Here we go.
This is the week my Lemtrada (alemtuzumab) infusions begin. A few weeks ago I wrote about how Lemtrada has been successful in stopping disease progression in folks with relapsing-remitting multiple sclerosis, and those who have transitioned to secondary progressive MS but continue to have relapses. There have also been many reports of people who have had some of their MS symptoms improved after being treated with the drug. But then, I was writing about reports. Now, it’s personal.
Treatment starts before the IV
Two days before my first infusion, I began to pre-medicate to reduce the chance of some side effects. I’m taking Acyclovir to reduce the chance of contracting the herpes virus. Doctors say that Lemtrada treatments raise the chance of getting this virus for some people. The allergy drugs Zantac and Zyrtec are being taken to limit hives and rashes. I also have on hand ibuprofen, Benadryl and hydrocortisone creme to use, if necessary, to treat any pain, rash, hives or fever.
The five days of infusions actually involve three drugs. First comes Solumedrol. My neurologist tells that it serves two purposes. As a steroid it calms the body’s immune system. But it’s also a histamine blocker, serving as another barrier to hives, rashes and the like. I’m to receive 1,000 mg on the first three days, 500 mg on the second, third and fourth day, and 250 mg on the final day.
Next comes 25–50 mg of Benadryl by IV. Finally, the star of the show … Lemtrada — 12 mg over four hours. Oops, not done yet. After all the drugs are finished, there’s a two-hour “watch” period, during which IV fluids continue. In all, 7–8 hours each day. Whew!
For the next few months I’ll be drinking lots of water. (That’s going to be tough for this MSer who has spent the past 35 years trying to avoid drinking the stuff). My neuro, and most “Lemmies” who’ve had these infusions, say it’s the best thing to do to limit uncomfortable side effects. Consistently flushing the toxins and dying cells out of my system, they say, is the best approach to feeling as good as I can.
Watch what you eat
There are some foods that I’ve been told to avoid for the first month after my infusions. This is to reduce the risk of Listeria. They include:
- Hot dogs and deli meats (This will be a hardship)
- Refrigerated pâtés and meat spreads
- Unpasteurized milk and dairy products
- Soft cheese made with unpasteurized milk, e.g. feta, Brie, queso fresco and Camembert
- Raw sprouts
- Smoked seafood
- Raw fish, e.g. sushi (I wouldn’t, anyway)
- Raw eggs or meat
- Prepared salads, e.g., chicken salad, ham salad and egg salad
- Wash all vegetables and fruits thoroughly
And after the infusions
I’ve been told to expect a roller coaster ride of good and bad days for a week or two — headache, body aches and fever — some days feeling like I’ve crashed and burned, and others where I’m feeling very well. After a month I’ll be scheduling physical therapy. After four or five months I’ve been told that I should see an improvement in my overall endurance.
That’s quite a ride for a 68-year-old guy to anticipate, but, as I’ve said several times in writing about Lemtrada, the potential benefit makes the risk and discomfort worthwhile.
If you’re a Lemmie, or planning to become one, your treatment plan may vary, but the basic infusion process should be pretty much what I’ve described.
Now, my fingers are crossed. Unless I’m really dragging, and at the bottom of the roller coaster loop, I’ll be reporting on my ride in a column in another week, or so.
[Please check out my personal blog at: www.themswire.com]
Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to multiple sclerosis.