Plegridy Anniversary

Hello everyone,

One year has passed since starting plegridy, my very first DMT. My RRMS is not active, and I am so used to the treatment that I hardly think about it.

It wasn’t easy when I started this treatment. I recall the first 3 months, the fatigue, the headaches, the flu symptoms I experienced for a couple of days after injecting. Luckily, now, all I get is less than 20 hours of these symptoms, and they are normally mild. I get a migraine almost every time after injecting. It starts about 10 hours after the injection. I control it with paracetamol. Of course I get the red injection site (erethyma), but I apply some gel on it (witch hazel gel) and I can easily manage this problem. I have found out that eating porridge in the morning makes the erythema less itchy. I have no idea why, but it certainly helps. Apart from plegridy, I also take a high dosage of vitamin D.

Anyway, plegridy is definitely not the nightmare I though it would be. I may eventually swifch to something else, more effective, in a year or so, but for now, so far so good. I will see my neuro in March. Let’s see what happens.

Sending you all positive energy.

Maria

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Good to hear that Pledigry injections are now more or less a matter of routine and have few side effects.

I’ve been injecting Avonex for some 18 years now ( basically same as Pledigry but injected every week into muscle). In all those years I’ve never been able to work out why the after effects are worse some weeks than others but so be it. Might have had one relapse but no new lesions for years and years now ( just received my latest and more or less standard letter to say that my MRI in January showed no change compared to the one a year ago).

Think I might be drifting into so called Secondary Progressive but still mobile and active ( will be 71 in a few weeks).

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It’s great to hear Avonex has been working for you. Side effects may be worse because of heat, stress, etc. It’s good to hear you are active and mobile. Keep going strong.
Maria