[Congressional Record Volume 171, Number 91 (Thursday, May 29, 2025)]
[Extensions of Remarks]
[Pages E483-E484]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
RECOGNIZING MAY 2025 AS GBS|CIDP AWARENESS MONTH
______
HON. JOHN GARAMENDI
of california
in the house of representatives
Thursday, May 29, 2025
Mr. GARAMENDI. Mr. Speaker, I rise today to recognize the month of
May as GBS|CIDP Awareness Month.
Guillain-Barre Syndrome (GBS) is an inflammatory disorder of the
peripheral nerves outside the brain and spinal cord. GBS is
characterized by the rapid onset of numbness, weakness, and often
paralysis of the legs, arms, breathing muscles, and face. Paralysis is
ascending, meaning that it travels up the limbs from fingers and toes
towards the torso. Loss of reflexes, such as the knee jerk, are usually
found. Usually, a new case of GBS is admitted to ICU (Intensive Care)
to monitor breathing and other body functions until the disease is
stabilized. Plasma exchange (a blood ``cleansing'' procedure) and high
dose intravenous immune globulins are often helpful to shorten the
course of GBS. The acute phase of GBS typically varies in length from a
few days to months. Patient care involves the coordinated
[[Page E484]]
efforts of a team such as a neurologist, physiatrist (rehabilitation
physician), internist, family physician, physical therapist,
occupational therapist, social worker, nurse, and psychologist or
psychiatrist. Recovery may occur over six months to two years or
longer. A particularly frustrating consequence of GBS is long-term
recurrences of fatigue and/or exhaustion as well as abnormal sensations
including pain and muscle aches.
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is a rare
disorder of the peripheral nerves characterized by gradually increasing
weakness of the legs and, to a lesser extent, the arms. It is the
gradual onset as well as the chronic nature of CIDP that differentiates
it from GBS. Like GBS, CIDP is caused by damage to the covering of the
nerves, called myelin. It can start at any age and in both genders.
Weakness occurs over two or more months. Unlike GBS, CIDP is chronic,
with symptoms constantly waxing and waning. Left untreated, 30 percent
of CIDP patients will progress to wheelchair dependence. Early
recognition and treatment can avoid a significant amount of disability.
Post-treatment life depends on whether the disease was caught early
enough to benefit from treatment options. The gradual onset of CIDP can
delay diagnosis by several months or even years, resulting in
significant nerve damage that may take several courses of treatment
before benefits are seen. The chronic nature of CIDP differentiates
long-term care from GBS patients. Adjustments inside the home may need
to be made to facilitate a return to normal life.
I continue to champion key priorities of the GBS|CIDP community,
including cosponsoring H.R. 1143, the Medicare IVIG Access Enhancement
Act, that will facilitate home infusion for the treatment of CIDP and
MMN.
I call on my colleagues to join me in recognizing May as GBS|CIDP
Awareness Month and in supporting this important legislation by
becoming a cosponsor of H.R. 1143 that will help promote therapy
adherence, enhance quality of life, and promote positive health
outcomes for beneficiaries with CIDP and MMN.
____________________