Los Angeles Thievers T-shirts

 all over his body. (Lindsey Marson) “The MRI showed that he had a large plexiform tumor behind his eye, in his face and in part of his brain,” Marson said. By the Los Angeles Thievers T-shirts In addition,I will do this time Bryson was three months old, the large tumor had grown — so he was taken to Children’s Hospital of Philadelphia (CHOP) to start chemo. He was put on MEK chemotherapy, an oral form of chemo that can administered at home. CHILDREN BATTLING CANCER GET BOOST FROM VIRGINIA BOY WHO LOST HIS OWN MOM TO THE DISEASE While the chemo stabilized the tumor, side effects left Bryson with a severe rash — so Marson and Bryson’s oncologist decided to stop administering the chemo, Marson said. Bryson had to undergo surgery to try to remove the tumor from his eyelid because it was compromising visibility in his left eye. (Lindsey Marson) Surgery could not remove Bryson’s tumor in its entirety because his particular tumor is “like a spider web throughout his face, his brain [and] his eye,” Marson explained. The tumor in Bryson’s eye began compromising his vision, so a portion of the tumor was removed by his ophthalmologist. Marson is now over a year old, but the tumors in his face and brain have only continued to grow, Marson said after her son had another MRI in May. VIRGINIA 12-YEAR-OLD IS HELPING KIDS WITH CANCER AFTER LOSING HIS OWN MOM TO THE DISEASE Marson and her son went through genetic testing, and it lined up perfectly. They “have the exact same variant,” she stated — but they have completely different symptoms. Marson and Bryson

have the Los Angeles Thievers T-shirts In addition,I will do this same form of Neurofibromatosis Type 1, but it presents itself differently in each of them. (Lindsey Marson) “I saw that NF could be severe, but I totally thought, ‘I didn’t have it severe, so Bryson is not going to have it severe,'” she added. While seeing her son struggle with NF has been difficult, Marson said her own diagnosis of the same genetic disease has made it slightly easier because she has a level of understanding her own parents did not have when she was growing up. “We are definitely closer because of this. I mean, he is my little baby.” “It was still really scary, and I still felt extremely guilty,” Marson said. CLICK HERE TO SIGN UP FOR OUR LIFESTYLE NEWSLETTER She added, “It was still hard, but it wasn’t as hard because I knew all the terminology and I knew what to expect.” “I feel like we have a stronger bond because of [our condition],” Marson told Fox News Digital. (Lindsey Marson) Marson believes the best thing a parent can do for a child is be an advocate — and find moments of positivity. She started a Facebook page to educate others on the condition, hoping to bring awareness to NF and help others know how to recognize it in a child. “We are definitely closer because of this. I mean, he is my little baby,” Marson said of herself and her son. “I feel like we have a stronger bond because of it and I know what he is going through, and I will be there for him 100% of the time,” she said. This year, the Children’s Tumor Foundation featured Marson and Bryson in a photo series with other parents and their children who are fighting NF together. Sydney Borchers is a lifestyle production assistant with Fox News Digital.

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