a 7.5 x 7.5 mm saccular aneurysm located on the anterior communicating artery (ACOM). All other major arteries (internal carotid, middle cerebral, anterior cerebral, posterior cerebral, basilar, and vertebral) exhibit normal size and blood flow without any stenosis. **Radiologist’s Summary:** - Chronic alterations due to small vessel issues and gliosis likely from past vascular problems. - Mild early cerebral atrophy noted. - Presence of a 7.5 mm ACOM aneurysm that requires follow-up and further evaluation. I’m left wondering about the implications of a 7.5 mm aneurysm on the ACOM. How serious is this condition? What typically comes next—would it involve monitoring, coiling, or clipping? Should we prioritize a visit to a neurosurgeon, or is this something that can be scheduled without urgency? For anyone who has faced similar findings, I’d appreciate hearing about your experiences. The mention of the aneurysm has understandably made me quite anxious. Thank you in advance for any guidance you can provide!

FibromyalgiaCOPDInternal Medicine
Male25-34
8 minutes ago

Am I Left Without Alternatives?

Today, I visited a physician due to escalating discomfort in my right hip. I was diagnosed with Legg-Calve Perthes disease at the tender age of three, with the initial prognosis suggesting that I would need to rely on a wheelchair throughout my life. Fortunately, I defied that expectation and simply underwent regular monitoring by an orthopedic specialist who conducted annual X-rays. Having transitioned out of pediatric care, my hip is now presenting significant challenges. I find it difficult to rest on my right side, and have started limping intermittently while walking. Sleep evades me due to the pain, which seems to persist regardless of my position. At 19 years old, I received a rather disappointing response from the doctor. He indicated that my pain levels are not severe enough at this time and advised me to return for a follow-up once the discomfort intensifies. At that point, he would consider referring me to a specialist who could perform a hip replacement. Inquiring about interim pain relief strategies, I learned about a shoe lift that might help, given that my right leg is shorter than my left. Yet, the doctor characterized it as largely aesthetic, suggesting there are no meaningful solutions available right now. Can this be accurate? Am I truly out of options, or should I pursue a second opinion? I am a 19-year-old female residing in the United States, with primary diagnoses of Legg-Calve Perthes disease and Stickler Syndrome. Currently, I don’t take medications specifically for these conditions, apart from those prescribed for psychiatric issues and migraines.

ArthritisCrohn's DiseaseCOPD
Male25-34
9 minutes ago

Confusing Experience During Echo Examination: Is This Common?

Greetings. I'm a 21-year-old female, standing at 5'1" and weighing 240 pounds. My medical history, as noted in my patient portal, includes conditions such as Depression, Anxiety, ADHD, GERD, BRBPR, an elevated heart rate, DOE, Obesity, and Iron deficiency anemia caused by chronic blood loss. My current medications consist of Vyvanse, Pepcid, Iron supplements, Zoloft, and I've also been using NuvaRing. Recently, I underwent a Transthoracic Echocardiogram due to experiencing a rapid heartbeat and shortness of breath, particularly during activities like exercising or even playing with my nephew in a bounce house, which left me feeling faint and in need of a significant recovery period before my breathing and heart rate returned to normal. I have been under observation using a Zio Patch as well. Upon arriving for the echo, I was instructed to remove my shirt and lie on the examination table. The doctor proceeded with the procedure by applying gel to the transducer and beginning the scans on my chest, while also operating her computer. I was guided through a series of breathing techniques: short breaths followed by deep ones, ostensibly to help position my lungs for better imaging. This initial phase lasted around 15-20 minutes and was mostly quiet, aside from her reminders to hold my breath. She then indicated that the images weren't sufficient and that I would need to receive a medication to enhance the clarity of my heart images. A nurse came in to place an IV for administering this medication. Unfortunately, the experience was quite painful as he struggled to locate a suitable vein, resulting in discomfort with the needle moving around—which is something I usually find unpleasant, and this particular attempt left a strange bruise surrounding the entry point. After the IV was successfully placed, the doctor injected what I later learned was Difinity into the line. Communication about the procedure was lacking; she hadn’t provided much information as she resumed with the ultrasound. Almost immediately, I started to experience a tightening in my throat and chest, which made me visibly uneasy and caused me to lean back. When she asked about the tightness, I nodded, feeling too suffocated to respond verbally. Pain began to spread throughout my body, accompanied by dizziness and an intense heartbeat. I found myself twisting in discomfort and crying out, overwhelmed by the sensation, shouting "it hurts!" I genuinely felt like I was on the brink of collapse. She reassured me that what I was experiencing was typical and that I needed to remain calm, mentioning that it often feels worse before it gets better. Despite her reassurances, I couldn't help but feel frightened and exhausted as I laid there while she continued the exam by pushing more medication through the IV. This lasted for another ten minutes, during which my limbs felt strangely cold and I broke into a sweat. Eventually, she finished up and asked if I felt any relief before allowing me to dress. She offered no further explanation about my reaction or the procedure, stating that the doctor would reach out with the results. As we walked to the exit, she inquired again about my well-being, and I expressed that while I felt somewhat better, the ordeal was terrifying. She admitted that it was alarming and noted that the experience often feels worse than it actually is. I departed feeling both shocked and drained, recalling the experience as among the most distressing I’ve ever endured. I keep wondering why I wasn't forewarned about the potential side effects. Was her demeanor towards my discomfort too casual? Was my reaction typical? Am I right to be concerned? My feelings of frustration and confusion persist as I try to process everything that happened.

AsthmaCrohn's DiseaseInternal Medicine
Male25-34
39 minutes ago

Adolescent Male Seeking Guidance on Neuromuscular Concerns

I’m an 18-year-old male, standing at 5'11" and weighing approximately 167 pounds, and I’m reaching out because I have escalating concerns regarding my neuromuscular health. My struggle with muscular weakness began roughly five years ago, and I’ve also been on medication for depression. This is my first post in years, and I’d like to share my experience. It all started in 2021 when I began to notice a peculiar sensation—an overwhelming feeling of persistent cold enveloping my entire body, accompanied by a slight pain that reminded me of a migraine. Unfortunately, these symptoms have progressed significantly over time. I now face challenges like loss of coordination, noticeable muscle weakness, joint discomfort, and a troubling feeling of trembling at times, making me feel as if my ligaments have endured a tough workout, despite my muscles still growing in size. I struggle to harness my full strength, often dropping things and stumbling into various objects like walls and furniture. Moreover, I have noticed a decline in my ability to communicate effectively and a general inability to focus, which manifests as brain fog. I frequently forget where I placed items, lose track of my tasks, and struggle to recall faces and names—even those I should know well. These issues seem to persist irrespective of my medication status. To clarify, I do have myopia and currently show no significant outward signs of my condition. While I experience stress like many others, I ensure that I get plenty of sleep and maintain a wholesome diet. Interestingly, it appears I am the only one among my siblings grappling with these difficulties. I would be deeply grateful if anyone could offer guidance on what steps I should take next. Despite visiting numerous doctors over the years, I have yet to receive a clear diagnosis, and living in a developing country has made seeking help even more daunting. Thank you for taking the time to read my concerns.

ArthritisMultiple SclerosisLupus
Male25-34
49 minutes ago

Persistent Ear Sensation Following Influenza

Seven days ago, I received a positive diagnosis for the flu, despite having been vaccinated beforehand. After starting antiviral medication within the initial 24 hours, my severe symptoms seemed to diminish within roughly three days. Nevertheless, I'm still experiencing a continuous sensation of fullness or muffling in my ears, which hasn’t seen any sign of improvement. The intensity of this sensation varies, but overall, it appears to be worsening. Additionally, I have been having occasional bouts of dizziness linked to the pressure in my ears. This situation is concerning for me, especially considering my childhood history with poorly developed Eustachian tubes that were never treated. This condition caused repeated ear infections and temporary hearing loss until I was approximately 3 to 4 years old. Following that, I went through eight years of speech therapy to help me read and articulate properly. Considering my background and the escalation of my current symptoms, I am questioning whether I should seek a professional evaluation. Alternatively, could this just be a common post-viral inflammation that might resolve on its own? My fiancé also contracted the flu and mentioned that his muffled hearing disappeared two days after he exhibited his first symptoms.

ArthritisCOPDInternal Medicine
Male25-34
1 hour ago