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Mavenclad (Cladribine) 2nd week update - Multiple Sclerosis Medication

A bit later than expected but, here’s an update on second and final week of taking the Multiple Sclerosis medication Mavenclad (Cladribine) this year. I'm surprised and thankful, not too bad at all in terms of side effects. Some continued itching, a reduced winded feeling but extra nausea, with a decreased appetite. Extra fatigue and a little hair loss, more than usual for me. I know some people experience different side effects so I am thinking myself lucky and hope next years course will follow the same route. My neurologist has arranged an MRI for 6 months time to compare to my pre medication scan and I have my blood test to check liver, kidneys and lymphocyte levels soon. Remember the following may help if you are taking MS medication or are taking or thinking about Mavenclad… Medication monitoring app: https://www.mytherapyapp.com/ If you need any support from people who are taking Mavenclad for Multiple Sclerosis please head over to the Facebook group. I have found it to be very helpful:   / mavenclad   If you are taking this medication or are about to, please remember that the tablets are uncoated. Take extra precautions to not touch the tablet and clean all work surfaces that it does touch. Until next time, stay healthy x