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# The Zebra's Guide to Love and Relationships

Updated: Jun 15

Greetings, zebras! No doubt, you are well acquainted with the obstacles of navigating life with EDS, a rare genetic condition impacting the body's connective tissues. EDS manifests in hypermobile joints, elastic and delicate skin, and tissue vulnerability. Beyond these physical challenges, it significantly influences various facets of our well-being, including sleep, digestion, circulation, and immunity. Today, let's delve into a topic frequently sidelined or disregarded: the impact of EDS on our romantic relationships.


A couple in love

As a person with EDS, I know how hard it can be to find and maintain a romantic partner, a friend, or even a family member who understands and supports us. EDS can make us feel isolated, misunderstood, and rejected. It can also make us doubt our worth and attractiveness. We may struggle with intimacy, communication, and trust. We may face stigma, discrimination, and ignorance. We may have to deal with the impact of EDS on our mental health, such as anxiety, depression, and ADHD.


But I also know that EDS does not define us. We are more than our diagnosis. We are human beings who deserve love and happiness. We have strengths, talents, and passions. We have dreams and goals. We have feelings and needs. And we have the right to share them with someone who respects and appreciates us.

So, how can we find and manage love and relationships as a person with EDS? Here are some tips that I have learned from my own experience and from other zebras who have shared their stories with me:


- Be honest and open. One of the most important things in any relationship is honesty and openness. Don't be afraid to tell your partner, friend, or family member about your condition, symptoms, limitations, and needs. Explain to them what EDS is and how it affects you. Educate them about the signs and symptoms, the treatments, and the resources available. Share with them your feelings, your fears, and your hopes. Let them know how they can help you and support you. And don't forget to listen to them as well. They may have questions, concerns, or emotions that they want to express. Communication is a two-way street, and it can help you build trust and understanding.


- Be realistic and flexible. Another key thing in any relationship is realism and flexibility. Don't expect your partner, friend, or family member to be perfect or to know everything about EDS. They may make mistakes, say the wrong things, or do the wrong things. They may not always be able to meet your expectations or needs. They may have their issues or challenges that they are dealing with. Remember that they are human, too, and they are doing their best. Try to be patient, forgiving, and compassionate. And don't be too hard on yourself, either. You may not always be able to do what you want to do or what others want you to do. You may have to cancel plans, change routines, or compromise on some things. You may have to deal with pain, fatigue, or flare-ups. You may have to ask for help, accept help, or give help. Be kind to yourself and others. And be willing to adapt and adjust to different situations and circumstances.


- Be positive and hopeful. A third essential thing in any relationship is positivity and hope. Don't let EDS take away your joy and happiness. Don't let it make you feel hopeless or helpless. Don't let it stop you from pursuing your interests and hobbies. Don't let it prevent you from making new friends or finding new love. Don't let it ruin your existing relationships or your self-esteem. Instead, focus on the positive aspects of your life and your relationships. Celebrate your achievements and successes. Appreciate your partner, friend, or family member for their love and support. Enjoy the moments and memories that you share. Find humour and laughter in everyday things. Seek inspiration and motivation from other zebras who have overcome obstacles and achieved goals. And keep your faith and optimism for the future. Remember that you are not alone, and EDS does not define you. You are a zebra, and you are beautiful and strong.


I hope this blog post has helped you in some way. I know that finding and managing love and relationships as a person with EDS is not easy, but it is possible. And it is worth it. You deserve to be loved and to love yourself. You deserve to be happy and to make others happy. You deserve to live and to love. And you can do it. You are a zebra, and you are amazing.


Thank you for reading, and please feel free to comment, share, or contact me if you have any questions or feedback. I would love to hear from you and to connect with you. Until next time, stay zebra-tastic!


Disclaimer: Ehlers Danlos Boy is a dedicated platform offering news and information about the disease. We do not offer medical advice, diagnosis, or treatment. The content provided is for informational purposes only and should not replace professional medical advice. Always consult your physician or qualified health providers for personalized medical guidance. Any reliance on information from this website is at your own risk. For further inquiries, please contact us at ehlersdanlosboy@gmail.com. Based in South Africa.

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