Good day everyone. So it's been almost 3 years since I've been diagnosed. However, this is the first time that I would be travelling. Is there anything that I should be aware of? Like when I'm in the plane or flying? Landing? Anything specific I should look out for with respect to pain or nausea etc?
Or will it be okay?
Mind you, I usually have pains when it's about to rain.
Written by
Stephanie0210
To view profiles and participate in discussions please or .
Where are you going? I hope you'll have a lovely time
Definitely get travel insurance that will cover your Lupus or any other condition you have. I was lucky to find one through compare the market but I think there are a few specialist ones too. Sadly it is more expensive but it will be worth it if you do fall ill or flare up while on holiday.
If you are going somewhere sunny (or even not that sunny) bring sunscreen and hat! This can be important to protect you.
Check online if your drugs are allowed where you are going, ring your GP and get them to sign a copy of your prescription in case. I was not questioned at security but you could be and it's quicker if you can be like "I'm prescribed this, here is a signed prescription". I also brought my most recent letter from my Rheumy in case. Also make sure you have enough or extra medication for the trip.
I think one thing you may have to ask is if you have the sticky blood symptom (lupus anti colant). As high altitudes, like on planes, can increase risk of blood clots but if your not already they can give you blood thinner, such as aspirin just for the trip
A lot of people recommended using the special assistance service at the airport, especially if fatigue or any mobility issues impact you along with lupus. Apparently very helpful
Thank you so much for your insight! I will definitely get a signed prescription when I go on holidays to ensure I don't get my medication taken away. Thank you very very much.!
We have an article on our website about going on holiday with lupus which has lots of information and advice for travelling. You can read it at lupusuk.org.uk/going-on-hol...
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.