I've just been refused travel insurance from World First. The questions that throws me out is:
Do you have a high white cell count? high being 11 or 1100 per cubic millimetre. My stats show my WBC count as 78 so I answered yes. I've tried talking to them but it's all in the algorithms and so no one has any idea. They did insure me two years ago with same answers to all questions. I'm on W&W and other than CLL in good health.
Has anyone else had this problem and if so found a solution?
I'd just give up holidays but have family that live abroad.
Thanks Is
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is-sul
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I booked a holiday to San Francisco and managed to get travel insurance for me and my friend for £120 for 5 nights on the basis that i wasn't having treatment. I am at work now and cant remember the name of the company but i will let you know when i get home...
Unfortunately due to my increased WBC, 220, i have had to cancel the holiday as i have been advised not to fly....the long flight in an air conditioned plane plus the risk of DVT. gutted but better healthy.
I am not prepared to go against medical advice, its not worth the risk. At the time it was touch and go as to whether i needed to start treatment or not as my lymph nodes were greatly enlarged and my WBC had shot up dramatically.
At the meeting to discuss test results and possible treatment it was decided that treatment could be delayed but that i would need check ups more often, every 4 weeks.
I asked about my holiday and was strongly advised against it due to the length of the flights and the length of time spent in airports, the risk of DVT and due to the cost of health care in America and the possibility of the insurance company not paying out to get me home, ( insurance companies are very good at trying anything they can to get out of paying out, i know i used to work in the industry).
Given i have 2 very young grandchildren and a third due next March, i wasn't prepared to risk it for the sake of a 5 day holiday.
If everything settles down and i am still on W&W i will consider holidays next year, but probably ones with shorter flight times.
We Should be very careful about applying specific advice given to us by our doctors knowing the full details of our case to others who may have very different things going on that the doctor is aware of.
I use to travel abroad quite a bit and never purchased travel insurance. I haven't traveled abroad since I was diagnosed with CLL (nothing to do with CLL). Is this something you are doing because you have CLL, or is it something many people do even if they are perfectly healthy?
It’s a requirement in the U.K. particularly Patagozon because whilst we have reciprocal health arrangements for public medical care in EU countries (using a EHIC card), private insurance is needed for repatriation, additional costs, lost luggage and medical care that cannot be provided in public hospitals.
I’m not sure if you’re in the USA where people may have private health insurance and travel within the US but with a reliance on the NHS, we need to cover ourselves regardless of CLL. if we leave our own shores.
I'm now insured with World First and even better with no excess. I have always had an excess in past but that one change in answer has made all the difference - sanity and holiday now saved!
hi, as promised, but a little later than planned, the name of the travel company I used, HolidaySafe travel insurance.
They insured me to travel having CLL for £120 but the excesses on the policy were loaded, so as well as the £60 standard excess per person, it had an additional £200 per person excess,
When I called them re cancelling my holiday, the lady I spoke to was very helpful as because I had only paid the deposit for my holiday which was less than the excesses, she suggested I just cancel the policy and she would refund me half the cost of the policy.
I had explained why I was cancelling and a few days later I received flowers and a card with best wishes.
When I did a quote on their website for insurance with CLL and having treatment the cost sky rocketed to £973 for 5 days.
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