Short answer · Medically reviewed summary · Last updated: 2026-04-07

Anosmia is the total loss of the sense of smell, which can significantly impact quality of life, safety, and emotional well-being. While currently there is no singular cure, consistent "smell training" remains the gold-standard therapeutic intervention to help stimulate the olfactory system and potentially facilitate neural recovery. What should I prioritize immediately after an Anosmia diagnosis? First, please breathe and know that you are not alone; 513 members of the DiseaseMaps community have navigated this same path.

7 people with Anosmia have shared their first-person experience on this question at DiseaseMaps.

8

Which advice would you give to someone who has just been diagnosed with Anosmia?

Advice for the newly diagnosed with Anosmia, written by people who have lived it. What they wish they had known on day one.

Anosmia advice

Anosmia is the total loss of the sense of smell, which can significantly impact quality of life, safety, and emotional well-being. While currently there is no singular cure, consistent "smell training" remains the gold-standard therapeutic intervention to help stimulate the olfactory system and potentially facilitate neural recovery.



What should I prioritize immediately after an Anosmia diagnosis?


First, please breathe and know that you are not alone; 513 members of the DiseaseMaps community have navigated this same path. Your immediate priority is safety. Because Anosmia prevents you from detecting environmental hazards like smoke, gas leaks, or spoiled food, you must install high-quality smoke and carbon monoxide detectors throughout your home. Transition to using date-stamping labels for all refrigerated items to ensure food safety, as you can no longer rely on your nose to identify spoilage.



How do I build an effective medical care team for Anosmia?


Managing Anosmia often requires a multidisciplinary approach. Start by consulting an Otorhinolaryngologist (ENT specialist), ideally one who specializes in rhinology or chemosensory disorders. They can evaluate structural issues, such as nasal polyps or chronic sinusitis, that may be causing your Anosmia. Additionally, consider working with a clinical psychologist or counselor who specializes in chronic illness, as the loss of smell is deeply tied to memory and emotional regulation, often leading to feelings of isolation or "anhedonia"—the loss of pleasure in eating.



How can I manage daily life and symptoms effectively?


Living with Anosmia requires adapting your sensory environment. Here are practical strategies to help manage your condition:



  • Implement Olfactory Training: Engage in structured "smell training" twice daily, sniffing strong, distinct scents (such as rose, lemon, clove, and eucalyptus) for 20 seconds each to stimulate olfactory receptors.

  • Enhance Food Texture: Since flavor is primarily smell-dependent, focus on the "mouthfeel" of food—incorporating crunchy, spicy, or temperature-contrasting elements to make meals more satisfying.

  • Label Everything: Use a permanent marker to write purchase dates on food items.

  • Safety First: Ensure your home is equipped with hard-wired, interconnected smoke alarms.



How do I find community support and stay informed on research?


Connecting with others is vital for mental health. By joining platforms like DiseaseMaps.org, you can share experiences with the 513 other individuals currently living with Anosmia. Regarding research, keep an eye on clinical trials via ClinicalTrials.gov. New research into the regenerative capacity of the olfactory epithelium is ongoing, and participating in studies may provide you with access to emerging therapies for Anosmia before they are widely available.



What should caregivers and family members know?


For those supporting someone with Anosmia, empathy is the most important tool. Understand that Anosmia is not just about missing pleasant scents; it is a loss of a primary sensory connection to the world, which can lead to profound sadness. Encourage your loved one, but avoid minimizing the condition. Assist them in creating a safe home environment and remain patient during meals, as the social aspect of dining may feel diminished for them.



Next steps



  • Schedule an appointment with an Otorhinolaryngologist to rule out reversible causes.

  • Begin a consistent daily smell training regimen using essential oils.

  • Join the DiseaseMaps community to connect with others who understand the day-to-day challenges of Anosmia.

  • Install safety devices (gas and smoke detectors) immediately.



Medical disclaimer: This content is for informational purposes only and does not constitute medical advice, diagnosis, or treatment; always seek the advice of your physician with any questions regarding a medical condition.



References



  • NIH Genetic and Rare Diseases Information Center (GARD) - Anosmia resources

  • Orphanet: The portal for rare diseases and orphan drugs

  • PubMed: Current literature on olfactory training and recovery

  • AbScent: A global charity dedicated to supporting people with smell and taste disorders

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-04-07
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
8 answers
The best news I have had regarding this condition is that a percentage of people will recover their sense of smell, especially if it is caused by a virus. It is important to start Smell Training as soon as possible, as this will help the body-brain connection and exercise your brain to be attuned to scent.

Don't give up seeking answers! Doctors don't know everything about this condition yet, particularly because it involved the brain, which is a new frontier for science and research.

Posted Mar 20, 2017 by DebRose 1160
Learn to live with your limitations. Enjoy life. Reach out to others with the same conditions. Find out as much as you can about the disease. Don't ever feel that it limits your abilities, it also allows you to do tasks others can't/will not do due to the strong odor that those without anosmia are unwilling or unable to perform.

Posted Apr 24, 2017 by JHG010462 1000
As I said prior, anosmia is rarely diagnosed as doctors hardly ever have to deal with something like this (congenital). And when they do it's usually a "there's nothing that can be done, sorry, enjoy your life as an anosmiac!"

It is not the end of the world, it does not prevent you from living your life.

Posted Sep 11, 2017 by Katie 1800
The same answer as the question above.

Posted Jan 28, 2019 by Kerry 2550
As a congenital anosmic myself, my overall advice to other fellow anosmics, is to maintain a positive outlook on life. I have become aware of a lot of do's and don't when living with this condition and have written about several topics on my personal blog. Whether you have questions about personal hygiene, what to look for in a "designated nose" to lots of tips when taking care of pets, you may find additional information and support by clicking on the following links below:

https://www.girlwhocantsmell.com/tips-for-living-with-anosmia/

I also offer tips for teens living with anosmia. You may find the full article here:

https://www.girlwhocantsmell.com/tips-for-teens-living-with-anosmia/

Posted Jul 1, 2019 by Girl Who Can't Smell 1480
It is valid and don’t try and hide it there needs to be more awareness

Posted Oct 4, 2019 by Amy Somers 1600
It is tough to lose the sense of smell, it will take some time to "settle down" with the new situation, but you will get through it. Join groups on social media about Anosmia, see that you are not alone. It is not embarrassing to ask for help with things you can't do, when people know about your diagnosis they are usually glad to help.

Posted Feb 25, 2020 by Synne 300

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