As with you Sarah, I try not to mind when friends or family say things like this, because it means they’re still seeing me as me, not as the disease.
Hugs and many thanks for your indomitable spirit, and sharing your life with such honesty and rawness.
]]>Love,
Beth
I lost a close family member to ALS, somehow it is healing to read about your experiences. I have trouble even understanding why that is true sometimes as it often breaks my heart. I guess it is a combination of appreciation of how you persevere along with a need to understand this mean disease.
I write today because your point about appreciating what you can do and what you have is so true. Health is something we all take for granted until we do not have it. We do not even notice how we feel until we do not feel well. Today I won’t take it for granted, nor tomorrow probably, because what you wrote resonates. But how do we keep up that appreciation of our health every day? We should! It should be our duty if we are healthy, or even reasonably healthy, to honor you and others and appreciate what we have.
]]>