<div>
 My family and I have recently lost our insurance and any type of government assistance.
</div>
<div>
 <strong>My son has ADHD and takes medicine daily to help him focus and concentrate at school.</strong>
</div>
<div>
 So since we lost our insurance, his medicine is no longer being covered, and it falls on me.
</div>
<div>
 <strong>It is around $412!</strong>
</div>
<div>
 And the pharmacy will not accept any type of discount card.
</div>
<div>
 Along with needing his medicine, we are also struggling for food and groceries.
</div>
<div>
 My spouse works, but his paycheck is covering all the other bills we have and doesn't leave us with much of anything.
</div>
<div>
 I have never asked for help and hate putting my business out there, but I'm also a mother and will do anything I can to get us the help we need!
</div>
<div>
 Even a like or share would be greatly appreciated.
</div>
<div>
 Thank you and God bless
</div>

Urgent Help Needed for Son’s Medicine and Groceries

<p>Hello my name is Denise and I'm Kelley's sister in law and with a very broken heart I am creating this fundraiser to help raise funds to cover unexpected burial funds. 
</p>
<p>To know Kelley was to love him. He truly never met a stranger and was one of the most giving and kindest souls ever to grace this earth. Sadly he was called home Saturday afternoon on July 10th 2021. My brother Dean Sines and Kelley shared a love that most can only dream to find. They spent almost 25 years together and never let life's trials shatter them. This comes as a complete life altering shock to all of us for he was very healthy and active in activism. 
</p>
<p>Unfortunately as we went to plan his services today, we found out there was no policy to cover any of the cost. With the struggles of the pandemic hitting and barely making it by already this is a more devastating shock for Dean on top of the loss. I ask please no matter how much if you can please,help me help him,  in giving this amazing man a proper memorial. More than anything keep him and all the lives that were touched by Kelley, for we lost a sweet angel on earth and Heaven definitely gained one.  Thank you 
</p>
<p><br />
</p>
<p>Kelley John Hammock 
</p>
<p>March 7, 1949 to July 10,2021
</p>
<p>Forever in the arms of the Lord
</p>

Kelley Hammock Memorial and Burial Fund

I would like for you to meet Susan.  Susan and I met in elementary school and she is one of the most remarkable people I have ever met.  She is, by far, the fiercest fighter I have ever known.  Susan is a wife of 26 years to Chris Kiechel and the mother of three children- Christian age 25, Joshua age 23, and Sloan age 21.<br /><br />Growing up, Susan was alway active in sports.  Throughout Middle School and High School she played on the basketball, softball, and soccer teams.  At Auburn University, Susan played on the intramural soccer team.  The school did not have a Varsity Women’s Soccer team.  Susan saw the injustice in the difference of funding for men’s and women’s sports teams and she did something about it.  After two years of research, she determined that 12% of funds were being used for women’s sports teams while half the student population was female.  She also polled women on campus and found ample support for a women’s varsity soccer team.  She then appealed to the university to implement a varsity soccer team.  Upon their refusal, Susan took the issue to the Office of Civil Rights at the Education Department and sued Auburn under Title IX of the federal education code which bars discrimination on the basis of gender.  The University settled out of court in 1993 and agreed to fund a women’s varsity soccer team.  At this point, Susan was no longer eligible to play but today Auburn has a first class women’s varsity soccer team.  Recently, Susan returned to Auburn to see the team play on the field she helped to build.  She also bestowed the honor of naming rights to the field (that she held but never used) to current coach, Karen Hoppa.<br /><br />I tell you this story so you have a glimpse of the fighter that is Susan Kiechel.  Susan is now in a different fight - she is fighting for her life.<br /><br />You see, in December 2000 Susan began experiencing problems picking up her feet.  This was devastating to a star athlete.  After many tests, Susan was diagnosed with CMTX.  This is a genetically inherited, rare, progressive neurological disease that affects the myelin sheath that wraps around the peripheral nerves that control muscles and causes it to slowly shred apart.  Over time it causes the loss of normal function to the lower legs/feet and hands/arms.  Within 4 months she required leg braces and forearm crutches to walk.  The progression of her disease was much quicker and more severe than expected, so she sought additional care from the CMT clinic at Wayne State in Detroit in July 2001.  The specialists there quickly realized something wasn’t right and began further, more extensive testing.  Her illness was progressing too quickly and becoming too severe to be explained only by the CMT.<br /><br />In July 2001, Susan was diagnosed with another rare neurological disease called CIDP (Chronic Inflammatory Demyelinating Polyneuropathy).  The CIDP was in addition to the CMT.  Susan was now fighting two rare and progressive neurological diseases.  CIDP is an autoimmune disease that causes the immune system to think the myelin sheath around the nerves is a foreign body and causes the body’s immune system to aggressively attack it.  In most cases, CIDP only affects the limbs, though it generally causes paralysis.  However, in 5-10% of cases, CIDP progresses to affect the trunk and becomes a life threatening illness because it will affect the nerves around the vital organs.  In December 2002, Susan joined the 5-10% of CIDP patients with a life threatening version of the disease.<br /><br />To slow the progression of  CIDP, Susan began Intravenous immunoglobulin (IVIG) treatments on September 12, 2001.  These treatments require a hospital stay every 28 days.  Susan was determined to fight to slow the progression of these diseases so her children would have a mother alive to raise them.  While the treatments have slowed the progression and kept her alive, they have come at an extremely high price. Each month, the disease is able to make some progress.  The IVIG slows the progress but it does not stop it.  Complications of IVIG treatment include stripping the body of magnesium, Vitamin D, and iron.  To counter this, Susan must receive multiple infusions of magnesium and iron each month along with countless other medications to treat the side effects of the IVIG treatment.  Also, the IVIG treatments induce meningitis which is the swelling of the membrane surrounding the brain and spinal cord.  This swelling threatens Susan life constantly and causes excruciating pain.  Each month, Susan’s neurological team walks the line of giving enough treatment to keep her alive but not enough that it does more harm. <br /><br />Susan has endured 232 monthly treatments.  This far surpasses the amount of IVIG treatments any other patient in the world has completed.  While the treatments have slowed the progression of the CIDP, they are also damaging her body every month.  Susan’s body can not withstand many more treatments.  She will die soon.<br /><br />Susan has fought every day for over 17 years to stay alive until a treatment could be found.  That day has arrived.  Clinical trials show Stem Cell Transplant is a very effective treatment for her neurological disease.  She has gone through all the testing phases and has been APPROVED by doctors in Charlotte to received a Stem Cell Transplant.  This procedure will save her life.  It will end her 17 year struggle.  It will return her to her husband and children.  It will help her lead a normal life for the first time in 20 years.  The only thing standing in the way…….money.  Processing the stem cell transplant through insurance is not an option.  The only option the hospital is providing Susan is an upfront cash payment. Please help us raise the money for Susan to receive this Stem Cell Transplant.  Please don’t let money be the reason a wife, mother, advocate, fighter, hero dies.<br /><br /><br />We thank you for your participation.  Please donate and please spread the word.  To us, you too will join the rank of a hero.

Life Saving Treatment for Susan

If you enjoy the videos  consider helping. Making.  These videos and editing isnt cheap There’s always something that pops up the requires money I just want to make people laugh with the message satire with a message. I need to get the supplies camera computer outfits for my characters and it cost money to boost a post on Facebook they charge you to get your video some more news feeds

Raising money to dump Trump & laugh

On the morning of March 29th 2018, my wife and I were awakened by our 13 year old son who told us our house was on fire.  We all were able to escape but there is substantial damage to our porch and living room. We don’t have homeowners insurance, as we couldn’t afford it anymore after adding my daughter to our car insurance which tripled. I know thats not an excuse but one never honestly thinks something like this will happen.   All I’m asking for per person is a $5 donation so that I can have this repaired as soon as possible. It will not replace any possessions but will strictly be used to repair the structural damage. I honestly hate even to ask for anything from anyone but I need this help unlike any I’ve ever needed in my life. Thank you from the bottom of my heart for anything you might be able to give. <br /><br />God Bless,<br />Jason Lowery.

House Fire

<strong> “Mom and Dad’s house is flooded.  It’s bad.”</strong><br /><br />Nothing prepares you to receive that text.  Not poring over the news.  Not obsessively watching the weather.  That was at 3:44 pm on September 11, 2017.  Over the next twelve hours, the water continued to rise.  This was the worst flooding Middleburg, Florida, had seen in over 100 years, with Black Creek swelling 28.5 feet above normal.<br /><br />The community was entirely unprepared.  Families were stranded in their homes with no means of escape as the waters rushed in.  My brothers, Nyk and Clayton, and a group of others gathered the boats they had and began rowing their neighbors to safety.<br /><br />Texts from Clayton:<br /><br /><strong>“I never would have thought it would get that high.  It’s crazy.  It was weird going down the creek after those people today.  Rowing over people’s fences and plants.”</strong><br /><br />Even more difficult was rescuing Mama and Daddy (Debbie and Harry Peppard).  The water was rising 6 inches an hour in the house they had owned for 30 years.  A lifetime of memories, scrawled pictures from grandbabies, and the home where they had raised their children.  When Black Creek finally crested, over two feet of water stood in their home.  Everything it had touched was ruined, including a box of family photographs, some black and white from Mama’s childhood and her mother’s childhood.<br /><br />The most difficult part was hearing Daddy’s heart break as he watched his years of hard work be destroyed.  He had just finished laying the new floors that replaced the original carpet and its well-worn paths made by children’s feet.  The bathroom he had renovated to Mama’s exacting specifications was now covered with the backed-up contents of the toilets mixed with creek waters.  Nothing can describe that feeling of loss.<br /><br />I (Kristi (Peppard) Sargent) created this GoFundMe account for two reasons.  The first one is obvious:  Our parents need a place to live.  The second one though… Nyk, Casey, Clayton and I can’t watch Daddy try to piece this back together with blood and tears.  He and Mama have given so much; sacrificed so much.  It is our turn as their children to try to make this right for them, just like they placed band-aids and rushed us to the ER when necessary. Any help you can offer is so gratefully appreciated.

Stephen Bradley