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Mental Health

Resources

Welcome to our mental health resources page, specially designed for individuals who are navigating the challenges of CLAs while prioritizing their mental well-being. LGDA is committed to fostering a community where you can access the resources and guidance you need to achieve both physical and emotional well-being on your journey.

Supporting the Mental Health Needs of Rare Disease Patients, Families, and Communities: Recorded October 16, 2024 During this session, therapist Dr. Al Freedman (an SMA dad) provides tools and resources for supporting the mental health needs of rare disease patients, families and communities.


A rare disease diagnosis doesn’t just impact the individual—it affects the entire family. The emotional, physical, and mental strain can be overwhelming for patients, parents, caregivers, and siblings alike. Navigating the uncertainties of Complex Lymphatic Anomalies (CLAs) can bring feelings of fear, anxiety, stress, and isolation. That’s why taking care of your mental health is just as important as managing physical health.

Whether you are living with a CLA, caring for a loved one, or supporting a sibling, your mental well-being matters. Finding the right support and resources can help you cope, build resilience, and connect with others who understand what you’re going through.

On this page, you’ll find:

  • Reading Material – Articles and guides to help you understand and manage the emotional impact of living with a rare disease.
  • Expert Insights – A video by Al Freedman, PhD, a psychologist and rare disease parent, offering guidance on mental health and coping strategies.
  • Support Organizations – Links to trusted resources providing mental health support for patients, caregivers, and families.

You are not alone. Support is available to help you through every step of this journey. Explore the resources below and take care of your mental health today. 


Here are three recommended resources that provide tailored mental health care for individuals and families navigating complex health challenges:

Rareminds
Rareminds is a pioneering nonprofit organization based in the UK, offering specialized counselling and psychotherapy services specifically for the rare disease community. Established in 2014, Rareminds’ mission is to make affordable, accessible mental health care an integral part of rare disease treatment. Through online counselling and wellbeing services, they support individuals in navigating the psychological and emotional aspects of rare conditions. 

Rare Counselling - Dr. Albert Freedman
Dr. Albert Freedman, PhD, is a licensed psychologist with a specialized practice serving patients and families affected by rare diseases and complex medical conditions. With clients across 40 states in the USA, Dr. Freedman provides counselling services designed to meet the unique mental health needs of individuals and families dealing with rare diseases. 

Global Genes is committed to providing information, resources and connections to all communities affected by rare diseases.

Starting Conversations About Living With a Rare Condition

Living with a rare condition presents a unique set of challenges, not least of which is deciding how and when to share information about the condition with others. It’s a deeply personal decision, influenced by how comfortable we are with revealing personal details and our relationships with those around us.

The Challenge of Sharing

For those with rare conditions, retelling your 'story' to healthcare professionals is a common part of receiving appropriate care. However, in everyday interactions, you might not always feel the need or desire to share as much. Deciding whether to disclose details about your or your child's condition depends on several factors: the context, the nature of your relationship with the person, their likely response, and the necessity of the disclosure, especially in health crises or professional settings.

Managing Perceptions and Assumptions

A rare condition can sometimes lead to assumptions about physical appearance or behavior, which can be distressing. How you choose to respond or correct these misconceptions is a personal choice and can vary depending on the situation and your emotional state at the time. There may also be concerns about being treated differently or facing invasive questions that you prefer not to answer.

Preparation and Strategy

Thinking ahead about what you want to say can make these conversations easier. Consider who you are speaking to, what you want them to understand, the timing of the discussion, and your environment. Being clear on why you want to share information and what you hope their response will be can also guide the conversation.

Support in Professional and Educational Settings

For those affected by a rare condition, whether directly or as a carer, it's crucial to know that you can request 'reasonable adjustments' at work or in educational settings. These adjustments are meant to ensure that you are not at a disadvantage and can include modifications like a shorter workday, changes in responsibilities, or physical accommodations.

Communicating with Children About Their Condition

Talking to children about their rare condition should be handled delicately and thoughtfully, considering their age, awareness, and communication ability. It’s beneficial to first process your own feelings, as this affects how you discuss the condition with your child and helps you to provide reassurance and support.

Children’s concerns are often practical and based on how the condition affects their daily lives. They may wonder about hospital visits, differences in appearance, or limitations on activities. Using the name of the condition in everyday conversation can help normalize it, making it easier for them to understand and accept.

The Power of Community

Knowing that they are not alone can be incredibly comforting for someone with a rare condition. Engaging with community groups, whether through online platforms or in-person events, can provide significant emotional support and reduce feelings of isolation.

Conclusion

Ultimately, each conversation about a rare condition is unique. Balancing openness with the need for privacy, managing how others perceive the condition, and providing support are all part of navigating these complex interactions. By being prepared and understanding your rights and resources, you can handle these discussions more confidently, ensuring you and your loved ones receive the support and understanding you deserve.

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