Hi, I'm Jessi! I'm 33 years old and I live in Germany.
Life hasn't been quite the same since I had COVID-19. Living with Long COVID and ME/CFS has completely changed my everyday life. On top of that, I was diagnosed with Cold Agglutinin Disease (CAD), a condition that makes cold temperatures much more than just uncomfortable for me. I used to work as a horse groom, spending most of my days outdoors, no matter the weather. Back then, the cold was simply part of my daily routine. Today, it's become one of my biggest challenges
When Cold Becomes an Everyday Obstacle
With CAD, certain antibodies in the blood react to low temperatures. For me, this means that temperatures below around 18°C (64°F) can already trigger significant symptoms. Things that used to be completely normal now require a lot of planning. Simply going outside spontaneously, taking a trip or running errands – none of these things can be taken for granted anymore. What I miss most is the freedom to be spontaneous. I constantly have to consider: How cold will it be? How long can I stay outside? And what impact might it have on my health afterwards? The changes happened gradually. At first, there was no way of knowing just how severely my illnesses would eventually affect my everyday life. Over time, I had to accept more and more limitations.
Three Winters, Three Changes
The progression has become particularly noticeable when it comes to heated clothing. During my first winter, the heated hoodie was enough to help me cope with the cold. During the second winter, I realised that this was no longer sufficient. Heated gloves became a necessity. And now, as I approach my third winter, I need heated socks as well. What might seem like a small change to others clearly shows just how much my physical limitations have increased over time. It isn't always easy to deal with this progression. Beyond the physical symptoms, it also means emotionally having to let go of a little more independence and freedom each time.
Looking for a Better Quality of Life
Since cold temperatures have such a significant impact on my everyday life, I specifically started looking for high-quality heated clothing. That's how I discovered Bertschat. It was important to me to find products I could rely on – clothing that would genuinely support me in my everyday life. Of course, heated clothing cannot cure my illnesses. It doesn't take away the exhaustion caused by ME/CFS or the symptoms of CAD. But it creates opportunities that might otherwise no longer be possible. For some people, a heated jacket is simply a practical item of clothing for cold winter days.
''For me, it means a little more quality of life and independence.''
Keeping a Positive Outlook
Of course, there are days when I wish I could have my old life back. Days when accepting yet another limitation feels particularly difficult. Nevertheless, I try not to lose my positive outlook. I've learned that quality of life doesn't always mean being able to do everything. Sometimes, it means finding new ways to enjoy life despite all the limitations and appreciating the little opportunities and achievements along the way. I can't simply make my illnesses disappear. But I can try to create the best possible life for myself with the opportunities I still have.
''And if heated clothing helps me regain even a little bit of freedom, then that means an incredible amount to me.''
A Little Warmth and a Wonderful Connection
Finally, I'd like to say a heartfelt thank you to Bertschat. What started as a search for high-quality heated clothing has turned into a truly positive experience that goes far beyond the products themselves. I particularly appreciate the friendly and uncomplicated communication, as well as the understanding shown towards my individual situation. It's wonderful to meet people and companies where it's not just about the product, but also about the person behind it. Thank you for this lovely connection and for accompanying me on my journey, even if it's just a little part of the way.
Follow My Journey
If you'd like to follow my journey and get a glimpse into my everyday life with CAD, Long COVID and ME/CFS, you can find me on Instagram at @jessi.lebt, where I share my experiences, challenges and little moments of happiness along the way.
