As some of you will know my sister in law opted to use the services of dignitas 11 days ago after MS had taken away most of her physical abilities. To be able to use their services you have to be able to administer the drugs yourself with no outside assistance, I can imagine nothing worse than my brother having to watch his wife of 36yrs go through such a process on top of which he has to self isolate for 14days on returning from Switzerland and be interviewed under caution by the police tomorrow. He will get a swiss death certificate which I presume will state the final cause of death, rather than the MS & inoperable cancers which would have ended her life “naturally” in way less than 2yrs anyway. Luckily they were able to afford the Dignitas fees but my brother now has no income as he was her full time carer and clearly her allowances are now stopped. They were/are an active cycling family, from cycling to Israel and back for a honeymoon, going car free with two small kids in the 90’s and being pedalled around sat in her wheelchair in what I can only describe as a glorified ice cream trike this summer 😀 My heart goes out to all the MS sufferers and carers out there.
Not looking for or asking for any sympathy, just a reminder to love life and keep on doing what you love whilst you still can. Dignity in dying – my SIL had it by the bucketful. Thanks DB.