chronic lyme disease with a taste of nut
Grateful to read how another with chronic pain reaches out to the Lord – a good reminder that God is the only One to meet all our needs.
One of the most common statements among autoimmune disease sufferers is that those who haven’t experienced the disease themselves or seen a closed loved one suffer often do not believe the level of pain suffered is as severe as we say it is. Lay persons cannot comprehend in this age of medicine that someone would have to suffer as we do so they think that we are exaggerating our symptoms. It is easy to see how they would believe this when our pain and activity levels are so inconsistent. To the lay person it would seem we use our disease as a crutch. That judgement hurts. The lack of support among friends and family of autoimmune disease sufferers is high.
It would seem that loved ones want to fix us by offering remedies that worked for their grandma’s osteoarthritis, by recommending unconventional treatments that can do permanent damage to our…
View original post 622 more words
A Literary Magazine that gives platform to writers and artists with invisible illness.
Staying grounded while recovering from Lyme disease
A Blog About Living with Lyme Disease
Radical hope. Compassionate change. 501(c)3 non profit
My journey in getting treatment for Lyme Disease
Advocacy is FREE and its never-ending ripples spread awareness for all worthy causes!
A Lyme Disease Blog from Bruce county ontario
Recovery from Lyme Disease, chronic pain, and fatigue
How the light gets in.
My Journey With Bee Venom Therapy