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	<title>Family Stories Archives - Friends of Karen</title>
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	<title>Family Stories Archives - Friends of Karen</title>
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		<title>A Survivorship Story: Supporting the Transition After Treatment</title>
		<link>https://www.friendsofkaren.org/survivorship-story-supporting-transition-after-treatment/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=survivorship-story-supporting-transition-after-treatment</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Fri, 15 Sep 2023 19:50:00 +0000</pubDate>
				<category><![CDATA[All Content]]></category>
		<category><![CDATA[CCAM 2023]]></category>
		<category><![CDATA[Family Stories]]></category>
		<category><![CDATA[What's New]]></category>
		<guid isPermaLink="false">http://www.friendsofkaren.org/fokdev2022/?p=6160</guid>

					<description><![CDATA[<p>Friends of Karen began a pilot program in late 2022 to continue to provide a limited number of supports to children who have gone off formal treatment, but continue to have serious healthcare, social and educational needs. Olivia’s mother Johanna shares more below about how Friends of Karen has helped her family during this crucial stage, after Olivia was treated...</p>
<p>The post <a href="https://www.friendsofkaren.org/survivorship-story-supporting-transition-after-treatment/">A Survivorship Story: Supporting the Transition After Treatment</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<p><img fetchpriority="high" decoding="async" class="wp-image-6163 size-medium alignright" src="https://www.friendsofkaren.org/fokdev2022/wp-content/uploads/2023/08/olivia-ross-alyssa-02-e1693252313829-282x300.jpeg" alt="" width="282" height="300" srcset="https://www.friendsofkaren.org/wp-content/uploads/2023/08/olivia-ross-alyssa-02-e1693252313829-282x300.jpeg 282w, https://www.friendsofkaren.org/wp-content/uploads/2023/08/olivia-ross-alyssa-02-e1693252313829-768x816.jpeg 768w, https://www.friendsofkaren.org/wp-content/uploads/2023/08/olivia-ross-alyssa-02-e1693252313829.jpeg 910w" sizes="(max-width: 282px) 100vw, 282px" /><em>Friends of Karen began a pilot program in late 2022 to continue to provide a limited number of supports to children who have gone off formal treatment, but continue to have serious healthcare, social and educational needs. Olivia’s mother Johanna shares more below about how Friends of Karen has helped her family during this crucial stage, after Olivia was treated for Medulloblastoma, a brain cancer that occurs most often in young children.</em></p><p>“Olivia was three years old when she started to vomit all the time and was having balance issues. After several doctor visits with no resolution, we went to the Emergency Room and Olivia had a CAT scan that showed a brain tumor. I felt like my heart just stopped.</p><p>It took seven days to find out Olivia had Medulloblastoma, and then she needed two surgeries. The doctors tell you ahead of time about the side effects of the surgery, but we were barely surviving. It was hard to see that Olivia’s whole right side was paralyzed and she could not speak or walk.</p><p>I am the kind of person that needs to feel in control and illness isn’t something you can control. It made me look at the future differently, and at that moment my hopes and dreams changed for Olivia. I just wanted her to live. Nothing else really mattered.</p><p>While I spent many sleepless nights at the hospital, I got a look behind the curtain at what our life would become. I needed others who understood what we were going through, so I researched resources every night and near the end of Olivia’s treatment I found Friends of Karen. During Olivia’s treatment we received emergency food assistance and help paying COBRA for our health insurance, which lessened our worries. At this point, Olivia had endured eight months of inpatient care, and being discharged carried big emotions and new challenges for us all. We were trying to heal, cope and adjust to our new life while trying our best to parent and help our daughter process the trauma she experienced. I found a play therapist for Olivia, but it wasn’t helping. I had spoken to different counselors myself, but I found I spent so much of each session describing the medical terms or updating the therapist on my daughter’s care that I never got the help I needed.</p><p>I was in contact with Friends of Karen social worker Alyssa who suggested the organization’s Sibling Support Program and Olivia was paired with child life specialist Melissa. My hope was that Melissa would be able to provide resources in navigating Olivia’s behavioral changes, and how I could support her transition to living isolated at home. This transition has also been eased by Friends of Karen’s Survivorship Program paying for Olivia to have music therapy to help address separation anxiety and for developmental stimulation.</p><p>Melissa is different because she understands the medical procedures and the experiences we had. She helped me to anticipate and best prepare for new experiences and eliminate anxiety. She is a sounding board for decisions I am preparing to make and navigating conversations with Olivia’s care team and advocating for her. She is there to help me understand the issues for Olivia in school, and what our life will look like when the support finishes. We are so grateful for Friends of Karen helping us through this stage of Olivia’s life.”</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/survivorship-story-supporting-transition-after-treatment/">A Survivorship Story: Supporting the Transition After Treatment</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>A Mom Story: The gift of more time to care</title>
		<link>https://www.friendsofkaren.org/a-mom-story-the-gift-of-more-time-to-care/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=a-mom-story-the-gift-of-more-time-to-care</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 18 May 2023 14:51:20 +0000</pubDate>
				<category><![CDATA[All Content]]></category>
		<category><![CDATA[Family Stories]]></category>
		<guid isPermaLink="false">http://www.friendsofkaren.org/fokdev2022/?p=5098</guid>

					<description><![CDATA[<p>Logan is a four-year-old boy who was diagnosed in 2022 with Aplastic Anemia, which is characterized by bone marrow failure when the body stops producing enough new blood cells. His mother, Elizabeth, a registered nurse, shares how Friends of Karen helped her, Logan and his twin sister Gianna, his older siblings Jayda and Jeremy, and his father Ismael as they...</p>
<p>The post <a href="https://www.friendsofkaren.org/a-mom-story-the-gift-of-more-time-to-care/">A Mom Story: The gift of more time to care</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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													<img decoding="async" width="640" height="219" src="https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner-1024x351.png" class="attachment-large size-large wp-image-5101" alt="" srcset="https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner-1024x351.png 1024w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner-300x103.png 300w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner-768x263.png 768w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner-1536x526.png 1536w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/website-spring-newsletter-banner.png 1643w" sizes="(max-width: 640px) 100vw, 640px" />													</div>
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<p>Logan is a four-year-old boy who was diagnosed in 2022 with Aplastic Anemia, which is characterized by bone marrow failure when the body stops producing enough new blood cells. His mother, Elizabeth, a registered nurse, shares how Friends of Karen helped her, Logan and his twin sister Gianna, his older siblings Jayda and Jeremy, and his father Ismael as they coped with his diagnosis and treatment. Elizabeth was Logan’s donor for a bone marrow transplant and his condition is stable now.</p>

<p><img decoding="async" class="size-medium wp-image-5103 alignright" src="https://www.friendsofkaren.org/fokdev2022/wp-content/uploads/2023/05/IMG_2375-300x200.jpg" alt="" width="300" height="200" srcset="https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375-300x200.jpg 300w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375-1024x683.jpg 1024w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375-768x512.jpg 768w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375-1536x1024.jpg 1536w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375-600x400.jpg 600w, https://www.friendsofkaren.org/wp-content/uploads/2023/05/IMG_2375.jpg 2048w" sizes="(max-width: 300px) 100vw, 300px" />“One day last summer my husband Ismael called to tell me that he noticed Logan suddenly had broken blood vessels all over his face and bruises on his body. Then Logan asked us to go to the doctor saying he was not feeling well. Up until this point, we had been doing well in our careers and had just moved into a new apartment the month before.</p>

<p>I have worked in all kinds of roles and settings in my nursing career, including in a pediatric ICU and in medical research. Even with my knowledge and background, getting Logan diagnosed was a very difficult and frustrating journey. As the doctors worked to eliminate all kinds of diagnoses, we watched helplessly as Logan got sicker. At one point he was hospitalized in the ICU with literally zero platelets and his urine was the color of red wine. A bone marrow test showed Logan’s body was in bone marrow failure, but doctors did not know why.</p>

<p>At that point my whole world was falling apart as we were expecting the worst. I couldn’t stop crying every day and I was losing weight. During that month, Logan had more tests and after another hospital stay, we found out that he had Aplastic Anemia. This is not a kind of anemia like the kind from a poor diet, but much more serious and the treatment is similar to how children are treated for cancer. Logan even lost his hair during treatment.</p>

<p>We are thankful our hospital social worker told us about Friends of Karen as we were trying to juggle everything going on. Our 20-year-old daughter Jayda had to help Ismael take care of Gianna and keep our home together. I had to stop working at my full-time job to be there for Logan and pick up public health nursing shifts here and there.</p>

<p>Our finances started getting tight and I don’t know what we would have done without Friends of Karen’s help to pay our phone, cable and light bills. Our Friends of Karen social worker Alyssa was always there for us. She is amazing and I can call or text her anytime. Alyssa always tries to find a solution for whatever issue comes up, she keeps her word and always calls me back, and there is never any judgement when we speak.</p>

<p>Everything Friends of Karen does for our family is a big deal for us. When Christmas was coming, I had not been working and we worried about gifts for the kids. Friends of Karen sent gifts for the kids with wrapping paper, bows, and tape. Thinking about that it’s so moving it gives me chills. Logan and Gianna met with Siobhan, a Friends of Karen art therapist, who was so good at what she was doing to help them. I also joined the support group for parents whose children were recently diagnosed, and it has been really helpful.</p>

<p>We are thankful that Friends of Karen’s support has helped us live so we have more time for Logan and his care. Right now, everything is stable and knowing they are here for us gives me peace of mind.”</p>
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		<p>The post <a href="https://www.friendsofkaren.org/a-mom-story-the-gift-of-more-time-to-care/">A Mom Story: The gift of more time to care</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>A Father’s Story</title>
		<link>https://www.friendsofkaren.org/a-fathers-story/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=a-fathers-story</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Mon, 15 Aug 2022 19:11:14 +0000</pubDate>
				<category><![CDATA[Childhood Cancer Awareness Month]]></category>
		<category><![CDATA[Family Stories]]></category>
		<guid isPermaLink="false">http://www.friendsofkaren.org/fokdev2022/?p=2660</guid>

					<description><![CDATA[<p>Manuel is the father of 14-year-old Rashelle, who recently completed treatment for<br />
Rhabdomyosarcoma, a disease in which cancer cells form in muscle tissue. Rashelle<br />
was diagnosed in 2021 and relapsed in July 2022 after this article was written. The<br />
family lives in New York City.</p>
<p>The post <a href="https://www.friendsofkaren.org/a-fathers-story/">A Father’s Story</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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										<content:encoded><![CDATA[<p><em>Manuel is the father of 14-year-old Rashelle, who recently completed treatment for Rhabdomyosarcoma, a disease in which cancer cells form in muscle tissue. Rashelle was diagnosed in 2021 and relapsed in July 2022 after this article was written. The family lives in New York City.</em></p>
<p>“When you hear the words, ‘your daughter has cancer,’ your world turns upside down. I couldn’t believe it. After the news, the doctors gave me all that information about the illness and about the treatment. They tell you you must travel to the hospital three or four times weekly for chemotherapy, checkups, blood transfusions, etc. At home, you must pay attention to side effects or fevers. It was overwhelming.</p>
<p>Then, you arrive home, still in shock, looking at the mail and seeing the bills. I couldn’t sleep thinking, ‘how am I going to do this?’ I am a single father and Rashelle’s mother, Emilia, lives in the Dominican Republic. I have family in New York, but everyone is busy with their jobs and lives. Suddenly I couldn’t work anymore because the idea of leaving Rashelle alone at home or in the hospital was unimaginable.</p>
<p>I kept thinking, ‘how would I pay the bills if I couldn’t work? What happens to others in my situation? How do they manage?’ On top of all my worries, things are a little more complicated for me because I have hearing problems and my primary language is Spanish. I explained my situation to the hospital social worker, and she told me to call Friends of Karen because they would help me.</p>
<p>I was so relieved when Friends of Karen paired me with social worker Natalia, who speaks Spanish fluently. Natalia is like an angel. It is not only about the financial assistance Friends of Karen provides, but Natalia also cares and always made sure that we are okay. Natalia made sure we could speak on video calls so I could read lips and we texted every week.</p>
<p>From the first time we connected, Natalia made me feel comfortable. During our first video call, she reassured me that from now on Rashelle’s health will be my only concern, and Friends of Karen will help take care of the bills. When Natalia asked me to send her the bills for our rent, electricity, and cell phone, I got quiet for a minute because I got very emotional. Friends of Karen took a weight off my shoulders, and I felt relieved. Because of Natalia’s work, Rashelle always had what she needed during her treatment, from clothes to a new bed.</p>
<p>Natalia also ensured that Rashelle received emotional support through other programs at Friends of Karen, including one-on-one sessions with the sibling support specialist Naomi and participating in the virtual teen groups. Without Friends of Karen, we would have lost everything I had worked for, including the apartment where Rashelle grew up. We felt safe because we knew Friends of Karen was there to help us. Natalia knew how to guide me through any question, concern, or problem; and how to find us resources. She took the time to be there for us every step of this journey.” — Manuel</p>
<p>The post <a href="https://www.friendsofkaren.org/a-fathers-story/">A Father’s Story</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>A father&#8217;s story: Embracing Support When Things Got Tough</title>
		<link>https://www.friendsofkaren.org/a-fathers-story-embracing-support-when-things-got-tough/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=a-fathers-story-embracing-support-when-things-got-tough</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 01 Feb 2024 18:54:41 +0000</pubDate>
				<category><![CDATA[ARFY23]]></category>
		<category><![CDATA[Family Stories]]></category>
		<category><![CDATA[What's New]]></category>
		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=7414</guid>

					<description><![CDATA[<p>Celeste is 3 and 1/2-years-old and in the maintenance phase of treatment for Acute Lymphoblastic Leukemia that was diagnosed in October 2022. Her father Rafael shares how he and his wife Gwen coped through Friends of Karen’s support. “Everything was going well for us. We were expecting a new baby and we decided to send Celeste temporarily to my parents’...</p>
<p>The post <a href="https://www.friendsofkaren.org/a-fathers-story-embracing-support-when-things-got-tough/">A father&#8217;s story: Embracing Support When Things Got Tough</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<p>Celeste is 3 and 1/2-years-old and in the maintenance phase of treatment for Acute Lymphoblastic Leukemia that was diagnosed in October 2022. Her father Rafael shares how he and his wife Gwen coped through Friends of Karen’s support.</p><p>“Everything was going well for us. We were expecting a new baby and we decided to send Celeste temporarily to my parents’ house before the baby’s arrival. Things got very difficult very fast. Our new son, Mael, was born early via C-section and Gwen was recovering in my care while we were nursing our son from the Neonatal Intensive Care Unit (NICU) at Jamaica Hospital. In the meantime, Celeste had developed a slight limp while in the care of her grandparents, which was showing no signs of letting up and quickly worsening. Unlike many kids her age, Celeste was rarely sick, so when my parents told us she was looking pale and limping we thought maybe it was a bit of separation anxiety or an injury from roughhousing with her cousins.</p><p>The orthopedist was unable to find anything to worry about, nor did the general physician. We didn’t think much of it, until my mother informed me Celeste was pale and unwilling to walk or eat. Then, she developed a mild yet unrelenting fever. We flew her back earlier than planned as a precaution. When she arrived at the airport in my mother’s arms and unable to stand, we quickly knew something was really wrong. Celeste had developed bruises and complained of pain everywhere. We thought she might have an infection from a potential knee or hip injury, and we were shocked when she was diagnosed with Leukemia. This was just five days after my wife gave birth and now our children were in two different ICUs in two different boroughs of New York City. I quickly found myself shuttling from one hospital to the other, while also taking care of my wife. It was all a whirlwind of meetings about the children’s care, and it was hard to retain all the information. Fortunately, the social worker at the hospital introduced us to Friends of Karen a few weeks after Celeste’s diagnosis. Our Friends of Karen social worker Rhonda has been available whenever we need her, and she has helped support us emotionally. I have participated in Friends of Karen’s online group for parents of newly diagnosed children. It’s helpful to speak with other parents who understand our situation.</p><p>My wife and I both work in the hospitality industry and with her maternity leave and Celeste’s illness, I worked when possible. The loss of income has meant we needed Friends of Karen’s financial support to pay some bills like our rent, which allowed us to breathe easier and set aside a lot of worries. Things have improved quite a bit since those dark days in 2022. Celeste is doing better and in partial remission. Gwen and I are back at work and only need to take time off for the kids’ doctor appointments.</p><p>We are thankful that Friends of Karen got us through a tough year. Gwen and I don’t have much family in the United States and Friends of Karen has come to feel like an extension of our family. Without Rhonda we would not have fully understood much about Celeste’s treatment and what the experience would be like for our family. It would have been an even more stressful time.” – Rafael</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/a-fathers-story-embracing-support-when-things-got-tough/">A father&#8217;s story: Embracing Support When Things Got Tough</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>Picking up the pieces after a loss</title>
		<link>https://www.friendsofkaren.org/picking-up-the-pieces-after-a-loss/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=picking-up-the-pieces-after-a-loss</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 12 Mar 2024 13:25:02 +0000</pubDate>
				<category><![CDATA[ARFY23]]></category>
		<category><![CDATA[Family Stories]]></category>
		<category><![CDATA[What's New]]></category>
		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=7987</guid>

					<description><![CDATA[<p>Long Island couple Liz and Theodore attended the Living Alongside Grief Retreat in April 2023 to address the impact of losing their only son Jeyden one year ago. The Retreat is a new family bereavement education program on the range of experiences that grieving family members may go through. Jeyden was 13 when he was diagnosed and treated for an Astrocytoma brain tumor and passed away at age 14. Liz shares how her Friends of Karen social worker Marla and the Family Support Program helped, and continue to help, her family. </p>
<p>The post <a href="https://www.friendsofkaren.org/picking-up-the-pieces-after-a-loss/">Picking up the pieces after a loss</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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													<img loading="lazy" decoding="async" width="640" height="436" src="https://www.friendsofkaren.org/wp-content/uploads/2024/03/jeyden-1024x698.png" class="attachment-large size-large wp-image-7988" alt="" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/03/jeyden-1024x698.png 1024w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/jeyden-300x204.png 300w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/jeyden-768x523.png 768w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/jeyden.png 1468w" sizes="(max-width: 640px) 100vw, 640px" />													</div>
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							<p>Long Island couple Liz and Theodore attended the Living Alongside Grief Retreat in April 2023 to address the impact of losing their only son Jeyden one year ago. The Retreat is a new family bereavement education program on the range of experiences that grieving family members may go through. Jeyden was 13 when he was diagnosed and treated for an Astrocytoma brain tumor and passed away at age 14. Liz shares how her Friends of Karen social worker Marla and the Family Support Program helped, and continue to help, her family.</p>
<p>“Jeyden was the kind of boy that everyone was drawn to. He had a beautiful heart and always stepped in to defend other kids from bullies. Through all our ups and downs we had each other and he knew how to make me laugh &#8211; and we laughed a lot. It was terrible to see our strong boy go through chemo, but he even went through that with a smile on his face.</p>
<p>Jeyden really tried to keep our spirits up, but Theodore and I were trying to cope and having a hard time facing the reality of his condition. All this was happening during COVID, and my husband was a chef and wasn’t working during the pandemic. I had to stop working to help care for Jeyden, so things started to get difficult quickly. Thankfully, our hospital social worker referred us to Friends of Karen, and we were paired with their social worker Marla.</p>
<p>Working with Marla and getting Friends of Karen’s support was like having them as part of our family. You just don’t find that kind of humanity everywhere. I can call Marla anytime if I need to talk or if we need help. She was there for us throughout Jeyden’s treatment and has been since he passed away. At that time Theodore and I just fell apart, and we have been holding it together with Friends of Karen’s help.</p>
<p>When Marla encouraged us to attend the Living Alongside Grief Retreat, we were hesitant about going. We had already cried so much and we were scared we would just sit there and cry. We took Marla’s advice and read through the retreat information and decided to attend. That was a good decision.</p>
<p>Our family has been so supportive, but being at the retreat with other families who went through the same thing was something we needed. This program helped us to cleanse our souls. My husband expressed his feelings in ways he had not shared before because he had wanted to support me and not burden me with what he was feeling.</p>
<p>When we got home after the retreat, we felt like we were in a better place than when we left home that morning. I learned that day it is OK for us to go on and live and have some happiness. It is a long process, but we are making progress in adjusting to our ‘new normal.’ We could not have gotten to this point without Friends of Karen.” – Liz</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/picking-up-the-pieces-after-a-loss/">Picking up the pieces after a loss</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>Running towards better days</title>
		<link>https://www.friendsofkaren.org/running-towards-better-days/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=running-towards-better-days</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 14 Mar 2024 12:32:49 +0000</pubDate>
				<category><![CDATA[All Content]]></category>
		<category><![CDATA[Family Stories]]></category>
		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=8031</guid>

					<description><![CDATA[<p>Xavier is a 17-year-old from Westchester County, NY who is on maintenance treatment for T-cell Acute Lymphoblastic Leukemia. He lives with his mother Antheya and his 15-year-old brother Zach and shares how Friends of Karen helped him and his family.</p>
<p>The post <a href="https://www.friendsofkaren.org/running-towards-better-days/">Running towards better days</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<em>Xavier is a 17-year-old from Westchester County, NY who is on maintenance treatment for T-cell Acute Lymphoblastic Leukemia. He lives with his mother Antheya and his 15-year-old brother Zach and shares how Friends of Karen helped him and his family.</em>						</div>
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													<img loading="lazy" decoding="async" width="640" height="361" src="https://www.friendsofkaren.org/wp-content/uploads/2024/03/xavier2-1024x578.png" class="attachment-large size-large wp-image-8036" alt="" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/03/xavier2-1024x578.png 1024w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/xavier2-300x169.png 300w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/xavier2-768x434.png 768w, https://www.friendsofkaren.org/wp-content/uploads/2024/03/xavier2.png 1240w" sizes="(max-width: 640px) 100vw, 640px" />													</div>
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<p><span style="background-color: rgba(255, 255, 255, 0);">“I love to run and am on the cross country team at my high school and the season had just ended when I noticed over the next few weeks that it was getting harder to breathe. I started wheezing just sitting still. Things kept getting worse and even my friends noticed I looked sick. Then, a few days after Thanksgiving in 2022, I was in the shower and noticed that every time I took a breath there was a pain in my shoulder.</span></p>
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<p>Soon after I couldn’t sleep, and suddenly there was an orange-sized growth on my neck, so my mom took me to urgent care. The doctor there thought I might have a collapsed lung, so I went to the hospital where I had a ton of tests. The test results showed a grapefruit-sized mass pushing against my heart and my lungs were filled with fluid. The doctors were amazed I had been so active with all this going on.</p>
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<p>I was transferred to the children’s hospital, and they tested the fluid in my lungs and found that I had cancer. I had been hoping it was just an infection, so this news left me numb. I didn’t have much time to think as the next day they had a roadmap for my treatment and they started by putting in a chest tube, a PICC line in my arm, and I had to go through a spinal tap which was the worst pain of my life. Then I was able to start chemotherapy. For weeks I was afraid to tell my friends because I knew that if a friend told me they had cancer I’d be devastated. I did not want anyone to worry about me or treat me differently.</p>
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<p>My mom learned about Friends of Karen from a friend. Our Friends of Karen social worker Rhonda has been there for my mom. Whatever makes my mom feel better makes me feel better, so I am glad that Rhonda helped her deal with my health insurance which seemed to be very confusing. Friends of Karen also helped my mom pay some of the bills for my doctor visits, surgeries, and chemotherapy which can add up fast.</p>
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<p>Friends of Karen sent Zach and me gifts for Christmas which came at a very dark time for us after my diagnosis, so it was appreciated. I spoke weekly to my Friends of Karen sibling support specialist Melissa who has helped me quell any anxiety I am feeling. Without Friends of Karen our lives would have been a lot sadder, and things would have been tougher for my mom.” – Xavier</p>
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		<p>The post <a href="https://www.friendsofkaren.org/running-towards-better-days/">Running towards better days</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>A MOTHER’S STORY: Finding Help and Understanding</title>
		<link>https://www.friendsofkaren.org/a-mothers-storyfinding-help-and-understanding/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=a-mothers-storyfinding-help-and-understanding</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Mon, 17 Jun 2024 14:18:13 +0000</pubDate>
				<category><![CDATA[Family Stories]]></category>
		<category><![CDATA[Spring 2024 Newsletter]]></category>
		<category><![CDATA[What's New]]></category>
		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=8366</guid>

					<description><![CDATA[<p>Finest is a 20-year-old college student being treated for a recurrence of Synovial Sarcoma, a soft tissue tumor, that first occurred when he was 15 years old. His mother Melissa was interviewed about how Friends of Karen has helped her, Finest and his 18-year-old brother Malik.</p>
<p>The post <a href="https://www.friendsofkaren.org/a-mothers-storyfinding-help-and-understanding/">A MOTHER’S STORY: Finding Help and Understanding</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<p><em>Finest is a 20-year-old college student being treated for a recurrence of Synovial Sarcoma, a soft tissue tumor, that first occurred when he was 15 years old. His mother Melissa was interviewed about how Friends of Karen has helped her, Finest and his 18-year-old brother Malik.</em></p>						</div>
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<p><strong><img loading="lazy" decoding="async" class="size-medium wp-image-8448 alignright" src="https://www.friendsofkaren.org/wp-content/uploads/2024/04/finest-malik-297x300.png" alt="" width="297" height="300" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/04/finest-malik-297x300.png 297w, https://www.friendsofkaren.org/wp-content/uploads/2024/04/finest-malik.png 465w" sizes="(max-width: 297px) 100vw, 297px" />Connections: How has Finest’s treatment changed your daily life?</strong> <br /><strong>Melissa:</strong> After the first time Finest was treated, he went about his life and went back to high school. Later he graduated and went on to Hunter College in Manhattan to study anthropology and was living a normal life until he had a car accident in April 2023. After the accident he noticed pain in his leg and he was limping. He had an x-ray but that did not show any problem. My mother’s intuition kicked in and I insisted they give him an MRI, which showed a tumor in his knee This time my world came crashing in on me. When he was diagnosed at 15, the doctor told me that if the cancer came back it would need to be treated aggressively. Now he needed chemotherapy, radiation, knee replacement and femur reconstruction.</p>
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<p><strong>Connections: How did you find out about Friends of Karen?<br />Melissa:</strong> During this recurrence, the hospital social worker gave me a list of organizations to call for support. I found out that because Finest is 20 years old he was not in the age range of most organizations that serve kids up to 18 years old or adults 21 years old and over. I was relieved that Friends of Karen would accept someone his age.</p>
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<p><strong>Connections: How has Friends of Karen been there for your family? </strong><br /><strong>Melissa:</strong> I am thankful for everything Friends of Karen has done for our family. Without them, I believe I would have gotten into debt and not had some of my basic needs met. It was important that Friends of Karen was by our side because all our family is in Saint Lucia. Friends of Karen sent their social worker Rhonda to visit. She made sure that Friends of Karen helped us with groceries, transportation to treatment, and some of our monthly bills. I did not know Finest could get covered under Medicaid and Rhonda told me about it and helped us through the application process. Friends of Karen gave Finest some gift certificates for games and clothing for him to be comfortable. They even found a volunteer to coach Malik through writing his college essays and applications.</p>
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<p>Rhonda has been amazing in getting us whatever help we’ve needed. It’s been heartbreaking for me to see my six-foot tall, healthy son go through surgery and treatment. Rhonda understood I was struggling and arranged for Jane, a Friends of Karen creative arts therapist, to come see us. Jane really listened to what we were going through, and we worked on art projects to help us emotionally. And Rhonda encouraged me to participate in the parents’ virtual support group. It helps me to have hope when I hear other families that are going through this with good outcomes.</p>
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		<p>The post <a href="https://www.friendsofkaren.org/a-mothers-storyfinding-help-and-understanding/">A MOTHER’S STORY: Finding Help and Understanding</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>A MOTHER’S STORY: Finding Consistent Support</title>
		<link>https://www.friendsofkaren.org/a-mothers-story-finding-consistent-support/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=a-mothers-story-finding-consistent-support</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 23 Apr 2024 20:05:01 +0000</pubDate>
				<category><![CDATA[All Content]]></category>
		<category><![CDATA[Family Stories]]></category>
		<category><![CDATA[Spring 2024 Newsletter]]></category>
		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=8739</guid>

					<description><![CDATA[<p>Ellis is a five-year-old boy who was diagnosed in 2023 with Acute Lymphoblastic Leukemia (ALL), a cancer of the blood and bone marrow. His mother Jennifer shares how the diagnosis and Ellis’s treatment affected her, her husband Eric, and their four-year-old son Jay. “During the summer of 2023 things were going along well for our family. My husband Eric had...</p>
<p>The post <a href="https://www.friendsofkaren.org/a-mothers-story-finding-consistent-support/">A MOTHER’S STORY: Finding Consistent Support</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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													<img loading="lazy" decoding="async" width="640" height="640" src="https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465-1024x1024.jpg" class="attachment-large size-large wp-image-8742" alt="Ellis" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465-1024x1024.jpg 1024w, https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465-300x300.jpg 300w, https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465-150x150.jpg 150w, https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465-768x768.jpg 768w, https://www.friendsofkaren.org/wp-content/uploads/2024/04/Ellis-Lentz-03-e1713902744465.jpg 1512w" sizes="(max-width: 640px) 100vw, 640px" />													</div>
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							<p>Ellis is a five-year-old boy who was diagnosed in 2023 with Acute Lymphoblastic Leukemia (ALL), a cancer of the blood and bone marrow. His mother Jennifer shares how the diagnosis and Ellis’s treatment affected her, her husband Eric, and their four-year-old son Jay.</p>						</div>
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							<p>“During the summer of 2023 things were going along well for our family. My husband Eric had just started a new job and I was doing well in my job as a physical therapist. Ellis got sick soon after, and there was a month of not having any answer to what was going on until a bone marrow biopsy came back conclusive for Leukemia.</p><p>Ellis’s diagnosis meant medical bills we weren’t prepared for, which in our case came with a complication. We were paying for our family’s health insurance out of pocket because we were on COBRA insurance until my husband’s benefits started at his new job. That meant neither of us could stop working completely during Ellis’s treatment.</p><p>Because this was a major issue, the hospital social worker encouraged us to apply to Friends of Karen for financial assistance. We had no idea that once we were connected to our Friends of Karen social worker Rhonda, they would be such an important support to us in so many other ways.</p><p>The best part of working with Rhonda is she calls often and it’s nice having someone that understands what we are going through. From the start she had a concrete list of things she knew we needed and was always a step ahead to predict what we would need next.</p><p>Friends of Karen helped with everything from working with us on applying to Medicaid for Ellis and arranging for Ellis to have a volunteer tutor so he was on track for kindergarten, to making sure we had gift cards to shop for Thanksgiving dinner and wrapping paper for the holiday gifts they provided for Ellis and Jay.</p><p>Rhonda had Melissa, a Friends of Karen creative arts therapist, work with Ellis for additional emotional support. Melissa also worked with Jay to help him understand what was happening in terms he could understand and help him with his feelings. Both boys also benefit from participating in the Friends Having Fun weekly virtual activity group since they have few chances to socialize while Ellis is immunocompromised.</p><p>Friends of Karen also makes a difference because they are with us for the long haul. We are thankful because, without Friends of Karen, we’d be struggling to make ends meet and I’d have to work more and not be able to be with Ellis. I think of Rhonda as our director of traffic to keep things going as smoothly as possible and she always has suggestions of how to handle things.”</p><p>— Jennifer</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/a-mothers-story-finding-consistent-support/">A MOTHER’S STORY: Finding Consistent Support</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>When Treatment Ends, New Challenges Begin</title>
		<link>https://www.friendsofkaren.org/when-treatment-ends-new-challenges-begin/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=when-treatment-ends-new-challenges-begin</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Sun, 01 Sep 2024 20:36:56 +0000</pubDate>
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		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=10273</guid>

					<description><![CDATA[<p>Ty was 4 years old in June 2021 when he was diagnosed with B cell Acute Lymphoblastic Leukemia, a type of blood cancer. He has completed his course of treatment and is in the survivorship phase of his illness journey. Survivorship is the period after treatment including long-term follow-up for health issues and addressing remaining emotional and psychosocial issues</p>
<p>The post <a href="https://www.friendsofkaren.org/when-treatment-ends-new-challenges-begin/">When Treatment Ends, New Challenges Begin</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<p><img loading="lazy" decoding="async" class="wp-image-11028 size-medium alignright" src="https://www.friendsofkaren.org/wp-content/uploads/2024/08/ty-main-223x300.png" alt="" width="223" height="300" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/08/ty-main-223x300.png 223w, https://www.friendsofkaren.org/wp-content/uploads/2024/08/ty-main.png 697w" sizes="(max-width: 223px) 100vw, 223px" /></p><p><em>Ty was 4 years old in June 2021 when he was diagnosed with B cell Acute Lymphoblastic Leukemia, a type of blood cancer. He has completed his course of treatment and is in the survivorship phase of his illness journey. Survivorship is the period after treatment including long-term follow-up for health issues and addressing remaining emotional and psychosocial issues.</em></p><p> </p><p><i>Ty’s mother Samantha shares how their family of five -Ty, his six-year-old sister Ellyot, younger brother Bodhi and Ty’s father Aaron &#8211; are navigating the aftermath of treatment on their lives and new issues that have arisen during this phase.</i></p><p> </p><p>“My first reaction when Ty was diagnosed was complete and debilitating shock. My only concerns were how to help Ty get better and how we would manage our life, especially with Ellyot at home.</p><p> </p><p>Our family reminded us to think of questions to ask the doctors, but when you have no experience with cancer you have no clue what to ask. Then at the hospital everyone is talking at you a mile a minute as your whole world is turning upside down.</p><p> </p><p>As time passed and Ty was undergoing treatment our concern became his social development. He was a social beast that was outgoing and loved making friends and now he had to be isolated, especially since this was during COVID. We also realized that Ty’s diagnosis would have an impact on his sister Ellyot beyond the logistics of our day-to-day life during his treatment.</p><p> </p><p>I am grateful that my sisters did some research on the internet and found Friends of Karen so that we could all get the support we needed. Our Friends of Karen social worker Beth made sure we had help from the organization to pay for transportation to the hospital and Ty’s illness-related co-payments. She also connected us to Jen, a Friends of Karen child life specialist, to address Ty and Ellyot’s emotional needs.</p><p> </p><p>This has been especially important since Ty rang the bell when he completed treatment. Once it was done people expected to welcome us back and assumed everything would go back to normal. But it’s not like you snap your fingers and you’re back to your pre-cancer world.</p><p> </p><p>During this survivorship stage new issues have emerged as Ty has anxiety stemming from the trauma of treatment. For three years he was out of the world he knew, had zero control over his body, and experienced so much pain. He was always mature and wise beyond his years, but now so much time spent in the hospital left him playing catch up physically and socially with his peers. All of this affected his confidence and sense of belonging.</p><p> </p><p>Ellyot has also struggled as she was just three years old when Ty was diagnosed. Back then she was very attached to Ty, so when he got sick and was not at home it was like half of her was now missing. She also was thrust into Ty’s shadow as we had to focus on his getting well, which left her with nothing to call her own. Jen worked with her to explain Ty’s illness at her age level, something we did not have the tools to do. Jen is also helping Elly with the separation anxiety, feelings of jealousy and other emotional impacts that we’ve been told are typical for siblings. Elly’s time with Jen is something that is her own and just for her to talk about things that are bothering her and she learns ways to cope. Jen also sends me a write up of each session with the kids and suggestions of ways Aaron and I can help them.</p><p> </p><p>I can’t imagine what our lives would have been like without Friends of Karen. It is a good feeling to know we are not alone when we are struggling, and that Beth and Jen are there to share a different perspective on things.</p><p> </p><p>Friends of Karen gave us the valuable resource of ongoing support for these emotional issues throughout the phases of Ty’s illness. That is really something because no other organization offers that depth of support to families dealing with their child’s life-threatening illness.” &#8211; Samantha</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/when-treatment-ends-new-challenges-begin/">When Treatment Ends, New Challenges Begin</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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		<title>Paying it Forward</title>
		<link>https://www.friendsofkaren.org/paying-it-forward/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=paying-it-forward</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 24 Sep 2024 17:17:39 +0000</pubDate>
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		<guid isPermaLink="false">https://www.friendsofkaren.org/?p=10316</guid>

					<description><![CDATA[<p>When their five-year-old son, Taylor, was diagnosed with Non-Hodgkin’s Lymphoma in 2012, his parents Ron and Kesa were at a loss. How were they going to manage when Kesa had to give up her job as a human resources analyst to be Taylor’s primary caregiver? Like so many parents, Ron and Kesa didn’t know what to expect or what they...</p>
<p>The post <a href="https://www.friendsofkaren.org/paying-it-forward/">Paying it Forward</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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							<p>When their five-year-old son, Taylor, was diagnosed with Non-Hodgkin’s Lymphoma in 2012, his parents Ron and Kesa were at a loss. How were they going to manage when Kesa had to give up her job as a human resources analyst to be Taylor’s primary caregiver?</p><p><img loading="lazy" decoding="async" class="wp-image-11023 size-medium alignright" src="https://www.friendsofkaren.org/wp-content/uploads/2024/08/ron-and-taylor-232x300.png" alt="" width="232" height="300" srcset="https://www.friendsofkaren.org/wp-content/uploads/2024/08/ron-and-taylor-232x300.png 232w, https://www.friendsofkaren.org/wp-content/uploads/2024/08/ron-and-taylor.png 551w" sizes="(max-width: 232px) 100vw, 232px" /></p><p>Like so many parents, Ron and Kesa didn’t know what to expect or what they were going to need. Then their care team at the hospital where Taylor was being treated introduced them to Friends of Karen.</p><p> </p><p>As Ron explains, “Friends of Karen speaks to you face-to-face. Marla, our social worker, asked us ‘How are you doing?’ ‘What do you need?’ ‘What can Friends of Karen do to support you?’</p><p> </p><p>Besides covering mortgage payments, medical bills, travel expenses and utilities, Marla helped Ron and Kesa get on solid footing so they could focus on taking care of Taylor, and his then 13-year-old brother, Tilar.</p><p> </p><p>“I can’t imagine not having Friends of Karen when going through such a life-changing event,” asserts Ron. Taylor, who ended his treatment in 2015, is now thriving. He recently graduated high school and is college-bound, with plans to study engineering.</p><p> </p><p>Ron appreciates that not all family stories have the same outcome as his. He is grateful for the help that he and his family received because he “knows what it feels like to be overwhelmed financially and emotionally.”</p><p> </p><p>That’s what motivates him to pay it forward through his active support of Friends of Karen. In addition to making his own generous contributions, he takes full advantage of his employer’s matching gift program to increase the impact of his own giving. His support is not only financial, but he actively spreads the word among his friends, family and business associates, sharing the story of the ‘amazing things’ Friends of Karen did for his family.</p><p> </p><p>When Ron reaches out to support other parents, he reassures them, “At a time when things seem very dark, keep in mind there’s a family-friendly support system in Friends of Karen, a pillar of help I will never forget.”</p>						</div>
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		<p>The post <a href="https://www.friendsofkaren.org/paying-it-forward/">Paying it Forward</a> appeared first on <a href="https://www.friendsofkaren.org">Friends of Karen</a>.</p>
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